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Volumn 65, Issue 3, 2008, Pages 403-406

Amyotrophic lateral sclerosis with ragged-red fibers

Author keywords

[No Author keywords available]

Indexed keywords

CYTOCHROME C OXIDASE; MITOCHONDRIAL DNA; SURVIVAL MOTOR NEURON PROTEIN;

EID: 40849130169     PISSN: 00039942     EISSN: 15383687     Source Type: Journal    
DOI: 10.1001/archneurol.2007.65     Document Type: Article
Times cited : (28)

References (18)
  • 1
    • 25444474703 scopus 로고    scopus 로고
    • Mitochondria take center stage in aging and neurodegeneration
    • Beal MF. Mitochondria take center stage in aging and neurodegeneration. Ann Neurol. 2005;58(4):495-505.
    • (2005) Ann Neurol , vol.58 , Issue.4 , pp. 495-505
    • Beal, M.F.1
  • 2
    • 40849115655 scopus 로고    scopus 로고
    • Hays AP, Oskoui M, Tanji K, Kaufmann P, Bonilla E. Mitochondrial neurology, II: myopathies and peripheral neuropathies. In: DiMauro S, Hirano M, Schon EA, eds. Mitochondrial Medicine. London, England: Informa Healthcare; 2006:45-74.
    • Hays AP, Oskoui M, Tanji K, Kaufmann P, Bonilla E. Mitochondrial neurology, II: myopathies and peripheral neuropathies. In: DiMauro S, Hirano M, Schon EA, eds. Mitochondrial Medicine. London, England: Informa Healthcare; 2006:45-74.
  • 3
    • 0035222587 scopus 로고    scopus 로고
    • Optical imaging techniques (histochemical, immunohistochemical, and in situ hybridization staining methods) to visualize mitochondria
    • Tanji K, Bonilla E. Optical imaging techniques (histochemical, immunohistochemical, and in situ hybridization staining methods) to visualize mitochondria. Methods Cell Biol. 2001;65:311-332.
    • (2001) Methods Cell Biol , vol.65 , pp. 311-332
    • Tanji, K.1    Bonilla, E.2
  • 4
    • 0023429777 scopus 로고
    • Cytochrome c oxidase deficiency in Leigh syndrome
    • DiMauro S, Servidei S, Zeviani M, et al. Cytochrome c oxidase deficiency in Leigh syndrome. Ann Neurol. 1987;22(4):498-506.
    • (1987) Ann Neurol , vol.22 , Issue.4 , pp. 498-506
    • DiMauro, S.1    Servidei, S.2    Zeviani, M.3
  • 5
    • 0017175171 scopus 로고
    • Familial progressive bulbar and spinal muscular atrophy: Juvenile onset and late mortality with ragged-red fibers
    • Dobkin BH, Verity MA. Familial progressive bulbar and spinal muscular atrophy: juvenile onset and late mortality with ragged-red fibers. Neurology. 1976;26(8):754-763.
    • (1976) Neurology , vol.26 , Issue.8 , pp. 754-763
    • Dobkin, B.H.1    Verity, M.A.2
  • 6
    • 9744242736 scopus 로고    scopus 로고
    • Mitochondrial medicine
    • DiMauro S. Mitochondrial medicine. Biochim Biophys Acta. 2004;1659(2-3):107-114.
    • (2004) Biochim Biophys Acta , vol.1659 , Issue.2-3 , pp. 107-114
    • DiMauro, S.1
  • 7
    • 0025873627 scopus 로고
    • Clinical syndromes associated with ragged red fibers
    • Rowland LP, Blake D, Hirano M, et al. Clinical syndromes associated with ragged red fibers. Rev Neurol (Paris). 1991;147(6-7):467-473.
    • (1991) Rev Neurol (Paris) , vol.147 , Issue.6-7 , pp. 467-473
    • Rowland, L.P.1    Blake, D.2    Hirano, M.3
  • 8
    • 0030249589 scopus 로고    scopus 로고
    • Mitochondrial myopathy simulating spinal muscular atrophy
