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Pubmed for Handhelds

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Journal Abstract Search

110 related items for PubMed ID: 9645116

  • 1.
    ; . PubMed ID:
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  • 2. [Complex I (NADH-ubiquinone oxidoreductase) deficiency].
    Nonaka I.
    Ryoikibetsu Shokogun Shirizu; 2001; (36):129-31. PubMed ID: 11596342
    [No Abstract] [Full Text] [Related]

  • 3. Respiratory chain complex I deficiency.
    Triepels RH, Van Den Heuvel LP, Trijbels JM, Smeitink JA.
    Am J Med Genet; 2001; 106(1):37-45. PubMed ID: 11579423
    [Abstract] [Full Text] [Related]

  • 4. Mitochondrial disorders of the nervous system: clinical, biochemical, and molecular genetic features.
    Thyagarajan D, Byrne E.
    Int Rev Neurobiol; 2002; 53():93-144. PubMed ID: 12512338
    [No Abstract] [Full Text] [Related]

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  • 8. [Fatal infantile mitochondrial disease].
    Murakami N.
    Ryoikibetsu Shokogun Shirizu; 2001; (36):173-5. PubMed ID: 11596361
    [No Abstract] [Full Text] [Related]

  • 9. [Respiratory chain enzyme complex I].
    Koga Y, Ueki I.
    Nihon Rinsho; 2002 Apr; 60 Suppl 4():478-81. PubMed ID: 12013918
    [No Abstract] [Full Text] [Related]

  • 10. Low mutant load of mitochondrial DNA G13513A mutation can cause Leigh's disease.
    Kirby DM, Boneh A, Chow CW, Ohtake A, Ryan MT, Thyagarajan D, Thorburn DR.
    Ann Neurol; 2003 Oct; 54(4):473-8. PubMed ID: 14520659
    [Abstract] [Full Text] [Related]

  • 11. [Complex I deficiency due to mutations in nuclear-encoded subunit genes].
    Komaki H, Goto Y.
    Nihon Rinsho; 2002 Apr; 60 Suppl 4():371-5. PubMed ID: 12013889
    [No Abstract] [Full Text] [Related]

  • 12. [Complex III (ubiquinone-cytochrome c reductase) deficiency].
    Nonaka I.
    Ryoikibetsu Shokogun Shirizu; 2001 Apr; (36):135-6. PubMed ID: 11596344
    [No Abstract] [Full Text] [Related]

  • 13. Analysis of the mitochondrial encoded subunits of complex I in 20 patients with a complex I deficiency.
    Meulemans A, Lissens W, Van Coster R, De Meirleir L, Smet J, Nassogne MC, Liebaers I, Seneca S.
    Eur J Paediatr Neurol; 2004 Apr; 8(6):299-306. PubMed ID: 15542384
    [Abstract] [Full Text] [Related]

  • 14. Isolated complex I deficiency in children: clinical, biochemical and genetic aspects.
    Loeffen JL, Smeitink JA, Trijbels JM, Janssen AJ, Triepels RH, Sengers RC, van den Heuvel LP.
    Hum Mutat; 2000 Apr; 15(2):123-34. PubMed ID: 10649489
    [Abstract] [Full Text] [Related]

  • 15. CIA30 complex I assembly factor: a candidate for human complex I deficiency?
    Janssen R, Smeitink J, Smeets R, van Den Heuvel L.
    Hum Genet; 2002 Mar; 110(3):264-70. PubMed ID: 11935339
    [Abstract] [Full Text] [Related]

  • 16. Necrotizing encephalopathy and macrocephaly with mitochondrial complex I deficiency.
    Feillet F, Mousson B, Grignon Y, Leonard JV, Vidailhet M.
    Pediatr Neurol; 1999 Apr; 20(4):305-8. PubMed ID: 10328281
    [Abstract] [Full Text] [Related]

  • 17. Identification of a novel T398A mutation in the ND5 subunit of the mitochondrial complex I and of three novel mtDNA polymorphisms in two patients presenting ocular symptoms.
    Batandier C, Picard A, Tessier N, Lunardi J.
    Hum Mutat; 2000 Dec; 16(6):532. PubMed ID: 11102991
    [No Abstract] [Full Text] [Related]

  • 18. [Pure mitochondrial myopathy].
    Murakami N, Sakuta R.
    Ryoikibetsu Shokogun Shirizu; 2001 Dec; (36):186-9. PubMed ID: 11596366
    [No Abstract] [Full Text] [Related]

  • 19. [Complex III deficiency due to mutations in the cytochrome b gene].
    Ishii A, Ohkoshi N.
    Nihon Rinsho; 2002 Apr; 60 Suppl 4():337-40. PubMed ID: 12013880
    [No Abstract] [Full Text] [Related]

  • 20. [Complex I deficiency due to NDUFS8 gene mutation].
    Ito M.
    Nihon Rinsho; 2002 Apr; 60 Suppl 4():441-3. PubMed ID: 12013907
    [No Abstract] [Full Text] [Related]

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