نتایج جستجو برای: hemiplegic migraine

تعداد نتایج: 14930  

Journal: :Neuroscience letters 2009
Roser Corominas Marta Ribasés Ester Cuenca-León Bernat Narberhaus Selma A Serra Mireia del Toro Manuel Roig José M Fernández-Fernández Alfons Macaya Bru Cormand

Migraine is a common neurological disorder with a complex inheritance pattern. Mutations in genes encoding proteins that are involved in ion transport across the neuronal membrane have been linked to rare monogenic variants of migraine. These or other related genes and proteins are also candidates to be involved in the inherited predisposition to the more common forms of migraine without aura (...

ASHFAQ SHUAIB, KAVIAN GHANDEHARI,

Background: The sporadic type of Hemiplegic Migraine (HM) is sometimes observed among migrainous patients (MP) and mimics ischemic strokes. Methods: In an evaluation of two-hundred consecutive adult MP in the Mackenzie headache clinic, Canada during 2004 , 9% of the patients met the criteria established by the International Headache Society for sporadic HM. Female to male sex ratio, family...

Journal: :American family physician 2011
Benjamin Gilmore Magdalena Michael

Migraine headache is a common and potentially debilitating disorder often treated by family physicians. Before diagnosing migraine, serious intracranial pathology must be ruled out. Treating acute migraine is challenging because of substantial rates of nonresponse to medications and difficulty in predicting individual response to a specific agent or dose. Data comparing different drug classes a...

2014
Markus A. Dahlem Julia Schumacher Niklas Hübel

Familial hemiplegic migraine (FHM) is a rare subtype of migraine with aura. A mutation causing FHM type 3 (FHM3) has been identified in SCN1A encoding the Nav1.1 Na(+) channel. This genetic defect affects the inactivation gate. While the Na(+) tail currents following voltage steps are consistent with both hyperexcitability and hypoexcitability, in this computational study, we investigate functi...

2007
Maurice Vincent

Clinical and pathophysiological evidences connect migraine and the cerebellum. Literature on documented cerebellar abnormalities in migraine, however, is relatively sparse. Cerebellar involvement may be observed in 4 types of migraines: in the widespread migraine with aura (MWA) and migraine without aura (MWoA) forms; in particular subtypes of migraine such as basilar-type migraine (BTM); and i...

Journal: :Revista Headache Medicine 2022

IntroductionMigraine is a complex brain disorder that influenced by different pathophysiological aspects such as inflammation, structural changes, and dysfunctions in multisensory processing. Recent studies have showed possible mutations genes interfere with the excitability of ion channels linked to nociception are one key mechanisms for development migraine. In this sense, it known familial h...

Journal: :Rinsho shinkeigaku = Clinical neurology 2012
Hisanori Kowa Kenji Nakashima

Cortical spreading depression (CSD) is a slowly propagated wave of depolarization of neurons and glial cells, followed by a subsequent sustained suppression of spontaneous neuronal activity. Functional imaging studies of migraine patients have shown dramatic changes in blood flow and brain activity whose characteristics are similar to those of CSD, implicated in migraine visual aura. Although t...

Journal: :Acta neurologica Belgica 2001
A Ambrosini A M de Noordhout J Schoenen

P/Q Ca2+ channels are genetically abnormal in most cases of familial hemiplegic migraine (FHM) and may be involved in other types of migraine. They are also found at the neuromuscular junctions, where they control stimulation-induced acetylcholine release. Prolonged aura is a very frequent clinical feature in FHM patients. The objective of this study was thus to explore neuromuscular transmissi...

Journal: :The Journal of neuroscience : the official journal of the Society for Neuroscience 2014
Mariano N Di Guilmi Tiantian Wang Carlota Gonzalez Inchauspe Ian D Forsythe Michel D Ferrari Arn M J M van den Maagdenberg J Gerard G Borst Osvaldo D Uchitel

Specific missense mutations in the CACNA1A gene, which encodes a subunit of voltage-gated CaV2.1 channels, are associated with familial hemiplegic migraine type 1 (FHM1), a rare monogenic subtype of common migraine with aura. We used transgenic knock-in (KI) mice harboring the human pathogenic FHM1 mutation S218L to study presynaptic Ca(2+) currents, EPSCs, and in vivo activity at the calyx of ...

Journal: :Human molecular genetics 2008
Dale R Nyholt K Steven LaForge Mikko Kallela Kirsi Alakurtti Verneri Anttila Markus Färkkilä Eija Hämaläinen Jaakko Kaprio Mari A Kaunisto Andrew C Heath Grant W Montgomery Hartmut Göbel Unda Todt Michel D Ferrari Lenore J Launer Rune R Frants Gisela M Terwindt Boukje de Vries W M Monique Verschuren Jan Brand Tobias Freilinger Volker Pfaffenrath Andreas Straube Dennis G Ballinger Yiping Zhan Mark J Daly David R Cox Martin Dichgans Arn M J M van den Maagdenberg Christian Kubisch Nicholas G Martin Maija Wessman Leena Peltonen Aarno Palotie

The clinical overlap between monogenic Familial Hemiplegic Migraine (FHM) and common migraine subtypes, and the fact that all three FHM genes are involved in the transport of ions, suggest that ion transport genes may underlie susceptibility to common forms of migraine. To test this leading hypothesis, we examined common variation in 155 ion transport genes using 5257 single nucleotide polymorp...

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