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26. [Mucopolysaccharidosis VII: report of a case and review of the literature]. Huang YL; Li SY; Zhao XY; Liu HS; Ou XB; Liu L Zhonghua Er Ke Za Zhi; 2011 Jun; 49(6):455-8. PubMed ID: 21924061 [TBL] [Abstract][Full Text] [Related]
27. Infantile sialic acid storage disease in two siblings. Cooper A; Sardharwalla IB; Thornley M; Ward KP J Inherit Metab Dis; 1988; 11 Suppl 2():259-62. PubMed ID: 3141716 [No Abstract] [Full Text] [Related]
28. Correction of murine mucopolysaccharidosis VII by a human beta-glucuronidase transgene. Kyle JW; Birkenmeier EH; Gwynn B; Vogler C; Hoppe PC; Hoffmann JW; Sly WS Proc Natl Acad Sci U S A; 1990 May; 87(10):3914-8. PubMed ID: 2111021 [TBL] [Abstract][Full Text] [Related]
30. A recognition marker required for uptake of a lysosomal enzyme by cultured fibroblasts. Hickman S; Shapiro LJ; Neufeld EF Biochem Biophys Res Commun; 1974 Mar; 57(1):55-61. PubMed ID: 4364008 [No Abstract] [Full Text] [Related]
31. [Mucopolysaccharidoses. VI. Genetics of mucopolysaccharidosis. Transmission and frequency]. Romano C; Vianello MG Minerva Pediatr; 1972 Oct; 24(34):1634-41. PubMed ID: 4264145 [No Abstract] [Full Text] [Related]
32. [A new type of mucopolysaccharidosis with athetosis and urinary excretion of keratan sulfate]. Maroteaux P Nouv Presse Med; 1973 Apr; 2(15):975-9. PubMed ID: 4267565 [No Abstract] [Full Text] [Related]
33. Galactokinase deficiency: clinical and biochemical findings in a new kindred. Pickering WR; Howell RR J Pediatr; 1972 Jul; 81(1):50-5. PubMed ID: 5034870 [No Abstract] [Full Text] [Related]
34. [Electrophoretic and enzymatic analysis of urinary glycosaminoglycans. Application to the study of mucopolysaccharidosis]. Picard J; Gardais A; Esquivie C Pathol Biol (Paris); 1971 Mar; 19(5):285-91. PubMed ID: 4102384 [No Abstract] [Full Text] [Related]
35. Restoration of normal lysosomal function in mucopolysaccharidosis type VII cells by retroviral vector-mediated gene transfer. Wolfe JH; Schuchman EH; Stramm LE; Concaugh EA; Haskins ME; Aguirre GD; Patterson DF; Desnick RJ; Gilboa E Proc Natl Acad Sci U S A; 1990 Apr; 87(8):2877-81. PubMed ID: 2158095 [TBL] [Abstract][Full Text] [Related]
36. Hydrocephalus and papilledema in the Maroteaux-Lamy syndrome (mucopolysaccharidosis type VI). Goldberg MF; Scott CI; McKusick VA Am J Ophthalmol; 1970 Jun; 69(6):969-75. PubMed ID: 4246483 [No Abstract] [Full Text] [Related]
37. Mucopolysaccharidosis 3 A (Sanfilippo A disease): deficiency of a heparin sulfamidase in skin fibroblasts and leucocytes. Kresse H Biochem Biophys Res Commun; 1973 Oct; 54(3):1111-8. PubMed ID: 4201808 [No Abstract] [Full Text] [Related]
38. [Mucopolysaccharidosis type VII. Clinical, radiological and biochemical studies in a neonatal case (author's transl)]. Teyssier G; Maire I; Damon G; Boyer S; Lauras B; Freycon F Arch Fr Pediatr; 1981 Oct; 38(8):603-4. PubMed ID: 6797379 [TBL] [Abstract][Full Text] [Related]
39. Cellular metachromasia, a genetic marker for studying the mucopolysaccharidoses. Danes BS; Bearn AG Lancet; 1967 Feb; 1(7484):241-3. PubMed ID: 4163146 [No Abstract] [Full Text] [Related]
40. [Effect of mucopolysaccharides on the solubility of lysosomal enzymes]. Kint JA Arch Int Physiol Biochim; 1973 Dec; 81(5):973. PubMed ID: 4133551 [No Abstract] [Full Text] [Related] [Previous] [Next] [New Search]