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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

303 related items for PubMed ID: 6855803

  • 21.
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  • 22. [Infantile progressive spinal muscular atrophy. Werdnig-Hoffmann disease].
    Mohr W, Olischläger A, Carl H.
    Med Welt; 1971 Aug 28; 35():1317-9. PubMed ID: 5564452
    [No Abstract] [Full Text] [Related]

  • 23. [Clinical picture, pathogenesis and geneology of hereditary progressive spinal muscular atrophies].
    Nesterov LN, Sushcheva GP, Viatkina SIa, Novikova NP.
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1984 Aug 28; 84(3):321-30. PubMed ID: 6326437
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  • 24. Juvenile spinal muscular atrophy: a new hexosaminidase deficiency phenotype.
    Johnson WG, Wigger HJ, Karp HR, Glaubiger LM, Rowland LP.
    Ann Neurol; 1982 Jan 28; 11(1):11-6. PubMed ID: 6460466
    [Abstract] [Full Text] [Related]

  • 25. Normal vitamin E status in spinal muscular atrophy.
    Sokol RJ, Iannaccone ST.
    Ann Neurol; 1983 Mar 28; 13(3):328-30. PubMed ID: 6847148
    [Abstract] [Full Text] [Related]

  • 26. [Molecular basis of spinal muscular atrophy: th SMN gene].
    Tizzano E, Baiget M.
    Neurologia; 2000 Nov 28; 15(9):393-400. PubMed ID: 11195146
    [Abstract] [Full Text] [Related]

  • 27. Werdnig-Hoffmann's disease.
    Warpus JM.
    ONA J; 1979 Jul 28; 6(7):287-9. PubMed ID: 257292
    [No Abstract] [Full Text] [Related]

  • 28. Sensory ganglioneuropathy in infantile spinal muscular atrophy. Light and electronmicroscopic findings in two cases.
    Probst A, Ulrich J, Bischoff A, Boltshauser E.
    Neuropediatrics; 1981 Aug 28; 12(3):215-31. PubMed ID: 7290343
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  • 32. Diseases of the anterior horn cell.
    Wadia RS, Karandikar R, Pallod S, Grant KB, Sardesai HV.
    J Assoc Physicians India; 1972 Jun 28; 20(6):415-22. PubMed ID: 4655115
    [No Abstract] [Full Text] [Related]

  • 33. [Cumulative familial incidence of Kugelberg-Welander disease].
    Nemes A, Károly E, Csenkér E, Pintér S.
    Orv Hetil; 1986 Nov 09; 127(45):2735-9. PubMed ID: 3796971
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