Article
The contribution of CACNA1A, ATP1A2 and SCN1A mutations in hemiplegic migraine: A clinical and genetic study in Finnish migraine families.
Cephalalgia : an international journal of headache - 1 Oct 2018
Hiekkala Marjo Eveliina, Vuola Pietari, Artto Ville, Häppölä Paavo, Häppölä Elisa, Vepsäläinen Salli, Cuenca-León Ester, Lal Dennis, Gormley Padhraig, Hämäläinen Eija, Ilmavirta Matti, Nissilä Markku, Säkö Erkki, Sumelahti Marja-Liisa, Harno Hanna, Havanka Hannele, Keski-Säntti Petra, Färkkilä Markus, Palotie Aarno, Wessman Maija, Kaunisto Mari Anneli, Kallela Mikko
Abstract excerpt
Objective To study the position of hemiplegic migraine in the clinical spectrum of migraine with aura and to reveal the importance of CACNA1A, ATP1A2 and SCN1A in the development of hemiplegic migraine in Finnish migraine families. Methods The International Classification of Headache Disorders 3rd edition criteria were used to determine clinical characteristics and occurrence of hemiplegic migraine, based on...
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