Nerve excitability studies characterize K V 1.1 fast potassium channel dysfunction in patients with episodic ataxia type 1

By Tomlinson Susan E.  

Brain, Vol. 133, Iss. 12, 2010-12 ,pp. : 3530-3540

Oxford University Press

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A novel mutation in the human voltage-gated potassium channel gene ( Kv1.1 ) associates with episodic ataxia type 1 and sometimes with partial epilepsy

By Zuberi S. M.   Eunson L. H.   Spauschus A.   De Silva R.   Tolmie J.   Wood N. W.   McWilliam R. C.   Stephenson J. P. B.   Kullmann D. M.   Hanna M. G.  

Brain, Vol. 122, Iss. 5, 1999-05 ,pp. : 817-825

Oxford University Press

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Otolith function in cerebellar ataxia due to mutations in the calcium channel gene CACNA1A

By Wiest Gerald  

Brain, Vol. 124, Iss. 12, 2001-12 ,pp. : 2407-2416

Oxford University Press

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Spinocerebellar ataxia type 2: polyQ repeat variation in the CACNA1A calcium channel modifies age of onset

By Pulst Stefan-M.  

Brain, Vol. 128, Iss. 10, 2005-10 ,pp. : 2297-2303

Oxford University Press

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A TASK3 channel (KCNK9) mutation in a genetic model of absence epilepsy

By Holter Jethro   Carter David   Leresche Nathalie   Crunelli Vincenzo   Vincent Pierre  

Journal of Molecular Neuroscience, Vol. 25, Iss. 1, 2005-02 ,pp. : 37-51

Humana Press, Inc

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