메뉴 건너뛰기




Volumn 60, Issue 7 SUPPL. 2, 2003, Pages

Heritability of migraine: Genetic findings

Author keywords

[No Author keywords available]

Indexed keywords

CALCIUM CHANNEL;

EID: 0037426441     PISSN: 00283878     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Conference Paper
Times cited : (8)

References (50)
  • 1
    • 0346031709 scopus 로고
    • Classification and diagnostic criteria for headache disorders, cranial neuralgias and facial pain
    • Headache Classification Committee of the International Headache Society. Classification and diagnostic criteria for headache disorders, cranial neuralgias and facial pain. Cephalalgia 1988;8(suppl 7):1-96.
    • (1988) Cephalalgia , vol.8 , Issue.SUPPL. 7 , pp. 1-96
  • 2
    • 0029119352 scopus 로고
    • Increased familial risk and evidence of genetic factor in migraine
    • Russell MB, Olesen J. Increased familial risk and evidence of genetic factor in migraine. BMJ 1995;311:541-544.
    • (1995) BMJ , vol.311 , pp. 541-544
    • Russell, M.B.1    Olesen, J.2
  • 3
  • 5
    • 0032965665 scopus 로고    scopus 로고
    • Evidence of a genetic factor in migraine with aura: A population-based Danish twin study
    • Ulrich V, Gervil M, Kyvik KO, Olesen J, Russell MB. Evidence of a genetic factor in migraine with aura: a population-based Danish twin study. Ann Neurol 1999;45:242-246.
    • (1999) Ann Neurol , vol.45 , pp. 242-246
    • Ulrich, V.1    Gervil, M.2    Kyvik, K.O.3    Olesen, J.4    Russell, M.B.5
  • 6
    • 0033595437 scopus 로고    scopus 로고
    • The relative role of genetic and environmental factors in migraine without aura
    • Gervil M, Ulrich V, Kaprio J, Olesen J, Russell MB. The relative role of genetic and environmental factors in migraine without aura. Neurology 1999;53:995-999.
    • (1999) Neurology , vol.53 , pp. 995-999
    • Gervil, M.1    Ulrich, V.2    Kaprio, J.3    Olesen, J.4    Russell, M.B.5
  • 7
    • 0033022635 scopus 로고    scopus 로고
    • The inheritance of migraine with aura estimated by means of structural equation modelling
    • Ulrich V, Gervil M, Kyvik KO, Olesen J, Russell MB. The inheritance of migraine with aura estimated by means of structural equation modelling. J Med Genet 1999;36:225-227.
    • (1999) J Med Genet , vol.36 , pp. 225-227
    • Ulrich, V.1    Gervil, M.2    Kyvik, K.O.3    Olesen, J.4    Russell, M.B.5
  • 8
    • 16044370232 scopus 로고    scopus 로고
    • Familial hemiplegic migraine and episodic ataxia type-2 are caused by mutations in the Ca2+ channel gene CACNL1A4
    • Ophoff RA, Terwindt GM, Vergouwe MN, et al. Familial hemiplegic migraine and episodic ataxia type-2 are caused by mutations in the Ca2+ channel gene CACNL1A4. Cell 1996;87:543-552.
    • (1996) Cell , vol.87 , pp. 543-552
    • Ophoff, R.A.1    Terwindt, G.M.2    Vergouwe, M.N.3
  • 9
    • 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
  • 11
    • 0028142733 scopus 로고
    • Genetic heterogeneity of familial hemiplegic migraine
    • Ophoff RA, van Eijk R, Sandkuijl LA, et al. Genetic heterogeneity of familial hemiplegic migraine. Genomics 1994;22:21-26.
    • (1994) Genomics , vol.22 , pp. 21-26
    • Ophoff, R.A.1    Van Eijk, R.2    Sandkuijl, L.A.3
  • 12
    • 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
  • 13
    • 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
  • 14
    • 0002731790 scopus 로고    scopus 로고
    • The genetics of headache
    • Silberstein SD, Lipton RB, Dalessio DJ, eds. New York: Oxford University Press
    • Ferrari MD, Haan J. The genetics of headache. In: Silberstein SD, Lipton RB, Dalessio DJ, eds. Wolff's headache and other head pain, 7th ed. New York: Oxford University Press, 2001:73-84.
