Results 151 to 160 of about 2,519,053 (161)

Episodic Ataxia Type 2 (EA2) and Spinocerebellar Ataxia Type 6 (SCA6) Due to CAG Repeat Expansion in the CACNA1A Gene on Chromosome 19p

Human Molecular Genetics, 1997
Flavia Trettel, Liana Veneziano, Elide Mantuano   +2 more
exaly  

Is the CACNA1A gene involved in familial migraine with aura?

Neurological Sciences, 2014
Massimo Leone, Renato Mantegazza, Raffaella Brugnoni   +2 more
exaly  

Novel frameshift mutation in the CACNA1A gene causing a mixed phenotype of episodic ataxia and familiar hemiplegic migraine

European Journal of Paediatric Neurology, 2015
Alexander Storch, M von der Hagen, M Smitka   +2 more
exaly  

Phenotypic Variability in a Four Generation Family With a p.Thr666Met CACNA1A Gene Mutation

Pediatric Neurology, 2014
Maria García-Baró-Huarte, Marina Garcia Morin, Maria Slocker-Barrio   +2 more
exaly  

CACNA1A Nonsense Mutation is Associated With Basilar‐Type Migraine and Episodic Ataxia Type 2

Headache, 2009
Matthew Robbins
exaly  

Haplotype and linkage disequilibrium analysis to characterise a region in the calcium channel gene CACNA1A associated with idiopathic generalised epilepsy

European Journal of Human Genetics, 2002
Sham Pc, Lina Nashef, B A Chioza
exaly  

Late-onset episodic ataxia type 2 associated with a novel loss-of-function mutation in the CACNA1A gene

Journal of the Neurological Sciences, 2009
Bru Cormand, Alfons Macaya Ruiz, Roser Corominas   +2 more
exaly  

Case report of novel CACNA1A gene mutation causing episodic ataxia type 2

SAGE Open Medical Case Reports, 2017
Michael Bradshaw, Peter Hedera
exaly  

Pseudomigraine With Lymphocytic Pleocytosis: A Calcium Channelopathy? Clinical Description of 10 Cases and Genetic Analysis of the Familial Hemiplegic Migraine Gene CACNA1A

Headache, 2003
Terrance Snutch
exaly  

No Involvement of the Calcium Channel Gene (CACNA1A) in a Family with Cluster Headache

Cephalalgia, 2001
Michel D Ferrari, Gisela Terwindt, E E Kors   +2 more
exaly