Résultats de la recherche

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Movement disorders in mitochondrial diseases.
Pathophysiogical and therapeutic progress in Friedreich ataxia
The autosomal recessive cerebellar ataxias
Pitfalls in ataxia with ocular motor apraxia type 1: pseudodominant inheritance and very late onset
From anti-GAD to ataxia with ocular motor apraxia type 2: through the looking glass
Small fiber neuropathy in a woman with fragile X-associated tremor/ataxia syndrome (FXTAS)
SPG15: a cause of juvenile atypical levodopa responsive parkinsonism
Emerging topics in FXTAS
Dalfampridine in hereditary spastic paraplegia: a prospective, open study
Erratum: Emerging topics in FXTAS
A Recurrent Mutation in CACNA1G Alters Cav3.1 T-Type Calcium-Channel Conduction and Causes Autosomal-Dominant Cerebellar Ataxia
Genes for spinocerebellar ataxia with blindness and deafness (SCABD/SCAR3, MIM# 271250 and SCABD2)
Exonic deletions of FXN and early-onset Friedreich ataxia

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