Paroxysmal Cerebellar Ataxia
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When MRI is a Clue in Episodic Ataxia
Neurol 93:e2074-e2075, Dhawan, S.R.,et al, 2019
Primary Episodic Ataxias:Diagnosis, Pathogenesis and Treatment
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Clinical Spectrum of Episodic Ataxia Type 2
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Neurological Channelopathies, Dysfunctional Ion Channels May Cause Many Neurological Diseases
BMJ 316:1104-1105, Rose,M.R., 1998
Ion Channels and Neurological Disease:DNA Based Diagnosis is Now Possible,and Ion Channels May be Important in Common Paroxysmal Disorders
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Familial episodic Ataxia:Clinical Heterogeneity in Four Families Linked to Chromosome 19p
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Calcium Channels in Neurological Disease
Ann Neurol 42:275-282, Greenberg,D.A., 1997
Spinocerebellar Ataxia Type 6, Frequency of the Mutation & Genotype-Phenotype Correl
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The Inherited Ataxias and the New Genetics
JNNP 61:327-332, Hammans,S.R., 1996
A Gene for Hereditary Paroxysmal Cerebellar Ataxia Maps to Chromosome 19p
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Acetazolamide-Responsive Episodic Ataxia Syndrome
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Familial Periodic Ataxia
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Hereditary Paroxysmal Ataxia:Response to Acetazolamide
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