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 *

101 related articles for article (PubMed ID: 4212078)

  • 1. In vitro restoration of deficient beta-galactosidase activity in liver of patients with Hurler and Hunter disease.
    Kint JA
    Nature; 1974 Aug; 250(465):424-5. PubMed ID: 4212078
    [No Abstract]   [Full Text] [Related]  

  • 2. Hunter's syndrome: beta-galactosidase deficiency in skin.
    Gerich JE
    N Engl J Med; 1969 Apr; 280(15):799-802. PubMed ID: 4975290
    [No Abstract]   [Full Text] [Related]  

  • 3. The effect of glycosaminoglycans on the in vitro activity of human skin fibroblast glycosphingolipid beta-galactosidases and neuraminidases.
    Rushton AR; Dawson G
    Clin Chim Acta; 1977 Oct; 80(1):133-9. PubMed ID: 409573
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Mucopolysaccharidosis II (Hunter's syndrome).
    Arch Dermatol; 1970 Nov; 102(5):578-80. PubMed ID: 4248769
    [No Abstract]   [Full Text] [Related]  

  • 5. 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]  

  • 6. An altered hexosaminidase A in the liver affected by Hurler and Hunter syndromes.
    Minami R; Nakamura F; Kudoh T; Oyanagi K; Nakao T
    Tohoku J Exp Med; 1980 Nov; 132(3):329-35. PubMed ID: 6451055
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Beta-galactosidase deficiency in the hurler syndrome.
    MacBrinn M; Okada S; Woollacott M; Patel V; Ho MW; Tappel AL; O'Brien JS
    N Engl J Med; 1969 Aug; 281(7):338-43. PubMed ID: 4240150
    [No Abstract]   [Full Text] [Related]  

  • 8. 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; 122(2):103-5. PubMed ID: 817912
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Glycosidases in skin and plasma in Hunter's syndrome. Abnormality of a beta-galactosidase in skin.
    Ockerman PA; Köhlin P
    Acta Paediatr Scand; 1968 Jul; 57(4):281-4. PubMed ID: 4236601
    [No Abstract]   [Full Text] [Related]  

  • 10. The defect in the Hunter syndrome: deficiency of sulfoiduronate sulfatase.
    Bach G; Eisenberg F; Cantz M; Neufeld EF
    Proc Natl Acad Sci U S A; 1973 Jul; 70(7):2134-8. PubMed ID: 4269173
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Deficiency of 4-methyl umbelliferyl-beta-galactosidase activity in the liver of seven patients with Hurler's disease.
    van Gemund JJ; Giesberts MA; Gorsira MC; Willighagen RG
    Maandschr Kindergeneeskd; 1969 Apr; 36(12):377-83. PubMed ID: 4976672
    [No Abstract]   [Full Text] [Related]  

  • 12. An assay for iduronate sulfatase (Hunter corrective factor).
    Lim TW; Leder IG; Bach G; Neufeld EF
    Carbohydr Res; 1974 Oct; 37(1):103-9. PubMed ID: 4214613
    [No Abstract]   [Full Text] [Related]  

  • 13. Mucolipidosis II (I-cell disease). A clinical and biochemical study.
    Wiesmann UN; Vassella F; Herschkowitz NN
    Acta Paediatr Scand; 1974 Jan; 63(1):9-16. PubMed ID: 4275378
    [No Abstract]   [Full Text] [Related]  

  • 14. [Mucopolysaccharidosis type II (Hurler-Hunter) in siblings. Electron microscopic study].
    Tichý J; Cihula J; Vortel V
    Sb Ved Pr Lek Fak Karlovy Univerzity Hradci Kralove; 1972; 15(2):173-9. PubMed ID: 4209410
    [No Abstract]   [Full Text] [Related]  

  • 15. The Hurler and Hunter syndromes.
    Dorfman A; Matalon R
    Am J Med; 1969 Nov; 47(5):691-707. PubMed ID: 4243120
    [No Abstract]   [Full Text] [Related]  

  • 16. The defect in Hurler and Hunter syndromes. II. Deficiency of specific factors involved in mucopolysaccharide degradation.
    Fratantoni JC; Hall CW; Neufeld EF
    Proc Natl Acad Sci U S A; 1969 Sep; 64(1):360-6. PubMed ID: 4244031
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. The relative frequency of the Hurler and Hunter syndromes.
    McKusick VA
    N Engl J Med; 1970 Oct; 283(16):853-4. PubMed ID: 4989786
    [No Abstract]   [Full Text] [Related]  

  • 19. Relative frequency of the Hurler and Hunter syndromes.
    N Engl J Med; 1970 Dec; 283(26):1466-8. PubMed ID: 4991513
    [No Abstract]   [Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 6.