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    Results: 19

    1.

    Genetic association study of endothelin-1 and its receptors EDNRA and EDNRB in migraine with aura.

    Tikka-Kleemola P, Kaunisto MA, Hämäläinen E, Todt U, Göbel H, Kaprio J, Kubisch C, Färkkilä M, Palotie A, Wessman M, Kallela M.

    Cephalalgia. 2009 Nov;29(11):1224-31. Epub 2009 Apr 9.PMID: 19558538 [PubMed - in process]Related articles

    2.

    Elevated MBL concentrations are not an indication of association between the MBL2 gene and type 1 diabetes or diabetic nephropathy.

    Kaunisto MA, Sjölind L, Sallinen R, Pettersson-Fernholm K, Saraheimo M, Fröjdö S, Forsblom C, Fagerudd J, Hansen TK, Flyvbjerg A, Wessman M, Groop PH; FinnDiane Study Group.

    Diabetes. 2009 Jul;58(7):1710-4. Epub 2009 Apr 14.PMID: 19366862 [PubMed - indexed for MEDLINE]Related articlesFree article

    3.

    Findings from bipolar disorder genome-wide association studies replicate in a Finnish bipolar family-cohort.

    Ollila HM, Soronen P, Silander K, Palo OM, Kieseppä T, Kaunisto MA, Lönnqvist J, Peltonen L, Partonen T, Paunio T.

    Mol Psychiatry. 2009 Apr;14(4):351-3. No abstract available. PMID: 19308021 [PubMed - indexed for MEDLINE]Related articlesFree article

    4.

    A high-density association screen of 155 ion transport genes for involvement with common migraine.

    Nyholt DR, LaForge KS, Kallela M, Alakurtti K, Anttila V, Färkkilä M, Hämaläinen E, Kaprio J, Kaunisto MA, Heath AC, Montgomery GW, Göbel H, Todt U, Ferrari MD, Launer LJ, Frants RR, Terwindt GM, de Vries B, Verschuren WM, Brand J, Freilinger T, Pfaffenrath V, Straube A, Ballinger DG, Zhan Y, Daly MJ, Cox DR, Dichgans M, van den Maagdenberg AM, Kubisch C, Martin NG, Wessman M, Peltonen L, Palotie A.

    Hum Mol Genet. 2008 Nov 1;17(21):3318-31. Epub 2008 Aug 2.PMID: 18676988 [PubMed - indexed for MEDLINE]Related articlesFree article

    5.

    Consistently replicating locus linked to migraine on 10q22-q23.

    Anttila V, Nyholt DR, Kallela M, Artto V, Vepsäläinen S, Jakkula E, Wennerström A, Tikka-Kleemola P, Kaunisto MA, Hämäläinen E, Widén E, Terwilliger J, Merikangas K, Montgomery GW, Martin NG, Daly M, Kaprio J, Peltonen L, Färkkilä M, Wessman M, Palotie A.

    Am J Hum Genet. 2008 May;82(5):1051-63.PMID: 18423523 [PubMed - indexed for MEDLINE]Related articlesFree article

    6.

    Association analysis of podocyte slit diaphragm genes as candidates for diabetic nephropathy.

    Ihalmo P, Wessman M, Kaunisto MA, Kilpikari R, Parkkonen M, Forsblom C, Holthöfer H, Groop PH; FinnDiane Study Group.

    Diabetologia. 2008 Jan;51(1):86-90. Epub 2007 Oct 30.PMID: 17968527 [PubMed - indexed for MEDLINE]Related articles

    7.

    No association of migraine to the GABA-A receptor complex on chromosome 15.

    Oswell G, Kaunisto MA, Kallela M, Hämäläinen E, Anttila V, Kaprio J, Färkkilä M, Wessman M, Palotie A.

    Am J Med Genet B Neuropsychiatr Genet. 2008 Jan 5;147B(1):33-6.PMID: 17580321 [PubMed - indexed for MEDLINE]Related articles

    8.

    Migraine: a complex genetic disorder.

    Wessman M, Terwindt GM, Kaunisto MA, Palotie A, Ophoff RA.

