121 related articles for article (PubMed ID: 113163)
1. Post- and pre-natal assessment of alpha-L-iduronidase deficiency with a radiolabelled natural substrate.
Hopwood JJ; Muller V; Pollard AC
Clin Sci (Lond); 1979 Jan; 56(6):591-9. PubMed ID: 113163
[No Abstract] [Full Text] [Related]
2. Letter: Phenotypic variation in alpha-L-iduronidase deficiency.
Leisti J; Rimoin DL; Kaback MM; Hollister DW; DEn Tandt W; Neufeld E; Matalon R; Philippart M
Lancet; 1975 Jun; 1(7920):1344. PubMed ID: 49545
[No Abstract] [Full Text] [Related]
3. Proceedings: Alpha-L-iduronidase deficiency associated with chondroitin sulphate mucopolysaccharidosis.
Babarik A; Benson PF; Dean MF; Muir H
Arch Dis Child; 1975 Apr; 50(4):329-30. PubMed ID: 807169
[No Abstract] [Full Text] [Related]
4. Absence of alpha-L-iduronidase activity in various tissues from two sibs affected with presumably the Hurler-Scheie compound syndrome.
Thompson JN; Finley SC; Lorincz AE; Finley WH
Birth Defects Orig Artic Ser; 1975; 11(6):341-6. PubMed ID: 811284
[No Abstract] [Full Text] [Related]
5. Variation in neuronal storage in alpha-L-iduronidase deficiency.
Wassman ER
Am J Med Genet; 1985 Dec; 22(4):827-9. PubMed ID: 3934972
[No Abstract] [Full Text] [Related]
6. 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]
7. alpha-L-Iduronidase deficiency in mucopolysaccharidosis type I against a radiolabelled sulfated disaccharide substrate derived from dermatan sulfate.
Muller VJ; Hopwood JJ
Clin Genet; 1984 Nov; 26(5):414-21. PubMed ID: 6437709
[TBL] [Abstract][Full Text] [Related]
8. A method for alpha-L-iduronidase assay.
Singh J; Niebes P; Di Ferrante N
FEBS Lett; 1974 Sep; 45(1):248-51. PubMed ID: 4212889
[No Abstract] [Full Text] [Related]
9. Genetic complementation analysis in somatic cell hybrids of alpha-L-iduronidase deficient cells.
Wehnert M; Machill G; Petruschka L
Hum Genet; 1985; 69(3):287. PubMed ID: 3920140
[No Abstract] [Full Text] [Related]
10. Diagnosis of the mucopolysaccharidoses using cultured skin fibroblasts and amniotic fluid cells.
Butterworth J
J Inherit Metab Dis; 1978; 1(1):25-8. PubMed ID: 117232
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. Heparan sulfate and dermatan sulfate from the liver of a patient with Hurler syndrome: high performance liquid chromatography of their degradation products after incubation with alpha-L-iduronidase-deficient fibroblasts.
Minami R; Fujibayashi S; Igarashi C; Ishikawa Y; Wagatsuma K; Nakao T; Tsugawa S
Clin Chim Acta; 1984 Feb; 137(2):179-87. PubMed ID: 6231139
[TBL] [Abstract][Full Text] [Related]
13. Microtest for determination of alpha-L-iduronidase in plasma and leucocytes and its potential for diagnosing alpha-L-iduronidase deficiency.
Den Tandt WR; Scharpe S; Giesberts M; Poorthuis BJ
Lancet; 1984 Apr; 1(8380):794. PubMed ID: 6143109
[No 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. 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]
16. Variant of iduronidase deficient mucopolysaccharidoses: further evidence for genetic heterogeneity.
Danes BS
J Med Genet; 1977 Oct; 14(5):346-51. PubMed ID: 412969
[TBL] [Abstract][Full Text] [Related]
17. Alpha-L-iduronidase deficiency in a cat: a model of mucopolysaccharidosis I.
Haskins ME; Jezyk PF; Desnick RJ; McDonough SK; Patterson DF
Pediatr Res; 1979 Nov; 13(11):1294-7. PubMed ID: 117422
[No Abstract] [Full Text] [Related]
18. Canine alpha-L-iduronidase deficiency. A model of mucopolysaccharidosis I.
Shull RM; Munger RJ; Spellacy E; Hall CW; Constantopoulos G; Neufeld EF
Am J Pathol; 1982 Nov; 109(2):244-8. PubMed ID: 6215865
[No Abstract] [Full Text] [Related]
19. 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]
20. The clinical spectrum of alpha-L-iduronidase deficiency.
Roubicek M; Gehler J; Spranger J
Am J Med Genet; 1985 Mar; 20(3):471-81. PubMed ID: 3922223
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
