نتایج جستجو برای: hemiplegic migraine

تعداد نتایج: 14930  

Journal: :The Journal of biological chemistry 2005
Angelita Tottene Francesca Pivotto Tommaso Fellin Tiziana Cesetti Arn M J M van den Maagdenberg Daniela Pietrobon

Mutation S218L in the Ca(V)2.1 alpha(1) subunit of P/Q-type Ca(2+) channels produces a severe clinical phenotype in which typical attacks of familial hemiplegic migraine (FHM) triggered by minor head trauma are followed, after a lucid interval, by deep (even fatal) coma and long lasting severe cerebral edema. We investigated the functional consequences of this mutation on human Ca(V)2.1 channel...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2013
Sandrine Cestèle Emanuele Schiavon Raffaella Rusconi Silvana Franceschetti Massimo Mantegazza

Familial hemiplegic migraine (FHM) is a rare subtype of migraine with aura. Mutations causing FHM type 3 have been identified in SCN1A, the gene encoding the Nav1.1 Na(+) channel, which is also a major target of epileptogenic mutations and is particularly important for the excitability of GABAergic neurons. However, functional studies of NaV1.1 FHM mutations have generated controversial results...

Journal: :Cell 1996
Roel A Ophoff Gisela M Terwindt Monique N Vergouwe Ronald van Eijk Peter J Oefner Susan M.G Hoffman Jane E Lamerdin Harvey W Mohrenweiser Dennis E Bulman Maurizio Ferrari Joost Haan Dick Lindhout Gert-Jan B van Ommen Marten H Hofker Michel D Ferrari Rune R Frants

Genes for familial hemiplegic migraine (FHM) and episodic ataxia type-2 (EA-2) have been mapped to chromosome 19p13. We characterized a brain-specific P/Q-type Ca2+ channel alpha1-subunit gene, CACNL1A4, covering 300 kb with 47 exons. Sequencing of all exons and their surroundings revealed polymorphic variations, including a (CA)n-repeat (D19S1150), a (CAG)n-repeat in the 3'-UTR, and different ...

Journal: :Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease 2013

2013
Andrea M Harriott Nicole Dueker Yu-Ching Cheng Kathleen A Ryan Jeffrey R O’Connell O Colin Stine Patrick F McArdle Marcella A Wozniak Barney J Stern Braxton D Mitchell Steven J Kittner John W Cole

In a recent meta-analysis migraine was associated with a two-fold increase in stroke risk. While the mechanism driving this association is unknown, one intriguing hypothesis is that migraineurs are genetically predisposed to developing ischemic stroke. Mutations in the ATP1A2 gene are implicated in familial hemiplegic migraine type II and increase the severity of ischemic brain injury in animal...

Journal: :Brain & development 2017
Yoshiaki Saito Gaku Yamanaka Hideki Shimomura Kazuhiro Shiraishi Tomoyuki Nakazawa Fumihide Kato Yuko Shimizu-Motohashi Masayuki Sasaki Yoshihiro Maegaki

OBJECTIVE To provide insight into the wide spectrum of migraine during childhood to establish practical and comprehensive treatment strategies. BACKGROUND Although recent studies have confirmed the effect of anti-migraine agents in childhood headaches fulfilling the criteria of migraine without aura, there have been no studies regarding the efficacy of these drugs in childhood migraine withou...

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید