Wessman M - Search Results

1

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

2

Mapping ESTs by fiber-FISH.

Horelli-Kuitunen N, Aaltonen J, Yaspo ML, Eeva M, Wessman M, Peltonen L, Palotie A. Horelli-Kuitunen N, et al. Among authors: wessman m. Genome Res. 1999 Jan;9(1):62-71. Genome Res. 1999. PMID: 9927485 Free PMC article.

3

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

4

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

5

Assignment of laminin alpha 2-chain gene (Lama2) to mouse chromosome 10A4-B1 by fluorescence in situ hybridization.

Sallinen R, Kuang W, Engvall E, Palotie A, Wessman M, Horelli-Kuitunen N. Sallinen R, et al. Among authors: wessman m. Cytogenet Cell Genet. 1999;87(3-4):195-6. doi: 10.1159/000015464. Cytogenet Cell Genet. 1999. PMID: 10702665 No abstract available.

6

Assignment of a novel locus for autosomal recessive congenital ichthyosis to chromosome 19p13.1-p13.2.

Virolainen E, Wessman M, Hovatta I, Niemi KM, Ignatius J, Kere J, Peltonen L, Palotie A. Virolainen E, et al. Among authors: wessman m. Am J Hum Genet. 2000 Mar;66(3):1132-7. doi: 10.1086/302813. Am J Hum Genet. 2000. PMID: 10712223 Free PMC article.

7

Physical mapping of mouse collagen genes on chromosome 10 by high-resolution FISH.

Sallinen R, Latvanlehto A, Kvist AP, Rehn M, Eerola I, Chu ML, Bonaldo P, Saitta B, Bressan GM, Pihlajaniemi T, Vuorio E, Palotie A, Wessman M, Horelli-Kuitunen N. Sallinen R, et al. Among authors: wessman m. Mamm Genome. 2001 May;12(5):340-6. doi: 10.1007/s003350010271. Mamm Genome. 2001. PMID: 11331940

8

Quantitative-trait-locus analysis of body-mass index and of stature, by combined analysis of genome scans of five Finnish study groups.

Perola M, Ohman M, Hiekkalinna T, Leppävuori J, Pajukanta P, Wessman M, Koskenvuo M, Palotie A, Lange K, Kaprio J, Peltonen L. Perola M, et al. Among authors: wessman m. Am J Hum Genet. 2001 Jul;69(1):117-23. doi: 10.1086/321286. Epub 2001 Jun 15. Am J Hum Genet. 2001. PMID: 11410840 Free PMC article.

9

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

10

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

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