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Journal Abstract Search

244 related items for PubMed ID: 2546706

  • 21. [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; 62(8):506-11. PubMed ID: 1658669
    [Abstract] [Full Text] [Related]

  • 22. Expression of NCAM (neural cell adhesion molecule) in mitochondrial myopathy.
    Heuss D, Engelhardt A, Göbel H, Neundörfer B.
    Clin Neuropathol; 1995 Aug; 14(6):331-6. PubMed ID: 8605739
    [Abstract] [Full Text] [Related]

  • 23. Apoptosis-related changes in skeletal muscles of patients with mitochondrial diseases.
    Umaki Y, Mitsui T, Endo I, Akaike M, Matsumoto T.
    Acta Neuropathol; 2002 Feb; 103(2):163-70. PubMed ID: 11810183
    [Abstract] [Full Text] [Related]

  • 24. [A case of MELAS (mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes) with progressive cytochrome c oxidase deficiency].
    Sumi K, Nagaura T, Itagaki Y, Inui K, Abe J.
    Rinsho Shinkeigaku; 1989 Jul; 29(7):901-8. PubMed ID: 2553313
    [Abstract] [Full Text] [Related]

  • 25. In vivo magnetic resonance spectroscopy of brain and muscle in a type of mitochondrial encephalomyopathy (MERRF).
    Matthews PM, Berkovic SF, Shoubridge EA, Andermann F, Karpati G, Carpenter S, Arnold DL.
    Ann Neurol; 1991 Apr; 29(4):435-8. PubMed ID: 1929212
    [Abstract] [Full Text] [Related]

  • 26. [Mitochondrial encephalomyopathies. A comparison of Kearns-Sayre syndrome, MELAS and MERRF].
    Zenner K, Gold R, Meurers B, Reichmann H.
    Nervenarzt; 1990 Oct; 61(10):597-603. PubMed ID: 2177152
    [No Abstract] [Full Text] [Related]

  • 27. Immunocytological and histochemical correlation in Kearns-Sayre syndrome with mtDNA deletion and partial cytochrome c oxidase deficiency in skeletal muscle.
    Romero NB, Lestienne P, Marsac C, Paturneau-Jouas M, Nelson I, François D, Eymard B, Fardeau M.
    J Neurol Sci; 1989 Nov; 93(2-3):297-309. PubMed ID: 2556504
    [Abstract] [Full Text] [Related]

  • 28. Kearns-Sayre syndrome. A case report.
    Altunbaşak S, Bingöl G, Ozbarlas N, Akçören Z, Hergüner O.
    Turk J Pediatr; 1998 Nov; 40(2):255-9. PubMed ID: 9677732
    [Abstract] [Full Text] [Related]

  • 29. Clonal expansion of mitochondrial DNA with multiple deletions in autosomal dominant progressive external ophthalmoplegia.
    Moslemi AR, Melberg A, Holme E, Oldfors A.
    Ann Neurol; 1996 Nov; 40(5):707-13. PubMed ID: 8957011
    [Abstract] [Full Text] [Related]

  • 30. [Ophthalmoplegia plus and ragged red fibers. Description of a case manifested in childhood].
    De Langlade E, Corazza G, Minetti C, Bado M, Venzano V, Chiossi FM.
    Minerva Pediatr; 1983 Nov 30; 35(22):1117-23. PubMed ID: 6672599
    [No Abstract] [Full Text] [Related]

  • 31. [Disorders of mitochondrial energy metabolism in patients with the Kearns-Sayre syndrome].
    Capková M, Tesarová M, Wenchich L, Cerná L, Hansíková H, Hůlková H, Hrubá E, Elleder M, Zeman J.
    Cas Lek Cesk; 2002 Feb 01; 141(2):51-4. PubMed ID: 11925663
    [Abstract] [Full Text] [Related]

  • 32. [Mitochondrial respiratory chain diseases. Evaluation and variability in 52 patients].
    Arpa-Gutiérrez FJ, Cruz-Martínez A, Campos-González Y, Gutiérrez-Molina M, Santiago-Pérez S, Pérez-Conde MC, López-Pajares MR, Martín-Casarrubias MA, Rubio-Muñoz JC, del Hoyo P, Arpa-Fernández A, Arenas-Barbero J.
    Rev Neurol; 2002 Feb 01; 41(8):449-54. PubMed ID: 16224730
    [Abstract] [Full Text] [Related]

  • 33. Investigation of human mitochondrial myopathies by phosphorus magnetic resonance spectroscopy.
    Arnold DL, Taylor DJ, Radda GK.
    Ann Neurol; 1985 Aug 01; 18(2):189-96. PubMed ID: 4037759
    [Abstract] [Full Text] [Related]

  • 34. Oxidative damage to skeletal muscle DNA from patients with mitochondrial encephalomyopathies.
    Mitsui T, Kawai H, Nagasawa M, Kunishige M, Akaike M, Kimura Y, Saito S.
    J Neurol Sci; 1996 Jul 01; 139(1):111-6. PubMed ID: 8836981
    [Abstract] [Full Text] [Related]

  • 35. Mitochondrial myopathies.
    DiMauro S, Bonilla E, Zeviani M, Nakagawa M, DeVivo DC.
    Ann Neurol; 1985 Jun 01; 17(6):521-38. PubMed ID: 3927817
    [Abstract] [Full Text] [Related]

  • 36. [Mitochondrial encephalomyopathy (focal cytochrome c oxidase deficiency) with transient episodes of muscle weakness and elevation of serum creatine kinase activity].
    Ohno M, Kobayashi T, Tanaka K, Goto I, Nonaka I.
    Rinsho Shinkeigaku; 1990 Mar 01; 30(3):317-9. PubMed ID: 2163788
    [Abstract] [Full Text] [Related]

  • 37. Increased mitochondrial DNA in blood vessels and ragged-red fibers in mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS).
    Tokunaga M, Mita S, Sakuta R, Nonaka I, Araki S.
    Ann Neurol; 1993 Mar 01; 33(3):275-80. PubMed ID: 7684581
    [Abstract] [Full Text] [Related]

  • 38. 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 01; 14(4):462-70. PubMed ID: 6314875
    [Abstract] [Full Text] [Related]

  • 39. [Mitochondrial abnormalities and diseases].
    Goto Y, Sugita H.
    Nihon Naika Gakkai Zasshi; 1991 May 10; 80(5):775-80. PubMed ID: 1651974
    [No Abstract] [Full Text] [Related]

  • 40. Ragged red fibers in normal aging and inflammatory myopathy.
    Rifai Z, Welle S, Kamp C, Thornton CA.
    Ann Neurol; 1995 Jan 10; 37(1):24-9. PubMed ID: 7818253
    [Abstract] [Full Text] [Related]

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