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Journal Abstract Search

251 related items for PubMed ID: 1611773

  • 21. Cytochrome c oxidase activity in single muscle fibers: assay techniques and diagnostic applications.
    Johnson MA, Bindoff LA, Turnbull DM.
    Ann Neurol; 1993 Jan; 33(1):28-35. PubMed ID: 8388186
    [Abstract] [Full Text] [Related]

  • 22. 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.
    Muscle Nerve; 1995 Nov; 18(11):1321-5. PubMed ID: 7565930
    [Abstract] [Full Text] [Related]

  • 23. Vascular involvement in mitochondrial myopathy.
    Sakuta R, Nonaka I.
    Ann Neurol; 1989 Jun; 25(6):594-601. PubMed ID: 2500889
    [Abstract] [Full Text] [Related]

  • 24. Diagnosis of mitochondrial diseases: clinical and histological study of sixty patients with ragged red fibers.
    Challa S, Kanikannan MA, Murthy JM, Bhoompally VR, Surath M.
    Neurol India; 2004 Sep; 52(3):353-8. PubMed ID: 15472426
    [Abstract] [Full Text] [Related]

  • 25. [A case of chronic progressive external ophthalmoplegia presenting as inflammatory myopathy].
    Fujimoto S, Ueyama H, Mita S, Kumamoto T, Tsuda T.
    Rinsho Shinkeigaku; 1998 Mar; 38(3):228-32. PubMed ID: 9711119
    [Abstract] [Full Text] [Related]

  • 26. Mitochondrial cytochrome deficiency presenting as a myopathy with hypotonia, external ophthalmoplegia, and lactic acidosis in an infant and as fatal hepatopathy in a second cousin.
    Boustany RN, Aprille JR, Halperin J, Levy H, DeLong GR.
    Ann Neurol; 1983 Oct; 14(4):462-70. PubMed ID: 6314875
    [Abstract] [Full Text] [Related]

  • 27. A mutation in the tRNA(Leu)(UUR) gene associated with the MELAS subgroup of mitochondrial encephalomyopathies.
    Goto Y, Nonaka I, Horai S.
    Nature; 1990 Dec 13; 348(6302):651-3. PubMed ID: 2102678
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  • 35. Ragged red fibers in normal aging and inflammatory myopathy.
    Rifai Z, Welle S, Kamp C, Thornton CA.
    Ann Neurol; 1995 Jan 13; 37(1):24-9. PubMed ID: 7818253
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  • 36. [Delayed manifestation of mitochondrial myopathy--complex I and IV deficiency of the mitochondrial respiratory chain with progressive paresis].
    Beyenburg S, von Wersebe O, Zierz S.
    Nervenarzt; 1991 Aug 13; 62(8):506-11. PubMed ID: 1658669
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  • 37. Point mutations of muscle mitochondrial DNA from patients with mitochondrial encephalomyopathies.
    Song D, Zhang Y, Shi J, Lü Q, Chen J, Zhang H, Zhang W, Wang H, Cai Q.
    Chin Med J (Engl); 2001 Dec 13; 114(12):1273-5. PubMed ID: 11793851
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  • 38. Mitochondrial encephalomyopathies.
    Lombes A, Bonilla E, Dimauro S.
    Rev Neurol (Paris); 1989 Dec 13; 145(10):671-89. PubMed ID: 2682927
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  • 39. [Mitochondrial encephalomyopathy: clinical aspects, CT morphology and neuropathology].
    Wessel K, Poremba M, Pfeiffer J, Roggendorf W.
    Fortschr Neurol Psychiatr; 1988 May 13; 56(5):154-62. PubMed ID: 3397029
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  • 40. [Chronic progressive external ophthalmoplegia: clinical and electromyographic manifestations in a series of cases].
    Jiménez-Caballero PE, Serviá M, Cabeza CI, Marsal-Alonso C, Alvarez-Tejerina A.
    Rev Neurol; 1988 May 13; 43(12):724-8. PubMed ID: 17160922
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