Episodic ataxias
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Publisher
Elsevier
Reference69 articles.
1. Familial episodic ataxia: clinical heterogeneity in four families linked to chromosome 19p;Baloh;Ann Neurol,1997
2. Familial periodic ataxia responsive to flunarizine;Boel;Neuropediatrics,1988
3. Episodic ataxia/myokymia syndrome is associated with point mutations in the human potassium channel gene, KCNA1;Browne;Nat Genet,1994
4. Kv1.1 knock-in ataxic mice exhibit spontaneous myokymic activity exacerbated by fatigue, ischemia and low temperature;Brunetti;Neurobiol Dis,2012
5. Mutation of the Ca2+ channel beta subunit gene Cchb4 is associated with ataxia and seizures in the lethargic (lh) mouse;Burgess;Cell,1997
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