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Journal Abstract Search

132 related items for PubMed ID: 136068

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  • 2. 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 04; 122(2):103-5. PubMed ID: 817912
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  • 6. 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 01; 92(2):257-65. PubMed ID: 114339
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  • 7. alpha-L-Iduronidase activity in established lymphoblastoid cells from patients with Hurler and Scheie syndromes transformed by Epstein-Barr virus.
    Minami R, Suzuki M, Kudoh T, Sato S, Oyanagi K.
    Tohoku J Exp Med; 1977 Aug 01; 122(4):393-6. PubMed ID: 199964
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  • 8. Leucocyte values of alpha-L-iduronidase activity in mucopolysaccharidosis I.
    Kelly TE, Taylor HA.
    J Med Genet; 1976 Apr 01; 13(2):149-51. PubMed ID: 819651
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  • 9. Clinical features of Mexican patients with Mucopolysaccharidosis type I.
    Alonzo-Rojo A, García-Ortiz JE, Ortiz-Aranda M, Gallegos-Arreola MP, Figuera-Villanueva LE.
    Genet Mol Res; 2017 Sep 21; 16(3):. PubMed ID: 28973713
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  • 10. Molecular genetic defect underlying alpha-L-iduronidase pseudodeficiency.
    Aronovich EL, Pan D, Whitley CB.
    Am J Hum Genet; 1996 Jan 21; 58(1):75-85. PubMed ID: 8554071
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  • 14. Prenatal exclusion of Hurler's disease by leucocyte alpha-L-iduronidase assay.
    Rodeck CH, Tansley LR, Benson PF, Fensom AH, Ellis M.
    Prenat Diagn; 1983 Jan 21; 3(1):61-3. PubMed ID: 6405375
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  • 15. Reversal of clinical features of Hurler's disease and biochemical improvement after treatment by bone-marrow transplantation.
    Hobbs JR, Hugh-Jones K, Barrett AJ, Byrom N, Chambers D, Henry K, James DC, Lucas CF, Rogers TR, Benson PF, Tansley LR, Patrick AD, Mossman J, Young EP.
    Lancet; 1981 Oct 03; 2(8249):709-12. PubMed ID: 6116856
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  • 16. Prenatal diagnosis of mucopolysaccharidosis I: A special difficulty arising from an unusually low enzyme activity in mother's cells.
    Gatti R, Borrone C, Filocamo M, Pannone N, Di Natale P.
    Prenat Diagn; 1985 Oct 03; 5(2):149-54. PubMed ID: 3921950
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  • 17. 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 01; 69(2):305-10. PubMed ID: 819189
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