메뉴 건너뛰기




Volumn 23, Issue 2, 2000, Pages 155-161

Multiple mtDNA deletions: Clinical and molecular correlations

Author keywords

[No Author keywords available]

Indexed keywords

MITOCHONDRIAL DNA;

EID: 0034040515     PISSN: 01418955     EISSN: None     Source Type: Journal    
DOI: 10.1023/A:1005617916260     Document Type: Article
Times cited : (5)

References (10)
  • 1
    • 0029996721 scopus 로고    scopus 로고
    • Multiple mitochondrial DNA deletions associated with autosomal recessive ophthalmoplegia and severe cardiomyopathy
    • Bohlega S, Tanji K, Santorelli FM, Hirano M, al-Jishi A, DiMauro S (1996) Multiple mitochondrial DNA deletions associated with autosomal recessive ophthalmoplegia and severe cardiomyopathy. Neurology 46: 1329-1334.
    • (1996) Neurology , vol.46 , pp. 1329-1334
    • Bohlega, S.1    Tanji, K.2    Santorelli, F.M.3    Hirano, M.4    Al-Jishi, A.5    DiMauro, S.6
  • 2
    • 0031882208 scopus 로고    scopus 로고
    • Multiple mtDNA deletions features in autosomal dominant and recessive diseases suggest distinct pathogeneses
    • Carrozzo R, Hirano M, Fromenty B, et al (1998) Multiple mtDNA deletions features in autosomal dominant and recessive diseases suggest distinct pathogeneses. Neurology 50: 99-106.
    • (1998) Neurology , vol.50 , pp. 99-106
    • Carrozzo, R.1    Hirano, M.2    Fromenty, B.3
  • 3
    • 0028301915 scopus 로고
    • Mitochondrial neurogastrointestinal encephalomyopathy (MNGIE): Clinical, biochemical, and genetic features of an autosomal recessive mitochondrial disorder
    • Hirano M, Silvestri G, Blake DM, et al (1994) Mitochondrial neurogastrointestinal encephalomyopathy (MNGIE): clinical, biochemical, and genetic features of an autosomal recessive mitochondrial disorder. Neurology 44: 721-727.
    • (1994) Neurology , vol.44 , pp. 721-727
    • Hirano, M.1    Silvestri, G.2    Blake, D.M.3
  • 4
    • 0031004167 scopus 로고    scopus 로고
    • Increased prevalence of mitochondrial DNA deletions in skeletal muscle of older individuals with impaired glucose tolerance: Possible marker of glycemic stress
    • Liang P, Hughes V, Fukagawa NK (1997) Increased prevalence of mitochondrial DNA deletions in skeletal muscle of older individuals with impaired glucose tolerance: possible marker of glycemic stress. Diabetes 46: 920-923.
    • (1997) Diabetes , vol.46 , pp. 920-923
    • Liang, P.1    Hughes, V.2    Fukagawa, N.K.3
  • 5
    • 0033613865 scopus 로고    scopus 로고
    • Thymidine phosphorylase gene mutations in MNGIE, a human mitochondrial disorder
    • Nishino I, Spinazzola A, Hirano M (1999) Thymidine phosphorylase gene mutations in MNGIE, a human mitochondrial disorder. Science 283: 689-692.
    • (1999) Science , vol.283 , pp. 689-692
    • Nishino, I.1    Spinazzola, A.2    Hirano, M.3
  • 6
    • 8944243541 scopus 로고    scopus 로고
    • Multiple mitochondrial DNa deletions in sporadic inclusion body myositis: A study of 56 patients
    • Santorelli FM, Sciacco M, Tanji K, et al (1996) Multiple mitochondrial DNA deletions in sporadic inclusion body myositis: a study of 56 patients. Ann Neurol 39: 789-795.
    • (1996) Ann Neurol , vol.39 , pp. 789-795
    • Santorelli, F.M.1    Sciacco, M.2    Tanji, K.3
  • 7
    • 26344438618 scopus 로고    scopus 로고
    • Clinical, biochemical, and genetic features of patients with multiple mtDNA deletions
    • Santorelli FM, Hirano M, Shanske S, et al (1997) Clinical, biochemical, and genetic features of patients with multiple mtDNA deletions. Neurology 48: A354.
    • (1997) Neurology , vol.48
    • Santorelli, F.M.1    Hirano, M.2    Shanske, S.3
  • 8
    • 0026463567 scopus 로고
    • Inherited idiopathic dilated cardiomyopathy with multiple deletions of mitochondrial DNA
    • Suomalainen A, Paetau A, Leinonen H, Majander A, Peltonen L, Somer H (1992) Inherited idiopathic dilated cardiomyopathy with multiple deletions of mitochondrial DNA. Lancet 340: 1319-1320.
    • (1992) Lancet , vol.340 , pp. 1319-1320
    • Suomalainen, A.1    Paetau, A.2    Leinonen, H.3    Majander, A.4    Peltonen, L.5    Somer, H.6
  • 9
    • 0028849791 scopus 로고
    • Multiple mitochondrial DNa deletions in a patient with mitochondrial myopathy and cardiomyopathy but no ophthalmoplegia
    • Takei Y, Ikeda S, Yanagisawa N, Takahashi W, Sekiguchi M, Hayashi T (1995) Multiple mitochondrial DNA deletions in a patient with mitochondrial myopathy and cardiomyopathy but no ophthalmoplegia. Muscle Nerve 18: 1321-1325.
    • (1995) Muscle Nerve , vol.18 , pp. 1321-1325
    • Takei, Y.1    Ikeda, S.2    Yanagisawa, N.3    Takahashi, W.4    Sekiguchi, M.5    Hayashi, T.6
  • 10
    • 0030837619 scopus 로고    scopus 로고
    • Disorders of nuclear-mitochondrial intergen omic signalling
    • Zeviani M, Petruzzella V, Carrozzo R (1997) Disorders of nuclear-mitochondrial intergen omic signalling. J Bioenerg Biomembr 29: 121-130.
    • (1997) J Bioenerg Biomembr , vol.29 , pp. 121-130
    • Zeviani, M.1    Petruzzella, V.2    Carrozzo, R.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.