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Volumn 128, Issue 1, 2008, Pages

A surviving case of mitochondrial cardiomyopathy diagnosed from the symptoms of multiple organ dysfunction syndrome

Author keywords

Congestive heart failure; Lactic acidosis; MELAS syndrome; Mitochondrial myopathies; Multiple organ failure

Indexed keywords

ATRIAL NATRIURETIC FACTOR ALPHA; CATECHOLAMINE; MITOCHONDRIAL DNA; TRANSFER RNA; UBIDECARENONE;

EID: 46149107646     PISSN: 01675273     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.ijcard.2007.05.072     Document Type: Article
Times cited : (14)

References (6)
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    • Goto, Y.1    Nonaka, I.2    Horai, S.3
  • 2
    • 0026612942 scopus 로고
    • 31P NMR spectroscopy and ergometer exercise test as evidence for muscle oxidative performance improvement with coenzyme Q in mitochondrial myopathies
    • Bendahan D., Desnuelle C., Vanuxem D., et al. 31P NMR spectroscopy and ergometer exercise test as evidence for muscle oxidative performance improvement with coenzyme Q in mitochondrial myopathies. Neurology 42 (1992) 1203-1208
    • (1992) Neurology , vol.42 , pp. 1203-1208
    • Bendahan, D.1    Desnuelle, C.2    Vanuxem, D.3
  • 3
    • 33645326875 scopus 로고    scopus 로고
    • Myocardial dysfunction in mitochondrial diabetes treated with Coenzyme Q10
    • Salles J.E., Moises V.A., Almeida D.R., et al. Myocardial dysfunction in mitochondrial diabetes treated with Coenzyme Q10. Diabetes Res Clin Pract 72 (2006) 100-103
    • (2006) Diabetes Res Clin Pract , vol.72 , pp. 100-103
    • Salles, J.E.1    Moises, V.A.2    Almeida, D.R.3
  • 4
    • 0015309883 scopus 로고
    • Oculocraniosomatic neuromuscular disease with "ragged-red" fibers
    • Olson W., Engel W.K., Walsh G.O., et al. Oculocraniosomatic neuromuscular disease with "ragged-red" fibers. Arch Neurol 26 (1972) 193-211
    • (1972) Arch Neurol , vol.26 , pp. 193-211
    • Olson, W.1    Engel, W.K.2    Walsh, G.O.3
  • 5
    • 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 42 (1992) 545-550
    • (1992) Neurology , vol.42 , pp. 545-550
    • Goto, Y.1    Horai, S.2    Matsuoka, T.3
  • 6
    • 0026906885 scopus 로고
    • Mutation in mitochondrial tRNA(Leu)(UUR) gene in a large pedigree with maternally transmitted type II diabetes mellitus and deafness
    • van den Ouweland J.M., Lemkes H.H., Ruitenbeek W., et al. Mutation in mitochondrial tRNA(Leu)(UUR) gene in a large pedigree with maternally transmitted type II diabetes mellitus and deafness. Nat Genet 1 (1992) 368-371
    • (1992) Nat Genet , vol.1 , pp. 368-371
    • van den Ouweland, J.M.1    Lemkes, H.H.2    Ruitenbeek, W.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.