Keywords
Last Name

Martin H. Steinberg, MD

TitleProfessor
InstitutionBoston University School of Medicine
DepartmentMedicine
DivisionHematology & Medical Oncology
Address75 E. Newton St Evans Building
Boston MA 02118
Phone(617) 414-1020
ORCID ORCID Icon0000-0001-8800-8020
Other Positions
TitleGraduate Faculty (Primary Mentor of Grad Students)
InstitutionBoston University School of Medicine, Division of Graduate Medical Sciences

TitleProfessor
InstitutionBoston University School of Medicine
DepartmentPathology & Laboratory Medicine

TitleProfessor
InstitutionBoston University School of Medicine
DepartmentPediatrics

TitleActive Staff Privileges
InstitutionBoston Medical Center
DepartmentMedicine
DivisionHematology & Medical Oncology

 Research Expertise & Professional Interests
Expertise includes: Clinical aspects of hemoglobinopathies; Genetics of hemoglobin disorders.

 Self-Described Keywords
  • fetal hemoglobin
  • genomics
  • sickle cell
  • SNPs
 Publications
Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Faculty can login to make corrections and additions.
List All   |   Timeline
  1. Piel FB, Steinberg MH, Rees DC. Sickle Cell Disease. N Engl J Med. 2017 04 20; 376(16):1561-1573. PMID: 28423290.
    View in: PubMed
  2. Aleluia MM, Santiago RP, da Guarda CC, Fonseca TC, Neves FI, Quinto RS, Figueiredo CV, Yahouédéhou SC, Oliveira RM, Ferreira JR, Cerqueira BA, Barbosa CG, Milton JN, Steinberg MH, de Souza Gonçalves M. Genetic modulation of fetal hemoglobin in hydroxyurea-treated sickle cell anemia. Am J Hematol. 2017 May; 92(5):E70-E72. PMID: 28195442.
    View in: PubMed
  3. Kato GJ, Steinberg MH, Gladwin MT. Intravascular hemolysis and the pathophysiology of sickle cell disease. J Clin Invest. 2017 Mar 01; 127(3):750-760. PMID: 28248201.
    View in: PubMed
  4. Jiang Z, Luo HY, Farrell JJ, Zhang Z, Schulz VP, Albarawi D, Steinberg MH, Al-Allawi NA, Gallagher PG, Forget BG, Chui DH. A variant Sp1 (R218Q) transcription factor might enhance HbF expression in ß0 -thalassaemia homozygotes. Br J Haematol. 2017 Feb 27. PMID: 28240767.
    View in: PubMed
  5. Cyrus C, Vatte C, Borgio JF, Al-Rubaish A, Chathoth S, Nasserullah ZA, Jarrash SA, Sulaiman A, Qutub H, Alsaleem H, Alzahrani AJ, Steinberg MH, Ali AK. Existence of HbF Enhancer Haplotypes at HBS1L-MYB Intergenic Region in Transfusion-Dependent Saudi ß-Thalassemia Patients. Biomed Res Int. 2017; 2017:1972429. PMID: 28280727.
    View in: PubMed
  6. Steinberg MH. Go with the Flow. N Engl J Med. 2017 02 02; 376(5):485-487. PMID: 28146663.
    View in: PubMed
  7. Park S, Gianotti-Sommer A, Molina-Estevez FJ, Vanuytsel K, Skvir N, Leung A, Rozelle SS, Shaikho EM, Weir I, Jiang Z, Luo HY, Chui DHK, Figueiredo MS, Alsultan A, Al-Ali A, Sebastiani P, Steinberg MH, Mostoslavsky G, Murphy GJ. A Comprehensive, Ethnically Diverse Library of Sickle Cell Disease-Specific Induced Pluripotent Stem Cells. Stem Cell Reports. 2017 Apr 11; 8(4):1076-1085. PMID: 28111279.
    View in: PubMed
  8. Dai Y, Sangerman J, Nouraie M, Faller AD, Oneal P, Rock A, Owoyemi O, Niu X, Nekhai S, Maharaj D, Cui S, Taylor R, Steinberg M, Perrine S. Effects of hydroxyurea on F-cells in sickle cell disease and potential impact of a second fetal globin inducer. Am J Hematol. 2017 Jan; 92(1):E10-E11. PMID: 27766663.
    View in: PubMed
  9. Vathipadiekal V, Farrell JJ, Wang S, Edward HL, Shappell H, Al-Rubaish AM, Al-Muhanna F, Naserullah Z, Alsuliman A, Qutub HO, Simkin I, Farrer LA, Jiang Z, Luo HY, Huang S, Mostoslavsky G, Murphy GJ, Patra PK, Chui DH, Alsultan A, Al-Ali AK, Sebastiani P, Steinberg MH. A candidate transacting modulator of fetal hemoglobin gene expression in the Arab-Indian haplotype of sickle cell anemia. Am J Hematol. 2016 Nov; 91(11):1118-1122. PMID: 27501013.
    View in: PubMed
  10. Bae H, Monti S, Montano M, Steinberg MH, Perls TT, Sebastiani P. Learning Bayesian Networks from Correlated Data. Sci Rep. 2016 May 05; 6:25156. PMID: 27146517.
    View in: PubMed
  11. Vathipadiekal V, Alsultan A, Baltrusaitis K, Farrell JJ, Al-Rubaish AM, Al-Muhanna F, Naserullah Z, Suliman A, Patra PK, Milton JN, Farrer LA, Chui DH, Al-Ali AK, Sebastiani P, Steinberg MH. Homozygosity for a haplotype in the HBG2-OR51B4 region is exclusive to Arab-Indian haplotype sickle cell anemia. Am J Hematol. 2016 Jun; 91(6):E308-11. PMID: 27185208.
    View in: PubMed
  12. Shaikho EM, Habara AH, Alsultan A, Al-Rubaish AM, Al-Muhanna F, Naserullah Z, Alsuliman A, Qutub HO, Patra PK, Sebastiani P, Baltrusaitis K, Farrell JJ, Jiang Z, Luo HY, Chui DH, Al-Ali AK, Steinberg MH. Variants of ZBTB7A (LRF) and its ß-globin gene cluster binding motifs in sickle cell anemia. Blood Cells Mol Dis. 2016 Jul; 59:49-51. PMID: 27282567.
    View in: PubMed
  13. Liu L, Pertsemlidis A, Ding LH, Story MD, Steinberg MH, Sebastiani P, Hoppe C, Ballas SK, Pace BS. Original Research: A case-control genome-wide association study identifies genetic modifiers of fetal hemoglobin in sickle cell disease. Exp Biol Med (Maywood). 2016 Apr; 241(7):706-18. PMID: 27022141.
    View in: PubMed
  14. Habara A, Steinberg MH. Minireview: Genetic basis of heterogeneity and severity in sickle cell disease. Exp Biol Med (Maywood). 2016 Apr; 241(7):689-96. PMID: 26936084.
    View in: PubMed
  15. Borgio JF, AbdulAzeez S, Naserullah ZA, Al-Jarrash S, Al-Ali RA, Al-Madan MS, Al-Muhanna F, Al-Suliman AM, Al-Nafie A, Steinberg MH, Al-Ali AK. Mutations in the ß-globin gene from a Saudi population: an update. Int J Lab Hematol. 2016 Apr; 38(2):e38-40. PMID: 26822801.
    View in: PubMed
  16. Jiang Z, Luo HY, Huang S, Farrell JJ, Davis L, Théberge R, Benson KA, Riolueang S, Viprakasit V, Al-Allawi NA, Ünal S, Gümrük F, Akar N, Basak AN, Osorio L, Badens C, Pissard S, Joly P, Campbell AD, Gallagher PG, Steinberg MH, Forget BG, Chui DH. The genetic basis of asymptomatic codon 8 frame-shift (HBB:c25_26delAA) ß(0) -thalassaemia homozygotes. Br J Haematol. 2016 Mar; 172(6):958-65. PMID: 26771086.
    View in: PubMed
  17. Maron BJ, Harris KM, Thompson PD, Eichner ER, Steinberg MH. Eligibility and Disqualification Recommendations for Competitive Athletes With Cardiovascular Abnormalities: Task Force 14: Sickle Cell Trait: A Scientific Statement From the American Heart Association and American College of Cardiology. J Am Coll Cardiol. 2015 Dec 1; 66(21):2444-6. PMID: 26542668.
    View in: PubMed
  18. Maron BJ, Harris KM, Thompson PD, Eichner ER, Steinberg MH. Eligibility and Disqualification Recommendations for Competitive Athletes With Cardiovascular Abnormalities: Task Force 14: Sickle Cell Trait: A Scientific Statement From the American Heart Association and American College of Cardiology. Circulation. 2015 Dec 1; 132(22):e343-5. PMID: 26527715.
    View in: PubMed
  19. Akinbami AO, Campbell AD, Han ZJ, Luo HY, Chui DH, Steinberg MH. Hereditary Persistence of Fetal Hemoglobin Caused by Single Nucleotide Promoter Mutations in Sickle Cell Trait and Hb SC Disease. Hemoglobin. 2016; 40(1):64-5. PMID: 26372199.
    View in: PubMed
  20. Ngo DA, Steinberg MH. Genomic approaches to identifying targets for treating ß hemoglobinopathies. BMC Med Genomics. 2015; 8:44. PMID: 26215470.
    View in: PubMed
  21. Steinberg MH, Rodgers GP. HbA2 : biology, clinical relevance and a possible target for ameliorating sickle cell disease. Br J Haematol. 2015 Sep; 170(6):781-7. PMID: 26104837.
    View in: PubMed
  22. Zhang X, Zhang W, Saraf SL, Nouraie M, Han J, Gowhari M, Hassan J, Miasnikova G, Sergueeva A, Nekhai S, Kittles R, Machado RF, Garcia JG, Gladwin MT, Steinberg MH, Sebastiani P, McClain DA, Gordeuk VR. Genetic polymorphism of APOB is associated with diabetes mellitus in sickle cell disease. Hum Genet. 2015 Aug; 134(8):895-904. PMID: 26025476.
    View in: PubMed
  23. Sobota A, Sabharwal V, Fonebi G, Steinberg M. How we prevent and manage infection in sickle cell disease. Br J Haematol. 2015 Sep; 170(6):757-67. PMID: 26018640.
    View in: PubMed
  24. Al-Nafie AN, Borgio JF, AbdulAzeez S, Al-Suliman AM, Qaw FS, Naserullah ZA, Al-Jarrash S, Al-Madan MS, Al-Ali RA, AlKhalifah MA, Al-Muhanna F, Steinberg MH, Al-Ali AK. Co-inheritance of novel ATRX gene mutation and globin (a & ß) gene mutations in transfusion dependent beta-thalassemia patients. Blood Cells Mol Dis. 2015 Jun; 55(1):27-9. PMID: 25976463.
    View in: PubMed
  25. Bae H, Perls T, Steinberg M, Sebastiani P. Bayesian Polynomial Regression Models to Fit Multiple Genetic Models for Quantitative Traits. Bayesian Anal. 2015 Mar; 10(1):53-74. PMID: 26029316.
    View in: PubMed
  26. Sebastiani P, Farrell JJ, Alsultan A, Wang S, Edward HL, Shappell H, Bae H, Milton JN, Baldwin CT, Al-Rubaish AM, Naserullah Z, Al-Muhanna F, Alsuliman A, Patra PK, Farrer LA, Ngo D, Vathipadiekal V, Chui DH, Al-Ali AK, Steinberg MH. BCL11A enhancer haplotypes and fetal hemoglobin in sickle cell anemia. Blood Cells Mol Dis. 2015 Mar; 54(3):224-30. PMID: 25703683.
    View in: PubMed
  27. Milton JN, Steinberg MH, Sebastiani P. Evaluation of an ensemble of genetic models for prediction of a quantitative trait. Front Genet. 2014; 5:474. PMID: 25628649.
    View in: PubMed
  28. Steinberg MH. Nitric oxide-based treatment for sickle cell leg ulcers? Lancet Haematol. 2014 Dec; 1(3):e86-7. PMID: 27029231.
    View in: PubMed
  29. Edward HL, Pisani LA, Rodriguez-Romero WE, Chaves-Villalobos J, Garcia-Quesada J, Harris NS, Luo HY, Steinberg MH, Forget BG, Chui DH. Hb Youngstown [ß101(G3)Glu???Ala; HBB: c.305A > C]: An unstable hemoglobin variant causing severe hemolytic anemia. Hemoglobin. 2014; 38(6):381-4. PMID: 25347256.
    View in: PubMed
  30. Buch K, Watanabe M, Elias EJ, Liao JH, Jara H, Nadgir RN, Saito N, Steinberg MH, Sakai O. Quantitative magnetic resonance imaging analysis of the lacrimal gland in sickle cell disease. J Comput Assist Tomogr. 2014 Sep-Oct; 38(5):674-80. PMID: 24834886.
