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Journal Abstract Search

269 related items for PubMed ID: 4784980

  • 1. Mitochondria-lipid-glycogen (MLG) disease of muscle: a morphologically regressive congenital myopathy.
    Jerusalem F, Angelini C, Engel AG, Groover RV.
    Trans Am Neurol Assoc; 1973; 98():89-93. PubMed ID: 4784980
    [No Abstract] [Full Text] [Related]

  • 2. Mitochondria-lipid-glycogen (MLG) disease of muscle. A morphologically regressive congenital myopathy.
    Jerusalem F, Angelini C, Engel AG, Groover RV.
    Arch Neurol; 1973 Sep; 29(3):162-9. PubMed ID: 4273245
    [No Abstract] [Full Text] [Related]

  • 3. Fingerprint body myopathy, a newly recognized congenital muscle disease.
    Engel AG, Angelini C, Gomez MR.
    Mayo Clin Proc; 1972 Jun; 47(6):377-88. PubMed ID: 4339422
    [No Abstract] [Full Text] [Related]

  • 4. Benign congenital myopathy. A cause for mild, nonprogressive or slowly progressive muscle weakness.
    Saper JR.
    Am J Med; 1974 Aug; 57(2):157-60. PubMed ID: 4276677
    [No Abstract] [Full Text] [Related]

  • 5. Benign mitochondrial myopathy with deficiency of NADH-CoQ reductase and cytochrome c oxidase.
    Roodhooft AM, Van Acker KJ, Martin JJ, Ceuterick C, Scholte HR, Luyt-Houwen IE.
    Neuropediatrics; 1986 Nov; 17(4):221-6. PubMed ID: 3027606
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  • 7. Mitochondria-lipid-glycogen myopathy, hyperlactacidemia, and carnitine deficiency.
    Di Donato S, Cornelio F, Balestrini MR, Bertagnolio B, Peluchetti D.
    Neurology; 1978 Nov; 28(11):1110-6. PubMed ID: 568729
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  • 9. [Congenital ophthalmomyopathy].
    Frazzetto F, Streiff EB, Forssmann WG.
    Ann Ocul (Paris); 1969 Dec; 202(12):1217-53. PubMed ID: 5404748
    [No Abstract] [Full Text] [Related]

  • 10. [Mitochondrial myopathies].
    Reichmann H, Rohkamm R, Ricker K, Mertens HG.
    Dtsch Med Wochenschr; 1988 Jan 22; 113(3):106-13. PubMed ID: 2827983
    [No Abstract] [Full Text] [Related]

  • 11. Lipid storage myopathy responsive to prednisone.
    Engel AG, Siekert RG.
    Arch Neurol; 1972 Aug 22; 27(2):174-81. PubMed ID: 5040634
    [No Abstract] [Full Text] [Related]

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  • 14. The myopathology of the Kocher-Debré-Sémélaigne syndrome. Electromyography, light- and electron-microscopic study.
    Afifi AK, Najjar SS, Mire-Salman J, Bergman RA.
    J Neurol Sci; 1974 Aug 22; 22(4):445-70. PubMed ID: 4847305
    [No Abstract] [Full Text] [Related]

  • 15. [Experimental myopathy induced with cortisone. Histological, histochemical and ultrastructural study].
    Toga M, Gambarelli D, Pellissier JF, Berard M, Hassoun J.
    Ann Anat Pathol (Paris); 1973 Aug 22; 18(1):67-90. PubMed ID: 4716704
    [No Abstract] [Full Text] [Related]

  • 16. [Sudanophilic (mitochondria) myopathy (author's transl)].
    Gullotta F, Payk TR, Solbach A.
    Z Neurol; 1974 Apr 04; 206(4):309-26. PubMed ID: 4134756
    [No Abstract] [Full Text] [Related]

  • 17. [McArdle's metabolic myopathy].
    Shutov AA, Bessonov AV, Sidorov VV.
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1974 Apr 04; 74(10):1485-90. PubMed ID: 4530582
    [No Abstract] [Full Text] [Related]

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