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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

227 related items for PubMed ID: 5122052

  • 21.
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  • 22.
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  • 23. [Serum enzymatic activity in neuromuscular diseases].
    Strumień M.
    Neurol Neurochir Pol; 1975; 9(1):1-5. PubMed ID: 1121344
    [Abstract] [Full Text] [Related]

  • 24. [Type II proximal spinal muscular atrophy. Clinical, electrophysiological, histopathological and histochemical studies].
    Tangheroni W, Cao A, Cianchetti C, Calisti L.
    Minerva Pediatr; 1974 Jun 23; 26(22):1125-45. PubMed ID: 4276719
    [No Abstract] [Full Text] [Related]

  • 25. [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 23; 64(6):523-30. PubMed ID: 3190905
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  • 26.
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  • 28. 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 23; 120(5):525-35. PubMed ID: 6054585
    [No Abstract] [Full Text] [Related]

  • 29. [Changes in the activity of blood serum enzymes in relatives of children with myopathy].
    Grinio LP.
    Vopr Med Khim; 1966 Nov 23; 12(6):600-3. PubMed ID: 6000902
    [No Abstract] [Full Text] [Related]

  • 30. [Errors in the diagnosis of progressive muscular dystrophy and spinal muscular atrophy].
    Parnitzke C, Hagen EM.
    Z Arztl Fortbild (Jena); 1981 Jul 01; 75(13):577-81. PubMed ID: 7314671
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  • 31.
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  • 32. [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
    [Abstract] [Full Text] [Related]

  • 33.
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  • 34. [Clinico-morphologic characteristics of X-linked pseudohypertrophic myopathy].
    Demidov PV, Kop'eva TN, Potomskaia IZ, Grinio LP, Kopylova EN.
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1976 May 19; 76(5):641-6. PubMed ID: 936862
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  • 35.
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  • 36. [Autosomal recessive severe, proximal myopathy in children, common in Tunisia].
    Ben Hamida M, Attia N, Chabouni H, Fardeau M.
    Rev Neurol (Paris); 1983 May 19; 139(4):289-97. PubMed ID: 6612142
    [Abstract] [Full Text] [Related]

  • 37. Spinal muscular atrophy in childhood. Two clues to clinical diagnosis.
    Moosa A, Dubowitz V.
    Arch Dis Child; 1973 May 19; 48(5):386-8. PubMed ID: 4703068
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  • 40.
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