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.
111 related articles for article (PubMed ID: 11031994)
21. [Sanfilippo's disease of type B. Study of the enzymatic deficiency in a family]. Nobili B; Iolascon A; Bello L; Chianese C; Rasulo V; Iolascon G; Pinto L Pediatria (Napoli); 1983; 91(2-3):295-301. PubMed ID: 6420769 [No Abstract] [Full Text] [Related]
22. Sanfilippo syndrome type D: natural history and identification of 3 novel mutations in the GNS Gene. Jansen AC; Cao H; Kaplan P; Silver K; Leonard G; De Meirleir L; Lissens W; Liebaers I; Veilleux M; Andermann F; Hegele RA; Andermann E Arch Neurol; 2007 Nov; 64(11):1629-34. PubMed ID: 17998446 [TBL] [Abstract][Full Text] [Related]
23. Mild Sanfilippo syndrome: a further cause of hyperactivity and behavioural disturbance. Wraith JE; Danks DM; Rogers JG Med J Aust; 1987 Nov; 147(9):450-1. PubMed ID: 3118155 [TBL] [Abstract][Full Text] [Related]
24. Follow-up on seven adult patients with mild Sanfilippo B-disease. van Schrojenstein-de Valk HM; van de Kamp JJ Am J Med Genet; 1987 Sep; 28(1):125-9. PubMed ID: 3118713 [TBL] [Abstract][Full Text] [Related]
28. Molecular analysis of mucopolysaccharidosis type IIIB in Portugal: evidence of a single origin for a common mutation (R234C) in the Iberian Peninsula. Mangas M; Nogueira C; Prata MJ; Lacerda L; Coll MJ; Soares G; Ribeiro G; Amaral O; Ferreira C; Alves C; Coutinho MF; Alves S Clin Genet; 2008 Mar; 73(3):251-6. PubMed ID: 18218046 [TBL] [Abstract][Full Text] [Related]
29. Correction of mucopolysaccharidosis type IIIb fibroblasts by lentiviral vector-mediated gene transfer. Villani GR; Follenzi A; Vanacore B; Di Domenico C; Naldini L; Di Natale P Biochem J; 2002 Jun; 364(Pt 3):747-53. PubMed ID: 12049639 [TBL] [Abstract][Full Text] [Related]
30. Molecular defect of caprine N-acetylglucosamine-6-sulphatase deficiency. A single base substitution creates a stop codon in the 5'-region of the coding sequence. Cavanagh KT; Leipprandt JR; Jones MZ; Friderici K J Inherit Metab Dis; 1995; 18(1):96. PubMed ID: 7623459 [No Abstract] [Full Text] [Related]
31. Intravenous administration of human umbilical cord blood cells in an animal model of MPS III B. Garbuzova-Davis S; Klasko SK; Sanberg PR J Comp Neurol; 2009 Jul; 515(1):93-101. PubMed ID: 19399896 [TBL] [Abstract][Full Text] [Related]
32. Retrovirally transduced bone marrow has a therapeutic effect on brain in the mouse model of mucopolysaccharidosis IIIB. Zheng Y; Ryazantsev S; Ohmi K; Zhao HZ; Rozengurt N; Kohn DB; Neufeld EF Mol Genet Metab; 2004 Aug; 82(4):286-95. PubMed ID: 15308126 [TBL] [Abstract][Full Text] [Related]
33. Gene symbol: SGSH. Disease: Sanfilippo syndrome type A. Zhang W; Huiping S Hum Genet; 2008 Oct; 124(3):323. PubMed ID: 18846687 [No Abstract] [Full Text] [Related]
35. Sanfilippo B disease: a re-examination of a particular sibship after 12 years. Di Natale P J Inherit Metab Dis; 1991; 14(1):23-8. PubMed ID: 1907336 [TBL] [Abstract][Full Text] [Related]
36. [Neuroimaging features in mucopolysaccharidosis: their correlation with mental retardation]. Sá G; Teixeira JF; Cruz R; Barbot C; Martins E Rev Neurol; 2006 Dec 16-31; 43(12):760-2. PubMed ID: 17160929 [No Abstract] [Full Text] [Related]
37. [Hyperactivity and behavioral disorders in Sanfilippo A (mucopolysaccharidosis type IIIA)--case report and review of the literature]. Wolańczyk T; Banaszkiewicz A; Mierzewska H; Czartoryska B; Zdziennicka E Psychiatr Pol; 2000; 34(5):831-7. PubMed ID: 11202024 [TBL] [Abstract][Full Text] [Related]
38. Molecular genetics of mucopolysaccharidosis type IIIA and IIIB: Diagnostic, clinical, and biological implications. Yogalingam G; Hopwood JJ Hum Mutat; 2001 Oct; 18(4):264-81. PubMed ID: 11668611 [TBL] [Abstract][Full Text] [Related]
39. Metabolic studies in older mentally retarded patients: significance of metabolic testing and correlation with the clinical phenotype. Van Buggenhout GJ; Trijbels JM; Wevers R; Trommelen JC; Hamel BC; Brunner HG; Fryns JP Genet Couns; 2001; 12(1):1-21. PubMed ID: 11332972 [TBL] [Abstract][Full Text] [Related]