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2. alpha-L-iduronidase activity in leukocytes: diagnosis of homozygotes and heterozygotes of the Hurler syndrome. Omura K; Higami S; Tada K Eur J Pediatr; 1976 May; 122(2):103-5. PubMed ID: 817912 [TBL] [Abstract][Full Text] [Related]
3. The use of alpha-L-iduronidase activity determinations in leucocytes for the detection of Hurler and Scheie syndromes. Liem KO; Hooghwinkel GJ Clin Chim Acta; 1975 Apr; 60(2):259-62. PubMed ID: 805007 [No Abstract] [Full Text] [Related]
4. The Hurler syndrome: detection of patients and heterozygotes using a microassay for alpha-L-iduronidase in fibroblasts. Kleijer WJ; Hensing-Wolffers GM; Thompson EJ; Niermeijer MF Clin Chim Acta; 1981 Oct; 116(1):47-54. PubMed ID: 6797759 [TBL] [Abstract][Full Text] [Related]
5. The defect in the Hurler and Scheie syndromes: deficiency of -L-iduronidase. Bach G; Friedman R; Weissmann B; Neufeld EF Proc Natl Acad Sci U S A; 1972 Aug; 69(8):2048-51. PubMed ID: 4262258 [TBL] [Abstract][Full Text] [Related]
6. A fluorometric assay using 4-methylumbelliferyl alpha-L-iduronide for the estimation of alpha-L-iduronidase activity and the detection of Hurler and Scheie syndromes. Hopwood JJ; Muller V; Smithson A; Baggett N Clin Chim Acta; 1979 Mar; 92(2):257-65. PubMed ID: 114339 [TBL] [Abstract][Full Text] [Related]
7. alpha-L-Iduronidase activity in established lymphoblastoid cells from patients with Hurler and Scheie syndromes transformed by Epstein-Barr virus. Minami R; Suzuki M; Kudoh T; Sato S; Oyanagi K Tohoku J Exp Med; 1977 Aug; 122(4):393-6. PubMed ID: 199964 [TBL] [Abstract][Full Text] [Related]
8. Leucocyte values of alpha-L-iduronidase activity in mucopolysaccharidosis I. Kelly TE; Taylor HA J Med Genet; 1976 Apr; 13(2):149-51. PubMed ID: 819651 [TBL] [Abstract][Full Text] [Related]
9. Clinical features of Mexican patients with Mucopolysaccharidosis type I. Alonzo-Rojo A; GarcĂa-Ortiz JE; Ortiz-Aranda M; Gallegos-Arreola MP; Figuera-Villanueva LE Genet Mol Res; 2017 Sep; 16(3):. PubMed ID: 28973713 [TBL] [Abstract][Full Text] [Related]
11. A canine model of human alpha-L-iduronidase deficiency. Spellacy E; Shull RM; Constantopoulos G; Neufeld EF Proc Natl Acad Sci U S A; 1983 Oct; 80(19):6091-5. PubMed ID: 6412235 [TBL] [Abstract][Full Text] [Related]
12. [Fluorometric determination of alpha-L-iduronidase activity in leukocytes and blood plasma in Hurler's disease]. Gusina NB; Tsukerman GL Lab Delo; 1988; (7):46-9. PubMed ID: 2460681 [No Abstract] [Full Text] [Related]
13. Simplied assay method of alpha-L-iduronidase activity in leukocytes for detection of Hurler syndrome and its carriers. Momoi T; Sudo M; Tanioka KI; Kushida H Clin Chim Acta; 1977 Dec; 81(3):311-3. PubMed ID: 411615 [No Abstract] [Full Text] [Related]
15. Reversal of clinical features of Hurler's disease and biochemical improvement after treatment by bone-marrow transplantation. Hobbs JR; Hugh-Jones K; Barrett AJ; Byrom N; Chambers D; Henry K; James DC; Lucas CF; Rogers TR; Benson PF; Tansley LR; Patrick AD; Mossman J; Young EP Lancet; 1981 Oct; 2(8249):709-12. PubMed ID: 6116856 [TBL] [Abstract][Full Text] [Related]
16. Prenatal diagnosis of mucopolysaccharidosis I: A special difficulty arising from an unusually low enzyme activity in mother's cells. Gatti R; Borrone C; Filocamo M; Pannone N; Di Natale P Prenat Diagn; 1985; 5(2):149-54. PubMed ID: 3921950 [TBL] [Abstract][Full Text] [Related]
17. Detection of the carrier state of Hurler's syndrome by assay of alpha-L-iduronidase in leukocytes. Dulaney JT; Milunsky A; Moser HW Clin Chim Acta; 1976 Jun; 69(2):305-10. PubMed ID: 819189 [TBL] [Abstract][Full Text] [Related]
18. Fluorometric assay of alpha-L-iduronidase in serum for detection of affected and carrier animals in a canine model of mucopolysaccharidosis I. Shull RM; Hastings NE Clin Chem; 1985 Jun; 31(6):826-7. PubMed ID: 3922649 [TBL] [Abstract][Full Text] [Related]
19. Prenatal diagnosis of two Hurler fetuses using an improved assay for methylumbelliferyl-alpha-L-iduronidase. Stirling JL; Robinson D; Fensom AH; Benson PF; Baker JE; Button LR Lancet; 1979 Jul; 2(8132):37. PubMed ID: 87908 [No Abstract] [Full Text] [Related]
20. A nonpathologic allele (IW) for low alpha-L-iduronidase enzyme activity vis-a-vis prenatal diagnosis of Hurler syndrome. Whitley CB; Gorlin RJ; Krivit W Am J Med Genet; 1987 Sep; 28(1):233-43. PubMed ID: 3118714 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]