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

Access to resources Recommend Favorite

Smooth pursuit eye movements and otolith–ocular responses are differently impaired in cerebellar ataxia

By Anastasopoulos D   Haslwanter T   Fetter M   Dichgans J  

Brain, Vol. 121, Iss. 8, 1998-08 ,pp. : 1497-1505

Oxford University Press

Access to resources Recommend Favorite

Novel splice site CACNA1A mutation causing episodic ataxia type 2

By Kaunisto M.   Harno H.   Kallela M.   Somer H.   Sallinen R.   Hämäläinen E.   Miettinen P.J.   Vesa J.   Orpana A.   Palotie A.   Färkkilä M.   Wessman M.  

Neurogenetics, Vol. 5, Iss. 1, 2004-02 ,pp. : 69-73

Springer Publishing Company

Access to resources Recommend Favorite

Cerebellar ataxia with oculomotor apraxia type 1: clinical and genetic studies

By Le Ber Isabelle  

Brain, Vol. 126, Iss. 12, 2003-12 ,pp. : 2761-2772

Oxford University Press

Access to resources Recommend Favorite

Human lissencephaly with cerebellar hypoplasia due to mutations in : expansion of the foetal neuropathological phenotype

By Lecourtois Magalie   Poirier Karine   Friocourt Gaëlle   Jaglin Xavier   Goldenberg Alice   Saugier-Veber Pascale   Chelly Jamel   Laquerrière Annie  

Acta Neuropathologica, Vol. 119, Iss. 6, 2010-06 ,pp. : 779-789

Springer Publishing Company

Access to resources Recommend Favorite