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Journal Abstract Search

128 related items for PubMed ID: 2668777

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

  • 2. Fatal lipid storage with abnormal mitochondria in an infant.
    Angelini C, Battistella PA, Laverda A, Pierobon-Bormioli S, Salviati G, Vergani L.
    Acta Neuropathol Suppl; 1981 Jul; 7():221-5. PubMed ID: 6939240
    [Abstract] [Full Text] [Related]

  • 3. [Myopathy with carnitine deficiency and lactic acidosis. A contribution to differential diagnosis of carnitine deficiency myopathies and mitochondrial myopathies].
    Cammann R, Dunker H, Schumacher H, Ruitenbeek W, Sperner J.
    Z Arztl Fortbild (Jena); 1992 Jul 10; 86(13):667-71. PubMed ID: 1642019
    [No Abstract] [Full Text] [Related]

  • 4.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 5. Mitochondrial encephalomyopathies.
    DiMauro S, Bonilla E, Lombes A, Shanske S, Minetti C, Moraes CT.
    Neurol Clin; 1990 Aug 10; 8(3):483-506. PubMed ID: 2170831
    [Abstract] [Full Text] [Related]

  • 6. [Inborn errors of metabolism with preferred localization in the central nervous system].
    Peiffer J.
    Verh Dtsch Ges Pathol; 1982 Aug 10; 66():213-33. PubMed ID: 7184239
    [No Abstract] [Full Text] [Related]

  • 7. Muscle carnitine deficiency in old age. Case report and therapeutic results.
    Martin JJ, Vercruyssen A, de Barsy T, Ceuterick C.
    Clin Neurol Neurosurg; 1985 Aug 10; 87(4):275-81. PubMed ID: 4092408
    [Abstract] [Full Text] [Related]

  • 8. Hypotonia in infancy.
    Dubowitz V.
    Acta Univ Carol Med Monogr; 1976 Aug 10; (75):13-8. PubMed ID: 1077757
    [No Abstract] [Full Text] [Related]

  • 9. Simple biochemical methods for the study of lipidoses and aminoacidopathies.
    Adriaenssens K, Karcher D.
    Riv Patol Nerv Ment; 1970 Oct 10; 91(5):274-6. PubMed ID: 5525772
    [No Abstract] [Full Text] [Related]

  • 10. [A case of mitochondrial encephalomyopathy with a defect in electron transport at complex I and IV in skeletal muscle showing peripheral neuropathy].
    Ohnishi A, Nakano S, Hashimoto T, Tsuji S, Murai Y.
    Rinsho Shinkeigaku; 1988 Jan 10; 28(1):107-11. PubMed ID: 2838209
    [No Abstract] [Full Text] [Related]

  • 11. [Neuropathology of encephalopathies caused by inborn errors of lipid, carbohydrate and amino metabolism].
    Pellissier JF, Bérard-Badier M, Gambarelli D, Hassoun J, Tripier MF, Toga M.
    Rev Electroencephalogr Neurophysiol Clin; 1978 Jan 10; 8(1):19-44. PubMed ID: 96500
    [No Abstract] [Full Text] [Related]

  • 12. [Diagnostic significance of muscle biopsies in metabolic myopathies. I. Myopathology].
    Pongratz D, Hübner G, Deufel T, Paetzke I, Wieland OH.
    Klin Wochenschr; 1984 Jul 02; 62(13):603-12. PubMed ID: 6592394
    [Abstract] [Full Text] [Related]

  • 13. [Metabolic myopathies].
    Lössner J, Kühn HJ.
    Psychiatr Neurol Med Psychol (Leipz); 1984 Sep 02; 36(9):513-26. PubMed ID: 6595679
    [Abstract] [Full Text] [Related]

  • 14. [Contributions to clinical myology. The role of electron microscopy].
    Lehmann J.
    Psychiatr Neurol Med Psychol Beih; 1987 Sep 02; 38():108-19. PubMed ID: 2841706
    [No Abstract] [Full Text] [Related]

  • 15. [Retinal involvement in hereditary neurometabolic disorders (author's transl)].
    Sakuragawa M.
    No To Shinkei; 1979 May 02; 31(5):471-85. PubMed ID: 486266
    [No Abstract] [Full Text] [Related]

  • 16. Mitochondrial encephalomyopathies: a group of neuromuscular disorders with defects in oxidative metabolism.
    Shapira Y, Harel S, Russell A.
    Isr J Med Sci; 1977 Feb 02; 13(2):161-4. PubMed ID: 863679
    [No Abstract] [Full Text] [Related]

  • 17. [Mitochondrial myopathies and encephalomyopathies. Neuromuscular and central nervous system diseases caused by defects in mitochondrial oxidative metabolism].
    Siemes H.
    Monatsschr Kinderheilkd; 1985 Nov 02; 133(11):798-805. PubMed ID: 3935918
    [Abstract] [Full Text] [Related]

  • 18. Menkes kinky hair disease with 'ragged red' fibers.
    Morgello S, Peterson HD, Kahn LJ, Laufer H.
    Dev Med Child Neurol; 1988 Dec 02; 30(6):812-6. PubMed ID: 3234609
    [Abstract] [Full Text] [Related]

  • 19. Metabolic disorders and corneal changes.
    François J.
    Dev Ophthalmol; 1981 Dec 02; 4():1-69. PubMed ID: 6795067
    [No Abstract] [Full Text] [Related]

  • 20. [Lipid storage myopathy].
    Gáti I, Czopf J, Kuntár L, Trombitás K.
    Orv Hetil; 1985 Sep 15; 126(37):2285-8. PubMed ID: 4047634
    [No Abstract] [Full Text] [Related]

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