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Journal Abstract Search

216 related items for PubMed ID: 5747395

  • 1. [On Becker's benign muscular dystrophy: study of a family with 10 affected members in 6 generations].
    Caruso G, Campanella G.
    Acta Neurol (Napoli); 1968; 23(4):709-31. PubMed ID: 5747395
    [No Abstract] [Full Text] [Related]

  • 2. [Becker's benign muscular dystrophy. Observations on 1 family].
    Armocida G, Cottini R, Finavera L, Majeron MA.
    Minerva Med; 1978 May 19; 69(25):1745-8. PubMed ID: 662177
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  • 3. [Progressive muscular dystrophy: CPK, LDH, ALD (aldolase)--EMG, ECG in patients and their families].
    Diotallevi P, Bargilli E, Danni M, Dellantonio R, Tocchini M, Milani-Comparetti M.
    Boll Soc Ital Biol Sper; 1988 Jun 19; 64(6):523-30. PubMed ID: 3190905
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  • 6. [Progressive musclar dystrophy in the experience of the Pediatric Clinic of Florence. Longitudinal study of 43 subjects].
    Adami Lami Conti C, Calandi C, Nistri R, Aulisi A, Bucciolini MG, Vannelli G, Ragazzini F.
    Minerva Pediatr; 1981 May 15; 33(9):385-412. PubMed ID: 7019663
    [No Abstract] [Full Text] [Related]

  • 7. Clinical studies in progressive muscular dystrophy.
    Prot J.
    Pol Med J; 1972 May 15; 11(4):1004-12. PubMed ID: 5078704
    [No Abstract] [Full Text] [Related]

  • 8. [Muscular dystrophy and its problems].
    Ueda K, Ito T, Nakata T, Ohara T, Matsumoto K.
    Nihon Rinsho; 1968 Sep 15; 26(9):2184-98. PubMed ID: 5752294
    [No Abstract] [Full Text] [Related]

  • 9. [Evaluation of serum pyruvate kinase in patients with Duchenne's muscular dystrophy and carriers. Comparison with other enzyme determinations].
    Calandi C, Adami Lami C, Guidotti T, Nistri R, Papuzza S, Tozzi P, Poggi G.
    Minerva Pediatr; 1981 May 31; 33(10):453-64. PubMed ID: 7254147
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  • 11. [Serum aldolase and creatine phosphokinase in progressive muscular dystrophy].
    Ceccarelli A, Leone P.
    Clin Pediatr (Bologna); 1967 May 31; 49(5):237-45. PubMed ID: 6080497
    [No Abstract] [Full Text] [Related]

  • 12. [Differentiation and dedifferentiation of muscular dystrophy].
    Ueda K, Ito T, Nakata T, Ohara T, Matsumoto K.
    Nihon Rinsho; 1968 Oct 31; 26(10):2423-42. PubMed ID: 5752013
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  • 15. Benign congenital muscular dystrophy: a special form of congenital hypotonia.
    Zellweger H, Afifi A, McCormick WF, Mergner W.
    Clin Pediatr (Phila); 1967 Nov 31; 6(11):655-63. PubMed ID: 6058423
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  • 18. Blood enzymes in Duchene's progressive muscular dystrophy and their correlation with the clinical and histological pictures.
    Niebrój-Dobosz I, Jedrzejowska H, Hetnarska L.
    Acta Med Pol; 1970 Nov 31; 11(4):387-93. PubMed ID: 5493781
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  • 19. Slowly progressive X-linked recessive muscular dystrophy (type 3b). Report of cases and review of the literature.
    Zellweger H, Hanson JW.
    Arch Intern Med; 1967 Nov 31; 120(5):525-35. PubMed ID: 6054585
    [No Abstract] [Full Text] [Related]

  • 20. [Effects of administration of phosphocreatine on the clinical, biochemical and electromyographic evolution of Duchenne's progressive muscular dystrophy].
    Radu H, Keresztes L, Stenzel K.
    Minerva Med; 1968 Dec 12; 59(99):5524-9. PubMed ID: 5718841
    [No Abstract] [Full Text] [Related]

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