    • Pons R, Andreetta F, Wang CH, et al. Mitochondrial myopathy simulating spinal muscular atrophy. Pediatr Neurol. 1996;15(2):153-158.
    • (1996) Pediatr Neurol , vol.15 , Issue.2 , pp. 153-158
    • Pons, R.1    Andreetta, F.2    Wang, C.H.3
  • 9
    • 33747192567 scopus 로고    scopus 로고
    • Clinical spectrum of mitochondrial DNA depletion due to mutations in the thymidine kinase 2 gene
    • Oskoui M, Davidzon G, Pascual J, et al. Clinical spectrum of mitochondrial DNA depletion due to mutations in the thymidine kinase 2 gene. Arch Neurol. 2006;63(8):1122-1126.
    • (2006) Arch Neurol , vol.63 , Issue.8 , pp. 1122-1126
    • Oskoui, M.1    Davidzon, G.2    Pascual, J.3
  • 10
    • 0037159255 scopus 로고    scopus 로고
    • Mitochondrial DNA depletion: Mutations in thymidine kinase gene with myopathy and SMA
    • Mancuso M, Salviati L, Sacconi S, et al. Mitochondrial DNA depletion: mutations in thymidine kinase gene with myopathy and SMA. Neurology. 2002;59(8):1197-1202.
    • (2002) Neurology , vol.59 , Issue.8 , pp. 1197-1202
    • Mancuso, M.1    Salviati, L.2    Sacconi, S.3
  • 12
    • 0031915174 scopus 로고    scopus 로고
    • Cytochrome c oxidase subunit I microdeletion in a patient with motor neuron disease
    • Comi GP, Bordoni A, Salani S, et al. Cytochrome c oxidase subunit I microdeletion in a patient with motor neuron disease. Ann Neurol. 1998;43(1):110-116.
    • (1998) Ann Neurol , vol.43 , Issue.1 , pp. 110-116
    • Comi, G.P.1    Bordoni, A.2    Salani, S.3
  • 13
    • 0037254203 scopus 로고    scopus 로고
    • Mitochondriopathy mimicking amyotrophic lateral sclerosis
    • Finsterer J. Mitochondriopathy mimicking amyotrophic lateral sclerosis. Neurologist. 2003;9(1):45-48.
    • (2003) Neurologist , vol.9 , Issue.1 , pp. 45-48
    • Finsterer, J.1
  • 15
    • 0033556363 scopus 로고    scopus 로고
    • Spinal muscular atrophy-like picture, cardiomyopathy, and cytochrome c oxidase deficiency
    • Rubio-Gozalbo ME, Smeitink JAM, Ruitenbeek W, et al. Spinal muscular atrophy-like picture, cardiomyopathy, and cytochrome c oxidase deficiency. Neurology. 1999;52(2):383-386.
    • (1999) Neurology , vol.52 , Issue.2 , pp. 383-386
    • Rubio-Gozalbo, M.E.1    Smeitink, J.A.M.2    Ruitenbeek, W.3
  • 16
    • 0036096893 scopus 로고    scopus 로고
    • Cytochrome c oxidase deficiency due to a novel SCO2 mutation mimicking Werdnig-Hoffman disease
    • Salviati L, Sacconi S, Rasalam MM, et al. Cytochrome c oxidase deficiency due to a novel SCO2 mutation mimicking Werdnig-Hoffman disease. Arch Neurol. 2002;59:862-865.
    • (2002) Arch Neurol , vol.59 , pp. 862-865
    • Salviati, L.1    Sacconi, S.2    Rasalam, M.M.3
  • 17
    • 10744220944 scopus 로고    scopus 로고
    • Tarnopolsky MA, Bourgeois JM, Fu MH, et al. Novel SCO2 mutation (G1521A) presenting as a spinal muscular atrophy type I phenotype [published correction appears in Am J Med Genet A. 2004;130(2):218]. Am J Med Genet A. 2004;125(3):310-314.
    • Tarnopolsky MA, Bourgeois JM, Fu MH, et al. Novel SCO2 mutation (G1521A) presenting as a spinal muscular atrophy type I phenotype [published correction appears in Am J Med Genet A. 2004;130(2):218]. Am J Med Genet A. 2004;125(3):310-314.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.