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Volumn 251, Issue 6, 2004, Pages 755-756

Brain mitochondrial impairment in ethylmalonic encephalopathy [3]

Author keywords

[No Author keywords available]

Indexed keywords

ETHYLMALONIC ACID; MALONIC ACID DERIVATIVE; UNCLASSIFIED DRUG;

EID: 3042618926     PISSN: 03405354     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Letter
Times cited : (10)

References (10)
  • 2
    • 0035001589 scopus 로고    scopus 로고
    • Severe metabolic abnormalities in the white matter of patients with vacuolating megalencephalic leukoencephalopathy with subcortical cysts. A proton MR spectroscopic imaging study
    • De Stefane N, Balestri P, Dotti MT, Grosso S, Mortilla M, Morgese G, et al. (2001) Severe metabolic abnormalities in the white matter of patients with vacuolating megalencephalic leukoencephalopathy with subcortical cysts. A proton MR spectroscopic imaging study. J Neurol 248:403-409
    • (2001) J Neurol , vol.248 , pp. 403-409
    • De Stefane, N.1    Balestri, P.2    Dotti, M.T.3    Grosso, S.4    Mortilla, M.5    Morgese, G.6
  • 3
    • 0034113246 scopus 로고    scopus 로고
    • Proton MR spectroscopy to assess axonal damage in multiple sclerosis and other white matter disorders
    • De Stefano N, Narayanan S, Matthews PM, Mortilla M, Dotti MT, Federico A, et al. (2000) Proton MR spectroscopy to assess axonal damage in multiple sclerosis and other white matter disorders. J Neurovirol 6(Suppl 2):121-129
    • (2000) J Neurovirol , vol.6 , Issue.2 SUPPL. , pp. 121-129
    • De Stefano, N.1    Narayanan, S.2    Matthews, P.M.3    Mortilla, M.4    Dotti, M.T.5    Federico, A.6
  • 5
    • 0033950567 scopus 로고    scopus 로고
    • Oxidative phosphorylation defect in the brains of carriers of the tRNAleu(UUR) A3243G mutation in a MELAS pedigree
    • Dubeau F, De Stefano N, Zifkin BG, Arnold DL, Shoubridge EA (2000) Oxidative phosphorylation defect in the brains of carriers of the tRNAleu(UUR) A3243G mutation in a MELAS pedigree. Ann Neurol 47:179-185
    • (2000) Ann Neurol , vol.47 , pp. 179-185
    • Dubeau, F.1    De Stefano, N.2    Zifkin, B.G.3    Arnold, D.L.4    Shoubridge, E.A.5
  • 6
    • 0028033348 scopus 로고
    • Muscle cytochrome c oxidase deficiency in two Italian patients with ethylmalonic aciduria and peculiar clinical phenotype
    • Garavaglia B, Colamaria V, Carrara F, Tonin P, Rimoldi M, Uziel G (1994) Muscle cytochrome c oxidase deficiency in two Italian patients with ethylmalonic aciduria and peculiar clinical phenotype. J Inherit Metab Dis 17:301-303
    • (1994) J Inherit Metab Dis , vol.17 , pp. 301-303
    • Garavaglia, B.1    Colamaria, V.2    Carrara, F.3    Tonin, P.4    Rimoldi, M.5    Uziel, G.6
  • 9
    • 0027303309 scopus 로고
    • Ethylmalonic aciduria associated with progressive neurological disease and partial cytochrome c oxidase deficiency
    • Lehnert W, Ruitenbeek W (1993) Ethylmalonic aciduria associated with progressive neurological disease and partial cytochrome c oxidase deficiency. J Inherit Metab Dis 16:557-559
    • (1993) J Inherit Metab Dis , vol.16 , pp. 557-559
    • Lehnert, W.1    Ruitenbeek, W.2
  • 10
    • 0031863503 scopus 로고    scopus 로고
    • Ethylmalonic and methylsuccinic aciduria in ethylmalonic encephalopathy arise from abnormal isoleucine metabolism
    • Nowaczyk MJ, Lehotay DC, Platt BA, Fisher L, Tan R, Phillips H, et al. (1998) Ethylmalonic and methylsuccinic aciduria in ethylmalonic encephalopathy arise from abnormal isoleucine metabolism. Metabolism 47:836-839
    • (1998) Metabolism , vol.47 , pp. 836-839
    • Nowaczyk, M.J.1    Lehotay, D.C.2    Platt, B.A.3    Fisher, L.4    Tan, R.5    Phillips, H.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.