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Journal Abstract Search

126 related items for PubMed ID: 6354540

  • 1. Myoencephalopathies with abnormal mitochondria: a review.
    Walter GF.
    Clin Neuropathol; 1983; 2(3):101-13. PubMed ID: 6354540
    [Abstract] [Full Text] [Related]

  • 2. [Mitochondrial myopathies and encephalomyopathies. Neuromuscular and central nervous system diseases caused by defects in mitochondrial oxidative metabolism].
    Siemes H.
    Monatsschr Kinderheilkd; 1985 Nov; 133(11):798-805. PubMed ID: 3935918
    [Abstract] [Full Text] [Related]

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  • 5. [Neuromuscular mitochondriopathy. A morphological expression of disorders of the energy metabolism (author's transl)].
    Walter GF.
    Veroff Pathol; 1981 Nov; 117():1-111. PubMed ID: 6210998
    [No Abstract] [Full Text] [Related]

  • 6. [Central nervous system and neuromuscular diseases with abnormal mitochondria. Analysis and critical evaluation of the so-called "mitochondrial encephalomyopathies"].
    Schmitt HP.
    Nervenarzt; 1982 Aug; 53(8):427-34. PubMed ID: 7133243
    [No Abstract] [Full Text] [Related]

  • 7. Mitochondrial myopathies and myoencephalopathies.
    Byrne E.
    Curr Opin Rheumatol; 1990 Dec; 2(6):889-95. PubMed ID: 2083153
    [No Abstract] [Full Text] [Related]

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  • 9. Mitochondrial encephalomyopathies in childhood. I. Biochemical and morphologic investigations.
    Tulinius MH, Holme E, Kristiansson B, Larsson NG, Oldfors A.
    J Pediatr; 1991 Aug; 119(2):242-50. PubMed ID: 1861209
    [Abstract] [Full Text] [Related]

  • 10. Mitochondrial encephalomyopathies in childhood. II. Clinical manifestations and syndromes.
    Tulinius MH, Holme E, Kristiansson B, Larsson NG, Oldfors A.
    J Pediatr; 1991 Aug; 119(2):251-9. PubMed ID: 1861210
    [Abstract] [Full Text] [Related]

  • 11. Failure of brain and skeletal muscle energy metabolism in multiple system atrophy shown by in vivo phosphorous MR spectroscopy.
    Martinelli P, Giuliani S, Lodi R, Iotti S, Zaniol P, Barbiroli B.
    Adv Neurol; 1996 Aug; 69():271-7. PubMed ID: 8615139
    [No Abstract] [Full Text] [Related]

  • 12. [Mitochondrial diseases in children--a review].
    Holme E, Kristiansson B, Oldfors A, Tulinius M.
    Lakartidningen; 1987 Jul 22; 84(30-31):2411-5. PubMed ID: 3626706
    [No Abstract] [Full Text] [Related]

  • 13. The mitochondrial myopathies: 9 case reports and a literature review.
    Fitzsimons RB.
    Clin Exp Neurol; 1981 Jul 22; 17():185-210. PubMed ID: 7346199
    [Abstract] [Full Text] [Related]

  • 14. Electron cytochemistry of crystalline inclusions in human skeletal muscle mitochondria.
    Bonilla E, Schotland DL, DiMauro S, Aldover B.
    J Ultrastruct Res; 1975 Jun 22; 51(3):404-8. PubMed ID: 166198
    [No Abstract] [Full Text] [Related]

  • 15. Neuromuscular disorders with abnormal muscle mitochondria.
    Kamieniecka Z, Schmalbruch H.
    Int Rev Cytol; 1980 Jun 22; 65():321-57. PubMed ID: 6993406
    [No Abstract] [Full Text] [Related]

  • 16. [2 cases of mitochondrial encephalomyopathy].
    Parisi L, Mariorenzi R, Renato Valente GO, Caramia M, Palmieri G, Amabile G.
    Riv Neurol; 1988 Jun 22; 58(3):110-5. PubMed ID: 3175460
    [Abstract] [Full Text] [Related]

  • 17. Mitochondrial encephalomyopathies.
    DiMauro S, Bonilla E, Lombes A, Shanske S, Minetti C, Moraes CT.
    Neurol Clin; 1990 Aug 22; 8(3):483-506. PubMed ID: 2170831
    [Abstract] [Full Text] [Related]

  • 18. Mitochondrial encephalomyopathies: a group of neuromuscular disorders with defects in oxidative metabolism.
    Shapira Y, Harel S, Russell A.
    Isr J Med Sci; 1977 Feb 22; 13(2):161-4. PubMed ID: 863679
    [No Abstract] [Full Text] [Related]

  • 19. [Benign myopathy in children].
    Morooka K.
    Nihon Rinsho; 1982 Feb 22; 40(7):1534-46. PubMed ID: 6757481
    [No Abstract] [Full Text] [Related]

  • 20. Variability of mitochondrial cytochemistry in human neuromuscular diseases.
    Shah A, Sahgal V, Sahgal S, Subramani V, Kochar H.
    J Submicrosc Cytol Pathol; 1988 Apr 22; 20(2):287-95. PubMed ID: 3395968
    [Abstract] [Full Text] [Related]

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