    View in: PubMed
  31. Steinberg MH. More blood for sickle cell anemia? N Engl J Med. 2014 Aug 21; 371(8):775-6. PMID: 25140964.
    View in: PubMed
  32. Griffin PJ, Sebastiani P, Edward H, Baldwin CT, Gladwin MT, Gordeuk VR, Chui DH, Steinberg MH. The genetics of hemoglobin A2 regulation in sickle cell anemia. Am J Hematol. 2014 Nov; 89(11):1019-23. PMID: 25042611.
    View in: PubMed
  33. Borgio JF, AbdulAzeez S, Al-Nafie AN, Naserullah ZA, Al-Jarrash S, Al-Madan MS, Al-Muhanna F, Steinberg MH, Al-Ali AK. A novel HBA2 gene conversion in cis or trans: "a12 allele" in a Saudi population. Blood Cells Mol Dis. 2014 Dec; 53(4):199-203. PMID: 25065854.
    View in: PubMed
  34. Klings ES, Machado RF, Morris CR, Gordeuk VR, Kato GJ, Ataga KI, Castro O, Hsu L, Telen MJ, Krishnamurti L, Steinberg MH, Gladwin MT. Reply: Practice guideline for pulmonary hypertension in sickle cell: direct evidence needed before universal adoption. Am J Respir Crit Care Med. 2014 Jul 15; 190(2):238-40. PMID: 25025360.
    View in: PubMed
  35. Calvaruso G, Vitrano A, Di Maggio R, Ballas S, Steinberg MH, Rigano P, Sacco M, Telfer P, Renda D, Barone R, Maggio A. Deferiprone versus deferoxamine in sickle cell disease: results from a 5-year long-term Italian multi-center randomized clinical trial. Blood Cells Mol Dis. 2014 Dec; 53(4):265-71. PMID: 24814618.
    View in: PubMed
  36. Ngo D, Steinberg M. Hematology clinic. Sickle cell disease. Hematology. 2014 Jun; 19(4):244-5. PMID: 24666152.
    View in: PubMed
  37. Klings ES, Machado RF, Barst RJ, Morris CR, Mubarak KK, Gordeuk VR, Kato GJ, Ataga KI, Gibbs JS, Castro O, Rosenzweig EB, Sood N, Hsu L, Wilson KC, Telen MJ, Decastro LM, Krishnamurti L, Steinberg MH, Badesch DB, Gladwin MT. An official American Thoracic Society clinical practice guideline: diagnosis, risk stratification, and management of pulmonary hypertension of sickle cell disease. Am J Respir Crit Care Med. 2014 Mar 15; 189(6):727-40. PMID: 24628312.
    View in: PubMed
  38. Milton JN, Gordeuk VR, Taylor JG, Gladwin MT, Steinberg MH, Sebastiani P. Prediction of fetal hemoglobin in sickle cell anemia using an ensemble of genetic risk prediction models. Circ Cardiovasc Genet. 2014 Apr; 7(2):110-5. PMID: 24585758.
    View in: PubMed
  39. Zhang X, Zhang W, Ma SF, Desai AA, Saraf S, Miasniakova G, Sergueeva A, Ammosova T, Xu M, Nekhai S, Abbasi T, Casanova NG, Steinberg MH, Baldwin CT, Sebastiani P, Prchal JT, Kittles R, Garcia JG, Machado RF, Gordeuk VR. Hypoxic response contributes to altered gene expression and precapillary pulmonary hypertension in patients with sickle cell disease. Circulation. 2014 Apr 22; 129(16):1650-8. PMID: 24515990.
    View in: PubMed
  40. Belfer I, Youngblood V, Darbari DS, Wang Z, Diaw L, Freeman L, Desai K, Dizon M, Allen D, Cunnington C, Channon KM, Milton J, Hartley SW, Nolan V, Kato GJ, Steinberg MH, Goldman D, Taylor JG. A GCH1 haplotype confers sex-specific susceptibility to pain crises and altered endothelial function in adults with sickle cell anemia. Am J Hematol. 2014 Feb; 89(2):187-93. PMID: 24136375.
    View in: PubMed
  41. Steinberg MH, Chui DH. HbC disorders. Blood. 2013 Nov 21; 122(22):3698. PMID: 24263962.
    View in: PubMed
  42. Alsultan A, Alabdulaali MK, Griffin PJ, Alsuliman AM, Ghabbour HA, Sebastiani P, Albuali WH, Al-Ali AK, Chui DH, Steinberg MH. Sickle cell disease in Saudi Arabia: the phenotype in adults with the Arab-Indian haplotype is not benign. Br J Haematol. 2014 Feb; 164(4):597-604. PMID: 24224700.
    View in: PubMed
  43. Steinberg MH, Chui DH, Dover GJ, Sebastiani P, Alsultan A. Fetal hemoglobin in sickle cell anemia: a glass half full? Blood. 2014 Jan 23; 123(4):481-5. PMID: 24222332.
    View in: PubMed
  44. Pecoraro A, Rigano P, Troia A, Calzolari R, Scazzone C, Maggio A, Steinberg MH, Di Marzo R. Quantification of HBG mRNA in primary erythroid cultures: prediction of the response to hydroxyurea in sickle cell and beta-thalassemia. Eur J Haematol. 2014 Jan; 92(1):66-72. PMID: 24112139.
    View in: PubMed
  45. Bhatnagar P, Barron-Casella E, Bean CJ, Milton JN, Baldwin CT, Steinberg MH, Debaun M, Casella JF, Arking DE. Genome-wide meta-analysis of systolic blood pressure in children with sickle cell disease. PLoS One. 2013; 8(9):e74193. PMID: 24058526.
    View in: PubMed
  46. Barbosa CG, Aleluia AC, Pacheco AP, Paz SS, Zanette AM, Lyra IM, Steinberg MH, Milton JN, Goncalves MS. Genetic modulation of HbF in Brazilians with HbSC disease and sickle cell anemia. Am J Hematol. 2013 Oct; 88(10):923-4. PMID: 23828430.
    View in: PubMed
  47. Rigano P, Pecoraro A, Calvaruso G, Steinberg MH, Iannello S, Maggio A. Cerebrovascular events in sickle cell-beta thalassemia treated with hydroxyurea: a single center prospective survey in adult Italians. Am J Hematol. 2013 Nov; 88(11):E261-4. PMID: 23828131.
    View in: PubMed
  48. Smith BW, Rozelle SS, Leung A, Ubellacker J, Parks A, Nah SK, French D, Gadue P, Monti S, Chui DH, Steinberg MH, Frelinger AL, Michelson AD, Theberge R, McComb ME, Costello CE, Kotton DN, Mostoslavsky G, Sherr DH, Murphy GJ. The aryl hydrocarbon receptor directs hematopoietic progenitor cell expansion and differentiation. Blood. 2013 Jul 18; 122(3):376-85. PMID: 23723449.
    View in: PubMed
  49. Alsultan A, Ngo D, Bae H, Sebastiani P, Baldwin CT, Melista E, Suliman AM, Albuali WH, Nasserullah Z, Luo HY, Chui DH, Steinberg MH, Al-Ali AK. Genetic studies of fetal hemoglobin in the Arab-Indian haplotype sickle cell-ß(0) thalassemia. Am J Hematol. 2013 Jun; 88(6):531-2. PMID: 23483609.
    View in: PubMed
  50. Ngo D, Bae H, Steinberg MH, Sebastiani P, Solovieff N, Baldwin CT, Melista E, Safaya S, Farrer LA, Al-Suliman AM, Albuali WH, Al Bagshi MH, Naserullah Z, Akinsheye I, Gallagher P, Luo HY, Chui DH, Farrell JJ, Al-Ali AK, Alsultan A. Fetal hemoglobin in sickle cell anemia: genetic studies of the Arab-Indian haplotype. Blood Cells Mol Dis. 2013 Jun; 51(1):22-6. PMID: 23465615.
    View in: PubMed
  51. Milton JN, Rooks H, Drasar E, McCabe EL, Baldwin CT, Melista E, Gordeuk VR, Nouraie M, Kato GR, Minniti C, Taylor J, Campbell A, Luchtman-Jones L, Rana S, Castro O, Zhang Y, Thein SL, Sebastiani P, Gladwin MT. Genetic determinants of haemolysis in sickle cell anaemia. Br J Haematol. 2013 Apr; 161(2):270-8. PMID: 23406172.
    View in: PubMed
  52. Watanabe M, Saito N, Nadgir RN, Liao JH, Flower EN, Steinberg MH, Sakai O. Craniofacial bone infarcts in sickle cell disease: clinical and radiological manifestations. J Comput Assist Tomogr. 2013 Jan-Feb; 37(1):91-7. PMID: 23321839.
    View in: PubMed
  53. Liao J, Saito N, Ozonoff A, Jara H, Steinberg M, Sakai O. Quantitative MRI analysis of salivary glands in sickle cell disease. Dentomaxillofac Radiol. 2012 Dec; 41(8):630-6. PMID: 23166360.
    View in: PubMed
  54. Liao JH, Jara H, Nadgir R, Elias E, Nowrouzi N, Saito N, Steinberg MH, Sakai O. qMRI relaxometry of mandibular bone marrow: a monomodal distribution in sickle cell disease. J Magn Reson Imaging. 2013 May; 37(5):1182-8. PMID: 23086731.
    View in: PubMed
  55. Hartley SW, Monti S, Liu CT, Steinberg MH, Sebastiani P. Bayesian methods for multivariate modeling of pleiotropic SNP associations and genetic risk prediction. Front Genet. 2012; 3:176. PMID: 22973300.
    View in: PubMed
  56. Bae HT, Baldwin CT, Sebastiani P, Telen MJ, Ashley-Koch A, Garrett M, Hooper WC, Bean CJ, Debaun MR, Arking DE, Bhatnagar P, Casella JF, Keefer JR, Barron-Casella E, Gordeuk V, Kato GJ, Minniti C, Taylor J, Campbell A, Luchtman-Jones L, Hoppe C, Gladwin MT, Zhang Y, Steinberg MH. Meta-analysis of 2040 sickle cell anemia patients: BCL11A and HBS1L-MYB are the major modifiers of HbF in African Americans. Blood. 2012 Aug 30; 120(9):1961-2. PMID: 22936743.
    View in: PubMed
  57. Elias EJ, Liao JH, Jara H, Watanabe M, Nadgir RN, Sakai Y, Erbay K, Saito N, Ozonoff A, Steinberg MH, Sakai O. Quantitative MRI analysis of craniofacial bone marrow in patients with sickle cell disease. AJNR Am J Neuroradiol. 2013 Mar; 34(3):622-7. PMID: 22878006.
    View in: PubMed
  58. Alsultan A, Ngo DA, Farrell JJ, Akinsheye I, Solovieff N, Ghabbour HA, Al-Ali A, Alsuliman A, Al-Baghshi M, Albu-Ali W, Alabdulaali M, Baldwin CT, Farrer LA, Luo H, Melista E, Safaya S, Nwaru M, Chui DH, Steinberg MH. A functional promoter polymorphism of the d-globin gene is a specific marker of the Arab-Indian haplotype. Am J Hematol. 2012 Aug; 87(8):824-6. PMID: 22641479.
    View in: PubMed
  59. Steinberg MH, Sebastiani P. Genetic modifiers of sickle cell disease. Am J Hematol. 2012 Aug; 87(8):795-803. PMID: 22641398.
    View in: PubMed
  60. Milton JN, Sebastiani P, Solovieff N, Hartley SW, Bhatnagar P, Arking DE, Dworkis DA, Casella JF, Barron-Casella E, Bean CJ, Hooper WC, DeBaun MR, Garrett ME, Soldano K, Telen MJ, Ashley-Koch A, Gladwin MT, Baldwin CT, Steinberg MH, Klings ES. A genome-wide association study of total bilirubin and cholelithiasis risk in sickle cell anemia. PLoS One. 2012; 7(4):e34741. PMID: 22558097.
    View in: PubMed
  61. Goldsmith JC, Bonham VL, Joiner CH, Kato GJ, Noonan AS, Steinberg MH. Framing the research agenda for sickle cell trait: building on the current understanding of clinical events and their potential implications. Am J Hematol. 2012 Mar; 87(3):340-6. PMID: 22307997.
    View in: PubMed
  62. Verhovsek M, Shah NR, Wilcox I, Koenig SC, Barros T, Thornburg CD, Steinberg MH, Luo HY, Chui DH. Severe fetal and neonatal hemolytic anemia due to a 198 kb deletion removing the complete ß-globin gene cluster. Pediatr Blood Cancer. 2012 Nov; 59(5):941-4. PMID: 22294483.
