메뉴 건너뛰기




Volumn 11, Issue 3, 1998, Pages 217-226

The place of migraine as a channelopathy

Author keywords

[No Author keywords available]

Indexed keywords

CALCIUM CHANNEL; CHLORIDE CHANNEL; SODIUM CHANNEL;

EID: 0031837371     PISSN: 13507540     EISSN: None     Source Type: Journal    
DOI: 10.1097/00019052-199806000-00005     Document Type: Review
Times cited : (40)

References (60)
  • 1
    • 0027511236 scopus 로고
    • Genetics and physiology of the myotonic muscle disorders
    • Ptácek LJ, Johnson KJ, Griggs RC. Genetics and physiology of the myotonic muscle disorders. N Engl J Med 1993; 328:482-489.
    • (1993) N Engl J Med , vol.328 , pp. 482-489
    • Ptácek, L.J.1    Johnson, K.J.2    Griggs, R.C.3
  • 2
    • 0343488504 scopus 로고    scopus 로고
    • Channelopathies: Ion channel disorders of muscle as a paradigm for paroxysmal disorders of the nervous system
    • Ptácek LJ. Channelopathies: ion channel disorders of muscle as a paradigm for paroxysmal disorders of the nervous system. Neuromusc Disord 1997; 7:250-255.
    • (1997) Neuromusc Disord , vol.7 , pp. 250-255
    • Ptácek, L.J.1
  • 3
    • 0023140306 scopus 로고
    • Adynamia episodica hereditaria with myotonia : A non-inactivating sodium current and the effect of extracellular pH
    • Lehmann Horn F, Kuther G, Ricker K, Grate P, Ballanyi K, Rudel R. Adynamia episodica hereditaria with myotonia : a non-inactivating sodium current and the effect of extracellular pH. Muscle Nerve 1987; 10:363-374.
    • (1987) Muscle Nerve , vol.10 , pp. 363-374
    • Lehmann Horn, F.1    Kuther, G.2    Ricker, K.3    Grate, P.4    Ballanyi, K.5    Rudel, R.6
  • 4
  • 5
    • 0025774566 scopus 로고
    • A sodium channel defect in hyperkalemic periodic paralysis: Potassium-induced failure of inactivation
    • Cannon SC, Brown RH Jr, Corey DP. A sodium channel defect in hyperkalemic periodic paralysis: potassium-induced failure of inactivation. Neuron 1991; 6:619-626.
    • (1991) Neuron , vol.6 , pp. 619-626
    • Cannon, S.C.1    Brown Jr., R.H.2    Corey, D.P.3
  • 6
    • 0023179138 scopus 로고
    • Membrane defects in paramyotonia congenita (Eulenburg)
    • Lehmann Horn F, Rudel R, Ricker K. Membrane defects in paramyotonia congenita (Eulenburg). Muscle Nerve 1987; 10:633-641.
    • (1987) Muscle Nerve , vol.10 , pp. 633-641
    • Lehmann Horn, F.1    Rudel, R.2    Ricker, K.3
  • 11
    • 0026516209 scopus 로고
    • Temperature-sensitive mutations in the III-IV cytoplasmic loop region of the skeletal muscle sodium channel gene in paramyotonia congenita
    • McClatchey AI, Van den Bergh P, Pericak Vance MA, Raskind W, Verellen C, McKenna Yasek D, et al. Temperature-sensitive mutations in the III-IV cytoplasmic loop region of the skeletal muscle sodium channel gene in paramyotonia congenita. Cell 1992; 68:769-774.
    • (1992) Cell , vol.68 , pp. 769-774
    • McClatchey, A.I.1    Van Den Bergh, P.2    Pericak Vance, M.A.3    Raskind, W.4    Verellen, C.5    McKenna Yasek, D.6
  • 13
    • 0027409755 scopus 로고
    • Functional expression of sodium channel mutations identified in families with periodic paralysis
    • Cannon SC, Strittmatter SM. Functional expression of sodium channel mutations identified in families with periodic paralysis. Neuron 1993; 10:317-326.
    • (1993) Neuron , vol.10 , pp. 317-326
    • Cannon, S.C.1    Strittmatter, S.M.2
  • 15
    • 0028326016 scopus 로고
    • Sodium channel mutations in paramyotonia congenita uncouple inactivation from activation
    • Chahine M, George AL, Jr., Zhou M, Ji S, Sun W, Barchi RL, Horn R. Sodium channel mutations in paramyotonia congenita uncouple inactivation from activation. Neuron 1994; 12:281-294.
