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PUBMED FOR HANDHELDS

Journal Abstract Search


115 related items for PubMed ID: 929032

  • 21. [Spinal facioscapulo-peroneal (or facioscapulo-crural) muscular atrophy and facioscapulo-peroneal muscular dystrophy].
    Kazakov VM, Skoromets AA, Mikhaĭlov EP, Barantsevich ER.
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1986; 86(5):662-7. PubMed ID: 3739474
    [Abstract] [Full Text] [Related]

  • 22. The myogenic scapulo-peroneal syndrome. Muscular dystrophy in the K. kindred: clinical study and genetics.
    Kazakov VM, Bogorodinsky DK, Skorometz AA.
    Clin Genet; 1976 Jul; 10(1):41-50. PubMed ID: 949863
    [Abstract] [Full Text] [Related]

  • 23. Landouzy-Dejerine disease: a progressive metameric muscular dystrophy of autosomal dominant inheritance with a variable intrafamilial phenotype expression.
    Rossi A, Giannini F, D'Amore I, Guazzi GC.
    Acta Neurol (Napoli); 1985 Apr; 7(2):93-111. PubMed ID: 4013841
    [No Abstract] [Full Text] [Related]

  • 24. Early signs of Landouzy-Déjerine disease: wrist and finger weakness.
    Siegel IM.
    JAMA; 1972 Jul 17; 221(3):302. PubMed ID: 5067800
    [No Abstract] [Full Text] [Related]

  • 25. Scapulo-thoracic fusion.
    Bunch WH.
    Minn Med; 1973 May 17; 56(5):391-4. PubMed ID: 4698409
    [No Abstract] [Full Text] [Related]

  • 26. [Case of facio-scapulo-humeral dystrophy].
    Rózycki B.
    Wiad Lek; 1978 Dec 15; 31(24):1759-63. PubMed ID: 735090
    [No Abstract] [Full Text] [Related]

  • 27. [Infantile facioscapulohumeral muscular dystrophy].
    Badalian LO, Temin PA, Mukhin KIu, Bulaeva NV, Zavadenko NN, Nikanorova MIu, Shnaĭdman RV, Lysov VL.
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1992 Dec 15; 92(3):28-30. PubMed ID: 1332322
    [Abstract] [Full Text] [Related]

  • 28. [Identification of primary and secondary forms of progressive muscular dystrophy, from data of clinico-genetic and biochemical studies].
    Bondarenko ES, Tamarkina AD, Zakoshchikova LV.
    Vestn Akad Med Nauk SSSR; 1973 Dec 15; 28(7):38-44. PubMed ID: 4786657
    [No Abstract] [Full Text] [Related]

  • 29. [Facial-scapular-humeral myodystrophy (genetic and clinical features)].
    Bogorodinskiĭ DK, Znoĭko ZV, Kazakov VM, Skoromets AA.
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1973 Dec 15; 73(6):801-9. PubMed ID: 4753589
    [No Abstract] [Full Text] [Related]

  • 30. Facio-scapulo-humeral muscular dystrophy. Report of a case.
    Grewal HS, Mathur S, Thapar RK, Agarwal JK.
    Indian J Pediatr; 1967 May 15; 34(232):186-8. PubMed ID: 5594806
    [No Abstract] [Full Text] [Related]

  • 31. Poikiloderma atrophicans vasculare associated with muscular dystrophy.
    Woolfson H, McQueen A.
    Arch Dermatol; 1973 Jan 15; 107(1):115-7. PubMed ID: 4682534
    [No Abstract] [Full Text] [Related]

  • 32. Facio-scapulo-humeral Muscular Dystrophy (Landouzy-Déjerine) Type.
    Jewesbury RC.
    Proc R Soc Med; 1930 Jun 15; 23(8):1114-5. PubMed ID: 19987616
    [No Abstract] [Full Text] [Related]

  • 33. [So-called facio-scapulo-humeral myopathies. (Apropos of 14 cases)].
    Mouren P, Serratrice G, Tatossian A, Poinso Y.
    Sem Hop; 1965 Apr 08; 41(17):1030-4. PubMed ID: 4283968
    [No Abstract] [Full Text] [Related]

  • 34. Muscular dystrophy in Saskatchewan Hutterites.
    Shokeir MH, Rozdilsky B.
    Am J Med Genet; 1985 Nov 08; 22(3):487-93. PubMed ID: 4061485
    [Abstract] [Full Text] [Related]

  • 35. [Various features of muscle tissue metabolism in various muscular and neuromuscular diseases of a hereditary nature (clinico-histochemical study)].
    Anosov NN, Saĭkova LA.
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1982 Nov 08; 82(3):22-5. PubMed ID: 6952668
    [Abstract] [Full Text] [Related]

  • 36. [Chemiluminescence of blood plasma and functional status of the erythrocytes of patients with various hereditary neuromuscular diseases].
    Sitnikov VF, Khrennikov VIu, Teselkin IuO.
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1987 Nov 08; 87(3):376-81. PubMed ID: 3577527
    [Abstract] [Full Text] [Related]

  • 37. [Stark-Kaeser type of chronic scapulo-peroneal amyotrophy. Apropos of 10 cases].
    Serratrice G, Gastaut JL, Pellissier JF, Pouget J.
    Rev Neurol (Paris); 1976 Dec 08; 132(12):823-32. PubMed ID: 1013569
    [Abstract] [Full Text] [Related]

  • 38. The facio-scapulo-humeral type of primary myopathy; all females in three generations.
    NIELSEN JM, ANDERSON EA.
    Bull Los Angel Neuro Soc; 1954 Dec 08; 19(4):224-7. PubMed ID: 13230705
    [No Abstract] [Full Text] [Related]

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