    • (2001) Wolff's Headache and Other Head Pain, 7th Ed. , pp. 73-84
    • Ferrari, M.D.1    Haan, J.2
  • 15
    • 0000205562 scopus 로고    scopus 로고
    • A new mutation in the Chr19p calcium channel gene CACNL1A4 causing hemiplegic migraine with ataxia
    • Gardner K, Bernal O, Keegan M. A new mutation in the Chr19p calcium channel gene CACNL1A4 causing hemiplegic migraine with ataxia. Neurology 1999;52(suppl 2):A115-A116.
    • (1999) Neurology , vol.52 , Issue.SUPPL. 2
    • Gardner, K.1    Bernal, O.2    Keegan, M.3
  • 16
  • 17
    • 0003030177 scopus 로고    scopus 로고
    • Effect of mutations linked to familial hemiplegic migraine on the biophysical properties of human a1A-containing calcium channels
    • Pietrobon D, Luvisetto S, Spagnolo M. Effect of mutations linked to familial hemiplegic migraine on the biophysical properties of human a1A-containing calcium channels. Soc Neurosci Abst 1998;24:21.
    • (1998) Soc Neurosci Abst , vol.24 , pp. 21
    • Pietrobon, D.1    Luvisetto, S.2    Spagnolo, M.3
  • 18
    • 0033103648 scopus 로고    scopus 로고
    • Functional consequences of mutations in the human alpha1A calcium channel subunit linked to familial hemiplegic migraine
    • Hans M, Luvisetto S, Williams ME, et al. Functional consequences of mutations in the human alpha1A calcium channel subunit linked to familial hemiplegic migraine. J Neurosci 1999;19:1610-1619.
    • (1999) J Neurosci , vol.19 , pp. 1610-1619
    • Hans, M.1    Luvisetto, S.2    Williams, M.E.3
  • 20
    • 0032975258 scopus 로고    scopus 로고
    • High prevalence of CACNA1A truncations and broader clinical spectrum in episodic ataxia type 2
    • Denier C, Ducros A, Vahedi K, et al. High prevalence of CACNA1A truncations and broader clinical spectrum in episodic ataxia type 2. Neurology 1999;52:1816-1821.
    • (1999) Neurology , vol.52 , pp. 1816-1821
    • Denier, C.1    Ducros, A.2    Vahedi, K.3
  • 21
    • 0032557725 scopus 로고    scopus 로고
    • De novo mutation in CACNA1A caused acetazolamide-responsive episodic ataxia
    • Yue Q, Jen JC, Thwe MM, Nelson SF, Baloh RW. De novo mutation in CACNA1A caused acetazolamide-responsive episodic ataxia. Am J Med Genet 1998;77:298-301.
    • (1998) Am J Med Genet , vol.77 , pp. 298-301
    • Yue, Q.1    Jen, J.C.2    Thwe, M.M.3    Nelson, S.F.4    Baloh, R.W.5
  • 22
    • 0031012399 scopus 로고    scopus 로고
    • Autosomal dominant cerebellar ataxia (SCA6) associated with small polyglutamine expansions in the alpha 1A-voltage-dependent calcium channel
    • Zhuchenko O, Bailey J, Bonnen P, et al. Autosomal dominant cerebellar ataxia (SCA6) associated with small polyglutamine expansions in the alpha 1A-voltage-dependent calcium channel. Nat Genet 1997;15:62-69.
    • (1997) Nat Genet , vol.15 , pp. 62-69
    • Zhuchenko, O.1    Bailey, J.2    Bonnen, P.3
  • 23
    • 0031896548 scopus 로고    scopus 로고
    • Variable clinical expression of mutations in the P/Q-type calcium channel gene in familial hemiplegic migraine
    • Dutch Migraine Genetics Research Group
    • Terwindt GM, Ophoff RA, Haan J, et al. Variable clinical expression of mutations in the P/Q-type calcium channel gene in familial hemiplegic migraine. Dutch Migraine Genetics Research Group. Neurology 1998;50:1105-1110.
