Episodic Ataxia Syndrome: Longitudinal Study

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Familial Hemiplegic Migraine and Episodic Ataxia Type-2 Are Caused by Mutations in the Ca2+ Channel Gene CACNL1A4

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The MOS 36-ltem Short-Form Health Survey (SF-36): I. Conceptual Framework and Item Selection

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Episodic ataxia/myokymia syndrome is associated with point mutations in the human potassium channel gene, KCNA1

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Deletion of the KV1.1 Potassium Channel Causes Epilepsy in Mice

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Localization of Kv1.1 and Kv1.2, two K channel proteins, to synaptic terminals, somata, and dendrites in the mouse brain

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Clinical spectrum of episodic ataxia type 2

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Treatment of episodic ataxia type 2 with the potassium channel blocker 4-aminopyridine

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Familial episodic ataxia: Clinical heterogeneity in four families linked to chromosome 19p

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Familial paroxysmal kinesigenic ataxia and continuous myokymia.

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Hereditary paroxysmal ataxia

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Hereditary myokymia and periodic ataxia

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A gene for hereditary paroxysmal cerebellar ataxia maps to chromosome 19p

K. Vahedi, A. Joutel, P. van Bogaert, et al.. (1995). Annals of Neurology. Cited 126 times. https://doi.org/10.1002/ANA.410370304

Autosomal dominant episodic ataxia: A heterogeneous syndrome

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A gene for episodic ataxia/myokymia maps to chromosome 12p13.

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Familial periodic cerebellar ataxia: A problem of cerebellar intracellular pH homeostasis

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An autosomal dominant disorder with episodic ataxia, vertigo, and tinnitus

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Periodic vestibulocerebellar ataxia, an autosomal dominant ataxia with defective smooth pursuit, is genetically distinct from other autosomal dominant ataxias.

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Vestibulocerebellar ataxia. A newly defined hereditary syndrome with periodic manifestations.

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A locus for the nystagmus-associated form of episodic ataxia maps to an 11-cM region on chromosome 19p.

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Familial Periodic Ataxia Responsive to Flunarizine

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Sporadic late onset paroxysmal cerebellar ataxia in four unrelated patients: a new disease?

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Neurotological findings in a family with episodic ataxia

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