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Journal Abstract Search
118 related items for PubMed ID: 4283415
1. The biochemical basis for mucopolysaccharidoses and mucolipidoses. Neufeld EF. Prog Med Genet; 1974; 10():81-101. PubMed ID: 4283415 [No Abstract] [Full Text] [Related]
2. The mucopolysaccharidoses (a review). Dorfman A, Matalon R. Proc Natl Acad Sci U S A; 1976 Feb; 73(2):630-7. PubMed ID: 813230 [Abstract] [Full Text] [Related]
4. Heparan sulfate and dermatan sulfate from the liver of a patient with Hurler syndrome: high performance liquid chromatography of their degradation products after incubation with alpha-L-iduronidase-deficient fibroblasts. Minami R, Fujibayashi S, Igarashi C, Ishikawa Y, Wagatsuma K, Nakao T, Tsugawa S. Clin Chim Acta; 1984 Feb 28; 137(2):179-87. PubMed ID: 6231139 [Abstract] [Full Text] [Related]
12. Mucopolysaccharide storage diseases and lysosomal hydrolases in cultured fibroblasts. den Tandt WR, Schaberg A. Pathol Eur; 1973 Feb 28; 8(1):3-11. PubMed ID: 4269628 [No Abstract] [Full Text] [Related]
13. Clinical ultrastructural and tissue culture studies in a possible compound Hurler-Scheie case. Tondeur M, Vamos-Hurwitz E, Cantz M, Cremer N, Libert J, Pardou A. Acta Paediatr Belg; 1976 Feb 28; 29(2):109-15. PubMed ID: 826105 [No Abstract] [Full Text] [Related]
14. Proceedings: The defect in Maroteaux-Lamy disease (mucopolysaccharidosis VI, subtype A): deficiency of N-acetylgalactosamine-4-sulfatase. O'Brien JF, Spranger J, Cantz M. Hoppe Seylers Z Physiol Chem; 1974 Oct 28; 355(10):1235. PubMed ID: 4218834 [No Abstract] [Full Text] [Related]
15. Mucopolysaccharidoses and mucolipidoses. Van Hoof F. J Clin Pathol Suppl (R Coll Pathol); 1974 Oct 28; 8():64-93. PubMed ID: 4220223 [No Abstract] [Full Text] [Related]
18. Correction of mucopolysaccharidosis type I fibroblasts by retroviral-mediated transfer of the human alpha-L-iduronidase gene. Anson DS, Bielicki J, Hopwood JJ. Hum Gene Ther; 1992 Aug 28; 3(4):371-9. PubMed ID: 1525210 [Abstract] [Full Text] [Related]