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Journal Abstract Search

110 related items for PubMed ID: 9645116

  • 21. [Mitochondrial encephalopathies].
    Castro-Gago M, Novo-Rodríguez MI, Pintos-Martínez E, Campos Y, Arenas J, Eirís-Puñal J.
    Rev Neurol; ; 31(3):263-82. PubMed ID: 10996928
    [Abstract] [Full Text] [Related]

  • 22. Identification of a new mtDNA mutation (14724G>A) associated with mitochondrial leukoencephalopathy.
    Pereira C, Nogueira C, Barbot C, Tessa A, Soares C, Fattori F, Guimarães A, Santorelli FM, Vilarinho L.
    Biochem Biophys Res Commun; 2007 Mar 23; 354(4):937-41. PubMed ID: 17266923
    [Abstract] [Full Text] [Related]

  • 23. [Electron transfer complex III deficiency].
    Nishino I, Nonaka I.
    Ryoikibetsu Shokogun Shirizu; 1998 Mar 23; (19 Pt 2):494-6. PubMed ID: 9645118
    [No Abstract] [Full Text] [Related]

  • 24. Mitochondrial encephalomyopathy due to a novel mutation in the tRNAGlu of mitochondrial DNA.
    Pancrudo J, Shanske S, Bonilla E, Daras M, Akman HO, Krishna S, Malkin E, DiMauro S.
    J Child Neurol; 2007 Jul 23; 22(7):858-62. PubMed ID: 17715279
    [Abstract] [Full Text] [Related]

  • 25. [Mitochondrial dysfunction in Parkinson's disease].
    Hattori N, Mizuno Y.
    Nihon Rinsho; 2002 Apr 23; 60 Suppl 4():406-11. PubMed ID: 12013899
    [No Abstract] [Full Text] [Related]

  • 26. [Complex IV(cytochrome c oxidase)].
    Sugie K, Nishino I.
    Nihon Rinsho; 2002 Apr 23; 60 Suppl 4():490-4. PubMed ID: 12013921
    [No Abstract] [Full Text] [Related]

  • 27. [Mitochondrial diseases with recurrent myoglobinuria].
    Murakami N.
    Ryoikibetsu Shokogun Shirizu; 2001 Apr 23; (36):183-5. PubMed ID: 11596365
    [No Abstract] [Full Text] [Related]

  • 28. Mitochondrial myopathy of childhood associated with mitochondrial DNA depletion and a homozygous mutation (T77M) in the TK2 gene.
    Mancuso M, Filosto M, Bonilla E, Hirano M, Shanske S, Vu TH, DiMauro S.
    Arch Neurol; 2003 Jul 23; 60(7):1007-9. PubMed ID: 12873860
    [Abstract] [Full Text] [Related]

  • 29. The X-chromosomal NDUFA1 gene of complex I in mitochondrial encephalomyopathies: tissue expression and mutation detection.
    Loeffen J, Smeets R, Smeitink J, Ruitenbeek W, Janssen A, Mariman E, Sengers R, Trijbels F, van den Heuvel L.
    J Inherit Metab Dis; 1998 Jun 23; 21(3):210-5. PubMed ID: 9686359
    [No Abstract] [Full Text] [Related]

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  • 31. Rescue of a mitochondrial deficiency causing Leber Hereditary Optic Neuropathy.
    Guy J, Qi X, Pallotti F, Schon EA, Manfredi G, Carelli V, Martinuzzi A, Hauswirth WW, Lewin AS.
    Ann Neurol; 2002 Nov 23; 52(5):534-42. PubMed ID: 12402249
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  • 33. Biochemical analysis of cybrids expressing mitochondrial DNA from Contursi kindred Parkinson's subjects.
    Swerdlow RH, Parks JK, Cassarino DS, Binder DR, Bennett JP, Di Iorio G, Golbe LI, Parker WD.
    Exp Neurol; 2001 Jun 23; 169(2):479-85. PubMed ID: 11358461
    [Abstract] [Full Text] [Related]

  • 34. [Mitochondrial encephalomyopathies].
    Nonaka M.
    Nihon Naika Gakkai Zasshi; 1994 Sep 10; 83(9):1697-700. PubMed ID: 7798773
    [No Abstract] [Full Text] [Related]

  • 35. Combined enzymatic complex I and III deficiency associated with mutations in the nuclear encoded NDUFS4 gene.
    Budde SM, van den Heuvel LP, Janssen AJ, Smeets RJ, Buskens CA, DeMeirleir L, Van Coster R, Baethmann M, Voit T, Trijbels JM, Smeitink JA.
    Biochem Biophys Res Commun; 2000 Aug 18; 275(1):63-8. PubMed ID: 10944442
    [Abstract] [Full Text] [Related]

  • 36. Progressive exercise intolerance associated with a new muscle-restricted nonsense mutation (G142X) in the mitochondrial cytochrome b gene.
    Bruno C, Santorelli FM, Assereto S, Tonoli E, Tessa A, Traverso M, Scapolan S, Bado M, Tedeschi S, Minetti C.
    Muscle Nerve; 2003 Oct 18; 28(4):508-11. PubMed ID: 14506725
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  • 39. Mitochondrial cytopathies and neuromuscular disorders.
    Van Coster R, De Meirleir L.
    Acta Neurol Belg; 2000 Sep 18; 100(3):156-61. PubMed ID: 11098288
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