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PUBMED FOR HANDHELDS

Journal Abstract Search


128 related items for PubMed ID: 936862

  • 1.
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  • 2. Becker-type muscular dystrophy.
    Bradley WG, Jones MZ, Mussini JM, Fawcett PR.
    Muscle Nerve; 1978; 1(2):111-32. PubMed ID: 571527
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  • 4. [Clinico-biochemical and genetic studies of myopathy].
    Davidenkova EF, Droznina TA, Markelov IM.
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1966; 66(11):1623-8. PubMed ID: 6001049
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  • 6. [Contribution on the study of pseudohypertrophic muscular dystrophies. I. Benign pseudohypertrophic muscular dystrophy].
    Radu H, Stenzel K.
    Dtsch Z Nervenheilkd; 1969; 196(2):92-115. PubMed ID: 5800957
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  • 8. [Autosomal recessive severe, proximal myopathy in children, common in Tunisia].
    Ben Hamida M, Attia N, Chabouni H, Fardeau M.
    Rev Neurol (Paris); 1983; 139(4):289-97. PubMed ID: 6612142
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  • 10. [Changes in the activity of blood serum enzymes in relatives of children with myopathy].
    Grinio LP.
    Vopr Med Khim; 1966; 12(6):600-3. PubMed ID: 6000902
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  • 11. [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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  • 16. The detection of female carriers of pseudohypertrophic muscular dystrophy.
    Kakulas BA, Knight JO, Gubbay SS, Mastaglia FL.
    Proc Aust Assoc Neurol; 1968 May 31; 5(3):545-51. PubMed ID: 5709982
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  • 19. [Membrane effects of insulin in x-chromosome recessive hereditary progressive muscular dystrophy (Duchenne form)].
    Blietz R, Kruchten J, Riedl K, Wagner J.
    Hoppe Seylers Z Physiol Chem; 1967 Dec 31; 348(12):1609-15. PubMed ID: 5586908
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  • 20. Echinogenic action of L-alpha-lysophosphatidylcholine in Duchenne muscular dystrophy: a study on carrier detection.
    Tangorra A, Curatola G, Milani-Comparetti M, Ferretti G.
    Am J Med Genet; 1989 Apr 31; 32(4):540-4. PubMed ID: 2774000
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