    • (1994) Neuron , vol.12 , pp. 281-294
    • Chahine, M.1    George Jr., A.L.2    Zhou, M.3    Ji, S.4    Sun, W.5    Barchi, R.L.6    Horn, R.7
  • 19
    • 0028854326 scopus 로고
    • Hypokalemic periodic paralysis and the dihydropyridine receptor (CACNL1A3):genotype/phenotype correlations tor two predominant mutations and evidence for the absence of a founder effect in 16 caucasian families
    • Elbaz A, Vale Santos J, Jurkat Rott K, Lapie P, Ophoff RA, Bady B, et al. Hypokalemic periodic paralysis and the dihydropyridine receptor (CACNL1A3):genotype/phenotype correlations tor two predominant mutations and evidence for the absence of a founder effect in 16 caucasian families. Am J Hum Genet 1995; 56:374-380.
    • (1995) Am J Hum Genet , vol.56 , pp. 374-380
    • Elbaz, A.1    Vale Santos, J.2    Jurkat Rott, K.3    Lapie, P.4    Ophoff, R.A.5    Bady, B.6
  • 21
    • 0026705098 scopus 로고
    • The skeletal muscle chloride channel in dominant and recessive human myotonia
    • Koch MC, Steinmeyer K, Lorenz C, Ricker K, Wolf F, Otto M, et al. The skeletal muscle chloride channel in dominant and recessive human myotonia. Science 1992; 257:797-800.
    • (1992) Science , vol.257 , pp. 797-800
    • Koch, M.C.1    Steinmeyer, K.2    Lorenz, C.3    Ricker, K.4    Wolf, F.5    Otto, M.6
  • 23
    • 0028287533 scopus 로고
    • Proof of a non-functional muscle chloride channel in recessive myotonia congenita (Becker) by detection of a 4 base pair deletion
    • Heine R, George AL, Jr., Pika U, Deymeer F, Rudel R, Lehmann Horn F. Proof of a non-functional muscle chloride channel in recessive myotonia congenita (Becker) by detection of a 4 base pair deletion. Hum Mol Genet 1994; 3:1123-1128.
    • (1994) Hum Mol Genet , vol.3 , pp. 1123-1128
    • Heine, R.1    George Jr., A.L.2    Pika, U.3    Deymeer, F.4    Rudel, R.5    Lehmann Horn, F.6
  • 24
    • 0028093245 scopus 로고
    • Nonsense and missense mutations in the muscular chloride channel gene Clc-1 of myotonic mice
    • Gronemeier M, Condie A, Prosser J, Steinmeyer K, Jentsch TJ, Jockusch H. Nonsense and missense mutations in the muscular chloride channel gene Clc-1 of myotonic mice. J Biol Chem 1994; 269:5963-5967.
    • (1994) J Biol Chem , vol.269 , pp. 5963-5967
    • Gronemeier, M.1    Condie, A.2    Prosser, J.3    Steinmeyer, K.4    Jentsch, T.J.5    Jockusch, H.6
  • 25
    • 0029853212 scopus 로고    scopus 로고
    • Mutations in the human skeletal muscle chloride channel gene (CLCN1) associated with dominant and recessive myotonia congenita
    • Zhang J, George AL, Griggs RC, Fouad GT, Roberts J, Kwiecinski H, et al. Mutations in the human skeletal muscle chloride channel gene (CLCN1) associated with dominant and recessive myotonia congenita. Neurology 1996; 47:993-998.
    • (1996) Neurology , vol.47 , pp. 993-998
    • Zhang, J.1    George, A.L.2    Griggs, R.C.3    Fouad, G.T.4    Roberts, J.5    Kwiecinski, H.6
  • 26
    • 0029559938 scopus 로고
    • Mutations in dominant human myotonia congenita drastically alter the voltage dependence of the CIC-1 chloride channel
    • Pusch M, Steinmeyer K, Koch MC, Jentsch TJ. Mutations in dominant human myotonia congenita drastically alter the voltage dependence of the CIC-1 chloride channel. Neuron 1995; 15:1455-1463.
    • (1995) Neuron , vol.15 , pp. 1455-1463
    • Pusch, M.1    Steinmeyer, K.2    Koch, M.C.3    Jentsch, T.J.4
  • 27
    • 0029738742 scopus 로고    scopus 로고
    • Mechanism of voltage-dependent gating in skeletal muscle chloride channels
    • Fahlke C, Rosenbohm A, Mitrovic N, George AL, Jr., Rudel R. Mechanism of voltage-dependent gating in skeletal muscle chloride channels. Biophys J 1996; 71:695-706.
