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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

68 related items for PubMed ID: 943262

  • 21.
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  • 22. [Case of muscular dystrophy associated ith coincidental lower motor neuron lesion].
    Kondo K, Tsubaki T.
    No To Shinkei; 1969 Aug; 21(8):929-35. PubMed ID: 4309372
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  • 23. [Moebius' syndrome and amyotrophies of the extremities (5 cases)].
    Tridon P, André JM, André M, Brichet B, Arnould G.
    Rev Neurol (Paris); 1971 May; 124(5):367-78. PubMed ID: 5126782
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  • 30. [Abnormal head drooping in facioscapulohumeral muscular dystrophy].
    Ichikawa Y, Yamada H, Motoyoshi Y, Shimizu T, Kawai M.
    Rinsho Shinkeigaku; 1996 Mar; 36(3):503-6. PubMed ID: 8741360
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  • 31. [Pathogenetic considerations on congenital facial diplegia].
    Di Tizio A, D'Ambrosi D.
    Ann Ottalmol Clin Ocul; 1968 Dec; 94(12):1513-29. PubMed ID: 5735931
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  • 33. Diseases of the anterior horn cell.
    Wadia RS, Karandikar R, Pallod S, Grant KB, Sardesai HV.
    J Assoc Physicians India; 1972 Jun; 20(6):415-22. PubMed ID: 4655115
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  • 34. [Progressive deafness and facial paralysis as early symptoms of Camurati-Engelmann disease].
    Bormioli P, D'Alessandro A, Di Lella V.
    Clin Otorinolaringoiatr; 1970 Jun; 22(3):159-86. PubMed ID: 5526949
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  • 37. Atypical phenotypes in patients with facioscapulohumeral muscular dystrophy 4q35 deletion.
    Krasnianski M, Eger K, Neudecker S, Jakubiczka S, Zierz S.
    Arch Neurol; 2003 Oct; 60(10):1421-5. PubMed ID: 14568813
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  • 39. [A family with facioscapulohumeral muscular dystrophy and hereditary long QT syndrome].
    Kimura T, Moriwaki T, Sawada J, Naka T, Hazama T, Nakata T.
    Rinsho Shinkeigaku; 1997 Aug; 37(8):690-2. PubMed ID: 9404145
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  • 40. [Heredity of myopathy, with special reference to progressive muscular dystrophy].
    Sugita H.
    Naika; 1970 Apr; 25(4):611-9. PubMed ID: 4912548
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