161 related articles for article (PubMed ID: 817912)
1. 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]
2. 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]
3. 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]
4. 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]
5. 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]
6. Hurler syndrome: alpha-L-iduronidase activity in leukocytes as a method for heterozygote detection.
Wappner RS; Brandt IK
Pediatr Res; 1976 Jun; 10(6):629-32. PubMed ID: 818611
[TBL] [Abstract][Full Text] [Related]
7. Apparent allelism of the Hurler, Scheie, and Hurler/Scheie syndromes.
Mueller OT; Shows TB; Opitz JM
Am J Med Genet; 1984 Jul; 18(3):547-56. PubMed ID: 6433708
[TBL] [Abstract][Full Text] [Related]
8. [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]
9. Molecular genetic defect underlying alpha-L-iduronidase pseudodeficiency.
Aronovich EL; Pan D; Whitley CB
Am J Hum Genet; 1996 Jan; 58(1):75-85. PubMed ID: 8554071
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. 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]
12. 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]
13. 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]
14. Fluorometric measurement of alpha-L-iduronidase activity using 4-methylumbelliferyl-alpha-L-iduronide.
Minami R; Watanabe Y; Kudoh T; Oyanagi K; Nakao T
Tohoku J Exp Med; 1980 Apr; 130(4):381-4. PubMed ID: 6781103
[TBL] [Abstract][Full Text] [Related]
15. Properties of alpha-L-iduronidase in cultured skin fibroblasts from alpha-L-iduronidase-deficient patients.
Fujibayashi S; Minami R; Ishikawa Y; Wagatsuma K; Nakao T; Tsugawa S
Hum Genet; 1984; 65(3):268-72. PubMed ID: 6421718
[TBL] [Abstract][Full Text] [Related]
16. Atypical Hurler syndrome without alpha-L-iduronidase deficiency.
Orii T; Sukegawa K; Minami R; Matsuura Y; Tsugawa S
Tohoku J Exp Med; 1976 Oct; 120(2):113-23. PubMed ID: 136068
[TBL] [Abstract][Full Text] [Related]
17. Bone marrow transplantation for Hurler syndrome: assessment of metabolic correction.
Whitley CB; Ramsay NK; Kersey JH; Krivit W
Birth Defects Orig Artic Ser; 1986; 22(1):7-24. PubMed ID: 3083887
[No Abstract] [Full Text] [Related]
18. 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]
19. Use of 4-trifluoromethylumbelliferyl-alpha-L-iduronide as a new substrate for detection of alpha-L-iduronidase deficiency in human tissues and for rapid prenatal diagnosis of Hurler disease.
Tsvetkova IV; Karpova EA; Voznyi YV; Zolotukhina TV; Biryukov VV; Semyachkina AN
J Inherit Metab Dis; 1991; 14(2):134-9. PubMed ID: 1909400
[TBL] [Abstract][Full Text] [Related]
20. Detection of mucopolysaccharidosis type I heterozygotes on the basis of the biochemical properties of plasma alpha-L-iduronidase.
Mandelli J; Wajner A; Pires R; Giugliani R; Coelho JC
Clin Chim Acta; 2001 Oct; 312(1-2):81-6. PubMed ID: 11580912
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]