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Volumn 48, Issue 1, 2013, Pages 140-144

Ethambutol Toxicity Exacerbating The Phenotype Of CMT2A2

Author keywords

CMT; Ethambutol; Mitochondria; Mitofusin; Neurotoxicity

Indexed keywords

AZITHROMYCIN; ETHAMBUTOL; MITOFUSIN 2; RIFABUTIN;

EID: 84879550022     PISSN: 0148639X     EISSN: 10974598     Source Type: Journal    
DOI: 10.1002/mus.23766     Document Type: Article
Times cited : (18)

References (30)
  • 2
    • 22544465572 scopus 로고    scopus 로고
    • Clinical and electrophysiologic features of CMT2A with mutations in the mitofusin 2 gene
    • Lawson VH, Graham BV, Flanigan KM. Clinical and electrophysiologic features of CMT2A with mutations in the mitofusin 2 gene. Neurology 2005;65:197-204.
    • (2005) Neurology , vol.65 , pp. 197-204
    • Lawson, V.H.1    Graham, B.V.2    Flanigan, K.M.3
  • 3
    • 77951096150 scopus 로고    scopus 로고
    • Mitochondrial dynamics- fusion, fission, movement, and mitophagy- in neurodegenerative diseases
    • Chen H, Chan DC. Mitochondrial dynamics- fusion, fission, movement, and mitophagy- in neurodegenerative diseases. Hum Mol Genet 2009;18:169-176.
    • (2009) Hum Mol Genet , vol.18 , pp. 169-176
    • Chen, H.1    Chan, D.C.2
  • 4
    • 77955287381 scopus 로고    scopus 로고
    • Physiological functions of mitochondrial fusion
    • Chen H, Chan DC. Physiological functions of mitochondrial fusion. Ann N Y Acad Sci 2010;1201:21-25.
    • (2010) Ann N Y Acad Sci , vol.1201 , pp. 21-25
    • Chen, H.1    Chan, D.C.2
  • 6
    • 0015519743 scopus 로고
    • Vincristine neurotoxicity
    • Weiden PL, Wright SE. Vincristine neurotoxicity. N Engl J Med 1972;286:1369-1370.
    • (1972) N Engl J Med , vol.286 , pp. 1369-1370
    • Weiden, P.L.1    Wright, S.E.2
  • 7
    • 33644544788 scopus 로고    scopus 로고
    • Medication-induced exacerbation of neuropathy in Charcot Mare Tooth disease
    • Weimer HL, Podwall D. Medication-induced exacerbation of neuropathy in Charcot Mare Tooth disease. J Neurol Sci 2006;242:47-54.
    • (2006) J Neurol Sci , vol.242 , pp. 47-54
    • Weimer, H.L.1    Podwall, D.2
  • 9
    • 0004266448 scopus 로고
    • AMA Department of Drugs AMA Department of Drugs: Chicago, IL: American Medical Association; .
    • AMA Department of Drugs AMA Department of Drugs: AMA drug evaluations subscriptions. Chicago, IL: American Medical Association; 1986.
    • (1986) AMA drug evaluations subscriptions
  • 10
    • 19944425973 scopus 로고    scopus 로고
    • Mitochondrial GTPase mitofusin 2 mutation in Charcot-Marie-Tooth neuropathy type 2A
    • Kijima K, Numakura C, Izumino H, Umetsu K, Nezu A, Shiiki T, et al. Mitochondrial GTPase mitofusin 2 mutation in Charcot-Marie-Tooth neuropathy type 2A. Hum Genet 2005;116:23-27.
    • (2005) Hum Genet , vol.116 , pp. 23-27
    • Kijima, K.1    Numakura, C.2    Izumino, H.3    Umetsu, K.4    Nezu, A.5    Shiiki, T.6
  • 11
    • 42749094176 scopus 로고    scopus 로고
    • Mitochondrial fusion and function in Charcot-Marie-Tooth type 2A patient fibroblasts with mitofusin 2 mutations
    • Amiott EA, Lott P, Soto J, Kang PB, DiMauro S, Abel ED, et al. Mitochondrial fusion and function in Charcot-Marie-Tooth type 2A patient fibroblasts with mitofusin 2 mutations. Exp Neurol 2008;211:115-127.
    • (2008) Exp Neurol , vol.211 , pp. 115-127
