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2. 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]
3. 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]
4. Letter: Chondroitinsulphaturia with alpha-L-iduronidase deficiency. Babarik A; Benson PF; Dean MF; Muir H Lancet; 1974 Aug; 2(7878):464-5. PubMed ID: 4136880 [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. 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]
7. 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]
8. 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]
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. 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]
11. 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]
12. 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]
13. Neurochemical characterization of canine alpha-L-iduronidase deficiency disease (model of human mucopolysaccharidosis I). Constantopoulos G; Shull RM; Hastings N; Neufeld EF J Neurochem; 1985 Oct; 45(4):1213-7. PubMed ID: 3928817 [TBL] [Abstract][Full Text] [Related]
14. 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]