Search Results (144)
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Spinocerebellar ataxia type 8: molecular genetic comparisons and haplotype analysis of 37 families with ataxia.Academic Article Why?
Psychosis in Spinocerebellar Ataxias: a Case Series and Study of Tyrosine Hydroxylase in Substantia Nigra.Academic Article Why?
Knee Stability and Movement Coordination Impairments: Knee Ligament Sprain Revision 2017.Academic Article Why?
Protein kinase C gamma, a protein causative for dominant ataxia, negatively regulates nuclear import of recessive-ataxia-related aprataxin.Academic Article Why?
A novel AFG3L2 mutation in a Somalian patient with spinocerebellar ataxia type 28.Academic Article Why?
Fragile X carrier screening and spinocerebellar ataxia in older males.Academic Article Why?
Acute Ataxia in Children: A Review of the Differential Diagnosis and Evaluation in the Emergency Department.Academic Article Why?
Myoclonic Cerebellar DyssynergiaConcept Why?
Treatment with a catalytic antioxidant corrects the neurobehavioral defect in ataxia-telangiectasia mice.Academic Article Why?
Abnormal processing of transfected plasmid DNA in cells from patients with ataxia telangiectasia.Academic Article Why?
Ataxia after pontine stroke: insights from pontocerebellar fibers in monkey.Academic Article Why?
Ataxia and vision loss: flow cytometric diagnosis of primary central nervous system lymphoma.Academic Article Why?
Ataxia without telangiectasia.Academic Article Why?
Ataxia, dementia, and hypogonadotropism caused by disordered ubiquitination.Academic Article Why?
Cerebrospinal fluid GABA and homocarnosine concentrations in patients with Friedreich's ataxia, Parkinson's disease, and Huntington's chorea.Academic Article Why?
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