These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
94 related articles for article (PubMed ID: 101485)
1. Unusually mild course of beta-glucuronidase deficiency in two brothers (mucopolysaccharidosis VII). Gitzelmann R; Wiesmann UN; Spycher MA; Herschkowitz N; Giedion A Helv Paediatr Acta; 1978 Nov; 33(4-5):413-28. PubMed ID: 101485 [TBL] [Abstract][Full Text] [Related]
2. Mucopolysaccharidosis type VII (beta-glucuronidase deficiency): a chronic variant with an oligosymptomatic severe skeletal dysplasia. de Kremer RD; Givogri I; Argaraña CE; Hliba E; Conci R; Boldini CD; Capra AP Am J Med Genet; 1992 Sep; 44(2):145-52. PubMed ID: 1456283 [TBL] [Abstract][Full Text] [Related]
3. Beta-glucuronidase deficiency in a girl with unusual clinical features. Pfeiffer RA; Kresse H; Bäumer N; Sattinger E Eur J Pediatr; 1977 Oct; 126(3):155-61. PubMed ID: 144057 [TBL] [Abstract][Full Text] [Related]
4. Feline mucopolysaccharidosis VII due to beta-glucuronidase deficiency. Gitzelmann R; Bosshard NU; Superti-Furga A; Spycher MA; Briner J; Wiesmann U; Lutz H; Litschi B Vet Pathol; 1994 Jul; 31(4):435-43. PubMed ID: 7941232 [TBL] [Abstract][Full Text] [Related]
5. 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]
6. [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]
7. 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]
9. Mucopolysaccharidosis type VII. A morphologic, cytochemical, and ultrastructural study of the blood and bone marrow. Peterson L; Parkin J; Nelson A Am J Clin Pathol; 1982 Oct; 78(4):544-8. PubMed ID: 6814236 [TBL] [Abstract][Full Text] [Related]
10. 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]
11. Deficiency of arylsulfatase B in 2 brothers aged 40 and 38 years (Maroteaux-Lamy syndrome, type B). Pilz H; von Figura K; Goebel HH Ann Neurol; 1979 Oct; 6(4):315-25. PubMed ID: 122048 [TBL] [Abstract][Full Text] [Related]
12. Low beta-glucuronidase enzyme activity and mutations in the human beta-glucuronidase gene in mild mucopolysaccharidosis type VII, pseudodeficiency and a heterozygote. Vervoort R; Gitzelmann R; Bosshard N; Maire I; Liebaers I; Lissens W Hum Genet; 1998 Jan; 102(1):69-78. PubMed ID: 9490302 [TBL] [Abstract][Full Text] [Related]
17. Low beta-glucuronidase activity in a healthy member of a family with mucopolysaccharidosis VII. Chabas A; Giros ML; Guardiola A J Inherit Metab Dis; 1991; 14(6):908-14. PubMed ID: 1779649 [TBL] [Abstract][Full Text] [Related]
18. Beta-glucuronidase deficiency: enzyme studies in an affected family and prenatal diagnosis. Maire I; Mandon G; Zabot MT; Mathieu M; Guibaud P J Inherit Metab Dis; 1980; 2(2):29-34. PubMed ID: 6796758 [TBL] [Abstract][Full Text] [Related]