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.
121 related articles for article (PubMed ID: 6786801)
1. An improved assay for iduronate 2-sulphate sulphatase in serum and its use in the detection of carriers of the Hunter syndrome. Archer IM; Harper PS; Wusteman FS Clin Chim Acta; 1981 Apr; 112(1):107-12. PubMed ID: 6786801 [TBL] [Abstract][Full Text] [Related]
2. The iduronate sulphatase activities of cells and tissue fluids from patients with Hunter syndrome and normal controls. Dean MF J Inherit Metab Dis; 1983; 6(3):108-11. PubMed ID: 6422140 [TBL] [Abstract][Full Text] [Related]
3. Iduronate sulfatase activity in serum, lymphocytes, and fibroblasts--simplified diagnosis of the Hunter syndrome. Liebaers I; Neufeld E Pediatr Res; 1976 Aug; 10(8):733-6. PubMed ID: 821034 [TBL] [Abstract][Full Text] [Related]
4. Detection of hunter heterozygotes by enzymatic analysis of hair roots. Nwokoro N; Neufeld EF Am J Hum Genet; 1979 Jan; 31(1):42-9. PubMed ID: 107796 [TBL] [Abstract][Full Text] [Related]
5. Iduronate sulfatase analysis of hair roots for identification of Hunter syndrome heterozygotes. Yutaka T; Fluharty AL; Stevens RL; Kihara H Am J Hum Genet; 1978 Nov; 30(6):575-82. PubMed ID: 106723 [TBL] [Abstract][Full Text] [Related]
6. Iduronate sulfatase determination for the diagnosis of the Hunter syndrome and the detection of the carrier state. Neufeld EF; Liebaers I; Lim TW Adv Exp Med Biol; 1976; 68():253-60. PubMed ID: 820168 [No Abstract] [Full Text] [Related]
7. Hunter syndrome: prenatal diagnosis in maternal serum. Zlotogora J; Bach G Am J Hum Genet; 1986 Feb; 38(2):253-60. PubMed ID: 3080875 [TBL] [Abstract][Full Text] [Related]
8. Carrier detection in Hunter syndrome. Archer IM; Young ID; Rees DW; Oladimeji A; Wusteman FS; Harper PS Am J Med Genet; 1983 Sep; 16(1):61-9. PubMed ID: 6227239 [TBL] [Abstract][Full Text] [Related]
9. Heterozygote detection in Hunter syndrome. Zlotogora J; Bach G Am J Med Genet; 1984 Mar; 17(3):661-5. PubMed ID: 6424473 [TBL] [Abstract][Full Text] [Related]
10. A fluorimetric enzyme assay for the diagnosis of MPS II (Hunter disease). Voznyi YV; Keulemans JL; van Diggelen OP J Inherit Metab Dis; 2001 Nov; 24(6):675-80. PubMed ID: 11768586 [TBL] [Abstract][Full Text] [Related]
11. [Postnatal and prenatal diagnosis of mucopolysaccharidosis type II (Hunter syndrome)]. Zhang WM; Shi HP; Li BT; Zhao SM; Qi QW; Sun NH; Huang SZ Zhonghua Er Ke Za Zhi; 2006 Sep; 44(9):644-7. PubMed ID: 17217652 [TBL] [Abstract][Full Text] [Related]
12. Polyclonal antibodies against iduronate 2-sulphate sulphatase from human urine. Lissens W; Zenati A; Liebaers I Biochim Biophys Acta; 1984 Oct; 801(3):365-71. PubMed ID: 6386054 [TBL] [Abstract][Full Text] [Related]
13. alpha-L-iduronidase, beta-D-glucuronidase, and 2-sulfo-L-iduronate 2-sulfatase: preparation and characterization of radioactive substrates from heparin. Hopwood JJ Carbohydr Res; 1979 Mar; 69():203-16. PubMed ID: 106967 [TBL] [Abstract][Full Text] [Related]
14. Gene diagnosis and carrier detection in Hunter syndrome by the iduronate-2-sulphatase cDNA probe. Gal A; Beck M; Sewell AC; Morris CP; Schwinger E; Hopwood JJ J Inherit Metab Dis; 1992; 15(3):342-6. PubMed ID: 1357230 [No Abstract] [Full Text] [Related]
15. Hunter's syndrome: activity of iduronate sulfate sulfatase in the serum of pregnant heterozygotes. Zlotogora J; Bach G N Engl J Med; 1984 Aug; 311(5):331-2. PubMed ID: 6429538 [No Abstract] [Full Text] [Related]