250 related articles for article (PubMed ID: 4260316)
1. Hurler's syndrome, an -L-iduronidase deficiency.
Matalon R; Dorfman A
Biochem Biophys Res Commun; 1972 May; 47(4):959-64. PubMed ID: 4260316
[No Abstract] [Full Text] [Related]
2. 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]
3. Alpha-L-iduronidase activity in cultured skin fibroblasts and amniotic fluid cells.
Hall CW; Neufeld EF
Arch Biochem Biophys; 1973 Oct; 158(2):817-21. PubMed ID: 4205743
[No Abstract] [Full Text] [Related]
4. Enzyme measurements of hair follicles in the study of some inborn erros of metabolism, with particular reference to Hurler's disease.
Gibbs DA
Ann Clin Biochem; 1977 May; 14(3):157-60. PubMed ID: 405918
[No Abstract] [Full Text] [Related]
5. Arylsulfatase B deficiency in Maroteaux-Lamy syndrome cultured fibroblasts.
Fluharty AL; Stevens RL; Sanders DL; Kihara H
Biochem Biophys Res Commun; 1974 Jul; 59(2):455-61. PubMed ID: 4277366
[No Abstract] [Full Text] [Related]
6. Acid hydrolases in the serum and liver in mucopolysaccharidoses types I and 3.
Gordon BA; Feleki V
Clin Biochem; 1970 Sep; 3(3):193-202. PubMed ID: 4258597
[No Abstract] [Full Text] [Related]
7. Lysosomal enzymes in cultured cells from mucopolysaccharidoses.
Keyser AJ; Priest RE; Priest JH
Lab Invest; 1972 Dec; 27(6):600-5. PubMed ID: 4264608
[No Abstract] [Full Text] [Related]
8. A recognition marker required for uptake of a lysosomal enzyme by cultured fibroblasts.
Hickman S; Shapiro LJ; Neufeld EF
Biochem Biophys Res Commun; 1974 Mar; 57(1):55-61. PubMed ID: 4364008
[No Abstract] [Full Text] [Related]
9. Deficiency of lysosomal enzymes in storage diseases.
Den Tandt WR; Giesberts MA
Biochem Med; 1973 Jun; 7(3):441-51. PubMed ID: 4268487
[No Abstract] [Full Text] [Related]
10. Beta-galactosidases in fibroblasts: Hurler and Sanfilippo syndromes.
Benson PF; Bowser-Riley F; Giannelli F
N Engl J Med; 1970 Oct; 283(18):999-1000. PubMed ID: 4248669
[No Abstract] [Full Text] [Related]
11. Enzyme patterns in tissues and body fluids in mucopolysaccharidoses.
Ockerman PA; Hultberg B; Eriksson O
Clin Chim Acta; 1969 Jul; 25(1):97-102. PubMed ID: 4240390
[No Abstract] [Full Text] [Related]
12. Leroy's l-cell disease: markedly increased activity of plasma acid hydrolases.
Den Tandt WR; Lassila E; Philippart M
J Lab Clin Med; 1974 Mar; 83(3):403-8. PubMed ID: 4359899
[No Abstract] [Full Text] [Related]
13. Acid glycosidases in mucopolysaccharidoses fibroblasts.
Fluharty AL; Porter MT; Lassila EL; Trammell J; Carrel RE; Kihara H
Biochem Med; 1970 Sep; 4(2):110-20. PubMed ID: 4257448
[No Abstract] [Full Text] [Related]
14. Sanfilippo syndrome: profound deficiency of alpha-acetylglucosaminidase activity in organs and skin fibroblasts from type-B patients.
O'Brien JS
Proc Natl Acad Sci U S A; 1972 Jul; 69(7):1720-2. PubMed ID: 4261742
[TBL] [Abstract][Full Text] [Related]
15. The biochemistry of Hurler's syndrome.
Harmel RP
Enzymol Biol Clin (Basel); 1969; 10(6):534-48. PubMed ID: 4243200
[No Abstract] [Full Text] [Related]
16. Comparison of the substrate 4-methylumbelliferyl-alpha-l-iduronide with phenyl-alpha-L-iduronide for the diagnosis of Hurler's disease in cultured cells.
Butterworth J; Broadhead DM
J Inherit Metab Dis; 1980; 2(3):71-4. PubMed ID: 6796763
[TBL] [Abstract][Full Text] [Related]
17. Lysosomes and mucopolysaccharidoses.
Hers HG; van Hoof F
Biochem J; 1969 Dec; 115(5):34P-36P. PubMed ID: 4243352
[No Abstract] [Full Text] [Related]
18. Mucopolysaccharidosis.
Levin B; Jacoby NM
Proc R Soc Med; 1972 Apr; 65(4):339-41. PubMed ID: 4260161
[No Abstract] [Full Text] [Related]
19. 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]
20. -Galactosidase, N-acetyl- -glucosaminidase, and -glucuronidase activity in fibroblast cultures from patients with mucopolysaccharide storage disease.
Lagunoff D; Pritzl P; Scott CR
Biochem Med; 1973 Jun; 7(3):343-9. PubMed ID: 4268484
[No Abstract] [Full Text] [Related]
[Next] [New Search]
