Zobrazeno 1 - 4
of 4
pro vyhledávání: '"S M Zuberi"'
Autor:
A. Jollands, Angela Vincent, E Reavey, S MacLeod, M Kirkpatrick, M O'Regan, B Lang, K. Stewart, A McLellan, T Moloney, Joseph D. Symonds, L Dorris, N. Williams, S M Zuberi, Rachael Ellis
Publikováno v:
Scottish Medical Journal. 63:35-37
Autor:
S M, Zuberi, L H, Eunson, A, Spauschus, R, De Silva, J, Tolmie, N W, Wood, R C, McWilliam, J B, Stephenson, J P, Stephenson, D M, Kullmann, M G, Hanna
Publikováno v:
Brain. 122:817-825
Episodic ataxia type 1 (EA1) is a rare autosomal dominant disorder characterized by brief episodes of ataxia associated with continuous interattack myokymia. Point mutations in the human voltage-gated potassium channel (Kv1.1) gene on chromosome 12p1
Autor:
S. M. Zuberi, J. D. Symonds
Publikováno v:
Epilepsy and Intellectual Disabilities ISBN: 9781848002586
Epilepsy and Intellectual Disabilities ISBN: 9783319391427
Epilepsy and Intellectual Disabilities ISBN: 9783319391427
Misdiagnosis of epilepsy in both adult and pediatric populations is unfortunately very common. Accurate diagnosis of epilepsy relies primarily on sound history taking. Having a thorough knowledge of the many imitators of epileptic seizures helps the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::100fe1241fa121c45c0aefee67151413
https://doi.org/10.1007/978-1-84800-259-3_5
https://doi.org/10.1007/978-1-84800-259-3_5
Autor:
L H, Eunson, R, Rea, S M, Zuberi, S, Youroukos, C P, Panayiotopoulos, R, Liguori, P, Avoni, R C, McWilliam, J B, Stephenson, M G, Hanna, D M, Kullmann, A, Spauschus
Publikováno v:
Annals of neurology. 48(4)
Episodic ataxia type 1 (EA1) is an autosomal dominant central nervous system potassium channelopathy characterized by brief attacks of cerebellar ataxia and continuous interictal myokymia. Point mutations in the voltage-gated potassium channel gene K