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  1. Article

    Open Access

    Comorbidity in Finnish migraine families

    The objective of the study was to investigate comorbidity of migraine in Finnish migraine families. One thousand consecutive participants in the Finnish Migraine Gene Project reported their medical illnesses i...

    V. Artto, M. Wessman, M. Nissilä, E. Säkö, J. Liukkonen… in The Journal of Headache and Pain (2006)

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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)

  3. No Access

    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)

  4. No Access

    Article

    Wernicke's encephalopathy: is diffusion-weighted MRI useful?

    We present the clinical and magnetic resonance imaging (MRI) findings of five patients with acute Wernicke's encephalopathy. T2-weighted and fluid-attenuated inversion recovery (FLAIR) images demonstrated symm...

    J. Halavaara, A. Brander, J. Lyytinen, K. Setälä, M. Kallela in Neuroradiology (2003)