    • (1996) Biophys J , vol.71 , pp. 695-706
    • Fahlke, C.1    Rosenbohm, A.2    Mitrovic, N.3    George Jr., A.L.4    Rudel, R.5
  • 28
    • 0029162517 scopus 로고
    • An aspartic acid residue important for voltage-dependent gating of human muscle chloride channels
    • Fahlke C, Rudel R, Mitrovic N, Zhou M, George AL, Jr. An aspartic acid residue important for voltage-dependent gating of human muscle chloride channels. Neuron 1995; 15:463-472.
    • (1995) Neuron , vol.15 , pp. 463-472
    • Fahlke, C.1    Rudel, R.2    Mitrovic, N.3    Zhou, M.4    George Jr., A.L.5
  • 29
    • 0028124225 scopus 로고
    • Episodic ataxia/myokymia syndrome is associated with point mutations in the human potassium channel gene, KCNA1
    • Browne DL, Gancher ST, Nutt JG, Brunt ER, Smith EA, Kramer P, Litt M. Episodic ataxia/myokymia syndrome is associated with point mutations in the human potassium channel gene, KCNA1. Nat Genet 1994; 8:136-140.
    • (1994) Nat Genet , vol.8 , pp. 136-140
    • Browne, D.L.1    Gancher, S.T.2    Nutt, J.G.3    Brunt, E.R.4    Smith, E.A.5    Kramer, P.6    Litt, M.7
  • 32
    • 0028887901 scopus 로고
    • Familial hemiplegic migraine versus migraine with prolonged aura: An uncertain diagnosis in a family report
    • Marchioni E, Galimberti CA, Soragna D, Ferrandi D, Maurelli M, Ratti MT, et al. Familial hemiplegic migraine versus migraine with prolonged aura: an uncertain diagnosis in a family report. Neurology 1995; 45:33-37.
    • (1995) Neurology , vol.45 , pp. 33-37
    • Marchioni, E.1    Galimberti, C.A.2    Soragna, D.3    Ferrandi, D.4    Maurelli, M.5    Ratti, M.T.6
  • 33
    • 17344372328 scopus 로고    scopus 로고
    • A novel potassium channel gene. KCNQ2, is mutated in an inherited epilepsy of newborns
    • Singh NA, Charlier C, Stauffer D, DuPont BR, Leach RJ, Melis R, et al. •• A novel potassium channel gene. KCNQ2, is mutated in an inherited epilepsy of newborns. Nature Genet 1998; 18:25-29. This paper represents the first strong genetic data implicating an ion channel gene in a human epilepsy, benign familial neonatal convulsions. The gene encodes a voltage-gated potassium channel.
    • (1998) Nature Genet , vol.18 , pp. 25-29
    • Singh, N.A.1    Charlier, C.2    Stauffer, D.3    DuPont, B.R.4    Leach, R.J.5    Melis, R.6
  • 34
    • 0031974209 scopus 로고    scopus 로고
    • A pore mutation in a novel KQT-like potassium channel gene in an idiopathic epilepsy family
    • ••], the physical map of a second benign familial neonatal convulsion locus was examined for a gene homologous to the BFNC1 potassium channel. A second potassium channel causing a human epilepsy was characterized and shown to be mutated in a family mapping to this locus.
    • (1998) Nature Genet , vol.18 , pp. 53-55
    • Charlier, C.1    Singh, N.A.2    Ryan, S.G.3    Lewis, T.B.4    Reus, B.E.5    Leach, R.J.6    Leppert, M.7
  • 35
    • 0027330927 scopus 로고
    • Mutations in the alpha1 subunit of the inhibitory glycine receptor cause the dominant neurologic disorder, hyperekplexia
    • Shiang R, Ryan SG, Zhu YZ, Hahn AF, O'Connell P, Wasmuth JJ. Mutations in the alpha1 subunit of the inhibitory glycine receptor cause the dominant neurologic disorder, hyperekplexia. Nature Genet 1993; 5:351-358.
    • (1993) Nature Genet , vol.5 , pp. 351-358
    • Shiang, R.1    Ryan, S.G.2    Zhu, Y.3    Hahn, A.F.4    O'Connell, P.5    Wasmuth, J.J.6
  • 36
    • 10144229353 scopus 로고    scopus 로고
    • New mutations in acetylcholine receptor subunit genes reveal heterogeneity in the slow-channel congenital myasthenic syndrome
    • Engel AG, Ohno K, Milone M, Wang HL, Nakano S, Bouzat C, et al. New mutations in acetylcholine receptor subunit genes reveal heterogeneity in the slow-channel congenital myasthenic syndrome. Hum Mol Genet 1996; 5:1217-1227.