    View in: PubMed
  63. Safaya S, Steinberg MH, Klings ES. Monocytes from sickle cell disease patients induce differential pulmonary endothelial gene expression via activation of NF-?B signaling pathway. Mol Immunol. 2012 Feb; 50(1-2):117-23. PMID: 22264835.
    View in: PubMed
  64. Sebastiani P, Solovieff N, Dewan AT, Walsh KM, Puca A, Hartley SW, Melista E, Andersen S, Dworkis DA, Wilk JB, Myers RH, Steinberg MH, Montano M, Baldwin CT, Hoh J, Perls TT. Genetic signatures of exceptional longevity in humans. PLoS One. 2012; 7(1):e29848. PMID: 22279548.
    View in: PubMed
  65. Sebastiani P, Riva A, Montano M, Pham P, Torkamani A, Scherba E, Benson G, Milton JN, Baldwin CT, Andersen S, Schork NJ, Steinberg MH, Perls TT. Whole genome sequences of a male and female supercentenarian, ages greater than 114?years. Front Genet. 2011; 2:90. PMID: 22303384.
    View in: PubMed
  66. Akinsheye I, Solovieff N, Ngo D, Malek A, Sebastiani P, Steinberg MH, Chui DH. Fetal hemoglobin in sickle cell anemia: molecular characterization of the unusually high fetal hemoglobin phenotype in African Americans. Am J Hematol. 2012 Feb; 87(2):217-9. PMID: 22139998.
    View in: PubMed
  67. Verhovsek M, So CC, O'Shea T, Gibney GT, Ma ES, Steinberg MH, Chui DH. Is HbA2 level a reliable diagnostic measurement for ß-thalassemia trait in people with iron deficiency? Am J Hematol. 2012 Jan; 87(1):114-6. PMID: 22038702.
    View in: PubMed
  68. Ngo DA, Aygun B, Akinsheye I, Hankins JS, Bhan I, Luo HY, Steinberg MH, Chui DH. Fetal haemoglobin levels and haematological characteristics of compound heterozygotes for haemoglobin S and deletional hereditary persistence of fetal haemoglobin. Br J Haematol. 2012 Jan; 156(2):259-64. PMID: 22017641.
    View in: PubMed
  69. Saito N, Watanabe M, Liao J, Flower EN, Nadgir RN, Steinberg MH, Sakai O. Clinical and radiologic findings of inner ear involvement in sickle cell disease. AJNR Am J Neuroradiol. 2011 Dec; 32(11):2160-4. PMID: 21960497.
    View in: PubMed
  70. Steinberg MH. In the clinic. Sickle cell disease. Ann Intern Med. 2011 Sep 6; 155(5):ITC31-15; quiz ITC316. PMID: 21893620.
    View in: PubMed
  71. Sebastiani P, Solovieff N, Puca A, Hartley SW, Melista E, Andersen S, Dworkis DA, Wilk JB, Myers RH, Steinberg MH, Montano M, Baldwin CT, Perls TT. Retraction. Science. 2011 Jul 22; 333(6041):404. PMID: 21778381.
    View in: PubMed
  72. Castro OL, Gordeuk VR, Gladwin MT, Steinberg MH. Senicapoc trial results support the existence of different sub-phenotypes of sickle cell disease with possible drug-induced phenotypic shifts. Br J Haematol. 2011 Dec; 155(5):636-8. PMID: 21732927.
    View in: PubMed
  73. Alsultan A, Solovieff N, Aleem A, AlGahtani FH, Al-Shehri A, Osman ME, Kurban K, Bahakim H, Al-Momen AK, Baldwin CT, Chui DH, Steinberg MH. Fetal hemoglobin in sickle cell anemia: Saudi patients from the Southwestern province have similar HBB haplotypes but higher HbF levels than African Americans. Am J Hematol. 2011 Jul; 86(7):612-4. PMID: 21630302.
    View in: PubMed
  74. Solovieff N, Hartley SW, Baldwin CT, Klings ES, Gladwin MT, Taylor JG, Kato GJ, Farrer LA, Steinberg MH, Sebastiani P. Ancestry of African Americans with sickle cell disease. Blood Cells Mol Dis. 2011 Jun 15; 47(1):41-5. PMID: 21546286.
    View in: PubMed
  75. Akinsheye I, Alsultan A, Solovieff N, Ngo D, Baldwin CT, Sebastiani P, Chui DH, Steinberg MH. Fetal hemoglobin in sickle cell anemia. Blood. 2011 Jul 7; 118(1):19-27. PMID: 21490337.
    View in: PubMed
  76. Smith WR, Ballas SK, McCarthy WF, Bauserman RL, Swerdlow PS, Steinberg MH, Waclawiw MA. The association between hydroxyurea treatment and pain intensity, analgesic use, and utilization in ambulatory sickle cell anemia patients. Pain Med. 2011 May; 12(5):697-705. PMID: 21481164.
    View in: PubMed
  77. Farrell JJ, Sherva RM, Chen ZY, Luo HY, Chu BF, Ha SY, Li CK, Lee AC, Li RC, Li CK, Yuen HL, So JC, Ma ES, Chan LC, Chan V, Sebastiani P, Farrer LA, Baldwin CT, Steinberg MH, Chui DH. A 3-bp deletion in the HBS1L-MYB intergenic region on chromosome 6q23 is associated with HbF expression. Blood. 2011 May 5; 117(18):4935-45. PMID: 21385855.
    View in: PubMed
  78. Miller ST, Milton J, Steinberg MH. G6PD deficiency and stroke in the CSSCD. Am J Hematol. 2011 Mar; 86(3):331. PMID: 21328436.
    View in: PubMed
  79. Dworkis DA, Klings ES, Solovieff N, Li G, Milton JN, Hartley SW, Melista E, Parente J, Sebastiani P, Steinberg MH, Baldwin CT. Severe sickle cell anemia is associated with increased plasma levels of TNF-R1 and VCAM-1. Am J Hematol. 2011 Feb; 86(2):220-3. PMID: 21264913.
    View in: PubMed
  80. Wang W, Brugnara C, Snyder C, Wynn L, Rogers Z, Kalinyak K, Brown C, Qureshi A, Bigelow C, Neumayr L, Smith-Whitley K, Chui DH, Delahunty M, Woolson R, Steinberg M, Telen M, Kesler K. The effects of hydroxycarbamide and magnesium on haemoglobin SC disease: results of the multi-centre CHAMPS trial. Br J Haematol. 2011 Mar; 152(6):771-6. PMID: 21275961.
    View in: PubMed
  81. Solovieff N, Hartley SW, Baldwin CT, Perls TT, Steinberg MH, Sebastiani P. Clustering by genetic ancestry using genome-wide SNP data. BMC Genet. 2010; 11:108. PMID: 21143920.
    View in: PubMed
  82. Verhovsek M, Henderson MP, Cox G, Luo HY, Steinberg MH, Chui DH. Unexpectedly low pulse oximetry measurements associated with variant hemoglobins: a systematic review. Am J Hematol. 2010 Nov; 85(11):882-5. PMID: 20890907.
    View in: PubMed
  83. Minniti CP, Eckman J, Sebastiani P, Steinberg MH, Ballas SK. Leg ulcers in sickle cell disease. Am J Hematol. 2010 Oct; 85(10):831-3. PMID: 20872960.
    View in: PubMed
  84. Gladwin MT, Barst RJ, Castro OL, Gordeuk VR, Hillery CA, Kato GJ, Kim-Shapiro DB, Machado R, Morris CR, Steinberg MH, Vichinsky EP. Pulmonary hypertension and NO in sickle cell. Blood. 2010 Aug 5; 116(5):852-4. PMID: 20688967.
    View in: PubMed
  85. Sebastiani P, Solovieff N, Puca A, Hartley SW, Melista E, Andersen S, Dworkis DA, Wilk JB, Myers RH, Steinberg MH, Montano M, Baldwin CT, Perls TT. Genetic signatures of exceptional longevity in humans. Science. 2010 Jul 1; 2010. PMID: 20595579.
    View in: PubMed
  86. Steinberg MH, McCarthy WF, Castro O, Ballas SK, Armstrong FD, Smith W, Ataga K, Swerdlow P, Kutlar A, DeCastro L, Waclawiw MA. The risks and benefits of long-term use of hydroxyurea in sickle cell anemia: A 17.5 year follow-up. Am J Hematol. 2010 Jun; 85(6):403-8. PMID: 20513116.
    View in: PubMed
  87. Sebastiani P, Solovieff N, Hartley SW, Milton JN, Riva A, Dworkis DA, Melista E, Klings ES, Garrett ME, Telen MJ, Ashley-Koch A, Baldwin CT, Steinberg MH. Genetic modifiers of the severity of sickle cell anemia identified through a genome-wide association study. Am J Hematol. 2010 Jan; 85(1):29-35. PMID: 20029952.
    View in: PubMed
  88. Rao V, Rosenberg P, Miles QS, Patadia D, Treiber K, Bertrand M, Norton M, Steinberg M, Tschanz J, Lyketsos C. Neuropsychiatric symptoms in dementia patients with and without a history of traumatic brain injury. J Neuropsychiatry Clin Neurosci. 2010; 22(2):166-72. PMID: 20463110.
    View in: PubMed
  89. Solovieff N, Milton JN, Hartley SW, Sherva R, Sebastiani P, Dworkis DA, Klings ES, Farrer LA, Garrett ME, Ashley-Koch A, Telen MJ, Fucharoen S, Ha SY, Li CK, Chui DH, Baldwin CT, Steinberg MH. Fetal hemoglobin in sickle cell anemia: genome-wide association studies suggest a regulatory region in the 5' olfactory receptor gene cluster. Blood. 2010 Mar 4; 115(9):1815-22. PMID: 20018918.
    View in: PubMed
  90. Sebastiani P, Montano M, Puca A, Solovieff N, Kojima T, Wang MC, Melista E, Meltzer M, Fischer SE, Andersen S, Hartley SH, Sedgewick A, Arai Y, Bergman A, Barzilai N, Terry DF, Riva A, Anselmi CV, Malovini A, Kitamoto A, Sawabe M, Arai T, Gondo Y, Steinberg MH, Hirose N, Atzmon G, Ruvkun G, Baldwin CT, Perls TT. RNA editing genes associated with extreme old age in humans and with lifespan in C. elegans. PLoS One. 2009; 4(12):e8210. PMID: 20011587.
    View in: PubMed
  91. Koenig SC, Becirevic E, Hellberg MS, Li MY, So JC, Hankins JS, Ware RE, McMahon L, Steinberg MH, Luo HY, Chui DH. Sickle cell disease caused by heterozygosity for Hb S and novel LCR deletion: Report of two patients. Am J Hematol. 2009 Sep; 84(9):603-6. PMID: 19650141.
    View in: PubMed
  92. Kato GJ, Hebbel RP, Steinberg MH, Gladwin MT. Vasculopathy in sickle cell disease: Biology, pathophysiology, genetics, translational medicine, and new research directions. Am J Hematol. 2009 Sep; 84(9):618-25. PMID: 19610078.
    View in: PubMed
  93. Smith WR, Bauserman RL, Ballas SK, McCarthy WF, Steinberg MH, Swerdlow PS, Waclawiw MA, Barton BA. Climatic and geographic temporal patterns of pain in the Multicenter Study of Hydroxyurea. Pain. 2009 Nov; 146(1-2):91-8. PMID: 19683393.
    View in: PubMed
  94. Sebastiani P, Timofeev N, Dworkis DA, Perls TT, Steinberg MH. Genome-wide association studies and the genetic dissection of complex traits. Am J Hematol. 2009 Aug; 84(8):504-15. PMID: 19569043.
    View in: PubMed
  95. Thornburg CD, Steinberg MH, Chui DH. Hemoglobin SE disease in Maine, and severe thalassemia in New Hampshire. J Pediatr Hematol Oncol. 2009 Apr; 31(4):307. PMID: 19346889.
    View in: PubMed
  96. Safaya S, Klings ES, Odhiambo A, Li G, Farber HW, Steinberg MH. Effect of sodium butyrate on lung vascular TNFSF15 (TL1A) expression: differential expression patterns in pulmonary artery and microvascular endothelial cells. Cytokine. 2009 Apr; 46(1):72-8. PMID: 19251437.
    View in: PubMed
  97. Chen Z, Luo HY, Steinberg MH, Chui DH. BCL11A represses HBG transcription in K562 cells. Blood Cells Mol Dis. 2009 Mar-Apr; 42(2):144-9. PMID: 19153051.
    View in: PubMed
  98. Steinberg MH. Genetic etiologies for phenotypic diversity in sickle cell anemia. ScientificWorldJournal. 2009; 9:46-67. PMID: 19151898.
