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Year | Number of Results |
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2002 | 1 |
2003 | 1 |
2004 | 3 |
2005 | 1 |
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Page 1
Chromosome 19p13 loci in Finnish migraine with aura families.
Am J Med Genet B Neuropsychiatr Genet. 2005 Jan 5;132B(1):85-9. doi: 10.1002/ajmg.b.30082.
Am J Med Genet B Neuropsychiatr Genet. 2005.
PMID: 15449251
Free PMC article.
A novel missense ATP1A2 mutation in a Finnish family with familial hemiplegic migraine type 2.
Kaunisto MA, Harno H, Vanmolkot KR, Gargus JJ, Sun G, Hämäläinen E, Liukkonen E, Kallela M, van den Maagdenberg AM, Frants RR, Färkkilä M, Palotie A, Wessman M.
Kaunisto MA, et al.
Neurogenetics. 2004 Jun;5(2):141-6. doi: 10.1007/s10048-004-0178-z. Epub 2004 May 7.
Neurogenetics. 2004.
PMID: 15133718
Item in Clipboard
Acetazolamide improves neurotological abnormalities in a family with episodic ataxia type 2 (EA-2).
Harno H, Hirvonen T, Kaunisto MA, Aalto H, Levo H, Isotalo E, Somer H, Kallela M, Palotie A, Wessman M, Färkkilä M.
Harno H, et al.
J Neurol. 2004 Feb;251(2):232-4. doi: 10.1007/s00415-004-0299-1.
J Neurol. 2004.
PMID: 14991363
No abstract available.
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Novel splice site CACNA1A mutation causing episodic ataxia type 2.
Kaunisto MA, Harno H, Kallela M, Somer H, Sallinen R, Hämäläinen E, Miettinen PJ, Vesa J, Orpana A, Palotie A, Färkkilä M, Wessman M.
Kaunisto MA, et al.
Neurogenetics. 2004 Feb;5(1):69-73. doi: 10.1007/s10048-003-0161-0. Epub 2003 Oct 7.
Neurogenetics. 2004.
PMID: 14530926
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A susceptibility locus for migraine with aura, on chromosome 4q24.
Wessman M, Kallela M, Kaunisto MA, Marttila P, Sobel E, Hartiala J, Oswell G, Leal SM, Papp JC, Hämäläinen E, Broas P, Joslyn G, Hovatta I, Hiekkalinna T, Kaprio J, Ott J, Cantor RM, Zwart JA, Ilmavirta M, Havanka H, Färkkilä M, Peltonen L, Palotie A.
Wessman M, et al.
Am J Hum Genet. 2002 Mar;70(3):652-62. doi: 10.1086/339078. Epub 2002 Feb 8.
Am J Hum Genet. 2002.
PMID: 11836652
Free PMC article.
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