Adapted Finnish Migraine-Specific Questionnaire for family studies (FMSQFS): A validation study in two languages

European Journal of Neurology

Volumn 15, Issue 10, 2008, Pages 1071-1074

  Facheris, M F ^a,b   Vogl, F D ^c   Hollmann, S ^d   Sixt, G ^b   Pattaro, C ^a   Schonhuber R ^b   Pramstaller, P P ^a,b  

^a INSTITUTE FOR RENEWABLE ENERGY   (Italy)

^b CENTRAL HOSPITAL OF BOLZANO   (Italy)

^c F Tappeiner Hospital   (Italy)

^d UNIVERSITY OF LÜBECK   (Germany)

Author keywords

German; Italian; Migraine; Neuroepidemiology; Questionnaire validation

Indexed keywords

ADULT; AGED; ARTICLE; DIFFERENTIAL DIAGNOSIS; FAMILY STUDY; FEMALE; FINNISH MIGRAINE SPECIFIC QUESTIONNAIRE; GERMANY; HUMAN; ITALY; LANGUAGE; MAJOR CLINICAL STUDY; MALE; MIGRAINE; MIGRAINE WITH AURA; MIGRAINE WITHOUT AURA; PRIMARY HEADACHE; PRIORITY JOURNAL; QUESTIONNAIRE; VALIDATION STUDY;

ADOLESCENT; ADULT; AGED; DIAGNOSIS, DIFFERENTIAL; FAMILY HEALTH; FEMALE; FINLAND; GENETIC PREDISPOSITION TO DISEASE; GERMANY; HEADACHE; HUMANS; ITALY; LANGUAGE; MALE; MIDDLE AGED; MIGRAINE DISORDERS; QUESTIONNAIRES;

EID: 51349124009     PISSN: 13515101     EISSN: 14681331     Source Type: Journal    
DOI: 10.1111/j.1468-1331.2008.02248.x     Document Type: Article

References (18)

1. 2+ channel gene CACNL1A4. Cell 1996 87 : 543 552.
2. Russel MB. Genetics in primary headaches. The Journal of Headache and Pain 2007 8 : 190 195.
3. Russel MB, Olesen J. Increased familial risk and evidence of genetic factor in migraine. British Medical Journal 1995 311 : 541 544.
4. Russel MB. Genetic epidemiology of migraine and cluster headache. University of Copenhagen. Cephalalgia 1997 17 : 683 701.
5. Russel MB. Tension-type headache in 40-year-olds: a Danish population-based sample of 4000. The Journal of Headache and Pain 2005 6 : 441 447.
6. Kallela M, Wessman M, Färkkilä M. Validation of a migraine-specific questionnaire for use in family studies. European Journal of Neurology 2001 8 : 61 66.
7. Pattaro C, Marroni F, Riegler A, et al. The genetic study of three population microisolates in South Tyrol (MICROS): study design and epidemiological perspectives. BMC Medical Genetics 2007 8 : 29.
8. Headache Classification Subcommittee of the International Headache Society. The international classification of headache disorders. Cephalalgia 2004 24 (Suppl. 1 9 160.
9. Bernatsky S, Pineau CA, Lee JL, et al. Headache, Raynaud's syndrome and serotonin receptor agonists in systemic lupus erythematosus. Lupus 2006 15 : 671 674.
10. Hottenga JJ, Vanmolkot KR, Kors EE, et al. The 3p21.1-p21.3 hereditary vascular retinopathy locus increases the risk for Raynaud's phenomenon and migraine. Cephalalgia 2005 25 : 1168 1172.
11. Rains JC, Poceta JS. Headache and sleep disorders: review and clinical implications for headache management. Headache 2006 46 : 1344 1363.
12. Evers S, Goadsby PJ. Hypnic headache: clinical features, pathophysiology, and treatment. Neurology 2003 60 : 905 909.
13. Fleiss JL, Levin B, Paik MC. Statistical Methods for Rates and Proportions, 3rd edn. Hoboken, NJ : John Wiley & sons, 2003.
14. Altman DG. Practical Statistics for Medical Research. London, UK : Chapman & Hall, 1991.
15. Estevez M, Gardner KL. Update on the genetics of migraine. Human Genetics 2004 114 : 225 235.
16. Jen JC, Wan J, Paolos TP, Howard BD, Baloh RW. Mutation in the glutamate transporter EAAT1 causes episodic ataxia, hemiplegic, and seizures. Neurology 2005 65 : 529 534.
17. Gardner KL. Genetics of migraine: an update. Headache 2006 46 (Suppl. 1 S19 S24.
18. Wessman M, Terwindt GM, Kaunisto MA, Palotie A, Ophoff RA. Migraine: a complex genetic disorder. Lancet Neurology 2007 6 : 521 532.