    View in: PubMed
  99. Steinberg MH, Forget BG, Higgs DR, Weatherall DJ eds. Disorders of Hemoglobin: Genetics, Pathophysiology, Clinical Management, 2nd ed. Cambridge University Press. Cambridge. 2009; 826.
  100. Wilcox I, Boettger K, Greene L, Malek A, Davis L, Steinberg MH, Luo HY, Chui DH. Hemoglobin Kenya composed of alpha- and ((A)gammabeta)-fusion-globin chains, associated with hereditary persistence of fetal hemoglobin. Am J Hematol. 2009 Jan; 84(1):55-8. PMID: 19006227.
    View in: PubMed
  101. Steinberg MH. Sickle cell anemia, the first molecular disease: overview of molecular etiology, pathophysiology, and therapeutic approaches. ScientificWorldJournal. 2008; 8:1295-324. PMID: 19112541.
    View in: PubMed
  102. Zhao Z, Timofeev N, Hartley SW, Chui DH, Fucharoen S, Perls TT, Steinberg MH, Baldwin CT, Sebastiani P. Imputation of missing genotypes: an empirical evaluation of IMPUTE. BMC Genet. 2008; 9:85. PMID: 19077279.
    View in: PubMed
  103. Nolan VG, Zhang Y, Lash T, Sebastiani P, Steinberg MH. Association between wind speed and the occurrence of sickle cell acute painful episodes: results of a case-crossover study. Br J Haematol. 2008 Nov; 143(3):433-8. PMID: 18729854.
    View in: PubMed
  104. Sedgewick AE, Timofeev N, Sebastiani P, So JC, Ma ES, Chan LC, Fucharoen G, Fucharoen S, Barbosa CG, Vardarajan BN, Farrer LA, Baldwin CT, Steinberg MH, Chui DH. BCL11A is a major HbF quantitative trait locus in three different populations with beta-hemoglobinopathies. Blood Cells Mol Dis. 2008 Nov-Dec; 41(3):255-8. PMID: 18691915.
    View in: PubMed
  105. Klings ES, Anton Bland D, Rosenman D, Princeton S, Odhiambo A, Li G, Bernard SA, Steinberg MH, Farber HW. Pulmonary arterial hypertension and left-sided heart disease in sickle cell disease: clinical characteristics and association with soluble adhesion molecule expression. Am J Hematol. 2008 Jul; 83(7):547-53. PMID: 18383329.
    View in: PubMed
  106. Steinberg MH. SNPing away at sickle cell pathophysiology. Blood. 2008 Jun 15; 111(12):5420-1. PMID: 18544690.
    View in: PubMed
  107. Gibney GT, Panhuysen CI, So JC, Ma ES, Ha SY, Li CK, Lee AC, Li CK, Yuen HL, Lau YL, Johnson DM, Farrell JJ, Bisbee AB, Farrer LA, Steinberg MH, Chan LC, Chui DH. Variation and heritability of Hb F and F-cells among beta-thalassemia heterozygotes in Hong Kong. Am J Hematol. 2008 Jun; 83(6):458-64. PMID: 18266208.
    View in: PubMed
  108. Taylor JG, Nolan VG, Mendelsohn L, Kato GJ, Gladwin MT, Steinberg MH. Chronic hyper-hemolysis in sickle cell anemia: association of vascular complications and mortality with less frequent vasoocclusive pain. PLoS One. 2008; 3(5):e2095. PMID: 18461136.
    View in: PubMed
  109. Chen Z, Luo HY, Basran RK, Hsu TH, Mang DW, Nuntakarn L, Rosenfield CG, Patrinos GP, Hardison RC, Steinberg MH, Chui DH. A T-to-G transversion at nucleotide -567 upstream of HBG2 in a GATA-1 binding motif is associated with elevated hemoglobin F. Mol Cell Biol. 2008 Jul; 28(13):4386-93. PMID: 18443038.
    View in: PubMed
  110. Adewoye AH, Chen TC, Ma Q, McMahon L, Mathieu J, Malabanan A, Steinberg MH, Holick MF. Sickle cell bone disease: response to vitamin D and calcium. Am J Hematol. 2008 Apr; 83(4):271-4. PMID: 17924548.
    View in: PubMed
  111. Sebastiani P, Wang L, Nolan VG, Melista E, Ma Q, Baldwin CT, Steinberg MH. Fetal hemoglobin in sickle cell anemia: Bayesian modeling of genetic associations. Am J Hematol. 2008 Mar; 83(3):189-95. PMID: 17918249.
    View in: PubMed
  112. Sebastiani P, Zhao Z, Abad-Grau MM, Riva A, Hartley SW, Sedgewick AE, Doria A, Montano M, Melista E, Terry D, Perls TT, Steinberg MH, Baldwin CT. A hierarchical and modular approach to the discovery of robust associations in genome-wide association studies from pooled DNA samples. BMC Genet. 2008; 9:6. PMID: 18194558.
    View in: PubMed
  113. Steinberg MH. Clinical trials in sickle cell disease: adopting the combination chemotherapy paradigm. Am J Hematol. 2008 Jan; 83(1):1-3. PMID: 17724701.
    View in: PubMed
  114. Morris CR, Suh JH, Hagar W, Larkin S, Bland DA, Steinberg MH, Vichinsky EP, Shigenaga M, Ames B, Kuypers FA, Klings ES. Erythrocyte glutamine depletion, altered redox environment, and pulmonary hypertension in sickle cell disease. Blood. 2008 Jan 1; 111(1):402-10. PMID: 17848621.
    View in: PubMed
  115. Masiello D, Heeney MM, Adewoye AH, Eung SH, Luo HY, Steinberg MH, Chui DH. Hemoglobin SE disease: a concise review. Am J Hematol. 2007 Jul; 82(7):643-9. PMID: 17278112.
    View in: PubMed
  116. Sebastiani P, Nolan VG, Baldwin CT, Abad-Grau MM, Wang L, Adewoye AH, McMahon LC, Farrer LA, Taylor JG, Kato GJ, Gladwin MT, Steinberg MH. A network model to predict the risk of death in sickle cell disease. Blood. 2007 Oct 1; 110(7):2727-35. PMID: 17600133.
    View in: PubMed
  117. Adewoye AH, Nolan V, McMahon L, Ma Q, Steinberg MH. Effectiveness of a dedicated day hospital for management of acute sickle cell pain. Haematologica. 2007 Jun; 92(6):854-5. PMID: 17550862.
    View in: PubMed
  118. Steinberg MH. Pneumococcus and sickle cell disease: the beginning of the end? Clin Infect Dis. 2007 Jun 1; 44(11):1434-5. PMID: 17479938.
    View in: PubMed
  119. Nolan VG, Ma Q, Cohen HT, Adewoye A, Rybicki AC, Baldwin C, Mahabir RN, Homan EP, Wyszynski DF, Fabry ME, Nagel RL, Farrer LA, Steinberg MH. Estimated glomerular filtration rate in sickle cell anemia is associated with polymorphisms of bone morphogenetic protein receptor 1B. Am J Hematol. 2007 Mar; 82(3):179-84. PMID: 17034027.
    View in: PubMed
  120. Ma Q, Wyszynski DF, Farrell JJ, Kutlar A, Farrer LA, Baldwin CT, Steinberg MH. Fetal hemoglobin in sickle cell anemia: genetic determinants of response to hydroxyurea. Pharmacogenomics J. 2007 Dec; 7(6):386-94. PMID: 17299377.
    View in: PubMed
  121. Luo HY, Adewoye AH, Pilichowska M, Li MY, Basran RK, Steinberg MH, Chui DH. Two new alpha-thalassemia frameshift mutations. Hemoglobin. 2007; 31(2):135-9. PMID: 17486494.
    View in: PubMed
  122. Odhiambo A, Perlman DH, Huang H, Costello CE, Farber HW, Steinberg MH, McComb ME, Klings ES. Identification of oxidative post-translational modification of serum albumin in patients with idiopathic pulmonary arterial hypertension and pulmonary hypertension of sickle cell anemia. Rapid Commun Mass Spectrom. 2007; 21(14):2195-203. PMID: 17569101.
    View in: PubMed
  123. Kato GJ, Gladwin MT, Steinberg MH. Deconstructing sickle cell disease: reappraisal of the role of hemolysis in the development of clinical subphenotypes. Blood Rev. 2007 Jan; 21(1):37-47. PMID: 17084951.
    View in: PubMed
  124. Adewoye AH, Ramsey J, McMahon L, Sakai O, Steinberg MH. Lacrimal gland enlargement in sickle cell disease. Am J Hematol. 2006 Nov; 81(11):888-9. PMID: 16929543.
    View in: PubMed
  125. Andersson BA, Wering ME, Luo HY, Basran RK, Steinberg MH, Smith HP, Chui DH. Sickle cell disease due to compound heterozygosity for Hb S and a novel 7.7-kb beta-globin gene deletion. Eur J Haematol. 2007 Jan; 78(1):82-5. PMID: 17038017.
    View in: PubMed
  126. Machado RF, Anthi A, Steinberg MH, Bonds D, Sachdev V, Kato GJ, Taveira-DaSilva AM, Ballas SK, Blackwelder W, Xu X, Hunter L, Barton B, Waclawiw M, Castro O, Gladwin MT. N-terminal pro-brain natriuretic peptide levels and risk of death in sickle cell disease. JAMA. 2006 Jul 19; 296(3):310-8. PMID: 16849664.
    View in: PubMed
  127. Adewoye AH, Nolan VG, Ma Q, Baldwin C, Wyszynski DF, Farrell JJ, Farrer LA, Steinberg MH. Association of polymorphisms of IGF1R and genes in the transforming growth factor- beta /bone morphogenetic protein pathway with bacteremia in sickle cell anemia. Clin Infect Dis. 2006 Sep 1; 43(5):593-8. PMID: 16886151.
    View in: PubMed
  128. Nolan VG, Adewoye A, Baldwin C, Wang L, Ma Q, Wyszynski DF, Farrell JJ, Sebastiani P, Farrer LA, Steinberg MH. Sickle cell leg ulcers: associations with haemolysis and SNPs in Klotho, TEK and genes of the TGF-beta/BMP pathway. Br J Haematol. 2006 Jun; 133(5):570-8. PMID: 16681647.
    View in: PubMed
  129. Luo HY, Heeney M, Wang WC, Eung SH, Ware RE, Steinberg MH, Chui DH. Hemoglobinopathies mimicking Hb S/beta-thalassemia: Hb S/S with alpha-thalassemia and Hb S/Volga. Am J Hematol. 2006 May; 81(5):361-5. PMID: 16628724.
    View in: PubMed
  130. Steinberg MH, Adewoye AH. Modifier genes and sickle cell anemia. Curr Opin Hematol. 2006 May; 13(3):131-6. PMID: 16567954.
    View in: PubMed
  131. Klings ES, Wyszynski DF, Nolan VG, Steinberg MH. Abnormal pulmonary function in adults with sickle cell anemia. Am J Respir Crit Care Med. 2006 Jun 1; 173(11):1264-9. PMID: 16556694.
    View in: PubMed
  132. Steinberg MH. Pathophysiologically based drug treatment of sickle cell disease. Trends Pharmacol Sci. 2006 Apr; 27(4):204-10. PMID: 16530854.
    View in: PubMed
  133. Law HY, Luo HY, Wang W, Ho JF, Najmabadi H, Ng IS, Steinberg MH, Chui DH, Chong SS. Determining the cause of patchwork HBA1 and HBA2 genes: recurrent gene conversion or crossing over fixation events. Haematologica. 2006 Mar; 91(3):297-302. PMID: 16503550.
    View in: PubMed
  134. Chui DH, Cunningham MJ, Luo HY, Wolfe LC, Neufeld EJ, Steinberg MH. Screening and counseling for thalassemia. Blood. 2006 Feb 15; 107(4):1735-7. PMID: 16461765.
    View in: PubMed
  135. Luo HY, Tang W, Eung SH, Coad JE, Canfield P, Keller F, Crowell EH, Steinberg MH, Chui DH. Dominantly inherited beta thalassaemia intermedia caused by a new single nucleotide deletion in exon 2 of the beta globin gene: Hb morgantown (beta91 CTG>CG). J Clin Pathol. 2005 Oct; 58(10):1110-2. PMID: 16189162.
    View in: PubMed
  136. Nolan VG, Wyszynski DF, Farrer LA, Steinberg MH. Hemolysis-associated priapism in sickle cell disease. Blood. 2005 Nov 1; 106(9):3264-7. PMID: 15985542.
    View in: PubMed
  137. Luo HY, Boudreaux J, Steinberg MH, Chui DH. Patients with thalassemia in the United States. Blood. 2005 Jun 15; 105(12):4896-7. PMID: 15933066.
