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Volumn 243, Issue 4, 2005, Pages 380-382

Diagnostic value of mitochondrial DNA mutation analysis in juvenile unilateral ptosis

Author keywords

[No Author keywords available]

Indexed keywords

MITOCHONDRIAL DNA;

EID: 20444458389     PISSN: 0721832X     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00417-004-1000-1     Document Type: Article
Times cited : (7)

References (10)
  • 1
    • 0037321655 scopus 로고    scopus 로고
    • Neuro-ophthalmology of mitochondrial diseases
    • 10.1097/00019052-200302000-00005
    • Biousse V, Newman NJ (2003) Neuro-ophthalmology of mitochondrial diseases. Curr Opin Neurol 16:35-43 10.1097/00019052-200302000-00005
    • (2003) Curr. Opin. Neurol. , vol.16 , pp. 35-43
    • Biousse, V.1    Newman, N.J.2
  • 2
    • 0030670573 scopus 로고    scopus 로고
    • Clinical features, investigation, and management of patients with defects of mitochondrial DNA
    • Chinnery PF, Turnbull DM (1997) Clinical features, investigation, and management of patients with defects of mitochondrial DNA. J Neurol Neurosurg Psychiatry 63:559-563
    • (1997) J. Neurol. Neurosurg. Psychiatry , vol.63 , pp. 559-563
    • Chinnery, P.F.1    Turnbull, D.M.2
  • 3
    • 0034951327 scopus 로고    scopus 로고
    • Mitochondrial DNA mutations in human disease
    • 10.1002/ajmg.1392
    • DiMauro S, Schon EA (2001) Mitochondrial DNA mutations in human disease. Am J Med Genet 106:18-26 10.1002/ajmg.1392
    • (2001) Am. J. Med. Genet. , vol.106 , pp. 18-26
    • DiMauro, S.1    Schon, E.A.2
  • 4
    • 0034770537 scopus 로고    scopus 로고
    • Diseases of oxidative phosphorylation due to mtDNA mutations
    • 10.1055/s-2001-17942
    • DiMauro S, Andreu AL, Musumeci O, Bonilla E (2001) Diseases of oxidative phosphorylation due to mtDNA mutations. Semin Neurol 21:251-260 10.1055/ s-2001-17942
    • (2001) Semin. Neurol. , vol.21 , pp. 251-260
    • DiMauro, S.1    Andreu, A.L.2    Musumeci, O.3    Bonilla, E.4
  • 7
    • 0035956482 scopus 로고    scopus 로고
    • ANT1, Twinkle, POLG, and TP: New genes open our eyes to ophthalmoplegia
    • 1:STN:280:DC%2BD38%2FksF2mtA%3D%3D
    • Hirano M, DiMauro S (2001) ANT1, Twinkle, POLG, and TP: New genes open our eyes to ophthalmoplegia. Neurology 57:2163-2165 1:STN:280:DC%2BD38%2FksF2mtA%3D%3D
    • (2001) Neurology , vol.57 , pp. 2163-2165
    • Hirano, M.1    DiMauro, S.2
  • 9
    • 0032980279 scopus 로고    scopus 로고
    • Mitochondrial disorders: Clinical and genetic features
    • 10.1146/annurev.med.50.1.111
    • Simon DK, Johns DR (1999) Mitochondrial disorders: Clinical and genetic features. Annu Rev Med 50:111-127 10.1146/annurev.med.50.1.111
    • (1999) Annu. Rev. Med. , vol.50 , pp. 111-127
    • Simon, D.K.1    Johns, D.R.2
  • 10
    • 0033525773 scopus 로고    scopus 로고
    • Mitochondrial diseases in man and mouse
    • Wallace DC (1999) Mitochondrial diseases in man and mouse. Science 283:1482-1488
    • (1999) Science , vol.283 , pp. 1482-1488
    • Wallace, D.C.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.