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2. Arylsulfatase B deficiency in Maroteaux-Lamy syndrome cultured fibroblasts. Fluharty AL; Stevens RL; Sanders DL; Kihara H Biochem Biophys Res Commun; 1974 Jul; 59(2):455-61. PubMed ID: 4277366 [No Abstract] [Full Text] [Related]
3. Variation in the phenotypic expression of beta-glucuronidase deficiency. Beaudet AL; DiFerrante NM; Ferry GD; Nichols BL; Mullins CE J Pediatr; 1975 Mar; 86(3):388-94. PubMed ID: 803560 [TBL] [Abstract][Full Text] [Related]
4. Lysosomal enzymes of cultured fibroblasts of cystic fibrosis patients. Butterworth J; Scott F; McCrae WM; Bain AD Clin Chim Acta; 1972 Aug; 40(1):139-42. PubMed ID: 4262514 [No Abstract] [Full Text] [Related]
5. Mucolipidosis. 3. New studies. Robinow M; Soukup SM Birth Defects Orig Artic Ser; 1974; 10(8):129-34. PubMed ID: 4376425 [No Abstract] [Full Text] [Related]
6. Mucopolysaccharide storage diseases and lysosomal hydrolases in cultured fibroblasts. den Tandt WR; Schaberg A Pathol Eur; 1973; 8(1):3-11. PubMed ID: 4269628 [No Abstract] [Full Text] [Related]
7. 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]
8. Beta-glucuronidase deficiency in a dog: a model of human mucopolysaccharidosis VII. Haskins ME; Desnick RJ; DiFerrante N; Jezyk PF; Patterson DF Pediatr Res; 1984 Oct; 18(10):980-4. PubMed ID: 6436780 [TBL] [Abstract][Full Text] [Related]
9. Genetic heterogeneity within the chondroitinsulphaturias. Danes BS; Rottell BK; Eviatar L; Stolzenberg J J Med Genet; 1977 Apr; 14(2):103-7. PubMed ID: 404409 [TBL] [Abstract][Full Text] [Related]
11. [Radiological characteristics of the pelvic girdle in mucopolysaccharidoses]. Romano C; Pelizza A; Cordone G; Gargani GF Minerva Pediatr; 1975 Mar; 27(9):515-23. PubMed ID: 806777 [No Abstract] [Full Text] [Related]
12. A hypothesis for I-cell disease: defective hydrolases that do not enter lysosomes. Hickman S; Neufeld EF Biochem Biophys Res Commun; 1972 Nov; 49(4):992-9. PubMed ID: 4345092 [No Abstract] [Full Text] [Related]
13. Mucopolysaccharidosis. VII. Beta-glucuronidase deficiency. Gehler J; Cantz M; Tolksdorf M; Spranger J; Gilbert E; Drube H Humangenetik; 1974 Jul; 23(2):149-58. PubMed ID: 4277583 [No Abstract] [Full Text] [Related]
14. Mucopolysaccharidosis: secondarily induced abnormal distribution of lysosomal isoenzymes. Kint JA; Dacremont G; Carton D; Orye E; Hooft C Science; 1973 Jul; 181(4097):352-4. PubMed ID: 4268963 [TBL] [Abstract][Full Text] [Related]
15. Prenatal diagnosis of mucolipidosis II (I-cell disease). Gehler J; Cantz M; Stoeckenius M; Spranger J Eur J Pediatr; 1976 Jun; 122(3):201-6. PubMed ID: 819273 [TBL] [Abstract][Full Text] [Related]
16. [Mucolipidosis. biologic characteristics (author's transl)]. Gatti R; Borrone C; Torreblanca J; Cavalieri S; de Martini I; Filocamo M; Antelo MC An Esp Pediatr; 1979; 12(8-9):563-74. PubMed ID: 115347 [TBL] [Abstract][Full Text] [Related]
17. Atypical radiological features of beta-glucuronidase deficiency (mucopolysaccharidosis VII) occurring in an elderly patient from an inbred kindred. Chapman S; Gray RG; Constable TJ; Bundey S Br J Radiol; 1989 May; 62(737):491-4. PubMed ID: 2496886 [No Abstract] [Full Text] [Related]
19. A -glucuronidase deficiency mucopolysaccharidosis: studies in cultured fibroblasts. Hall CW; Cantz M; Neufeld EF Arch Biochem Biophys; 1973 Mar; 155(1):32-8. PubMed ID: 4268215 [No Abstract] [Full Text] [Related]
20. Morphological and biochemical findings in a case of mucopolysaccharidosis type III A (Sanfilippo's disease type A). Witting C; Müller KM; Kresse H; Figura KV; Marx H Beitr Pathol; 1975; 154(3):324-38. PubMed ID: 805586 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]