Zobrazeno 1 - 10
of 3 417
pro vyhledávání: '"Hemiplegic migraine"'
Publikováno v:
Pharmacogenomics and Personalized Medicine, Vol Volume 17, Pp 437-442 (2024)
Dong-Mei Guan,1,* Yuan-Zhuang Shan,1,* Hao-Tian Zhao,2 Ying Meng,2 Zhong-Rui Yan,2 Hai-Lin Zhang2 1Shandong University of Tradition Chinese Medicine, Jinan, Shandong, People’s Republic of China; 2Department of Neurology, Jining No.1 People
Externí odkaz:
https://doaj.org/article/2e7a8edc068c4d70b574c8eb655f238b
Autor:
Nico A. Jansen, Chelsey Linnenbank, Maarten Schenke, Rob A. Voskuyl, Maria S. Jorge, Georgii Krivoshein, Cor Breukel, Margot M. Linssen, Jill W.C. Claassens, Conny Brouwers, Sandra H. van Heiningen, Anders Heuck, Karin Lykke-Hartmann, Else A. Tolner, Arn M.J.M. van den Maagdenberg
Publikováno v:
Neurobiology of Disease, Vol 202, Iss , Pp 106714- (2024)
The mechanisms of initiation of spreading depolarization (SD) are understudied due to a paucity of disease models with spontaneously occurring events. We here present a novel mouse model of familial hemiplegic migraine type 2 (FHM2), expressing the m
Externí odkaz:
https://doaj.org/article/06ea3f35c9c3417aa35517e998fb1500
Autor:
Donna Schaare, Kendra Allison, Kara Skorge, Pangkong Fox, Laina Lusk, Sara M. Sarasua, Ingo Helbig, Luigi Boccuto
Publikováno v:
Frontiers in Neurology, Vol 15 (2024)
IntroductionCACNA1A-related Hemiplegic Migraine (HM) is a rare neurological disorder distinguished by paroxysmal episodes of hemiparesis/hemiplegia with and without headache. Clinical features have been widely characterized, yet the impacts of the pa
Externí odkaz:
https://doaj.org/article/82917b19e876457ca4a512a089e9799f
Publikováno v:
The Journal of Pediatric Academy, Vol 5, Iss 2, Pp 70-72 (2024)
Moyamoya disease (MMD) is a chronic progressive steno-occlusive disease of the intracranial arterial vessels and their branches characterized by puff smoke appearance on angiography. Multifocal neurological insults and deficits are commonly observed
Externí odkaz:
https://doaj.org/article/0531ddca72144397877a53bbb993216a
Autor:
Jakob Paungarttner, Martina Quartana, Lucrezia Patti, Barbora Sklenárová, Fatemeh Farham, Inés Hernando Jiménez, M. Gokcen Soylu, Irina Maria Vlad, Semih Tasdelen, Teresa Mateu, Oreste Marsico, Federica Reina, Viktoria Tischler, Christian Lampl, on behalf of the European Headache Federation School of Advanced Studies (EHF – SAS)
Publikováno v:
The Journal of Headache and Pain, Vol 25, Iss 1, Pp 1-23 (2024)
Abstract Background Migraine and epilepsy are two paroxysmal chronic neurological disorders affecting a high number of individuals and being responsible for a high individual and socioeconomic burden. The link between these disorders has been of inte
Externí odkaz:
https://doaj.org/article/31ae079e119a41428e0a892c286bf6ad
Autor:
Stuart M. Cain, Sascha R. A. Alles, Ray Gopaul, Louis-Philippe Bernier, Andrew C. Yung, Andrew Bauman, Yi Yang, Glen B. Baker, Piotr Kozlowski, Brian A. MacVicar, Terrance P. Snutch
Publikováno v:
Molecular Brain, Vol 16, Iss 1, Pp 1-14 (2023)
Abstract Familial hemiplegic migraine type-1 (FHM-1) is a form of migraine with aura caused by mutations in the P/Q-type (Cav2.1) voltage-gated calcium channel. Pregabalin, used clinically in the treatment of chronic pain and epilepsy, inhibits P/Q-t
Externí odkaz:
https://doaj.org/article/7f60fbce64114253a4fc70c967d52dd5
Akademický článek
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Publikováno v:
Frontiers in Neurology, Vol 15 (2024)
This case study describes a 57-year-old woman with a six-year history of recurrent episodes characterized by visual, sensory, speech disturbances, hemiparesis and severe one-sided headaches accompanied by fever and altered consciousness. Initially mi
Externí odkaz:
https://doaj.org/article/78c45fb69a6547afa14d6f500fc16a6e
Publikováno v:
Frontiers in Neurology, Vol 15 (2024)
This study presents a case report of a male adolescent diagnosed with familial hemiplegic migraine type 2 (FHM2), an autosomal dominant inheritance disorder caused by ATP1A2 mutation. We report the patient who presented with headache, aphasia, and le
Externí odkaz:
https://doaj.org/article/17e0e631fe4c43a583dcd408670f71ac
Akademický článek
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