Wessman M - Search Results

1

Migraine with aura is a risk factor for cervical artery dissection: a case-control study.

Artto V, Metso TM, Metso AJ, Putaala J, Haapaniemi E, Wessman M, Färkkilä M, Kallela M, Tatlisumak T. Artto V, et al. Among authors: wessman m. Cerebrovasc Dis. 2010;30(1):36-40. doi: 10.1159/000313608. Epub 2010 Apr 29. Cerebrovasc Dis. 2010. PMID: 20431287

2

Clinical characteristics of migraine in a population-based twin sample: similarities and differences between migraine with and without aura.

Kallela M, Wessman M, Färkkilä M, Palotie A, Koskenvuo M, Honkasalo ML, Kaprio J. Kallela M, et al. Among authors: wessman m. Cephalalgia. 1999 Apr;19(3):151-8. doi: 10.1046/j.1468-2982.1999.1903151.x. Cephalalgia. 1999. PMID: 10234462

3

Clinical characteristics of migraine concordant monozygotic twin pairs.

Kallela M, Wessman M, Färkkilä M, Palotie A, Koskenvuo M, Honkasalo ML, Kaprio J. Kallela M, et al. Among authors: wessman m. Acta Neurol Scand. 1999 Oct;100(4):254-9. doi: 10.1111/j.1600-0404.1999.tb00390.x. Acta Neurol Scand. 1999. PMID: 10510686

4

Validation of a migraine-specific questionnaire for use in family studies.

Kallela M, Wessman M, Färkkilä M. Kallela M, et al. Among authors: wessman m. Eur J Neurol. 2001 Jan;8(1):61-6. doi: 10.1046/j.1468-1331.2001.00165.x. Eur J Neurol. 2001. PMID: 11509082

5

Familial migraine with and without aura: clinical characteristics and co-occurrence.

Kallela M, Wessman M, Havanka H, Palotie A, Färkkilä M. Kallela M, et al. Among authors: wessman m. Eur J Neurol. 2001 Sep;8(5):441-9. doi: 10.1046/j.1468-1331.2001.00260.x. Eur J Neurol. 2001. PMID: 11554907

6

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. Among authors: wessman m. Neurogenetics. 2004 Feb;5(1):69-73. doi: 10.1007/s10048-003-0161-0. Epub 2003 Oct 7. Neurogenetics. 2004. PMID: 14530926

7

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. Harno H, et al. Among authors: wessman m. Neurology. 2003 Dec 23;61(12):1748-52. doi: 10.1212/01.wnl.0000098882.82690.65. Neurology. 2003. PMID: 14694041

8

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. Among authors: wessman m. Neurogenetics. 2004 Jun;5(2):141-6. doi: 10.1007/s10048-004-0178-z. Epub 2004 May 7. Neurogenetics. 2004. PMID: 15133718

9

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. Harno H, et al. Among authors: wessman m. Neurology. 2005 Feb 8;64(3):542-4. doi: 10.1212/01.WNL.0000150589.26350.3D. Neurology. 2005. PMID: 15699392

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. Anttila V, et al. Among authors: wessman m. Am J Hum Genet. 2006 Jul;79(1):85-99. doi: 10.1086/504814. Epub 2006 May 10. Am J Hum Genet. 2006. PMID: 16773568 Free PMC article.

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