    View in: PubMed
  138. Steinberg MH. Predicting clinical severity in sickle cell anaemia. Br J Haematol. 2005 May; 129(4):465-81. PMID: 15877729.
    View in: PubMed
  139. Baldwin C, Nolan VG, Wyszynski DF, Ma QL, Sebastiani P, Embury SH, Bisbee A, Farrell J, Farrer L, Steinberg MH. Association of klotho, bone morphogenic protein 6, and annexin A2 polymorphisms with sickle cell osteonecrosis. Blood. 2005 Jul 1; 106(1):372-5. PMID: 15784727.
    View in: PubMed
  140. Sebastiani P, Ramoni MF, Nolan V, Baldwin CT, Steinberg MH. Genetic dissection and prognostic modeling of overt stroke in sickle cell anemia. Nat Genet. 2005 Apr; 37(4):435-40. PMID: 15778708.
    View in: PubMed
  141. Adewoye AH, Klings ES, Farber HW, Palaima E, Bausero MA, McMahon L, Odhiambo A, Surinder S, Yoder M, Steinberg MH, Asea A. Sickle cell vaso-occlusive crisis induces the release of circulating serum heat shock protein-70. Am J Hematol. 2005 Mar; 78(3):240-2. PMID: 15726596.
    View in: PubMed
  142. Klings ES, Safaya S, Adewoye AH, Odhiambo A, Frampton G, Lenburg M, Gerry N, Sebastiani P, Steinberg MH, Farber HW. Differential gene expression in pulmonary artery endothelial cells exposed to sickle cell plasma. Physiol Genomics. 2005 May 11; 21(3):293-8. PMID: 15741505.
    View in: PubMed
  143. Zandi PP, Sparks DL, Khachaturian AS, Tschanz J, Norton M, Steinberg M, Welsh-Bohmer KA, Breitner JC. Do statins reduce risk of incident dementia and Alzheimer disease? The Cache County Study. Arch Gen Psychiatry. 2005 Feb; 62(2):217-24. PMID: 15699299.
    View in: PubMed
  144. Nolan VG, Baldwin C, Ma Q, Wyszynski DF, Amirault Y, Farrell JJ, Bisbee A, Embury SH, Farrer LA, Steinberg MH. Association of single nucleotide polymorphisms in klotho with priapism in sickle cell anaemia. Br J Haematol. 2005 Jan; 128(2):266-72. PMID: 15638863.
    View in: PubMed
  145. Luo HY, Irving I, Prior J, Lim E, Eung SH, Skelton TP, Erber WN, Steinberg MH, Chui DH. Hemoglobin Titusville, a low oxygen affinity variant hemoglobin, in a family of Northern European background. Am J Hematol. 2004 Dec; 77(4):384-6. PMID: 15551405.
    View in: PubMed
  146. Luo HY, Adewoye AH, Eung SH, Skelton TP, Quillen K, McMahon L, Steinberg MH, Chui DH. A novel sickle hemoglobin: hemoglobin S-south end. J Pediatr Hematol Oncol. 2004 Nov; 26(11):773-6. PMID: 15543018.
    View in: PubMed
  147. Saleh M, Vaillancourt JP, Graham RK, Huyck M, Srinivasula SM, Alnemri ES, Steinberg MH, Nolan V, Baldwin CT, Hotchkiss RS, Buchman TG, Zehnbauer BA, Hayden MR, Farrer LA, Roy S, Nicholson DW. Differential modulation of endotoxin responsiveness by human caspase-12 polymorphisms. Nature. 2004 May 6; 429(6987):75-9. PMID: 15129283.
    View in: PubMed
  148. Wyszynski DF, Baldwin CT, Cleves MA, Amirault Y, Nolan VG, Farrell JJ, Bisbee A, Kutlar A, Farrer LA, Steinberg MH. Polymorphisms near a chromosome 6q QTL area are associated with modulation of fetal hemoglobin levels in sickle cell anemia. Cell Mol Biol (Noisy-le-grand). 2004 Feb; 50(1):23-33. PMID: 15040424.
    View in: PubMed
  149. Ingle J, Adewoye A, Dewan R, Okoli M, Rollins L, Eung SH, Luo HY, Chui DH, Steinberg MH. Hb Hope [beta136(H14)Gly-->Asp (GGT-->GAT)]: interactions with Hb S [beta6(A3)Glu-->Val (GAG-->GTG)], other variant hemoglobins and thalassemia. Hemoglobin. 2004; 28(4):277-85. PMID: 15658184.
    View in: PubMed
  150. Steinberg M, Tschanz JT, Corcoran C, Steffens DC, Norton MC, Lyketsos CG, Breitner JC. The persistence of neuropsychiatric symptoms in dementia: the Cache County Study. Int J Geriatr Psychiatry. 2004 Jan; 19(1):19-26. PMID: 14716695.
    View in: PubMed
  151. Buchanan GR, DeBaun MR, Quinn CT, Steinberg MH. Sickle cell disease. Hematology Am Soc Hematol Educ Program. 2004; 35-47. PMID: 15561675.
    View in: PubMed
  152. Eberhardt RT, McMahon L, Duffy SJ, Steinberg MH, Perrine SP, Loscalzo J, Coffman JD, Vita JA. Sickle cell anemia is associated with reduced nitric oxide bioactivity in peripheral conduit and resistance vessels. Am J Hematol. 2003 Oct; 74(2):104-11. PMID: 14508796.
    View in: PubMed
  153. Nagel RL, Fabry ME, Steinberg MH. The paradox of hemoglobin SC disease. Blood Rev. 2003 Sep; 17(3):167-78. PMID: 12818227.
    View in: PubMed
  154. Steinberg MH. Bone marrow transplantation in sickle cell disease: indications and successes. Clin Adv Hematol Oncol. 2003 Jul; 1(7):406-7. PMID: 16258422.
    View in: PubMed
  155. Steinberg MH, Barton F, Castro O, Pegelow CH, Ballas SK, Kutlar A, Orringer E, Bellevue R, Olivieri N, Eckman J, Varma M, Ramirez G, Adler B, Smith W, Carlos T, Ataga K, DeCastro L, Bigelow C, Saunthararajah Y, Telfer M, Vichinsky E, Claster S, Shurin S, Bridges K, Waclawiw M, Bonds D, Terrin M. Effect of hydroxyurea on mortality and morbidity in adult sickle cell anemia: risks and benefits up to 9 years of treatment. JAMA. 2003 Apr 2; 289(13):1645-51. PMID: 12672732.
    View in: PubMed
  156. Steinberg MH. Therapies to increase fetal hemoglobin in sickle cell disease. Curr Hematol Rep. 2003 Mar; 2(2):95-101. PMID: 12901139.
    View in: PubMed
  157. Steinberg MH, Voskaridou E, Kutlar A, Loukopoulos D, Koshy M, Ballas SK, Castro O, Barton F. Concordant fetal hemoglobin response to hydroxyurea in siblings with sickle cell disease. Am J Hematol. 2003 Feb; 72(2):121-6. PMID: 12555216.
    View in: PubMed
  158. Steinberg MH. Hydroxyurea treatment for sickle cell disease. ScientificWorldJournal. 2002 Jun 25; 2:1706-28. PMID: 12806165.
    View in: PubMed
  159. Steinberg MH, Brugnara C. Developing treatment for sickle cell disease. Expert Opin Investig Drugs. 2002 May; 11(5):645-59. PMID: 11996646.
    View in: PubMed
  160. Steinberg MH, Brugnara C. Pathophysiological-based approaches to treatment of sickle cell disease. Annu Rev Med. 2003; 54:89-112. PMID: 12359829.
    View in: PubMed
  161. Orringer EP, Casella JF, Ataga KI, Koshy M, Adams-Graves P, Luchtman-Jones L, Wun T, Watanabe M, Shafer F, Kutlar A, Abboud M, Steinberg M, Adler B, Swerdlow P, Terregino C, Saccente S, Files B, Ballas S, Brown R, Wojtowicz-Praga S, Grindel JM. Purified poloxamer 188 for treatment of acute vaso-occlusive crisis of sickle cell disease: A randomized controlled trial. JAMA. 2001 Nov 7; 286(17):2099-106. PMID: 11694150.
    View in: PubMed
  162. Steinberg MH, Rodgers GP. Pathophysiology of sickle cell disease: role of cellular and genetic modifiers. Semin Hematol. 2001 Oct; 38(4):299-306. PMID: 11605164.
    View in: PubMed
  163. Steinberg MH, Rodgers GP. Pharmacologic modulation of fetal hemoglobin. Medicine (Baltimore). 2001 Sep; 80(5):328-44. PMID: 11552087.
    View in: PubMed
  164. Steinberg MH. Modulation of fetal hemoglobin in sickle cell anemia. Hemoglobin. 2001 May; 25(2):195-211. PMID: 11480781.
    View in: PubMed
  165. Nagel RL, Steinberg MH. Role of epistatic (modifier) genes in the modulation of the phenotypic diversity of sickle cell anemia. Pediatr Pathol Mol Med. 2001 Mar-Apr; 20(2):123-36. PMID: 12673837.
    View in: PubMed
  166. Qu G, Elkins S, Steinberg MH. Thalassemia intermedia and extramedullary hematopoiesis associated with compound heterozygosity for the 532 bp deletion of the beta-globin gene and gene deletion hereditary persistence of fetal hemoglobin. Hemoglobin. 2001 Feb; 25(1):91-6. PMID: 11300354.
    View in: PubMed
  167. Mitchell T, Plonczynski M, McCollum A, Hardy CL, Safaya S, Steinberg MH. Gene expression profiling during erythroid differentiation of K562 cells. Blood Cells Mol Dis. 2001 Jan-Feb; 27(1):309-19. PMID: 11358393.
    View in: PubMed
  168. Steinberg MH, Forget BG, Higgs D, Nagel RL eds. Disorders of Hemoglobin: Genetics, Pathophysiology, Clinical Management. Cambridge University Press. Cambridge. 2001; 1268.
  169. Steinberg MH. Southern Society for Clinical Investigation Founders Medal recipient's address. Am J Med Sci. 2000 Sep; 320(3):161-2. PMID: 11014369.
    View in: PubMed
  170. Kopetz S, Steele CD, Brandt J, Baker A, Kronberg M, Galik E, Steinberg M, Warren A, Lyketsos CG. Characteristics and outcomes of dementia residents in an assisted living facility. Int J Geriatr Psychiatry. 2000 Jul; 15(7):586-93. PMID: 10918338.
    View in: PubMed
  171. Iyer R, Baliga R, Nagel RL, Brugnara C, Kirchner K, Hogan S, Steinberg MH. Maximum urine concentrating ability in children with Hb SC disease: effects of hydroxyurea. Am J Hematol. 2000 May; 64(1):47-52. PMID: 10815787.
    View in: PubMed
  172. Swedberg K, Bergh CH, Dickstein K, McNay J, Steinberg M. The effects of moxonidine, a novel imidazoline, on plasma norepinephrine in patients with congestive heart failure. Moxonidine Investigators. J Am Coll Cardiol. 2000 Feb; 35(2):398-404. PMID: 10676687.
    View in: PubMed
  173. Rosse WF, Narla M, Petz LD, Steinberg MH. New Views of Sickle Cell Disease Pathophysiology and Treatment. Hematology Am Soc Hematol Educ Program. 2000; 2-17. PMID: 11701532.
    View in: PubMed
  174. Steinberg MH, Mitchell TE. Novel approaches to treatment of sickle cell anaemia. Expert Opin Investig Drugs. 1999 Nov; 8(11):1823-1836. PMID: 11139827.
    View in: PubMed
  175. Solovey A, Gui L, Ramakrishnan S, Steinberg MH, Hebbel RP. Sickle cell anemia as a possible state of enhanced anti-apoptotic tone: survival effect of vascular endothelial growth factor on circulating and unanchored endothelial cells. Blood. 1999 Jun 1; 93(11):3824-30. PMID: 10339489.
    View in: PubMed
  176. Plonczynski M, Hardy CL, Safaya S, Harrell A, McCoy L, Brinson A, Agwarangbo L, Steinberg MH. Induction of globin synthesis in K562 cells is associated with differential expression of transcription factor genes. Blood Cells Mol Dis. 1999 Jun-Aug; 25(3-4):156-65. PMID: 10575541.
    View in: PubMed
  177. Belcher JD, Marker PH, Geiger P, Girotti AW, Steinberg MH, Hebbel RP, Vercellotti GM. Low-density lipoprotein susceptibility to oxidation and cytotoxicity to endothelium in sickle cell anemia. J Lab Clin Med. 1999 Jun; 133(6):605-12. PMID: 10360636.
