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

Access to resources Recommend Favorite

Cortical thickness abnormality in juvenile myoclonic epilepsy

By Tae W.  

Journal of Neurology, Vol. 255, Iss. 4, 2008-04 ,pp. : 561-566

Springer Publishing Company

Access to resources Recommend Favorite

In cis autosomal dominant mutation of Senataxin associated with tremor/ataxia syndrome

By Bassuk A.   Chen Y.   Batish S.   Nagan N.   Opal P.   Chance P.   Bennett C.  

Neurogenetics, Vol. 8, Iss. 1, 2007-01 ,pp. : 45-49

Springer Publishing Company

Access to resources Recommend Favorite

Autosomal dominant epilepsy with febrile seizures plus with missense mutations of the (Na + )-channel 1 subunit gene, SCN1A

By Ito M.   Nagafuji H.   Okazawa H.   Yamakawa K.   Sugawara T.   Mazaki-Miyazaki E.   Hirose S.   Fukuma G.   Mitsudome A.   Wada K.   Kaneko S.  

Epilepsy Research, Vol. 48, Iss. 1, 2002-01 ,pp. : 15-23

Elsevier

Access to resources Recommend Favorite

A new autosomal recessive spastic ataxia associated with frequent white matter changes maps to 2q33–34

By Thiffault I.   Rioux M. F.   Tetreault M.   Jarry J.   Loiselle L.   Poirier J.   Gros-Louis F.   Mathieu J.   Vanasse M.   Rouleau G. A.   Bouchard J. P.   Lesage J.   Brais B.  

Brain, Vol. 129, Iss. 9, 2006-09 ,pp. : 2332-2340

Oxford University Press

Access to resources Recommend Favorite