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Gomez, ChristopherPerson Why?
(1)H MR spectroscopy in Friedreich's ataxia and ataxia with oculomotor apraxia type 2.Academic Article Why?
Prevalence of RFC1-mediated spinocerebellar ataxia in a North American ataxia cohort.Academic Article Why?
Measuring Friedreich ataxia: complementary features of examination and performance measures.Academic Article Why?
Ophthalmologic features of the common spinocerebellar ataxias.Academic Article Why?
Postural Tremor and Ataxia Progression in Spinocerebellar Ataxias.Academic Article Why?
The Initial Symptom and Motor Progression in Spinocerebellar Ataxias.Academic Article Why?
C9orf72 repeat expansions as genetic modifiers for depression in spinocerebellar ataxias.Academic Article Why?
Clinical evaluation of eye movements in spinocerebellar ataxias: a prospective multicenter study.Academic Article Why?
Coenzyme Q10 and spinocerebellar ataxias.Academic Article Why?
Depression and clinical progression in spinocerebellar ataxias.Academic Article Why?
Distinct neurochemical profiles of spinocerebellar ataxias 1, 2, 6, and cerebellar multiple system atrophy.Academic Article Why?
Dystonia and ataxia progression in spinocerebellar ataxias.Academic Article Why?
Neurochemical abnormalities in premanifest and early spinocerebellar ataxias.Academic Article Why?
The autosomal dominant spinocerebellar ataxias: emerging mechanistic themes suggest pervasive Purkinje cell vulnerability.Academic Article Why?
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