    • (1998) Neurology , vol.50 , pp. 1105-1110
    • Terwindt, G.M.1    Ophoff, R.A.2    Haan, J.3
  • 24
    • 9844263366 scopus 로고    scopus 로고
    • Episodic ataxia type 2 (EA2) and spinocerebellar ataxia type 6 (SCA6) due to CAG repeat expansion in the CACNA1A gene on chromosome 19p
    • Jodice C, Mantuano E, Veneziano L, et al. Episodic ataxia type 2 (EA2) and spinocerebellar ataxia type 6 (SCA6) due to CAG repeat expansion in the CACNA1A gene on chromosome 19p. Hum Mol Genet 1997;6:1973-1978.
    • (1997) Hum Mol Genet , vol.6 , pp. 1973-1978
    • Jodice, C.1    Mantuano, E.2    Veneziano, L.3
  • 25
    • 0031726082 scopus 로고    scopus 로고
    • Spinocerebellar ataxia type 6 with positional vertigo and acetazolamide responsive episodic ataxia
    • Jen JC, Yue Q, Karrim J, Nelson SF, Baloh RW. Spinocerebellar ataxia type 6 with positional vertigo and acetazolamide responsive episodic ataxia. J Neurol Neurosurg Psychiatry 1998;65:565-568.
    • (1998) J Neurol Neurosurg Psychiatry , vol.65 , pp. 565-568
    • Jen, J.C.1    Yue, Q.2    Karrim, J.3    Nelson, S.F.4    Baloh, R.W.5
  • 26
    • 0030776159 scopus 로고    scopus 로고
    • Progressive ataxia due to a missense mutation in a calcium-channel gene
    • Yue Q, Jen JC, Nelson SF, Baloh RW. Progressive ataxia due to a missense mutation in a calcium-channel gene. Am J Hum Genet 1997;61:1078-1087.
    • (1997) Am J Hum Genet , vol.61 , pp. 1078-1087
    • Yue, Q.1    Jen, J.C.2    Nelson, S.F.3    Baloh, R.W.4
  • 27
    • 0033551468 scopus 로고    scopus 로고
    • A novel nonsense mutation in CACNA1A causes episodic ataxia and hemiplegia
    • Jen J, Yue Q, Nelson SF, et al. A novel nonsense mutation in CACNA1A causes episodic ataxia and hemiplegia. Neurology 1999;53:34-37.
    • (1999) Neurology , vol.53 , pp. 34-37
    • Jen, J.1    Yue, Q.2    Nelson, S.F.3
  • 28
    • 0031064169 scopus 로고    scopus 로고
    • Mutations in the CACNL1A4 calcium channel gene are associated with seizures, cerebellar degeneration, and ataxia in tottering and leaner mutant mice
    • Doyle J, Ren X, Lennon G, Stubbs L. Mutations in the CACNL1A4 calcium channel gene are associated with seizures, cerebellar degeneration, and ataxia in tottering and leaner mutant mice. Mamm Genome 1997;8:113-120.
    • (1997) Mamm Genome , vol.8 , pp. 113-120
    • Doyle, J.1    Ren, X.2    Lennon, G.3    Stubbs, L.4
  • 29
    • 0032526434 scopus 로고    scopus 로고
    • Altered calcium channel currents in Purkinje cells of the neurological mutant mouse leaner
    • Lorenzon NM, Lutz CM, Frankel WN, Beam KG. Altered calcium channel currents in Purkinje cells of the neurological mutant mouse leaner. J Neurosci 1998;18:4482-4489.
    • (1998) J Neurosci , vol.18 , pp. 4482-4489
    • Lorenzon, N.M.1    Lutz, C.M.2    Frankel, W.N.3    Beam, K.G.4
  • 30
    • 0034988145 scopus 로고    scopus 로고
    • Delayed cerebral edema and fatal coma after minor head trauma: Role of the CACNA1A calcium channel subunit gene and relationship with familial hemiplegic migraine
    • Kors EE, Terwindt GM, Vermeulen FL, et al. Delayed cerebral edema and fatal coma after minor head trauma: role of the CACNA1A calcium channel subunit gene and relationship with familial hemiplegic migraine. Ann Neurol 2001;49:753-760.
