Results 141 to 150 of about 2,519,053 (161)

EEG patterns in each phase of hemiplegic migraine: a systematic review and pooled prevalence meta-analysis. [PDF]

J Headache Pain
Kedgan P, Anukoolwittaya P, Surawattanawong T, Thanprasertsuk S, Rattanawong W, Limotai C.   +5 more
europepmc   +1 more source

A Bioinformatic Study of Genetics Involved in Determining Mild Traumatic Brain Injury Severity and Recovery. [PDF]

Biomedicines
Tajik M, Noseworthy MD.
europepmc   +1 more source

Genotype mutations and phenotypes of 30 cases with epilepsy related to fever sensitivity in children. [PDF]

Front Neurol
Wang Y, Zhang L, Ma J, Jing M, Hua Y, Liu Y, Fan X.   +6 more
europepmc   +1 more source

Unbiased human genomic characterization of polyglutamine disorder genes to guide biological understanding and therapeutic strategies. [PDF]

HGG Adv
Namuli KL, Drögemöller BI, Wright GEB.
europepmc   +1 more source

Sporadic hemiplegic migraine and epilepsy associated with CACNA1A gene mutation

Epilepsy and Behavior, 2010
Familial hemiplegic migraine (FHM) is a clinically and genetically heterogeneous disease most commonly linked to CACNA1A gene mutation. Epilepsy rarely occurs in FHM and is seen predominantly with specific CACNA1A gene mutations.
A A Asadi-Pooya
exaly   +2 more sources

Identification of novel and recurrent CACNA1A gene mutations in fifteen patients with episodic ataxia type 2

Journal of the Neurological Sciences, 2010
Episodic ataxia type 2 is a rare autosomal dominant disease characterized by recurrent attacks of vertigo and cerebellar ataxia. The disease was caused by mutations in the CACNA1A gene, on chromosome 19p.
Giovanna Zorzi, Marina Frontali, Cinzia Gellera   +2 more
exaly   +2 more sources

Second Cistron in CACNA1A Gene Encodes a Transcription Factor Mediating Cerebellar Development and SCA6 [PDF]

Cell, 2013
SummaryThe CACNA1A gene, encoding the voltage-gated calcium channel subunit α1A, is involved in pre- and postsynaptic Ca2+ signaling, gene expression, and several genetic neurological disorders.
Christian Hansel, Kay-Marie Lamar, Christopher Gomez   +2 more
exaly   +2 more sources

Electroencephalographic changes and seizures in familial hemiplegic migraine patients with the CACNA1A gene S218L mutation

Journal of Clinical Neuroscience, 2008
The S218L CACNA1A mutation has been previously described in two families with familial hemiplegic migraine. We present three siblings with the mutation with the novel association of childhood seizures, and highlight the dynamic changes seen on ...
Jean-Marc Burgunder, Vijay Sharma, Einar Wilder-Smith   +2 more
exaly   +2 more sources

Recurrence of the T666M Calcium Channel CACNA1A Gene Mutation in Familial Hemiplegic Migraine with Progressive Cerebellar Ataxia [PDF]

American Journal of Human Genetics, 1999
SummaryFamilial hemiplegic migraine (HM) is an autosomal dominant migraine with aura. In 20% of HM families, HM is associated with a mild permanent cerebellar ataxia (PCA).
Anne Ducros, Elisabeth Tournier-Lasserve, Anne Joutel   +2 more
exaly   +2 more sources

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Phenotypic Characterization of Larval Zebrafish (Danio rerio) with Partial Knockdown of the cacna1a Gene

Molecular Neurobiology, 2019
Camila Esguerra, Kinga Gawel, Waldemar Turski   +2 more
exaly