    View in: PubMed
  178. Rhodes SL, Plonczynski M, Harrell A, Li J, Safaya S, Files JC, Steinberg MH. Double heterozygosity for the codon beta 39 C-to-T nonsense mutation and a triplicate alpha-globin gene locus can cause "dominantly" inherited beta-thalassemia intermedia. Am J Med Sci. 1999 May; 317(5):341-5. PMID: 10334122.
    View in: PubMed
  179. Steinberg MH. Management of sickle cell disease. N Engl J Med. 1999 Apr 1; 340(13):1021-30. PMID: 10099145.
    View in: PubMed
  180. Li J, Wilson D, Plonczynski M, Harrell A, Cook CB, Scheer WD, Zeng YT, Coleman MB, Steinberg MH. Genetic studies suggest a multicentric origin for Hb G-Coushatta [beta22(B4)Glu-->Ala]. Hemoglobin. 1999 Feb; 23(1):57-67. PMID: 10081986.
    View in: PubMed
  181. Steinberg MH, Lu ZH, Nagel RL, Venkataramani S, Milner PF, Huey L, Safaya S, Rieder RF. Hematological effects of atypical and Cameroon beta-globin gene haplotypes in adult sickle cell anemia. Am J Hematol. 1998 Oct; 59(2):121-6. PMID: 9766796.
    View in: PubMed
  182. Li J, Plonczynski M, Steinberg MH, Kheradpour A, Alter BP. Severe Hb S-beta+ thalassemia caused by IVS-I splice site mutations. Hemoglobin. 1998 Jul; 22(4):383-6. PMID: 9730369.
    View in: PubMed
  183. Steinberg MH. Pathophysiology of sickle cell disease. Baillieres Clin Haematol. 1998 Mar; 11(1):163-84. PMID: 10872477.
    View in: PubMed
  184. Adams-Graves P, Kedar A, Koshy M, Steinberg M, Veith R, Ward D, Crawford R, Edwards S, Bustrack J, Emanuele M. RheothRx (poloxamer 188) injection for the acute painful episode of sickle cell disease: a pilot study. Blood. 1997 Sep 1; 90(5):2041-6. PMID: 9292541.
    View in: PubMed
  185. Steinberg MH, Nagel RL, Brugnara C. Cellular effects of hydroxyurea in Hb SC disease. Br J Haematol. 1997 Sep; 98(4):838-44. PMID: 9326175.
    View in: PubMed
  186. Figueiredo MS, Steinberg MH. Fetal hemoglobin in sickle cell anemia: examination of phylogenetically conserved sequences within the locus control region but outside the cores of hypersensitive sites 2 and 3. Blood Cells Mol Dis. 1997 Aug; 23(2):188-200. PMID: 9236157.
    View in: PubMed
  187. Steinberg MH. Determinants of fetal hemoglobin response to hydroxyurea. Semin Hematol. 1997 Jul; 34(3 Suppl 3):8-14. PMID: 9317196.
    View in: PubMed
  188. Merritt D, Jones RT, Head C, Thibodeau SN, Fairbanks VF, Steinberg MH, Coleman MB, Rodgers GP. Hb Seal Rock [(alpha 2)142 term-->Glu, codon 142 TAA-->GAA]: an extended alpha chain variant associated with anemia, microcytosis, and alpha-thalassemia-2 (-3.7 Kb). Hemoglobin. 1997 Jul; 21(4):331-44. PMID: 9255612.
    View in: PubMed
  189. Steinberg MH, Lu ZH, Barton FB, Terrin ML, Charache S, Dover GJ. Fetal hemoglobin in sickle cell anemia: determinants of response to hydroxyurea. Multicenter Study of Hydroxyurea. Blood. 1997 Feb 1; 89(3):1078-88. PMID: 9028341.
    View in: PubMed
  190. Pegelow CH, Colangelo L, Steinberg M, Wright EC, Smith J, Phillips G, Vichinsky E. Natural history of blood pressure in sickle cell disease: risks for stroke and death associated with relative hypertension in sickle cell anemia. Am J Med. 1997 Feb; 102(2):171-7. PMID: 9217567.
    View in: PubMed
  191. Figueirido MS, Steinberg MH. 5' hypersensitive site-2 and fetal hemoglobin in Brazilians. Hemoglobin. 1996 Nov; 20(4):435-8. PMID: 8936469.
    View in: PubMed
  192. Charache S, Barton FB, Moore RD, Terrin ML, Steinberg MH, Dover GJ, Ballas SK, McMahon RP, Castro O, Orringer EP. Hydroxyurea and sickle cell anemia. Clinical utility of a myelosuppressive "switching" agent. The Multicenter Study of Hydroxyurea in Sickle Cell Anemia. Medicine (Baltimore). 1996 Nov; 75(6):300-26. PMID: 8982148.
    View in: PubMed
  193. Steinberg MH. Review: sickle cell disease: present and future treatment. Am J Med Sci. 1996 Oct; 312(4):166-74. PMID: 8853065.
    View in: PubMed
  194. Steinberg MH, Nagel RL, Lawrence C, Swaminathan V, Lu ZH, Plonczynski M, Harrell A. Beta-globin gene haplotype in Hb SC disease. Am J Hematol. 1996 Jul; 52(3):189-91. PMID: 8756085.
    View in: PubMed
  195. Browne PV, Mosher DF, Steinberg MH, Hebbel RP. Disturbance of plasma and platelet thrombospondin levels in sickle cell disease. Am J Hematol. 1996 Apr; 51(4):296-301. PMID: 8602630.
    View in: PubMed
  196. Lu ZH, Steinberg MH. Fetal hemoglobin in sickle cell anemia: relation to regulatory sequences cis to the beta-globin gene. Multicenter Study of Hydroxyurea. Blood. 1996 Feb 15; 87(4):1604-11. PMID: 8608254.
    View in: PubMed
  197. Steinberg MH. Modulation of the phenotypic diversity of sickle cell anemia. Hemoglobin. 1996 Feb; 20(1):1-19. PMID: 8745428.
    View in: PubMed
  198. Lee T, Esterhuyse T, Steinberg M, Schneider H. Demographic modelling of the HIV/AIDS epidemic on the Soweto population--results and health policy implications. S Afr Med J. 1996 Jan; 86(1):60-3. PMID: 8685784.
    View in: PubMed
  199. Steinberg MH, Ballas SK, Brunson CY, Bookchin R. Sickle cell anemia in septuagenarians. Blood. 1995 Nov 15; 86(10):3997-8. PMID: 7579371.
    View in: PubMed
  200. Ware RE, Steinberg MH, Kinney TR. Hydroxyurea: an alternative to transfusion therapy for stroke in sickle cell anemia. Am J Hematol. 1995 Oct; 50(2):140-3. PMID: 7572993.
    View in: PubMed
  201. Steinberg MH. Transient disappearance of sickle hemoglobin after transfusion. Blood. 1995 Jun 15; 85(12):3766-7. PMID: 7780160.
    View in: PubMed
  202. Steinberg MH. Genetic modulation of sickle cell anemia. Proc Soc Exp Biol Med. 1995 May; 209(1):1-13. PMID: 7724611.
    View in: PubMed
  203. Steinberg MH, Hsu H, Nagel RL, Milner PF, Adams JG, Benjamin L, Fryd S, Gillette P, Gilman J, Josifovska O, et al. Gender and haplotype effects upon hematological manifestations of adult sickle cell anemia. Am J Hematol. 1995 Mar; 48(3):175-81. PMID: 7532353.
    View in: PubMed
  204. Coleman MB, Lu ZH, Smith CM, Adams JG, Harrell A, Plonczynski M, Steinberg MH. Two missense mutations in the beta-globin gene can cause severe beta thalassemia. Hemoglobin Medicine Lake (beta 32[B14]leucine-->glutamine; 98 [FG5] valine-->methionine). J Clin Invest. 1995 Feb; 95(2):503-9. PMID: 7860732.
    View in: PubMed
  205. Coleman MB, Adams JG, Steinberg MH, Winter WP. A four base pair deletion 5' to the A gamma T gene is associated not only with decreased expression of the A gamma T-globin gene, but also of the G gamma-globin gene in cis. Am J Hematol. 1994 Dec; 47(4):307-11. PMID: 7526681.
    View in: PubMed
  206. Steinberg MH. Sickle cell anemia and fetal hemoglobin. Am J Med Sci. 1994 Nov; 308(5):259-65. PMID: 7526687.
    View in: PubMed
  207. Lu ZH, Steinberg MH. A new alpha alpha alpha anti-3.7 alpha-globin allele. Hemoglobin. 1994 Nov; 18(6):445-8. PMID: 7713750.
    View in: PubMed
  208. Waye JS, Eng B, Coleman MB, Steinberg MH, Alter BP. Delta beta-thalassemia in an African-American: identification of the deletion endpoints and PCR-based diagnosis. Hemoglobin. 1994 Nov; 18(6):389-99. PMID: 7713743.
    View in: PubMed
  209. Wethers DL, Ramirez GM, Koshy M, Steinberg MH, Phillips G, Siegel RS, Eckman JR, Prchal JT. Accelerated healing of chronic sickle-cell leg ulcers treated with RGD peptide matrix. RGD Study Group. Blood. 1994 Sep 15; 84(6):1775-9. PMID: 8080985.
    View in: PubMed
  210. Platt OS, Brambilla DJ, Rosse WF, Milner PF, Castro O, Steinberg MH, Klug PP. Mortality in sickle cell disease. Life expectancy and risk factors for early death. N Engl J Med. 1994 Jun 9; 330(23):1639-44. PMID: 7993409.
    View in: PubMed
  211. Embury SH, Hebbel RP, Mohandas N, Steinberg MH, eds. . Sickle Cell Disease: Basic Principles and Clinical Practice. Raven Press. New York. 1994; 902.
  212. Merat A, Haghshenas M, Pour ZM, Plonczynski MW, Harrell AN, Coleman MB, Steinberg MH. Beta-thalassemia in southwestern Iran. Hemoglobin. 1993 Oct; 17(5):427-37. PMID: 8294202.
    View in: PubMed
  213. Steinberg MH. DNA diagnosis for the detection of sickle hemoglobinopathies. Am J Hematol. 1993 Jun; 43(2):110-5. PMID: 8342537.
    View in: PubMed
  214. Steinberg MH. Sickle cell trait vs disease. Hosp Pract (Off Ed). 1993 May 15; 28(5):21. PMID: 8338571.
    View in: PubMed
  215. Steinberg MH. Case report: effects of iron deficiency and the -88 C-->T mutation on HbA2 levels in beta-thalassemia. Am J Med Sci. 1993 May; 305(5):312-3. PMID: 8484391.
    View in: PubMed
  216. Coleman MB, Adams JG, Steinberg MH, Plonczynski MW, Harrell AH, Castro O, Winter WP. G gamma A gamma (beta+) hereditary persistence of fetal hemoglobin: the G gamma -158 C-->T mutation in cis to the -175 T-->C mutation of the A gamma-globin gene results in increased G gamma-globin synthesis. Am J Hematol. 1993 Feb; 42(2):186-90. PMID: 7679879.
    View in: PubMed
  217. West MS, Wethers D, Smith J, Steinberg M. Laboratory profile of sickle cell disease: a cross-sectional analysis. The Cooperative Study of Sickle Cell Disease. J Clin Epidemiol. 1992 Aug; 45(8):893-909. PMID: 1624972.
    View in: PubMed
  218. Coleman MB, Adams JG, Plonczynski MW, Harrell AH, Walker AM, Fairbanks V, Steinberg MH. Beta-thalassemia intermedia with exceptionally high hemoglobin A2: relationship to mutations in the beta-gene promoter. Am J Med Sci. 1992 Aug; 304(2):73-8. PMID: 1380206.
    View in: PubMed
  219. Coleman MB, Steinberg MH, Harrell AH, Plonczynski MW, Walker AM, Adams JG. The -87 (C----A) beta(+)-thalassemia mutation in a black family. Hemoglobin. 1992; 16(5):399-401. PMID: 1428943.
    View in: PubMed
  220. Gupta AK, Kirchner KA, Nicholson R, Adams JG, Schechter AN, Noguchi CT, Steinberg MH. Effects of alpha-thalassemia and sickle polymerization tendency on the urine-concentrating defect of individuals with sickle cell trait. J Clin Invest. 1991 Dec; 88(6):1963-8. PMID: 1752955.
    View in: PubMed
  221. Coleman MB, Steinberg MH, Adams JG. A four-base deletion 5' to the A gamma globin gene is a common polymorphism. Blood. 1991 Nov 1; 78(9):2473-4. PMID: 1681964.
    View in: PubMed
  222. Steinberg MH. Prospects of gene therapy for hemoglobinopathies. Am J Med Sci. 1991 Nov; 302(5):298-303. PMID: 1750450.
