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Journal Abstract Search

222 related items for PubMed ID: 4260161

  • 21. Urinary amino acids in storage disorders: mucopolysaccharidosis, Gaucher's disease and metachromatic leucodystrophy.
    Hultberg B, Ockerman PA, Eriksson O.
    Metabolism; 1969 Aug; 18(8):713-9. PubMed ID: 4241013
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  • 30. [Diseases caused by genetic defects in lysosomal muco-polysaccharide-catabolism. Mucopolysaccharidoses].
    Passarge E, Wendel U, Wöhler W, Rüdiger HW.
    Dtsch Med Wochenschr; 1974 Jan 25; 99(4):144 passim. PubMed ID: 4274189
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  • 32. Glycosaminoglycans. A biochemical and clinical review.
    Lamberg SI, Stoolmiller AC.
    J Invest Dermatol; 1974 Dec 25; 63(6):433-49. PubMed ID: 4139221
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  • 35. Acid glycosidases in mucopolysaccharidoses fibroblasts.
    Fluharty AL, Porter MT, Lassila EL, Trammell J, Carrel RE, Kihara H.
    Biochem Med; 1970 Sep 25; 4(2):110-20. PubMed ID: 4257448
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  • 38. [Clinical variants of hereditary mucopolysaccharidosis].
    Geller LI.
    Klin Med (Mosk); 1970 Jul 25; 48(7):16-9. PubMed ID: 4250220
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  • 39. Mucopolysaccharide storage diseases and lysosomal hydrolases in cultured fibroblasts.
    den Tandt WR, Schaberg A.
    Pathol Eur; 1973 Jul 25; 8(1):3-11. PubMed ID: 4269628
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  • 40. Urinary hyaluronidase activity in mucopolysaccharidosis.
    Józsa L, Szabó L.
    Acta Paediatr Acad Sci Hung; 1969 Jul 25; 10(1):73-8. PubMed ID: 4240053
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