Kallela M - Search Results

1

The contribution of CACNA1A, ATP1A2 and SCN1A mutations in hemiplegic migraine: A clinical and genetic study in Finnish migraine families.

Hiekkala ME, Vuola P, Artto V, Häppölä P, Häppölä E, Vepsäläinen S, Cuenca-León E, Lal D, Gormley P, Hämäläinen E, Ilmavirta M, Nissilä M, Säkö E, Sumelahti ML, Harno H, Havanka H, Keski-Säntti P, Färkkilä M, Palotie A, Wessman M, Kaunisto MA, Kallela M. Hiekkala ME, et al. Among authors: kallela m. Cephalalgia. 2018 Oct;38(12):1849-1863. doi: 10.1177/0333102418761041. Epub 2018 Feb 27. Cephalalgia. 2018. PMID: 29486580

2

Familial migraine: exclusion of the susceptibility gene from the reported locus of familial hemiplegic migraine on 19p.

Hovatta I, Kallela M, Färkkilä M, Peltonen L. Hovatta I, et al. Among authors: kallela m. Genomics. 1994 Oct;23(3):707-9. doi: 10.1006/geno.1994.1563. Genomics. 1994. PMID: 7851903

3

Endothelin in migraine patients.

Kallela M, Färkkilä M, Saijonmaa O, Fyhrquist F. Kallela M, et al. Cephalalgia. 1998 Jul-Aug;18(6):329-32. doi: 10.1046/j.1468-2982.1998.1806329.x. Cephalalgia. 1998. PMID: 9731937

4

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. Cephalalgia. 1999 Apr;19(3):151-8. doi: 10.1046/j.1468-2982.1999.1903151.x. Cephalalgia. 1999. PMID: 10234462

5

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. Acta Neurol Scand. 1999 Oct;100(4):254-9. doi: 10.1111/j.1600-0404.1999.tb00390.x. Acta Neurol Scand. 1999. PMID: 10510686

6

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

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

7

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. Eur J Neurol. 2001 Sep;8(5):441-9. doi: 10.1046/j.1468-1331.2001.00260.x. Eur J Neurol. 2001. PMID: 11554907

8

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. Among authors: kallela m. 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.

9

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

10

Genetic and environmental influences on migraine: a twin study across six countries.

Mulder EJ, Van Baal C, Gaist D, Kallela M, Kaprio J, Svensson DA, Nyholt DR, Martin NG, MacGregor AJ, Cherkas LF, Boomsma DI, Palotie A. Mulder EJ, et al. Among authors: kallela m. Twin Res. 2003 Oct;6(5):422-31. doi: 10.1375/136905203770326420. Twin Res. 2003. PMID: 14624726

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