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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

355 related items for PubMed ID: 7135141

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  • 25. [Systematic neonatal detection of Duchenne's muscular dystrophy. Results after 10 years' of experience in Lyons (France)].
    Plauchu H, Cordier MP, Carrier HN, Dellamonica C, Dorche C, Guibaud P, Lauras B, Cotte J, Robert JM.
    J Genet Hum; 1987 Aug; 35(4):217-30. PubMed ID: 3655748
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  • 27. Rhabdomyolysis in association with Duchenne's muscular dystrophy.
    Obata R, Yasumi Y, Suzuki A, Nakajima Y, Sato S.
    Can J Anaesth; 1999 Jun; 46(6):564-6. PubMed ID: 10391604
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  • 29. [Critical evaluation of changes of serum CK after exertion in the identification of carriers of Duchenne's muscular dystrophy].
    Cordone G, Venzano V, Rossi G, Cavallero G, Minetti C.
    Pediatr Med Chir; 1984 Jun; 6(6):819-22. PubMed ID: 6545595
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  • 30. Fetal-blood creatine phosphokinase in the diagnosis of Duchenne's muscular dystrophy.
    N Engl J Med; 1978 Jun 29; 298(26):1479-80. PubMed ID: 652021
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  • 31. Prenatal diagnosis of Duchenne's muscular dystrophy.
    Stengel-Rutkowski L, Scheuerbrandt G, Beckmann R, Pongratz D.
    Lancet; 1977 Jun 25; 1(8026):1359-60. PubMed ID: 69071
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  • 39. [Importance of recombinant DNA studies for the identification of carriers of Duchenne's muscular dystrophy].
    Veenema H, Leschot NJ, van Ommen GJ, Pearson PL.
    Ned Tijdschr Geneeskd; 1985 Jun 15; 129(24):1137-41. PubMed ID: 4022155
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