Click the Why column to see why an item matched the search.
| Match | Type | Why |
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| Genetic variation of the transthyretin gene in wild-type transthyretin amyloidosis (ATTRwt). | Academic Article |
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| Structural Characterization of Cardiac Ex Vivo Transthyretin Amyloid: Insight into the Transthyretin Misfolding Pathway In Vivo. | Academic Article |
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| Identification of novel transthyretin variants in familial transthyretin amyloidosis by mass spectrometric peptide mapping | Academic Article |
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| Pressure-volume relationships in patients with transthyretin (ATTR) cardiac amyloidosis secondary to V122I mutations and wild-type transthyretin: Transthyretin Cardiac Amyloid Study (TRACS). | Academic Article |
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| The prealbumin nature of the amyloid protein in familial amyloid polyneuropathy (FAP)-swedish variety. | Academic Article |
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| Characterization of transthyretin variants in familial transthyretin amyloidosis by mass spectrometric peptide mapping and DNA sequence analysis. | Academic Article |
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| Identification of a novel transthyretin Thr59Lys/Arg104His. A case of compound heterozygosity in a Chinese patient diagnosed with familial transthyretin amyloidosis. | Academic Article |
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| Identification of S-sulfonation and S-thiolation of a novel transthyretin Phe33Cys variant from a patient diagnosed with familial transthyretin amyloidosis. | Academic Article |
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| Prospective evaluation of the morbidity and mortality of wild-type and V122I mutant transthyretin amyloid cardiomyopathy: the Transthyretin Amyloidosis Cardiac Study (TRACS). | Academic Article |
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| Use of Serum Transthyretin as a Prognostic Indicator and Predictor of Outcome in Cardiac Amyloid Disease Associated With Wild-Type Transthyretin. | Academic Article |
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| A new amyloidogenic transthyretin variant (Val122Ala) found in a compound heterozygous patient. | Academic Article |
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| A new transthyretin variant (Glu61Gly) associated with cardiomyopathy. | Academic Article |
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| A new transthyretin variant (Ser23Asn) associated with familial amyloidosis in a Portuguese patient. | Academic Article |
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| A rare transthyretin mutation (Asp18Glu) associated with cardiomyopathy. | Academic Article |
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| A second transthyretin mutation at position 33 (Leu/Phe) associated with familial amyloidotic polyneuropathy. | Academic Article |
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