Neuroimaging Features of Biotinidase Deficiency
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Clinicopathologic Conference, Biotinthiamine-Responsive Basal Ganglia Disease Due to Mutation SLC19A3
NEJM 377:2376-2385, Case 38-2017, 2017
MRI Findings of Biotin-Responsive Basal Ganglia Disease Before and After Treatment
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The Autosomal Recessive Cerebellar Ataxias
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The Clinical Spectrum of Familial Hemiplegic Migraine Associated with Mutations in a Neuronal Calcium Channel
NEJM 345:17-24,57, Ducros,A.,et al, 2001
A Gene for Hereditary Paroxysmal Cerebellar Ataxia Maps to Chromosome 19p
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Narcolspey
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