    View in: PubMed
  223. Steinberg MH, Adams JG. Hemoglobin A2: origin, evolution, and aftermath. Blood. 1991 Nov 1; 78(9):2165-77. PMID: 1932737.
    View in: PubMed
  224. Waye JS, Chui DH, Eng B, Cai SP, Coleman MB, Adams JG, Steinberg MH. Hb S/beta zero-thalassemia due to the approximately 1.4-kb deletion is associated with a relatively mild phenotype. Am J Hematol. 1991 Oct; 38(2):108-12. PMID: 1719807.
    View in: PubMed
  225. Steinberg MH, Coleman MB, Adams JG, Waye JS, Chui DH. High hemoglobin A2 beta-thalassemia. J Lab Clin Med. 1991 Oct; 118(4):382. PMID: 1940581.
    View in: PubMed
  226. Adams JG, Hardy CL, Steinberg MH. Disappearance of the protein of a somatic mutation: a possible example of stem cell inactivation. Am J Physiol. 1991 Sep; 261(3 Pt 1):C448-54. PMID: 1887872.
    View in: PubMed
  227. Steinberg MH. The interactions of alpha-thalassemia with hemoglobinopathies. Hematol Oncol Clin North Am. 1991 Jun; 5(3):453-73. PMID: 1864819.
    View in: PubMed
  228. Steinberg MH. Erythropoietin for anemia of renal failure in sickle cell disease. N Engl J Med. 1991 May 9; 324(19):1369-70. PMID: 1759999.
    View in: PubMed
  229. Tsevat J, Wong JB, Pauker SG, Steinberg MH. Neonatal screening for sickle cell disease: a cost-effectiveness analysis. J Pediatr. 1991 Apr; 118(4 Pt 1):546-54. PMID: 1901081.
    View in: PubMed
  230. Coleman MB, Steinberg MH, Adams JG. Hemoglobin Terre Haute arginine beta 106. A posthumous correction to the original structure of hemoglobin Indianapolis. J Biol Chem. 1991 Mar 25; 266(9):5798-800. PMID: 2005117.
    View in: PubMed
  231. Waye JS, Cai SP, Eng B, Clark C, Adams JG, Chui DH, Steinberg MH. High hemoglobin A2 beta 0-thalassemia due to a 532-basepair deletion of the 5' beta-globin gene region. Blood. 1991 Mar 1; 77(5):1100-3. PMID: 1995096.
    View in: PubMed
  232. Rieder RF, Safaya S, Gillette P, Fryd S, Hsu H, Adams JG, Steinberg MH. Effect of beta-globin gene cluster haplotype on the hematological and clinical features of sickle cell anemia. Am J Hematol. 1991 Mar; 36(3):184-9. PMID: 1996558.
    View in: PubMed
  233. Steinberg MH. Sickle cell anemia: pathophysiology, management, and prospects for the future. J Clin Apher. 1991; 6(4):221-3. PMID: 1816243.
    View in: PubMed
  234. Weiss I, Cash FE, Coleman MB, Pressley A, Adams JG, Sanguansermsri T, Liebhaber SA, Steinberg MH. Molecular basis for alpha-thalassemia associated with the structural mutant hemoglobin Suan-Dok (alpha 2 109leu----arg) Blood. 1990 Dec 15; 76(12):2630-6. PMID: 2265255.
    View in: PubMed
  235. Adams JG, Steinberg MH, Kazazian HH. Isolation and characterization of the translation product of a beta-globin gene nonsense mutation (beta 121 GAA----TAA). Br J Haematol. 1990 Aug; 75(4):561-7. PMID: 2207008.
    View in: PubMed
  236. Steinberg MH. Sickle cell anaemia in a septuagenarian. Br J Haematol. 1989 Feb; 71(2):297-8. PMID: 2923816.
    View in: PubMed
  237. Steinberg MH. Thalassemia: molecular pathology and management. Am J Med Sci. 1988 Nov; 296(5):308-21. PMID: 3057912.
    View in: PubMed
  238. Kennedy AP, Williams B, Meydrech EF, Steinberg MH. Regional and temporal variation in oscillatory blood flow in sickle cell disease. Am J Hematol. 1988 Jun; 28(2):92-4. PMID: 2969189.
    View in: PubMed
  239. Steinberg MH, West MS, Gallagher D, Mentzer W. Effects of glucose-6-phosphate dehydrogenase deficiency upon sickle cell anemia. Blood. 1988 Mar; 71(3):748-52. PMID: 3345344.
    View in: PubMed
  240. Steinberg MH, Kelton JG, Coller BS. Plasma glycocalicin. An aid in the classification of thrombocytopenic disorders. N Engl J Med. 1987 Oct 22; 317(17):1037-42. PMID: 3657867.
    View in: PubMed
  241. Liebhaber SA, Coleman MB, Adams JG, Cash FE, Steinberg MH. Molecular basis for nondeletion alpha-thalassemia in American blacks. Alpha 2(116GAG----UAG). J Clin Invest. 1987 Jul; 80(1):154-9. PMID: 3597771.
    View in: PubMed
  242. Meyer LM, Adams JG, Steinberg MH, Miller IE, Stokes N. Screening for sickle cell trait: the Veterans Administration National Sickle Cell Program. Am J Hematol. 1987 Apr; 24(4):429-32. PMID: 3551591.
    View in: PubMed
  243. Steinberg MH, Adams JG, Morrison WT, Pullen DJ, Abney R, Ibrahim A, Rieder RF. Hemoglobin Mississippi (beta 44ser----cys). Studies of the thalassemic phenotype in a mixed heterozygote with beta +-thalassemia. J Clin Invest. 1987 Mar; 79(3):826-32. PMID: 2434529.
    View in: PubMed
  244. Steinberg MH, Embury SH. Alpha-thalassemia in blacks: interactions with the sickle hemoglobin gene. Birth Defects Orig Artic Ser. 1987; 23(5A):43-8. PMID: 3689929.
    View in: PubMed
  245. Adams JG, Morrison WT, Barlow RL, Steinberg MH. Hb Mississippi [beta 44(CD3)Ser----Arg]: a new variant with anomalous properties. Hemoglobin. 1987; 11(5):435-52. PMID: 3429243.
    View in: PubMed
  246. Steinberg MH. Determinants of vaso-occlusive severity in sickle cell disease. Prog Clin Biol Res. 1987; 240:413-28. PMID: 3303060.
    View in: PubMed
  247. Adams JG, Newman MV, Steinberg MH, DeSimone J. Effect of lead and ethanol upon gamma-globin synthesis in sickle reticulocytes. Am J Med Sci. 1986 Nov; 292(5):299-305. PMID: 2430453.
    View in: PubMed
  248. Steinberg MH, Embury SH. Alpha-thalassemia in blacks: genetic and clinical aspects and interactions with the sickle hemoglobin gene. Blood. 1986 Nov; 68(5):985-90. PMID: 3533181.
    View in: PubMed
  249. Steinberg MH, Gill F, Emanuel BS. Expression of two G-6-PD genes in an XX phenotypic male. Br J Haematol. 1986 Sep; 64(1):107-10. PMID: 3756097.
    View in: PubMed
  250. Kennedy AP, Walsh DA, Nicholson R, Adams JG, Steinberg MH. Influence of HbS levels upon the hematological and clinical characteristics of sickle cell trait. Am J Hematol. 1986 May; 22(1):51-4. PMID: 3953566.
    View in: PubMed
  251. Steinberg MH, Coleman MB, Adams JG, Hartmann RC, Saba H, Anagnou NP. A new gene deletion in the alpha-like globin gene cluster as the molecular basis for the rare alpha-thalassemia-1(--/alpha alpha) in blacks: HbH disease in sickle cell trait. Blood. 1986 Feb; 67(2):469-73. PMID: 3942832.
    View in: PubMed
  252. Adams JG, Coleman MB, Hayes J, Morrison WT, Steinberg MH. Modulation of fetal hemoglobin synthesis by iron deficiency. N Engl J Med. 1985 Nov 28; 313(22):1402-5. PMID: 2414661.
    View in: PubMed
  253. Steinberg MH. Sickle cell trait and splenic syndrome. JAMA. 1985 Oct 11; 254(14):1901-2. PMID: 4046113.
    View in: PubMed
  254. Steinberg MH. Role of hemoglobin instability in premature red cell destruction. Prog Clin Biol Res. 1985; 195:149-57. PMID: 4059266.
    View in: PubMed
  255. Steinberg MH, Coleman MB, Adams JG, Rosenstock W. Interaction between HBS-beta-o-thalassemia and alpha-thalassemia. Am J Med Sci. 1984 Dec; 288(5):195-9. PMID: 6083725.
    View in: PubMed
  256. Steinberg MH. Review: the sickle hemoglobinopathies--genetic analyses of common phenocopies and new molecular approaches to treatment. Am J Med Sci. 1984 Nov; 288(4):169-74. PMID: 6208780.
    View in: PubMed
  257. Dreiling BJ, Steinberg MH. Neglected iron deficiency. J Miss State Med Assoc. 1984 Sep; 25(9):231-3. PMID: 6492150.
    View in: PubMed
  258. Steinberg MH, Rosenstock W, Coleman MB, Adams JG, Platica O, Cedeno M, Rieder RF, Wilson JT, Milner P, West S. Effects of thalassemia and microcytosis on the hematologic and vasoocclusive severity of sickle cell anemia. Blood. 1984 Jun; 63(6):1353-60. PMID: 6722353.
    View in: PubMed
  259. Balducci L, Little DD, Khansur T, Steinberg MH. Carcinomatous meningitis in small cell lung cancer. Am J Med Sci. 1984 Jan-Feb; 287(1):31-3. PMID: 6322586.
    View in: PubMed
  260. Balducci L, Hardy C, Dreiling B, Tavassoli M, Steinberg MH. Pure red blood cell aplasia associated with paraproteinemia: in vitro studies of erythropoiesis. Haematologia (Budap). 1984; 17(3):353-7. PMID: 6442912.
    View in: PubMed
  261. Steinberg MH, Adams JG. Thalassemic hemoglobinopathies. Am J Pathol. 1983 Dec; 113(3):396-409. PMID: 6359893.
    View in: PubMed
  262. Steinberg MH, Coleman MB, Adams JG, Platica O, Gillette P, Rieder RF. The effects of alpha-thalassaemia in HbSC disease. Br J Haematol. 1983 Nov; 55(3):487-92. PMID: 6639890.
    View in: PubMed
  263. Steinberg MH, Gatling RR, Tavassoli M. Evidence of hyposplenism in the presence of splenomegaly. Scand J Haematol. 1983 Nov; 31(5):437-9. PMID: 6685914.
    View in: PubMed
  264. Steinberg MH, Hebbel RP. Clinical diversity of sickle cell anemia: genetic and cellular modulation of disease severity. Am J Hematol. 1983 Jun; 14(4):405-16. PMID: 6190397.
    View in: PubMed
  265. Balducci L, Little DD, Glover NG, Hardy CS, Steinberg MH. Granulocyte reserve in cancer and malnutrition. Ann Intern Med. 1983 May; 98(5 Pt 1):610-1. PMID: 6405668.
    View in: PubMed
  266. Teetson W, Cartwright C, Dreiling BJ, Steinberg MH. The leukocyte composition of peripheral blood buffy coat. Am J Clin Pathol. 1983 Apr; 79(4):500-1. PMID: 6837515.
    View in: PubMed
  267. Smith CM, Hedlund B, Cich JA, Tukey DP, Olson M, Steinberg MH, Adams JG. Hemoglobin North Shore: a variant hemoglobin associated with the phenotype of beta-thalassemia. Blood. 1983 Feb; 61(2):378-83. PMID: 6821704.
    View in: PubMed
  268. Steinberg MH, Dreiling BJ. Microcytosis. Its significance and evaluation. JAMA. 1983 Jan 7; 249(1):85-7. PMID: 6848788.
    View in: PubMed
  269. Hebbel RP, Eaton JW, Balasingam M, Steinberg MH. Spontaneous oxygen radical generation by sickle erythrocytes. J Clin Invest. 1982 Dec; 70(6):1253-9. PMID: 6294138.
    View in: PubMed
  270. Steinberg MH, Adams JG. beta-thalassemia-? Selected pseudogenes. Med Hypotheses. 1982 Dec; 9(6):599-604. PMID: 6820119.
    View in: PubMed
  271. Steinberg MH. Sickle cell anemia and iron deficiency. JAMA. 1982 Nov 5; 248(17):2112-3. PMID: 7120637.
    View in: PubMed
  272. Steinberg MH, Adams JG, Hendrix R. Sickle cell-beta-thalassemia: a common phenocopy of sickle cell anemia. J Miss State Med Assoc. 1982 Nov; 23(11):319-21. PMID: 7175930.
