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Journal Abstract Search

152 related items for PubMed ID: 7357655

  • 1. [Spinal amyotonia-amyotrophy (Werdnig-Hoffman disease) on the basis of observation of 40 cases].
    Lesný I, Kocura P, Jirásek A, Krahulec B.
    Cesk Neurol Neurochir; 1980 Jan; 43(1):26-31. PubMed ID: 7357655
    [No Abstract] [Full Text] [Related]

  • 2. [Contribution of electromyography to the diagnosis of Werdnig-Hoffmann infantile spinal amyotrophy].
    Raimbault J, Laget P.
    Pathol Biol (Paris); 1972 Mar; 20(5):287-96. PubMed ID: 4556213
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  • 7. [Catamnestic inquiries in conditions of hypertonia in early childhood. With a critical contribution to the differential diagnosis of infantile spinal progressive muscular atrophy (Werdnig-Hoffman disease--myatonia congenital Oppenheilm)].
    HORSTMANN W.
    Z Kinderheilkd; 1959 Mar; 82():649-67. PubMed ID: 13848453
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  • 10. Infantile motor neuron diseases.
    Pearn JH.
    Adv Neurol; 1982 Mar; 36():121-30. PubMed ID: 7180678
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  • 13. [Muscular pseudohypertrophy caused by chronic radiculopathy].
    Soriano G, Bujanda M, Gállego J, Villanueva JA.
    Neurologia; 1992 May; 7(5):123-4. PubMed ID: 1389294
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  • 14. [Werdnig-Hoffman disease in a 2-month-old infant].
    Balcar-Boroń A, Sawa H, Robaszewska U, Słowik J.
    Wiad Lek; 1978 Mar 15; 31(6):417-20. PubMed ID: 654293
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  • 15. Benign focal amyotrophy. Variant of chronic spinal muscular atrophy.
    Riggs JE, Schochet SS, Gutmann L.
    Arch Neurol; 1984 Jun 15; 41(6):678-9. PubMed ID: 6721743
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  • 16. [Progressive infantile spinal atrophy. Werdnig-Hoffmann disease].
    Sotelo-Cruz N, Torres-Cárdenas O, Gallegos-Gardner M.
    Bol Med Hosp Infant Mex; 1984 Jul 15; 41(7):387-92. PubMed ID: 6477703
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  • 19. [Progressive spinal amyotrophy type I or Werdnig-Hoffman disease. Apropos of 5 cases in Dakar (Senegal)].
    Ndiaye O, Sall G, Sylla A, Diouf S, Diagne I, Kuakuvi N.
    Bull Soc Pathol Exot; 2002 Jun 15; 95(2):81-2. PubMed ID: 12145964
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