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Journal Abstract Search

129 related items for PubMed ID: 2769294

  • 1. Psychiatric disturbance in mitochondrial encephalomyopathy.
    Suzuki T, Koizumi J, Shiraishi H, Ofuku K, Sasaki M, Hori T, Oskoshi N.
    J Neurol Neurosurg Psychiatry; 1989 Jul; 52(7):920-2. PubMed ID: 2769294
    [No Abstract] [Full Text] [Related]

  • 2. [Mitochondrial encephalomyopathy: clinical aspects, CT morphology and neuropathology].
    Wessel K, Poremba M, Pfeiffer J, Roggendorf W.
    Fortschr Neurol Psychiatr; 1988 May; 56(5):154-62. PubMed ID: 3397029
    [Abstract] [Full Text] [Related]

  • 3. [Contributions to clinical myology. The role of electron microscopy].
    Lehmann J.
    Psychiatr Neurol Med Psychol Beih; 1987 May; 38():108-19. PubMed ID: 2841706
    [No Abstract] [Full Text] [Related]

  • 4. [2 cases of mitochondrial encephalomyopathy].
    Parisi L, Mariorenzi R, Renato Valente GO, Caramia M, Palmieri G, Amabile G.
    Riv Neurol; 1988 May; 58(3):110-5. PubMed ID: 3175460
    [Abstract] [Full Text] [Related]

  • 5. Mitochondrial oculoskeletal myopathy: case report.
    Colombo A, Merelli E, Sola P, Panzetti P, Quaglino D, Fornieri C.
    Ital J Neurol Sci; 1988 Aug; 9(4):385-9. PubMed ID: 2851565
    [Abstract] [Full Text] [Related]

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

  • 7. [Familial neural mitochondrial deafness].
    Marangos N, Mausolf A.
    HNO; 1990 Sep; 38(9):322-5. PubMed ID: 2262349
    [Abstract] [Full Text] [Related]

  • 8. Concentric laminated bodies in muscle pathology.
    Gambarelli D, Hassoun J, Pellissier JF, Berard M, Toga M.
    Pathol Eur; 1974 Sep; 9(4):289-96. PubMed ID: 4457782
    [Abstract] [Full Text] [Related]

  • 9. Congenital neuromuscular disorder with predominant mitochondrial changes in type II muscle fibers.
    Fardeau M, Tomé FM, Rolland JC.
    Acta Neuropathol Suppl; 1981 Sep; 7():279-82. PubMed ID: 6452787
    [Abstract] [Full Text] [Related]

  • 10. Deficiency of subunits of Complex I and mitochondrial encephalomyopathy.
    Ichiki T, Tanaka M, Nishikimi M, Suzuki H, Ozawa T, Kobayashi M, Wada Y.
    Ann Neurol; 1988 Mar; 23(3):287-94. PubMed ID: 3132077
    [Abstract] [Full Text] [Related]

  • 11. Familial oculocranioskeletal neuromuscular disease with abnormal muscle mitochondria.
    Tamura K, Santa T, Kuroiwa Y.
    Brain; 1974 Dec; 97(4):665-72. PubMed ID: 4154795
    [No Abstract] [Full Text] [Related]

  • 12. [Mitochondrial myopathies and encephalomyelopathies].
    Zierz S, Jerusalem F.
    Nervenarzt; 1989 Jul; 60(7):394-400. PubMed ID: 2668777
    [No Abstract] [Full Text] [Related]

  • 13. Familial mitochondrial myopathies.
    Walter GF, Tassin S, Brucher JM.
    Acta Neuropathol Suppl; 1981 Jul; 7():283-6. PubMed ID: 6939253
    [No Abstract] [Full Text] [Related]

  • 14. [Recent diagnostic and pathogenetic aspects of neuromuscular diseases].
    Gullotta F.
    Pathologica; 1985 Jul; 77(1048):121-31. PubMed ID: 3909086
    [No Abstract] [Full Text] [Related]

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

  • 16. Nemaline myopathy and a mitochondrial neuromuscular disorder in one family.
    Shapira YA, Yarom R, Blank A.
    Neuropediatrics; 1981 May; 12(2):152-65. PubMed ID: 6267500
    [Abstract] [Full Text] [Related]

  • 17. [A case of oculocraniosomatic neuromuscular disease with "ragged-red" fibers].
    Matsubara S, Yasuda A, Komai K, Okumura S, Takamori M.
    Rinsho Shinkeigaku; 1984 Mar; 24(3):221-9. PubMed ID: 6467743
    [No Abstract] [Full Text] [Related]

  • 18. Morphogenesis of the mitochondrial alterations in muscle diseases.
    Shah AJ, Sahgal V, Muschler G, Subramani V, Singh H.
    J Neurol Sci; 1982 Jul; 55(1):25-37. PubMed ID: 7108562
    [Abstract] [Full Text] [Related]

  • 19. Mitochondrial myopathy in Marinesco-Sjögren syndrome.
    Torbergsen T, Aasly J, Borud O, Lindal S, Mellgren SI.
    J Ment Defic Res; 1991 Apr; 35 ( Pt 2)():154-9. PubMed ID: 2072394
    [Abstract] [Full Text] [Related]

  • 20. Electron microscopy and histochemistry in primary and secondary neuromuscular mitochondriopathies.
    Walter GF.
    Acta Histochem Suppl; 1983 Apr; 28():249-52. PubMed ID: 6412305
    [No Abstract] [Full Text] [Related]

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