    View in: PubMed
  273. Adams JG, Morrison WT, Steinberg MH. Hemoglobin Parchman: double crossover within a single human gene. Science. 1982 Oct 15; 218(4569):291-3. PMID: 7123235.
    View in: PubMed
  274. Steinberg MH, Coleman MB, Adams JG. Beta-thalassemia with exceptionally high hemoglobin A2. Differential expression of the delta-globin gene in the presence of beta-thalassemia. J Lab Clin Med. 1982 Oct; 100(4):548-57. PMID: 6288819.
    View in: PubMed
  275. Steinberg MH, Adams JG. Thalassemia: recent insights into molecular mechanisms. Am J Hematol. 1982 Feb; 12(1):81-92. PMID: 6278929.
    View in: PubMed
  276. Hebbel RP, Eaton JW, Steinberg MH, White JG. Erythrocyte/endothelial interactions in the pathogenesis of sickle-cell disease: a "real logical" assessment. Blood Cells. 1982; 8(1):163-73. PMID: 7115974.
    View in: PubMed
  277. Hebbel RP, Moldow CF, Steinberg MH. Modulation of erythrocyte-endothelial interactions and the vasocclusive severity of sickling disorders. Blood. 1981 Nov; 58(5):947-52. PMID: 7296004.
    View in: PubMed
  278. Hebbel RP, Steinberg MH, Eaton JW. Erythrocyte calcium abnormalities in sickle cell disease. Prog Clin Biol Res. 1981; 51:321-32. PMID: 7022473.
    View in: PubMed
  279. Hebbel RP, Eaton JW, Steinberg MH, White JG. Erythrocyte/endothelial interactions and the vasocclusive severity of sickle cell disease. Prog Clin Biol Res. 1981; 55:145-62. PMID: 7291188.
    View in: PubMed
  280. Steinberg MH, Coleman MB, Garver FA, Grenett HE, Pressley A, Adams JG. Effects of dexamethasone on fetal hemoglobin synthesis in peripheral blood erythroid burst-forming units. Am J Hematol. 1981; 10(1):37-45. PMID: 6167163.
    View in: PubMed
  281. Adams JG, Steinberg MH. Low output hemoglobins which produce the phenotype of thalassemia. Prog Clin Biol Res. 1981; 55:81-98. PMID: 6895257.
    View in: PubMed
  282. Steinberg MH, Coleman MB, Pressley A, Adams JG. Globin biosynthesis in erythroid bursts of heterozygous alpha or beta thalassaemia. Br J Haematol. 1981 Jan; 47(1):57-65. PMID: 7437346.
    View in: PubMed
  283. Adams JG, Steinberg MH, Newman MV, Morrison WT, Benz EJ, Iyer R. beta-Thalassemia present in cis to a new beta-chain structural variant, Hb Vicksburg [beta 75 (E19)Leu leads to 0]. Proc Natl Acad Sci U S A. 1981 Jan; 78(1):469-73. PMID: 6165992.
    View in: PubMed
  284. Balducci L, Steinberg MH. Prolonged remission of metastatic rhabdomyosarcoma: The use of chemotherapy and nutritional support. J Miss State Med Assoc. 1980 Sep; 21(9):181-3. PMID: 6777498.
    View in: PubMed
  285. Hebbel RP, Boogaerts MA, Eaton JW, Steinberg MH. Erythrocyte adherence to endothelium in sickle-cell anemia. A possible determinant of disease severity. N Engl J Med. 1980 May 1; 302(18):992-5. PMID: 7366623.
    View in: PubMed
  286. Hebbel RP, Boogaerts MA, Koresawa S, Jacob HS, Eaton JW, Steinberg MH. Erytrocyte adherence to endothelium as a determinant of vasocclusive severity in sickle cell disease. Trans Assoc Am Physicians. 1980; 93:94-9. PMID: 7245585.
    View in: PubMed
  287. Balducci L, Dreiling B, Steinberg MH, Kakaiya RM, Morrison FS. Multifocal eosinophilic granuloma: description of an unusual case. South Med J. 1979 Jul; 72(7):884-5. PMID: 451705.
    View in: PubMed
  288. Adams JG, Steinberg MH, Boxer LA, Baehner RL, Forget BG, Tsistrakis GA. The structure of hemoglobin Indianapolis [beta112(G14) arginine]. An unstable variant detectable only by isotopic labeling. J Biol Chem. 1979 May 10; 254(9):3479-82. PMID: 429365.
    View in: PubMed
  289. Adams JG, Boxer LA, Baehner RL, Forget BG, Tsistrakis GA, Steinberg MH. Hemoglobin Indianapolis (beta 112[G14] arginine). An unstable beta-chain variant producing the phenotype of severe beta-thalassemia. J Clin Invest. 1979 May; 63(5):931-8. PMID: 447835.
    View in: PubMed
  290. Coleman MB, Steinberg MH, Oelshlegel FJ, Larson AD, Hart LT. Isolation of Plasmodium berghei by hemolysin lysis of infected erythrocytes and evidence for a parasite hexokinase. J Parasitol. 1979 Apr; 65(2):222-5. PMID: 376819.
    View in: PubMed
  291. Steinberg MH, Coleman MF, Pennebaker JB. Diamond-Blackfan syndrome: evidence for T-cell mediated suppression of erythroid development and a serum blocking factor associated with remission. Br J Haematol. 1979 Jan; 41(1):57-68. PMID: 311222.
    View in: PubMed
  292. Steinberg MH, Eaton JW, Berger E, Coleman MB, Oelshlegel FJ. Erythrocyte calcium abnormalities and the clinical severity of sickling disorders. Br J Haematol. 1978 Dec; 40(4):533-39. PMID: 728370.
    View in: PubMed
  293. Steinberg MH, Adams JG. Laboratory Diagnosis of sickling hemoglobinopathies. South Med J. 1978 Apr; 71(4):413-6. PMID: 635620.
    View in: PubMed
  294. Newcomb MM, Balducci L, Coleman MB, Steinberg MH. Erythroleukemia: in vitro studies of erythropoiesis. Am J Hematol. 1978; 5(4):291-5. PMID: 288310.
    View in: PubMed
  295. Steinberg MH, Adams JG. Hemoglobin F levels do not change during the painful crisis of sickle cell anemia. Am J Obstet Gynecol. 1977 Nov 15; 129(6):712-3. PMID: 920775.
    View in: PubMed
  296. Udomratn T, Steinberg MH, Campbell GD, Oelshlegel FJ. Effects of ascorbic acid on glucose-6-phosphate dehydrogenase-deficient erythrocytes: studies in an animal model. Blood. 1977 Mar; 49(3):471-5. PMID: 836955.
    View in: PubMed
  297. Steinberg MH, Dreiling BJ, Lovell WJ. Sickle cell anemia: erythrokinetics, blood volumes, and a study of possible determinants of severity. Am J Hematol. 1977; 2(1):17-23. PMID: 868865.
    View in: PubMed
  298. Adams JG, Steinberg MH. Alpha-thalassemia. Am J Hematol. 1977; 2(3):317-25. PMID: 596373.
    View in: PubMed
  299. Steinberg MH, Coleman M, Dreiling B. Unbalanced globin chain synthesis in erythroid precursor cells of heterozygous alpha-thalassaemia. Br J Haematol. 1976 Sep; 34(1):55-60. PMID: 952769.
    View in: PubMed
  300. Steinberg MH, Lovell WJ, Wells S, Coleman M, Dreiling BJ, Adams JG. Hemoglobin Hope: studies of oxygen equilibrium in heterozygotes, hemoglobin S-Hope disease, and isolated hemoglobin Hope. J Lab Clin Med. 1976 Jul; 88(1):125-31. PMID: 932531.
    View in: PubMed
  301. Udomratn T, Steinberg MH, Dreiling BJ, Lockhard V. Circulating micromegakaryocytes signaling blast transformation of chronic myeloid leukaemia. Scand J Haematol. 1976 May; 16(5):394-400. PMID: 1065956.
    View in: PubMed
  302. Steinberg MH, Dreiling BJ. Clinical, hematologic and biosynthetic studies in sickle cell-betao-thalassemia: a comparison with sickle cell anemia. Am J Hematol. 1976; 1(1):35-44. PMID: 984035.
    View in: PubMed
  303. Steinberg MH. Haemoglobin C/alpha thalassaemia: haematological and biosynthetic studies. Br J Haematol. 1975 Jul; 30(3):337-42. PMID: 1201216.
    View in: PubMed
  304. Campbell GD, Steinberg MH, Bower JD. Letter: Ascorbic acid-induced hemolysis in G-6-PD deficiency. Ann Intern Med. 1975 Jun; 82(6):810. PMID: 1138591.
    View in: PubMed
  305. Steinberg MH, Adams JG, Dreiling BJ. Alpha thalassaemia in adults with sickle-cell trait. Br J Haematol. 1975 May; 30(1):31-7. PMID: 1191571.
    View in: PubMed
  306. Steinberg MH, Adams JG, Thigpen JT, Morrison FS, Dreiling BJ. Hemoglobin Hope (alpha 2 beta 2(136-gly-asp))-S disease: clinical and biochemical studies. J Lab Clin Med. 1974 Nov; 84(5):632-42. PMID: 4283785.
    View in: PubMed
  307. Steinberg MH. Letter: Leukocyte alkaline phosphatase. Ann Intern Med. 1974 Aug; 81(2):274. PMID: 4843592.
    View in: PubMed
  308. Steinberg MH, Dreiling BJ. Glucose-6-phosphate dehydrogenase deficiency in Sickle-cell anemia. A study in adults. Ann Intern Med. 1974 Feb; 80(2):217-20. PMID: 4811795.
    View in: PubMed
  309. Thigpen JT, Steinberg MH, Beutler E, Gillespie GT, Dreiling BJ, Morrison FS. Glucose-6-phosphate dehydrogenase Jackson. A new variant associated with hemolytic anemia. Acta Haematol. 1974; 51(5):310-4. PMID: 4209318.
    View in: PubMed
  310. Steinberg MH, Breiling BJ. Vascular lesions in hemophilia B. N Engl J Med. 1973 Sep 13; 289(11):592. PMID: 4723113.
    View in: PubMed
  311. Willard RF, Lovell WJ, Dreiling BJ, Steinberg MH. Electrophoresis of hemoglobin on polyacrylamide gels: precise method for measurement of hemoglobin A2. Clin Chem. 1973 Sep; 19(9):1082-4. PMID: 4744815.
    View in: PubMed
  312. Steinberg MH, Dreiling BJ. Chronic granulocytic leukemia. Prolonged survival, muscle infiltration and sea-blue histiocytosis. Am J Med. 1973 Jul; 55(1):93-8. PMID: 4123736.
    View in: PubMed
  313. Steinberg MH, Dreiling BJ, Morrison FS, Necheles TF. Mild sickle cell disease. Clinical and laboratory studies. JAMA. 1973 Apr 16; 224(3):317-21. PMID: 4739533.
    View in: PubMed
  314. Steinberg MH, Dreiling BJ, Robinson F, Hallford C. The ultrastructure of developing bone marrow implants: a scanning electron microscope study. Acta Anat (Basel). 1973; 84(1):1-9. PMID: 4265082.
    View in: PubMed
  315. Morrison FS, Tatum WT, Dreiling BJ, Steinberg MH. Hodgkin's disease--a curable malignancy. J Miss State Med Assoc. 1972 Feb; 13(2):45-7. PMID: 5059229.
    View in: PubMed
  316. Steinberg MH, Charm SE. Effect of high concentrations of leukocytes on whole blood viscosity. Blood. 1971 Sep; 38(3):299-301. PMID: 5289281.
    View in: PubMed
  317. Steinberg MH, Necheles TF. Erythrocyte glutathione peroxidase deficiency. Biochemical studies on the mechanisms of drug-induced hemolysis. Am J Med. 1971 Apr; 50(4):542-6. PMID: 5572598.
    View in: PubMed
  318. Necheles TF, Steinberg MH, Cameron D. Erythrocyte glutathione-peroxidase deficiency. Br J Haematol. 1970 Nov; 19(5):605-12. PMID: 5481505.
    View in: PubMed
  319. Steinberg MH, Geary CG, Crosby WH. Acute granulocytic leukemia complicating Hodgkin's disease. Arch Intern Med. 1970 Mar; 125(3):496-8. PMID: 5264513.
    View in: PubMed
  320. Steinberg M, Brauer MJ, Necheles TF. Acute hemolytic anemia associated with erythrocyte glutathione-peroxidase deficiency. Arch Intern Med. 1970 Feb; 125(2):302-3. PMID: 5412019.
    View in: PubMed
Martin's Networks
Click the "See All" links for more information and interactive visualizations!
Concepts
_
BU Co-Authors
_
Similar BU People
_
Same Department