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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]
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]