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Journal Abstract Search

211 related items for PubMed ID: 9099526

  • 21. Mitochondrial genetics: principles and practice.
    Shoffner JM, Wallace DC.
    Am J Hum Genet; 1992 Dec; 51(6):1179-86. PubMed ID: 1463005
    [No Abstract] [Full Text] [Related]

  • 22. [Optical dual canal measuring system for the detection of disorders of mitochondrial metabolism in situ].
    Schneckenburger H, Sailer R, Gschwend MH, Strauss WS, Bauer M, Zipfl P, Steiner R.
    Biomed Tech (Berl); 1997 Dec; 42 Suppl():169-70. PubMed ID: 9517099
    [No Abstract] [Full Text] [Related]

  • 23. 'Secondary' 4216/ND1 and 13708/ND5 Leber's hereditary optic neuropathy mitochondrial DNA mutations do not further impair in vivo mitochondrial oxidative metabolism when associated with the 11778/ND4 mitochondrial DNA mutation.
    Lodi R, Montagna P, Cortelli P, Iotti S, Cevoli S, Carelli V, Barbiroli B.
    Brain; 2000 Sep; 123 ( Pt 9)():1896-902. PubMed ID: 10960053
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  • 24. Mitochondrial encephalomyopathies.
    DiMauro S, Moraes CT.
    Arch Neurol; 1993 Nov; 50(11):1197-208. PubMed ID: 8215979
    [Abstract] [Full Text] [Related]

  • 25. [Clinical and investigative approaches in mitochondrial diseases. A review of 15 cases].
    Arpa J, Campos Y, Cruz Martínez A, Gutiérrez Molina M, Arenas J, Alonso M, Plaza I, Morales C, Palomo F, Barreiro P.
    Neurologia; 1994 Oct; 9(8):324-36. PubMed ID: 7803049
    [Abstract] [Full Text] [Related]

  • 26. Human mitochondrial diseases: answering questions and questioning answers.
    Howell N.
    Int Rev Cytol; 1999 Oct; 186():49-116. PubMed ID: 9770297
    [Abstract] [Full Text] [Related]

  • 27. Mitochondrial involvement in Parkinson's disease, Huntington's disease, hereditary spastic paraplegia and Friedreich's ataxia.
    Schapira AH.
    Biochim Biophys Acta; 1999 Feb 09; 1410(2):159-70. PubMed ID: 10076024
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  • 33. Mitochondrial disorders in neuro-ophthalmology.
    Riordan-Eva P, Wood NW.
    Curr Opin Neurol; 1996 Feb 09; 9(1):1-4. PubMed ID: 8722656
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  • 34. Inborn and induced defects of mitochondria.
    Schapira AH.
    Arch Neurol; 1998 Oct 09; 55(10):1293-6. PubMed ID: 9779655
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  • 38. Mitochondrial gene mutations and human diseases: a prolegomenon.
    Howell N.
    Am J Hum Genet; 1994 Aug 09; 55(2):219-24. PubMed ID: 8037201
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