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  1. Article

    Open Access

    Migraine without aura: genome-wide association analysis identifies several novel susceptibility

    B Loci De Vries, T Freilinger, V Anttila, R Malik… in The Journal of Headache and Pain (2013)

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    Article

    A novel missense ATP1A2 mutation in a Finnish family with familial hemiplegic migraine type 2

    Familial hemiplegic migraine (FHM), a rare autosomal dominant subtype of migraine with aura, has been linked to two chromosomal loci, 19p13 and 1q23. Mutations in the Na+,K+-ATPase α2 subunit gene, ATP1A2, on 1q2...

    M. A. Kaunisto, H. Harno, K. R. J. Vanmolkot, J. J. Gargus, G. Sun… in Neurogenetics (2004)

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    Article

    Novel splice site CACNA1A mutation causing episodic ataxia type 2

    Episodic ataxia type 2 (EA-2) is an autosomal dominant neurological disorder, characterized by episodes of ataxia, vertigo, nausea, nystagmus, and fatigue, associated with acetazolamide responsiveness. The dis...

    M. A. Kaunisto, H. Harno, M. Kallela, H. Somer, R. Sallinen, E. Hämäläinen… in Neurogenetics (2004)