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PUBMED FOR HANDHELDS

Journal Abstract Search

175 related items for PubMed ID: 4843002

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  • 4. Ultrastructure of muscle in Werdnig-Hoffmann disease.
    Hughes JT, Brownell B.
    J Neurol Sci; 1969; 8(2):361-79. PubMed ID: 5805762
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  • 6. The nosology of the spinal muscular atrophies.
    Emery AE.
    J Med Genet; 1971 Dec; 8(4):481-95. PubMed ID: 4948374
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  • 7. Ultrastructural aspects of muscle and nerve in Werdnig-Hoffmann disease.
    Szliwowski HB, Drochmans P.
    Acta Neuropathol; 1975 Dec; 31(4):281-96. PubMed ID: 1155040
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  • 8. The role of histochemistry in muscle disease.
    Dubowitz V.
    Mod Trends Neurol; 1970 Dec; 5(0):189-208. PubMed ID: 4277721
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  • 11. [Ultrastructural findings and characterization of isoenzymes in the muscle in case of Werdnig-Hoffmann disease].
    Ferreli A, Cao A, Onnis C.
    Arch De Vecchi Anat Patol; 1967 Dec; 50(3):629-44. PubMed ID: 5634345
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  • 12. [Detection of hereditary factors in spinal muscular atrophy].
    Vacek J, Nevsímalová S, Dittrich J, Strelecková J.
    Cesk Neurol Neurochir; 1979 Jan; 42(1):42-8. PubMed ID: 761261
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  • 13. Benign infantile spinal muscular atrophy. A prospective study.
    van Wijngaarden GK, Bethlem J.
    Brain; 1973 Jan; 96(1):163-70. PubMed ID: 4695720
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  • 15. Ultrastructural and histochemical features of skeletal muscle in the Wohlfart-Kugelberg-Welander syndrome.
    Adachi M, Torii J, Sher J, Ratinoff E, Aronson SM, Lapovsky A.
    J Neurol Sci; 1971 May; 13(1):13-25. PubMed ID: 4254773
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  • 16. Electromyography and muscle biopsy in infantile spinal muscular atrophy.
    Buchthal F, Olsen PZ.
    Brain; 1970 May; 93(1):15-30. PubMed ID: 5418399
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  • 17. [Clinical aspects and differential diagnosis of Werding-Hoffmann spinal amyotrophy].
    Kondratenko OM, Tsvetnova NA.
    Vopr Okhr Materin Det; 1969 Apr; 14(4):56-60. PubMed ID: 5345274
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  • 19. Benign infantile spinal muscular atrophy.
    Dubowitz V.
    Dev Med Child Neurol; 1974 Oct; 16(5):672-5. PubMed ID: 4420627
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