    • (2001) Ann Neurol , vol.49 , pp. 753-760
    • Kors, E.E.1    Terwindt, G.M.2    Vermeulen, F.L.3
  • 31
    • 0028806580 scopus 로고
    • Familial hemiplegic migraine locus on 19p13 is involved in the common forms of migraine with and without aura
    • May A, Ophoff RA, Terwindt GM, et al. Familial hemiplegic migraine locus on 19p13 is involved in the common forms of migraine with and without aura. Hum Genet 1995;96:604-608.
    • (1995) Hum Genet , vol.96 , pp. 604-608
    • May, A.1    Ophoff, R.A.2    Terwindt, G.M.3
  • 32
    • 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
  • 33
    • 0031844375 scopus 로고    scopus 로고
    • Familial typical migraine: Linkage to chromosome 19p13 and evidence for genetic heterogeneity
    • Nyholt DR, Lea RA, Goadsby PJ, Brimage PJ, Griffiths LR. Familial typical migraine: linkage to chromosome 19p13 and evidence for genetic heterogeneity. Neurology 1998;50:1428-1432.
    • (1998) Neurology , vol.50 , pp. 1428-1432
    • Nyholt, D.R.1    Lea, R.A.2    Goadsby, P.J.3    Brimage, P.J.4    Griffiths, L.R.5
  • 34
    • 0031907348 scopus 로고    scopus 로고
    • Clinical and genetic analysis of a large Dutch family with autosomal dominant vascular retinopathy, migraine and Raynaud's phenomenon
    • Terwindt G, Haan J, Ophoff R, et al. Clinical and genetic analysis of a large Dutch family with autosomal dominant vascular retinopathy, migraine and Raynaud's phenomenon. Brain 1998;121:303-316.
    • (1998) Brain , vol.121 , pp. 303-316
    • Terwindt, G.1    Haan, J.2    Ophoff, R.3
  • 35
    • 0034920305 scopus 로고    scopus 로고
    • Hereditary vascular retinopathy, cerebroretinal vasculopathy, and hereditary endotheliopathy with retinopathy, nephropathy, and stroke map to a single locus on chromosome 3p21.1-p21.3
    • Ophoff RA, DeYoung J, Service SK, et al. Hereditary vascular retinopathy, cerebroretinal vasculopathy, and hereditary endotheliopathy with retinopathy, nephropathy, and stroke map to a single locus on chromosome 3p21.1-p21.3. Am J Hum Genet 2001;69:447-453.
    • (2001) Am J Hum Genet , vol.69 , pp. 447-453
    • Ophoff, R.A.1    DeYoung, J.2    Service, S.K.3
  • 36
    • 0031931027 scopus 로고    scopus 로고
    • Altered allelic distributions of the serotonin transporter gene in migraine without aura and migraine with aura
    • Ogilvie AD, Russell MB, Dhall P, et al. Altered allelic distributions of the serotonin transporter gene in migraine without aura and migraine with aura. Cephalalgia 1998;18:23-26.
    • (1998) Cephalalgia , vol.18 , pp. 23-26
    • Ogilvie, A.D.1    Russell, M.B.2    Dhall, P.3
  • 37
    • 0030818633 scopus 로고    scopus 로고
    • Clinical susceptibility to migraine with aura is modified by dopamine D2 receptor (DRD2) NcoI alleles
    • Peroutka SJ, Wilhoit T, Jones K. Clinical susceptibility to migraine with aura is modified by dopamine D2 receptor (DRD2) NcoI alleles. Neurology 1997;49:201-206.
    • (1997) Neurology , vol.49 , pp. 201-206
    • Peroutka, S.J.1    Wilhoit, T.2    Jones, K.3
  • 38
    • 0031916498 scopus 로고    scopus 로고
    • Comorbid migraine with aura, anxiety, and depression is associated with dopamine D2 receptor (DRD2) NcoI alleles
    • Peroutka SJ, Price SC, Wilhoit TL, Jones KW. Comorbid migraine with aura, anxiety, and depression is associated with dopamine D2 receptor (DRD2) NcoI alleles. Mol Med 1998;4:14-21.
