The contribution of CACNA1A, ATP1A2 and SCN1A mutations in hemiplegic migraine

A clinical and genetic study in Finnish migraine families

Marjo Eveliina Hiekkala, Pietari Vuola, Ville Artto, Paavo Häppölä, Elisa Häppölä, Salli Vepsäläinen, Ester Cuenca-Leon, Dennis Lal, Padhraig Gormley, Eija Hämäläinen, Matti Ilmavirta, Markku Nissilä, Erkki Säkö, Marja-Liisa Sumelahti, Hanna Harno, Hannele Havanka, Petra Keski-Säntti, Markus Färkkilä, Aarno Palotie, Maija Wessman & 2 others Mari Anneli Kaunisto, Mikko Kallela

Research output: Contribution to journalArticleScientificpeer-review

Original languageEnglish
JournalCephalalgia
Volume38
Issue number12
Pages (from-to)1849-1863
Number of pages15
ISSN0333-1024
DOIs
Publication statusPublished - Oct 2018
MoE publication typeA1 Journal article-refereed

Fields of Science

  • Migraine with aura
  • ICHD-3 beta criteria
  • clinical characteristics
  • ion channel
  • pathogenic variant
  • exome sequencing
  • FEBRILE SEIZURES PLUS
  • GENERALIZED EPILEPSY
  • CHANNEL
  • TYPE-2
  • VARIANTS
  • CONSEQUENCES
  • PROTEINS
  • SPECTRUM
  • 3112 Neurosciences
  • 3124 Neurology and psychiatry

Cite this

Hiekkala, Marjo Eveliina ; Vuola, Pietari ; Artto, Ville ; Häppölä, Paavo ; Häppölä, Elisa ; Vepsäläinen, Salli ; Cuenca-Leon, 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. / The contribution of CACNA1A, ATP1A2 and SCN1A mutations in hemiplegic migraine : A clinical and genetic study in Finnish migraine families. In: Cephalalgia. 2018 ; Vol. 38, No. 12. pp. 1849-1863.
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title = "The contribution of CACNA1A, ATP1A2 and SCN1A mutations in hemiplegic migraine: A clinical and genetic study in Finnish migraine families",
keywords = "Migraine with aura, ICHD-3 beta criteria, clinical characteristics, ion channel, pathogenic variant, exome sequencing, FEBRILE SEIZURES PLUS, GENERALIZED EPILEPSY, CHANNEL, TYPE-2, VARIANTS, CONSEQUENCES, PROTEINS, SPECTRUM, 3112 Neurosciences, 3124 Neurology and psychiatry",
author = "Hiekkala, {Marjo Eveliina} and Pietari Vuola and Ville Artto and Paavo H{\"a}pp{\"o}l{\"a} and Elisa H{\"a}pp{\"o}l{\"a} and Salli Veps{\"a}l{\"a}inen and Ester Cuenca-Leon and Dennis Lal and Padhraig Gormley and Eija H{\"a}m{\"a}l{\"a}inen and Matti Ilmavirta and Markku Nissil{\"a} and Erkki S{\"a}k{\"o} and Marja-Liisa Sumelahti and Hanna Harno and Hannele Havanka and Petra Keski-S{\"a}ntti and Markus F{\"a}rkkil{\"a} and Aarno Palotie and Maija Wessman and Kaunisto, {Mari Anneli} and Mikko Kallela",
year = "2018",
month = "10",
doi = "10.1177/0333102418761041",
language = "English",
volume = "38",
pages = "1849--1863",
journal = "Cephalalgia",
issn = "0333-1024",
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Hiekkala, ME, Vuola, P, Artto, V, Häppölä, P, Häppölä, E, Vepsäläinen, S, Cuenca-Leon, E, Lal, D, Gormley, P, Hämäläinen, E, Ilmavirta, M, Nissilä, M, Säkö, E, Sumelahti, M-L, Harno, H, Havanka, H, Keski-Säntti, P, Färkkilä, M, Palotie, A, Wessman, M, Kaunisto, MA & Kallela, M 2018, 'The contribution of CACNA1A, ATP1A2 and SCN1A mutations in hemiplegic migraine: A clinical and genetic study in Finnish migraine families', Cephalalgia, vol. 38, no. 12, pp. 1849-1863. https://doi.org/10.1177/0333102418761041

The contribution of CACNA1A, ATP1A2 and SCN1A mutations in hemiplegic migraine : A clinical and genetic study in Finnish migraine families. / Hiekkala, Marjo Eveliina; Vuola, Pietari; Artto, Ville; Häppölä, Paavo; Häppölä, Elisa; Vepsäläinen, Salli; Cuenca-Leon, 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.

In: Cephalalgia, Vol. 38, No. 12, 10.2018, p. 1849-1863.

Research output: Contribution to journalArticleScientificpeer-review

TY - JOUR

T1 - The contribution of CACNA1A, ATP1A2 and SCN1A mutations in hemiplegic migraine

T2 - A clinical and genetic study in Finnish migraine families

AU - Hiekkala, Marjo Eveliina

AU - Vuola, Pietari

AU - Artto, Ville

AU - Häppölä, Paavo

AU - Häppölä, Elisa

AU - Vepsäläinen, Salli

AU - Cuenca-Leon, Ester

AU - Lal, Dennis

AU - Gormley, Padhraig

AU - Hämäläinen, Eija

AU - Ilmavirta, Matti

AU - Nissilä, Markku

AU - Säkö, Erkki

AU - Sumelahti, Marja-Liisa

AU - Harno, Hanna

AU - Havanka, Hannele

AU - Keski-Säntti, Petra

AU - Färkkilä, Markus

AU - Palotie, Aarno

AU - Wessman, Maija

AU - Kaunisto, Mari Anneli

AU - Kallela, Mikko

PY - 2018/10

Y1 - 2018/10

KW - Migraine with aura

KW - ICHD-3 beta criteria

KW - clinical characteristics

KW - ion channel

KW - pathogenic variant

KW - exome sequencing

KW - FEBRILE SEIZURES PLUS

KW - GENERALIZED EPILEPSY

KW - CHANNEL

KW - TYPE-2

KW - VARIANTS

KW - CONSEQUENCES

KW - PROTEINS

KW - SPECTRUM

KW - 3112 Neurosciences

KW - 3124 Neurology and psychiatry

U2 - 10.1177/0333102418761041

DO - 10.1177/0333102418761041

M3 - Article

VL - 38

SP - 1849

EP - 1863

JO - Cephalalgia

JF - Cephalalgia

SN - 0333-1024

IS - 12

ER -