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Current Opinion in Neurology
Volumn 16, Issue 3, 2003, Pages 315-317
Migraine: Does one size fit all?
Author keywords

[No Author keywords available]
Indexed keywords

CLINICAL FEATURE; EDITORIAL; GENETIC PREDISPOSITION; GENETIC VARIABILITY; HEADACHE; HUMAN; MIGRAINE; PATHOPHYSIOLOGY;
EID: 0037782209     PISSN: 13507540     EISSN: None     Source Type: Journal    
DOI: 10.1097/00019052-200306000-00010     Document Type: Editorial
Times cited : (5)
References (9)
  • 1
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    • Migraine and concomitant symptoms among 8167 adult twin pairs
    • Honkasalo ML, Kaprio J, Winter T, et al. Migraine and concomitant symptoms among 8167 adult twin pairs. Headache 1995; 35:70-78.
    • (1995) Headache , vol.35 , pp. 70-78
    • Honkasalo, M.L.1    Kaprio, J.2    Winter, T.3
  • 2
    • 0027306090 scopus 로고
    • A gene for familial hemiplegic migraine maps to chromosome 19
    • Joutel A, Bousser MG, Biousse V, et al. A gene for familial hemiplegic migraine maps to chromosome 19. Nat Genet 1993; 5:40-45.
    • (1993) Nat Genet , vol.5 , pp. 40-45
    • Joutel, A.1    Bousser, M.G.2    Biousse, V.3
  • 3
    • 16044370232 scopus 로고    scopus 로고
    • Familial hemiplegic migraine and episodic ataxia type 2 are caused by mutations in the Ca2+ channel gene CACNLA4
    • Ophoff RA, Terwindt GM, Vergouwe MD, et al. Familial hemiplegic migraine and episodic ataxia type 2 are caused by mutations in the Ca2+ channel gene CACNLA4. Cell 1996; 87:543-552.
    • (1996) Cell , vol.87 , pp. 543-552
    • Ophoff, R.A.1    Terwindt, G.M.2    Vergouwe, M.D.3
  • 4
    • 0030657961 scopus 로고    scopus 로고
    • A new locus for hemiplegic migraine maps to chromosome 1q31
    • Gardner K, Barmada MM, Ptacek LJ, Hoffman EP. A new locus for hemiplegic migraine maps to chromosome 1q31. Neurology 1997; 49:1231-1238.
    • (1997) Neurology , vol.49 , pp. 1231-1238
    • Gardner, K.1    Barmada, M.M.2    Ptacek, L.J.3    Hoffman, E.P.4
  • 5
    • 0031470730 scopus 로고    scopus 로고
    • Mapping of a second locus for familial hemiplegic migraine to 1q21-q23 and evidence of further heterogeneity
    • Ducros A, Joutel A, Vahedi K, et al. Mapping of a second locus for familial hemiplegic migraine to 1q21-q23 and evidence of further heterogeneity. Ann Neurol 1997; 42:885-890.
    • (1997) Ann Neurol , vol.42 , pp. 885-890
    • Ducros, A.1    Joutel, A.2    Vahedi, K.3
  • 6
    • 0035942343 scopus 로고    scopus 로고
    • Involvement of the CACNA1A gene containing region on 19p13 in migraine with and without aura
    • Terwindt GM, Ophoff RA, van Eijk R, et al. Involvement of the CACNA1A gene containing region on 19p13 in migraine with and without aura. Neurology 2001; 56:1028-1032.
    • (2001) Neurology , vol.56 , pp. 1028-1032
    • Terwindt, G.M.1    Ophoff, R.A.2    Van Eijk, R.3
  • 7
    • 18244372492 scopus 로고    scopus 로고
    • A susceptibility locus for migraine with aura, on chromosome 4q24
    • Wessman M, Kallela M, Kaunisto MA, et al. A susceptibility locus for migraine with aura, on chromosome 4q24. Am J Hum Genet 2002; 70:652-662.
    • (2002) Am J Hum Genet , vol.70 , pp. 652-662
    • Wessman, M.1    Kallela, M.2    Kaunisto, M.A.3
  • 8
    • 0037058780 scopus 로고    scopus 로고
    • Identification of a susceptibility locus for migraine with and without aura on 6p12.2-p21.1
    • Carlsson A, Forsgren L, Nylander P-O, et al. Identification of a susceptibility locus for migraine with and without aura on 6p12.2-p21.1. Neurology 2002; 59:1804-1807.
    • (2002) Neurology , vol.59 , pp. 1804-1807
    • Carlsson, A.1    Forsgren, L.2    Nylander, P.-O.3
  • 9
    • 0031912334 scopus 로고    scopus 로고
    • Evidence for an X-lined genetic component in familial typical migraine
    • Nyholt DR, Dawkins JL, Brimage PJ, et al. Evidence for an X-lined genetic component in familial typical migraine. Hum Mol Genet 1998; 7:459-463.
    • (1998) Hum Mol Genet , vol.7 , pp. 459-463
    • Nyholt, D.R.1    Dawkins, J.L.2    Brimage, P.J.3

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.