    • Amiott, E.A.1    Lott, P.2    Soto, J.3    Kang, P.B.4    DiMauro, S.5    Abel, E.D.6
  • 13
    • 0141793758 scopus 로고    scopus 로고
    • Hereditary motor and sensory neuropathy type VI with optic atrophy
    • Voo I, Allf B, Udar N, et al. Hereditary motor and sensory neuropathy type VI with optic atrophy. Am J Ophthalmol 2003;136:670-677.
    • (2003) Am J Ophthalmol , vol.136 , pp. 670-677
    • Voo, I.1    Allf, B.2    Udar, N.3
  • 14
    • 67649803117 scopus 로고    scopus 로고
    • Role of mitofusin 2 mutations in the physiopathology of Charcot-Marie-Tooth disease type 2A
    • Cartoni R, Martinou JC. Role of mitofusin 2 mutations in the physiopathology of Charcot-Marie-Tooth disease type 2A. Exp Neurol 2009;218:268-273.
    • (2009) Exp Neurol , vol.218 , pp. 268-273
    • Cartoni, R.1    Martinou, J.C.2
  • 16
    • 38849151612 scopus 로고    scopus 로고
    • Mutation of OPA1 causes dominant optic atrophy with external ophthalmoplegia, ataxia, deafness and multiple mitochondrial DNA deletions: a novel disorder of mtDNA maintenance
    • Hudson G, Amati-Bonneau P, Blakely EL, Stewart JD, He L, Schaefer AM, et al. Mutation of OPA1 causes dominant optic atrophy with external ophthalmoplegia, ataxia, deafness and multiple mitochondrial DNA deletions: a novel disorder of mtDNA maintenance. Brain 2008;131:329-337.
    • (2008) Brain , vol.131 , pp. 329-337
    • Hudson, G.1    Amati-Bonneau, P.2    Blakely, E.L.3    Stewart, J.D.4    He, L.5    Schaefer, A.M.6
  • 17
    • 68149103297 scopus 로고    scopus 로고
    • Mitofusins and OPA1 mediate sequential steps in mitochondrial membrane fusion
    • Song Z, Ghochani M, McCaffery JM, Frey TG, Chan DC. Mitofusins and OPA1 mediate sequential steps in mitochondrial membrane fusion. Mol Biol Cell 2009;20:3525-3532.
    • (2009) Mol Biol Cell , vol.20 , pp. 3525-3532
    • Song, Z.1    Ghochani, M.2    McCaffery, J.M.3    Frey, T.G.4    Chan, D.C.5
  • 18
    • 77949801029 scopus 로고    scopus 로고
    • Mitofusin 2 is necessary for transport of axonal mitochondria and interacts with the Miro/Milton Complex
    • Misko A, Jiang S, Wegorzewska I, Milbrandt J, Baloh RH. Mitofusin 2 is necessary for transport of axonal mitochondria and interacts with the Miro/Milton Complex. J Neurosci 2010;30:4232-4240.
    • (2010) J Neurosci , vol.30 , pp. 4232-4240
    • Misko, A.1    Jiang, S.2    Wegorzewska, I.3    Milbrandt, J.4    Baloh, R.H.5
  • 21
    • 0031034482 scopus 로고    scopus 로고
    • Clustering of Caucasian Leber hereditary optic neuropathy patients containing the 11778 or 14484 mutations on an mtDNA lineage
    • Brown MD, Sun F, Wallace DC. Clustering of Caucasian Leber hereditary optic neuropathy patients containing the 11778 or 14484 mutations on an mtDNA lineage. Am J Hum Genet 1997;60:381-387.
    • (1997) Am J Hum Genet , vol.60 , pp. 381-387
    • Brown, M.D.1    Sun, F.2    Wallace, D.C.3
  • 22
    • 64049112293 scopus 로고    scopus 로고
    • Ethambutol optic neuropathy: how we can prevent 100,000 new cases of blindness each year
    • Sadun AA, Wang MY. Ethambutol optic neuropathy: how we can prevent 100, 000 new cases of blindness each year. J Neuroophthalmol 2008;28:265-268.
    • (2008) J Neuroophthalmol , vol.28 , pp. 265-268
    • Sadun, A.A.1    Wang, M.Y.2
  • 23
    • 64049085998 scopus 로고    scopus 로고
