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PUBMED FOR HANDHELDS

Journal Abstract Search

365 related items for PubMed ID: 5800957

  • 21. Diagnosis of occult muscular dystrophy: importance of the "chance" finding of elevated serum aminotransferase activities.
    Morse RP, Rosman NP.
    J Pediatr; 1993 Feb; 122(2):254-6. PubMed ID: 8429443
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  • 22. [Muscular dystrophies].
    Zellweger H, Ionasescu V, Conway TW.
    Schweiz Med Wochenschr; 1972 Jun 03; 102(22):753-9. PubMed ID: 5035931
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  • 24. Carrier detection in X-linked Duchenne type muscular dystrophy. A pluridimensional investigation.
    Radu H, Migea S, Török Z, Bordeianu L, Radu A.
    J Neurol Sci; 1968 Jun 03; 6(2):289-300. PubMed ID: 4179111
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  • 30. [Effect of drug administration on the child with progressive muscular dystrophy].
    Nakahara T, Annaka S, Baba T, Kanno M.
    Iryo; 1969 Oct 03; 23(10):1319-27. PubMed ID: 5364983
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  • 31. [CLINICAL AND BIOCHEMICAL STUDIES IN MYOPATHIES. I. SERUM ENZYMES IN PROGRESSIVE MUSCULAR DYSTROPHY (TYPE I, II, IIIA)].
    ROTTHAUWE HW, KOWALEWSKI S.
    Klin Wochenschr; 1965 Feb 01; 43():144-50. PubMed ID: 14258511
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  • 32. Distal muscular dystrophy with autosomal recessive inheritance.
    Scoppetta C, Vaccario ML, Casali C, Di Trapani G, Mennuni G.
    Muscle Nerve; 1984 Feb 01; 7(6):478-81. PubMed ID: 6543900
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  • 36. Calcium stimulated enzyme efflux from human skeletal muscle.
    Anand R, Emery AE.
    Res Commun Chem Pathol Pharmacol; 1980 Jun 01; 28(3):541-50. PubMed ID: 7403666
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  • 37. Inflammatory ocular myopathy in systemic sclerosis (scleroderma). A case report and review of the literature.
    Arnett FC, Michels RG.
    Arch Intern Med; 1973 Nov 01; 132(5):740-3. PubMed ID: 4750227
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  • 40. Clinical symptoms in a female carrier of Duchenne muscular dystrophy.
    Zatz M, Levisky RB, Levy JA, Valente BO, Gianotti M, Frota-Pessoa O.
    J Genet Hum; 1973 Dec 01; 21(4):297-305. PubMed ID: 4792239
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