    • (1998) Mol Med , vol.4 , pp. 14-21
    • Peroutka, S.J.1    Price, S.C.2    Wilhoit, T.L.3    Jones, K.W.4
  • 39
    • 0031782998 scopus 로고    scopus 로고
    • Association between dopamine receptor genes and migraine without aura in a Sardinian sample
    • Del Zompo M, Cherchi A, Palmas MA, et al. Association between dopamine receptor genes and migraine without aura in a Sardinian sample. Neurology 1998;51:781-786.
    • (1998) Neurology , vol.51 , pp. 781-786
    • Del Zompo, M.1    Cherchi, A.2    Palmas, M.A.3
  • 40
    • 0031752626 scopus 로고    scopus 로고
    • The D2 receptor NcoI allele: Absence of allelic association with migraine with aura
    • Letter
    • Dichgans M, Forderreuther S, Deiterich M, Pfaffenrath V, Gasser T. The D2 receptor NcoI allele: absence of allelic association with migraine with aura. Neurology 1998;51:928. Letter.
    • (1998) Neurology , vol.51 , pp. 928
    • Dichgans, M.1    Forderreuther, S.2    Deiterich, M.3    Pfaffenrath, V.4    Gasser, T.5
  • 42
    • 0028787008 scopus 로고
    • Mitochondria, magnesium and migraine
    • Welch KMA, Ramadan NM. Mitochondria, magnesium and migraine. J Neurol Sci 1995;134:9-14.
    • (1995) J Neurol Sci , vol.134 , pp. 9-14
    • Welch, K.M.A.1    Ramadan, N.M.2
  • 43
    • 0028957093 scopus 로고
    • Abnormal brain and muscle energy metabolism shown by 31P-MRS in familial hemiplegic migraine
    • Uncini A, Lodi R, Di Muzio A, et al. Abnormal brain and muscle energy metabolism shown by 31P-MRS in familial hemiplegic migraine. J Neurol Sci 1995;129:214-222.
    • (1995) J Neurol Sci , vol.129 , pp. 214-222
    • Uncini, A.1    Lodi, R.2    Di Muzio, A.3
  • 47
    • 0001784844 scopus 로고
    • Mutation in platelet mitochondrial gene in patients with migraine
    • Abstract
    • Shimomura T, Kitano A, Marukawa H, Takahashi K. Mutation in platelet mitochondrial gene in patients with migraine. Cephalalgia 1995;15(suppl 14):10. Abstract.
    • (1995) Cephalalgia , vol.15 , Issue.SUPPL. 14 , pp. 10
    • Shimomura, T.1    Kitano, A.2    Marukawa, H.3    Takahashi, K.4
  • 48
    • 0030869213 scopus 로고    scopus 로고
    • Genetic heterogeneity of migraine with and without aura in Danes cannot be explained by mutation in mtDNA nucleotide pair 11084
    • Russell MB, Diamant M, Norby S. Genetic heterogeneity of migraine with and without aura in Danes cannot be explained by mutation in mtDNA nucleotide pair 11084. Acta Neurol Scand 1997;96:171-173.
    • (1997) Acta Neurol Scand , vol.96 , pp. 171-173
    • Russell, M.B.1    Diamant, M.2    Norby, S.3
  • 49
    • 0027373654 scopus 로고
    • An A-to-G transition at nucleotide pair 11084 in the ND4 gene may be an mtDNA polymorphism
    • Letter
    • Sakuta R, Goto Y, Nonaka I, Horai S. An A-to-G transition at nucleotide pair 11084 in the ND4 gene may be an mtDNA polymorphism. Am J Hum Genet 1993;53:964-965. Letter.
    • (1993) Am J Hum Genet , vol.53 , pp. 964-965
    • Sakuta, R.1    Goto, Y.2    Nonaka, I.3    Horai, S.4
  • 50
    • 0032497128 scopus 로고    scopus 로고
    • Mitochondrial DNA haplogroup U as a risk factor for occipital stroke in migraine
    • Letter
    • Majamaa K, Finnila S, Turkka J, Hassinen IE. Mitochondrial DNA haplogroup U as a risk factor for occipital stroke in migraine. Lancet 1998;352:455-456. Letter.
    • (1998) Lancet , vol.352 , pp. 455-456
    • Majamaa, K.1    Finnila, S.2    Turkka, J.3    Hassinen, I.E.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.