    • Incidence and clinical features of ethambutol-induced optic neuropathy in Korea
    • Lee EJ, Kim SJ, Choung HK, Kim JH, Yu YS. Incidence and clinical features of ethambutol-induced optic neuropathy in Korea. J Neuroophthalmol 2008;28:269-277.
    • (2008) J Neuroophthalmol , vol.28 , pp. 269-277
    • Lee, E.J.1    Kim, S.J.2    Choung, H.K.3    Kim, J.H.4    Yu, Y.S.5
  • 24
    • 0018916699 scopus 로고
    • Peripheral neuropathy associated with ethambutol
    • Nair VS, LeBrun M, Kass I. Peripheral neuropathy associated with ethambutol. Chest 1980;77:98-100.
    • (1980) Chest , vol.77 , pp. 98-100
    • Nair, V.S.1    LeBrun, M.2    Kass, I.3
  • 25
    • 16844381836 scopus 로고    scopus 로고
    • Reliability and validity of the CMT neuropathy score as a measure of disability
    • Shy ME, Blake J, Krajewski K, Fuerst DR, Laura M, Hahn AF, et al. Reliability and validity of the CMT neuropathy score as a measure of disability. Neurology 2005;64:1209-1214.
    • (2005) Neurology , vol.64 , pp. 1209-1214
    • Shy, M.E.1    Blake, J.2    Krajewski, K.3    Fuerst, D.R.4    Laura, M.5    Hahn, A.F.6
  • 26
    • 53549104776 scopus 로고    scopus 로고
    • Diagnosis and treatment of infections due to Mycobacterium avium complex
    • Kasperbauer SH, Daley CL. Diagnosis and treatment of infections due to Mycobacterium avium complex. Semin Respir Crit Care Med 2008;29:569-576.
    • (2008) Semin Respir Crit Care Med , vol.29 , pp. 569-576
    • Kasperbauer, S.H.1    Daley, C.L.2
  • 27
    • 77958074597 scopus 로고    scopus 로고
    • Alphabet soup: making sense of genetic testing in CMT
    • Lawson VH, Gharibshahi S. Alphabet soup: making sense of genetic testing in CMT. Semin Neurol 2010;30:373-386.
    • (2010) Semin Neurol , vol.30 , pp. 373-386
    • Lawson, V.H.1    Gharibshahi, S.2
  • 28
    • 25444514731 scopus 로고    scopus 로고
    • Ganglioside-induced differentiation associated protein 1 is a regulator of the mitochondrial network: new implications for Charcot-Marie-Tooth disease
    • Niemann A, Ruegg M, La Padula V, Schenone A, Suter U. Ganglioside-induced differentiation associated protein 1 is a regulator of the mitochondrial network: new implications for Charcot-Marie-Tooth disease. J Cell Biol 2005;170:1067-1078.
    • (2005) J Cell Biol , vol.170 , pp. 1067-1078
    • Niemann, A.1    Ruegg, M.2    La Padula, V.3    Schenone, A.4    Suter, U.5
  • 29
    • 55749093730 scopus 로고    scopus 로고
    • Vocal cord paresis and diaphragmantic dysfunction are severe and frequent symptoms of GDAP-1 associated neuropathy
    • Sevilla T, Jaijo T, Nauffal D, Collado D, chumillas MJ, Vilchez JJ, et al. Vocal cord paresis and diaphragmantic dysfunction are severe and frequent symptoms of GDAP-1 associated neuropathy. Brain 2008;131:3051-3061.
    • (2008) Brain , vol.131 , pp. 3051-3061
    • Sevilla, T.1    Jaijo, T.2    Nauffal, D.3    Collado, D.4    chumillas, M.J.5    Vilchez, J.J.6
  • 30
    • 18544372631 scopus 로고    scopus 로고
    • Leber hereditary optic neuropathy: biochemical lights in a blurry scenario
    • Hirano M, DiMauro S. Leber hereditary optic neuropathy: biochemical lights in a blurry scenario. Arch Neurol 2005;62:711.
    • (2005) Arch Neurol , vol.62 , pp. 711
    • Hirano, M.1    DiMauro, S.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.