Results 211 to 217 of about 125,979 (217)
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Clinical and genetic spectrum of SCN2A-associated episodic ataxia
European Journal of Paediatric Neurology, 2019Kathleen M Gorman, G Kluger, T Bast
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De novo mutation in CACNA1A caused acetazolamide-responsive episodic ataxia
1998Stanley Nelson, Joanna Jen, Q Yue
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Episodic ataxia/myokymia mutations functionally expressed in the Shaker potassium channel
Neuroscience, 1999Linda M Boland, D L Price
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Episodic ataxia type 1: A neuronal potassium channelopathy
Neurotherapeutics, 2007Dimitri Kullmann +2 more
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Episodic Ataxia Type 1 with Distal Weakness: A Novel Manifestation of a Potassium Channelopathy
Neuropediatrics, 2004R W Baloh
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Familial episodic ataxia in lambs
New Zealand Veterinary Journal, 2013Anne Ridler, Hugh Blair, R D Jolly
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Case report of novel CACNA1A gene mutation causing episodic ataxia type 2
SAGE Open Medical Case Reports, 2017Michael Bradshaw, Peter Hedera
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