    Lancet Neurol. 2007 Jun;6(6):521-32. Review.PMID: 17509487 [PubMed - indexed for MEDLINE]Related articles

    9.

    Testing of variants of the MTHFR and ESR1 genes in 1798 Finnish individuals fails to confirm the association with migraine with aura.

    Kaunisto MA, Kallela M, Hämäläinen E, Kilpikari R, Havanka H, Harno H, Nissilä M, Säkö E, Ilmavirta M, Liukkonen J, Teirmaa H, Törnwall O, Jussila M, Terwilliger J, Färkkilä M, Kaprio J, Palotie A, Wessman M.

    Cephalalgia. 2006 Dec;26(12):1462-72.PMID: 17116097 [PubMed - indexed for MEDLINE]Related articles

    10.

    Trait components provide tools to dissect the genetic susceptibility of migraine.

    Anttila V, Kallela M, Oswell G, Kaunisto MA, Nyholt DR, Hamalainen E, Havanka H, Ilmavirta M, Terwilliger J, Sobel E, Peltonen L, Kaprio J, Farkkila M, Wessman M, Palotie A.

    Am J Hum Genet. 2006 Jul;79(1):85-99. Epub 2006 May 10.PMID: 16773568 [PubMed - indexed for MEDLINE]Related articlesFree article

    11.

    Decreased cerebellar total creatine in episodic ataxia type 2: a 1H MRS study.

    Harno H, Heikkinen S, Kaunisto MA, Kallela M, Häkkinen AM, Wessman M, Färkkilä M, Lundbom N.

    Neurology. 2005 Feb 8;64(3):542-4.PMID: 15699392 [PubMed - indexed for MEDLINE]Related articles

    12.

    The molecular genetics of migraine.

    Wessman M, Kaunisto MA, Kallela M, Palotie A.

    Ann Med. 2004;36(6):462-73. Review.PMID: 15513297 [PubMed - indexed for MEDLINE]Related articles

    13.

    Chromosome 19p13 loci in Finnish migraine with aura families.

    Kaunisto MA, Tikka PJ, Kallela M, Leal SM, Papp JC, Korhonen A, Hämäläinen E, Harno H, Havanka H, Nissilä M, Säkö E, Ilmavirta M, Kaprio J, Färkkilä M, Ophoff RA, Palotie A, Wessman M.

    Am J Med Genet B Neuropsychiatr Genet. 2005 Jan 5;132B(1):85-9.PMID: 15449251 [PubMed - indexed for MEDLINE]Related articles

    14.

    Kinetic alterations due to a missense mutation in the Na,K-ATPase alpha2 subunit cause familial hemiplegic migraine type 2.

    Segall L, Scanzano R, Kaunisto MA, Wessman M, Palotie A, Gargus JJ, Blostein R.

    J Biol Chem. 2004 Oct 15;279(42):43692-6. Epub 2004 Aug 11.PMID: 15308625 [PubMed - indexed for MEDLINE]Related articlesFree article

    15.

    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.

    Neurogenetics. 2004 Jun;5(2):141-6. Epub 2004 May 7.PMID: 15133718 [PubMed - indexed for MEDLINE]Related articles

    16.

    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.

    J Neurol. 2004 Feb;251(2):232-4. No abstract available. PMID: 14991363 [PubMed - indexed for MEDLINE]Related articles

    17.

    Subclinical vestibulocerebellar dysfunction in migraine with and without aura.

    Harno H, Hirvonen T, Kaunisto MA, Aalto H, Levo H, Isotalo E, Kallela M, Kaprio J, Palotie A, Wessman M, Färkkilä M.

    Neurology. 2003 Dec 23;61(12):1748-52.PMID: 14694041 [PubMed - indexed for MEDLINE]Related articles

    18.

    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.

    Neurogenetics. 2004 Feb;5(1):69-73. Epub 2003 Oct 7.PMID: 14530926 [PubMed - indexed for MEDLINE]Related articles

    19.

    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.

    Am J Hum Genet. 2002 Mar;70(3):652-62. Epub 2002 Feb 8.PMID: 11836652 [PubMed - indexed for MEDLINE]Related articlesFree article

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