    • (1996) Hum Mol Genet , vol.5 , pp. 1217-1227
    • Engel, A.G.1    Ohno, K.2    Milone, M.3    Wang, H.L.4    Nakano, S.5    Bouzat, C.6
  • 39
    • 0000738544 scopus 로고
    • Familial paroxysmal choreoathetosis
    • Mount L, Reback S. Familial paroxysmal choreoathetosis. Arch Neurol Psychiatry 1940; 44:841-847.
    • (1940) Arch Neurol Psychiatry , vol.44 , pp. 841-847
    • Mount, L.1    Reback, S.2
  • 40
    • 0001504349 scopus 로고
    • Oxford: Butterworth-Heinemann
    • Fahn S. The paroxysmal dyskinesias. Oxford: Butterworth-Heinemann 1994, pp 310-345.
    • (1994) The Paroxysmal Dyskinesias , pp. 310-345
    • Fahn, S.1
  • 41
    • 0029091303 scopus 로고
    • Paroxysmal dyskinesias: Clinical features and classification
    • Demirkiran M, Jankovic J. Paroxysmal dyskinesias: clinical features and classification. Ann Neurol 1995; 38:571-579.
    • (1995) Ann Neurol , vol.38 , pp. 571-579
    • Demirkiran, M.1    Jankovic, J.2
  • 42
    • 0002635506 scopus 로고    scopus 로고
    • Channelopathies: Ion Channels and paroxysmal disorders of the Nervous system
    • Genton P, ed. London: John Libbey, in press
    • Ptáček LJ. Channelopathies: Ion Channels and paroxysmal disorders of the Nervous system. In: Genton P, ed. Genetics of Focal Epilepsies. London: John Libbey, 1998; in press.
    • (1998) Genetics of Focal Epilepsies
    • Ptáček, L.J.1
  • 43
    • 0031018816 scopus 로고    scopus 로고
    • Migraine and epilepsy
    • Welch KM, Lewis D. Migraine and epilepsy. Neurol Clin 1997; 15: 107-114.
    • (1997) Neurol Clin , vol.15 , pp. 107-114
    • Welch, K.M.1    Lewis, D.2
  • 44
    • 16044370232 scopus 로고    scopus 로고
    • 2+ gene CACNL1A4
    • 2+ gene CACNL1A4. Cell 1996; 87:543-552. This publication established the CACNL1A4 gene (a gene homologous to the calcium channel known to cause hypokalemic periodic paralysis: see [18]) as the site of mutation in episodic ataxia type 2 and one form of familial hemiplegic migraine.
    • (1996) Cell , vol.87 , pp. 543-552
    • Ophoff, R.A.1    Taswindt, G.M.2    Vergouwe, M.N.3    Van Eijk, R.4    Oefner, P.J.5    Hoffman, S.M.G.6
  • 45
    • 0031470730 scopus 로고    scopus 로고
    • Mapping of a second locus for familial hemiplegic migraine to 1q21-q23 and evidence of further heterogeneity
    • Process Citation.
    • Ducros A, Joutel A, Vahedi K, Cecillon M, Ferreira A, Bernard E, et al. Mapping of a second locus for familial hemiplegic migraine to 1q21-q23 and evidence of further heterogeneity In Process Citation. Ann Neurol 1997; 42:885-90.
    • (1997) Ann Neurol , vol.42 , pp. 885-890
    • Ducros, A.1    Joutel, A.2    Vahedi, K.3    Cecillon, M.4    Ferreira, A.5    Bernard, E.6
  • 46
    • 0030657961 scopus 로고    scopus 로고
    • A new locus for hemiplegic migraine maps to chromosome 1q31
    • Gardner K, Barmada MM, Ptáček 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    Ptáček, L.J.3    Hoffman, E.P.4
  • 47
    • 9044240040 scopus 로고    scopus 로고
    • Positional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arrhythmias
    • Wang Q, Curran ME, Splawski I, Burn TC, Millholland JM, VanRaay TJ, et al. Positional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arrhythmias. Nat Genet 1996; 12:17-23.
    • (1996) Nat Genet , vol.12 , pp. 17-23
    • Wang, Q.1    Curran, M.E.2    Splawski, I.3    Burn, T.C.4    Millholland, J.M.5    VanRaay, T.J.6
  • 49
    • 0028905566 scopus 로고
    • SCN5A mutations associated with an inherited cardiac arrhythmia, long QT syndrome
    • Wang Q, Shen J, Splawski I, Atkinson D, Li Z, Robinson JL, et al. SCN5A mutations associated with an inherited cardiac arrhythmia, long QT syndrome. Cell 1995;80:805-811.
