These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

111 related articles for article (PubMed ID: 49545)

  • 1. 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]  

  • 2. 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]  

  • 3. 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]  

  • 4. 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]  

  • 5. 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]  

  • 6. 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]  

  • 7. 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]  

  • 8. 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]  

  • 9. 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]  

  • 10. Mucopolysaccharide storage disorders.
    Wappner RS
    J Indiana State Med Assoc; 1981 Feb; 74(2):81-4. PubMed ID: 6782167
    [No Abstract]   [Full Text] [Related]  

  • 11. 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]  

  • 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. [Possible genetic nature of phenotypical differences of mucopolysaccharidosis 1].
    Kobrinskiĭ BA
    Vopr Med Khim; 1982; 28(3):55-7. PubMed ID: 6808766
    [No Abstract]   [Full Text] [Related]  

  • 14. A new phenotypic variant of alpha-L-iduronidase deficiency.
    Kohn G; Bach G; Lasch E; Massri ME; Legum C; Cohen MM
    Monogr Hum Genet; 1978; 10():7-10. PubMed ID: 723907
    [No Abstract]   [Full Text] [Related]  

  • 15. 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]  

  • 16. 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]  

  • 17. 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]  

  • 18. 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]  

  • 19. 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]  

  • 20. 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]  

    [Next]    [New Search]
    of 6.