메뉴 건너뛰기




Volumn 19, Issue 1, 1999, Pages 20-22

Search for mitochondrial DNA mutations in migraine subgroups

Author keywords

MELAS; Migraine; Mitochondria; mtDNA mutations

Indexed keywords

MITOCHONDRIAL DNA;

EID: 0033019867     PISSN: 03331024     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1468-2982.1999.1901020.x     Document Type: Article
Times cited : (34)

References (17)
  • 1
    • 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
  • 4
    • 0001784844 scopus 로고
    • Mutation in platelet mitochondrial gene in patients with migraine
    • Shimomura T, Kitano A, Marukawa H, Takahashi K. Mutation in platelet mitochondrial gene in patients with migraine. Cephalalgia 1995;15 Suppl. 14:10
    • (1995) Cephalalgia , vol.15 , Issue.SUPPL. 14 , pp. 10
    • Shimomura, T.1    Kitano, A.2    Marukawa, H.3    Takahashi, K.4
  • 5
    • 0027373654 scopus 로고
    • An A-to-G transition at nucleotide pair 11084 in the ND4 gene may be an mtDNA polymorphism
    • 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;53:964-5
    • (1993) Am J Hum Genet , vol.53 , pp. 964-965
    • Sakuta, R.1    Goto, Y.2    Nonaka, I.3    Horai, S.4
  • 7
    • 0032497128 scopus 로고    scopus 로고
    • Mitochondrial DNA haplogroup U as a risk factor for occipital stroke in migraine
    • Majamaa K, Finnila S, Turkka J, Hassinen IE. Mitochondrial DNA haplogroup U as a risk factor for occipital stroke in migraine. Lancet 1998;352:455-6
    • (1998) Lancet , vol.352 , pp. 455-456
    • Majamaa, K.1    Finnila, S.2    Turkka, J.3    Hassinen, I.E.4
  • 9
    • 0030762172 scopus 로고    scopus 로고
    • The factor V Leiden mutation (R506Q) is not a major risk factor for migrainous cerebral infarction
    • Haan J, Kappelle LJ, de Ronde H, Ferrari MD, Bertina RM. The factor V Leiden mutation (R506Q) is not a major risk factor for migrainous cerebral infarction. Cephalalgia 1997;17:605-7
    • (1997) Cephalalgia , vol.17 , pp. 605-607
    • Haan, J.1    Kappelle, L.J.2    De Ronde, H.3    Ferrari, M.D.4    Bertina, R.M.5
  • 10
    • 0029960177 scopus 로고    scopus 로고
    • Heteroplasmy levels of a mitochondrial gene mutation associated with diabetes mellitus decrease in leucocyte DNA upon aging
    • 't Hart LM, Jansen JJ, Lemkes HHPJ, de Knijff P, Maassen JA. Heteroplasmy levels of a mitochondrial gene mutation associated with diabetes mellitus decrease in leucocyte DNA upon aging. Hum Mutat 1996;7:193-7
    • (1996) Hum Mutat , vol.7 , pp. 193-197
    • 'T Hart, L.M.1    Jansen, J.J.2    Lemkes, H.H.P.J.3    De Knijff, P.4    Maassen, J.A.5
  • 11
    • 0026708671 scopus 로고
    • Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS): A correlative study of the clinical features and mitochondrial DNA mutation
    • Goto Y, Horai S, Matsuoka T, et al. Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS): A correlative study of the clinical features and mitochondrial DNA mutation. Neurology 1992;42: 545-50
    • (1992) Neurology , vol.42 , pp. 545-550
    • Goto, Y.1    Horai, S.2    Matsuoka, T.3
  • 12
    • 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;96:171-3
    • (1997) Acta Neurol Scand , vol.96 , pp. 171-173
    • Russell, M.B.1    Diamant, M.2    Norby, S.3
  • 13
    • 0026641790 scopus 로고
    • A new disease-related mutation for mitochondrial encephalopathy lactic acidosis and stroke-like episodes (MELAS) affects the ND4 subunit of the respiratory complex I
    • Lertrit P, Noer AS, Jean-Francois MJB, Kapsa R, Dennett X, Thyagarajan D, et al. A new disease-related mutation for mitochondrial encephalopathy lactic acidosis and stroke-like episodes (MELAS) affects the ND4 subunit of the respiratory complex I. Am J Hum Genet 1992;51:457-68
    • (1992) Am J Hum Genet , vol.51 , pp. 457-468
    • Lertrit, P.1    Noer, A.S.2    Jean-Francois, M.J.B.3    Kapsa, R.4    Dennett, X.5    Thyagarajan, D.6
  • 14
    • 0029166941 scopus 로고
    • Leber's "plus": Neurological abnormalities in patients with Leber's hereditary optic neuropathy
    • Nikoskelainen EK, Marttila RJ, Huoponen K, et al. Leber's "plus": Neurological abnormalities in patients with Leber's hereditary optic neuropathy. J Neurol Neurosurg Psychiatry 1995;59:160-4
    • (1995) J Neurol Neurosurg Psychiatry , vol.59 , pp. 160-164
    • Nikoskelainen, E.K.1    Marttila, R.J.2    Huoponen, K.3
  • 16
    • 0027441181 scopus 로고
    • Variable retinal and neurological manifestations in patients harboring the mitochondrial DNA 8993 mutation
    • Ortiz RG, Newman NJ, Shoffner JM, Kaufman AE, Koontz DA, Wallace DC. Variable retinal and neurological manifestations in patients harboring the mitochondrial DNA 8993 mutation. Arch Ophthalmol 1993;111:1525-30
    • (1993) Arch Ophthalmol , vol.111 , pp. 1525-1530
    • Ortiz, R.G.1    Newman, N.J.2    Shoffner, J.M.3    Kaufman, A.E.4    Koontz, D.A.5    Wallace, D.C.6
  • 17
    • 0031024138 scopus 로고    scopus 로고
    • Wolfram (DIDMOAD) syndrome and Leber hereditary optic neuropathy (LHON) are associated with distinct mitochondrial DNA haplotypes
    • Hofmann S, Bezold R, Jaksch M, et al. Wolfram (DIDMOAD) syndrome and Leber hereditary optic neuropathy (LHON) are associated with distinct mitochondrial DNA haplotypes. Genomics 1997;39:8-18
    • (1997) Genomics , vol.39 , pp. 8-18
    • Hofmann, S.1    Bezold, R.2    Jaksch, M.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.