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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)

  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

    Novel method for in-flight particle temperature and velocity measurements in plasma spraying using a single CCD camera

    A novel, technically simple imaging system for individual, in-flight particle temperature and velocity measurements for plasma and other thermal spray processes is described. A custom double dichroic mirror is...

    J. Vattulainen, E. Hämäläinen, R. Hernberg… in Journal of Thermal Spray Technology (2001)