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Journal Abstract Search

129 related items for PubMed ID: 77096

  • 1. [Peripheral metabolic neuropathies in genetically dependent lysosomal enzyme defects].
    Pilz H, Goebel HH, Argyrakis A, Hopf HC.
    Verh Dtsch Ges Inn Med; ; 83():1075-7. PubMed ID: 77096
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  • 10. [Lysosomal enzyme defects].
    Spranger J.
    Monatsschr Kinderheilkd; 1983 Jun; 131(6):311-7. PubMed ID: 6888383
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  • 11. [Pathogenesis and pathomorphology of human leukodystrophies].
    Zhabotinskiĭ IuM, Shefer VF.
    Arkh Patol; 1981 Jun; 43(11):86-92. PubMed ID: 7032481
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  • 12. Hereditary and acquired polyneuropathies. Electrophysiologic aspects.
    Miller RG.
    Neurol Clin; 1985 Aug; 3(3):543-56. PubMed ID: 2413343
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  • 13. Clinical and biochemical pathophysiology of ataxia in the sphingolipidoses.
    Philippart M.
    Adv Neurol; 1978 Aug; 21():131-49. PubMed ID: 104554
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  • 14. [Animal models for inborn lysosomal storage diseases (author's transl)].
    Naiki M.
    Jikken Dobutsu; 1977 Jan; 26(1):65-77. PubMed ID: 404167
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  • 17. [Progressive neuronal degeneration and childhood cirrhosis].
    Kumada S, Okaniwa M.
    Ryoikibetsu Shokogun Shirizu; 1995 Jan; (8):442-5. PubMed ID: 8581675
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  • 18. Genetic disorders of lysosomes.
    Hirschhorn R, Weissmann G.
    Prog Med Genet; 1976 Jan; 1():49-101. PubMed ID: 180565
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  • 19. Biochemical approaches to the nosology of nervous system defects, III.
    Menkes JH.
    Birth Defects Orig Artic Ser; 1971 Feb; 7(1):37-41. PubMed ID: 5006214
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  • 20. Neuropathological changes in brain glycoproteins.
    Berra B, Brunngraber EG.
    Biochem Exp Biol; 1977 Feb; 13(1):31-9. PubMed ID: 26363
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