    • (1995) Cell , vol.80 , pp. 805-811
    • Wang, Q.1    Shen, J.2    Splawski, I.3    Atkinson, D.4    Li, Z.5    Robinson, J.L.6
  • 51
    • 0028980028 scopus 로고
    • A missense mutation in the neuronal nicotinic acetylcholine receptor alpha 4 subunit is associated with autosomal dominant nocturnal frontal lobe epilepsy
    • Steinliein OK, Mulley JC, Propping P, Wallace RH, Phillips HA, Sutherland GR, et al. A missense mutation in the neuronal nicotinic acetylcholine receptor alpha 4 subunit is associated with autosomal dominant nocturnal frontal lobe epilepsy. Nat Genet 1995; 11:201-203.
    • (1995) Nat Genet , vol.11 , pp. 201-203
    • Steinliein, O.K.1    Mulley, J.C.2    Propping, P.3    Wallace, R.H.4    Phillips, H.A.5    Sutherland, G.R.6
  • 52
    • 15844429136 scopus 로고    scopus 로고
    • Congenital myasthenic syndrome caused by decreased agonist binding affinity due to a mutation in the acetylcholine receptor epsilon subunit
    • Ohno K, Wang HL, Milone M, Bren N, Brengman JM, Nakano S, et al. Congenital myasthenic syndrome caused by decreased agonist binding affinity due to a mutation in the acetylcholine receptor epsilon subunit. Neuron 1996; 17:157-170.
    • (1996) Neuron , vol.17 , pp. 157-170
    • Ohno, K.1    Wang, H.L.2    Milone, M.3    Bren, N.4    Brengman, J.M.5    Nakano, S.6
  • 53
    • 0030027095 scopus 로고    scopus 로고
    • A gene for autosomal dominant paroxysmal choreoathetosis/spasticity (CSE) maps to the vicinity of a potassium channel gene cluster on chromosome 1p, probable within 2 cM between D1S443 and D1S197
    • Auburger G, Ratzlaff T, Lunkes A, Nelles H, Leube B, Binkofski F, Kugel H, et al. A gene for autosomal dominant paroxysmal choreoathetosis/spasticity (CSE) maps to the vicinity of a potassium channel gene cluster on chromosome 1p, probable within 2 cM between D1S443 and D1S197. Genomics 1996; 31:90-94.
    • (1996) Genomics , vol.31 , pp. 90-94
    • Auburger, G.1    Ratzlaff, T.2    Lunkes, A.3    Nelles, H.4    Leube, B.5    Binkofski, F.6    Kugel, H.7
  • 55
    • 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, Cecillon M, Ferreira A, Bernard E, et al. Mapping of a second locus for familial hemiplegic migraine to 1q21-q23 and evidence of further heterogeneity. Ann Neurol 1997; 47:885-890.
    • (1997) Ann Neurol , vol.47 , pp. 885-890
    • Ducros, A.1    Joutel, A.2    Vahedi, K.3    Cecillon, M.4    Ferreira, A.5    Bernard, E.6
  • 57
  • 58
    • 0029925480 scopus 로고    scopus 로고
    • +-channel dysfunction in an inherited cardiac arrhythmia
    • Published erratum appears in Proc Natl Acad Sci USA 1996; Aug 6; 93(16):8796
    • +-channel dysfunction in an inherited cardiac arrhythmia. Proc Natl Acad Sci USA 1996; 93:2208-2212. Published erratum appears in Proc Natl Acad Sci USA 1996; Aug 6; 93(16):8796.
    • (1996) Proc Natl Acad Sci USA , vol.93 , pp. 2208-2212
    • Sanguinetti, M.C.1    Curran, M.E.2    Spector, P.S.3    Keating, M.T.4
  • 59
    • 0029002969 scopus 로고
    • A mechanistic link between an inherited and an acquired cardiac arrhythmia: HERG encodes the IKr potassium channel
    • Sanguinetti MC, Jiang C, Curran ME, Keating MT. A mechanistic link between an inherited and an acquired cardiac arrhythmia: HERG encodes the IKr potassium channel. Cell 1995; 81:299-307.
    • (1995) Cell , vol.81 , pp. 299-307
    • Sanguinetti, M.C.1    Jiang, C.2    Curran, M.E.3    Keating, M.T.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.