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Journal Abstract Search

199 related items for PubMed ID: 6123259

  • 1. Placental steroid deficiency: association with arylsulfatase A deficiency.
    Vidgoff J, Buxman MM, Shapiro LJ, Dimond RL, Wilson TG, Hepburn CA, Tabei T, Heinrichs WR.
    Am J Hum Genet; 1982 May; 34(3):434-43. PubMed ID: 6123259
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  • 2. X-linked ichthyosis and X-linked placental sulfatase deficiency: a disease entity. Histochemical observations.
    Jöbsis AC, De Groot WP, Tigges AJ, De Bruijn HW, Rijken Y, Meijer AE, Marinkovic-Ilsen A.
    Am J Pathol; 1980 May; 99(2):279-89. PubMed ID: 6929654
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  • 3. [Microsomal sulfatase deficiency in X chromosome-linked ichthyosis].
    Meyer JC, Schnyder UW.
    Hautarzt; 1982 Feb; 33(2):82-8. PubMed ID: 6951821
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  • 8. Recognising placental steroid sulphatase deficiency.
    Harkness RA, Taylor NF, Crawfurd MA, Rose FA.
    Br Med J (Clin Res Ed); 1983 Jul 02; 287(6384):2-3. PubMed ID: 6407677
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  • 12. Foetal steroid sulphatase deficiency. A case report.
    Follett GF, Finn OA, Stewart K.
    Scott Med J; 1984 Jul 02; 29(3):193-5. PubMed ID: 6598228
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  • 13. [Steroid sulfatase and placental deficiency. Current data as instigators of new research].
    Bedin M, Pointis G.
    Ann Endocrinol (Paris); 1987 Jul 02; 48(4):323-33. PubMed ID: 3477995
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  • 14. X-linked recessive ichthyosis. Enzymatic diagnosis of affected males and female carriers.
    Piraud M, Maire I, Zabot MT.
    Enzyme; 1989 Jul 02; 41(4):227-34. PubMed ID: 2743959
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  • 15. Very low arylsulfatase A and cerebroside sulfatase activities in leukocytes of healthy members of metachromatic leukodystrophy family.
    Dubois G, Harzer K, Baumann N.
    Am J Hum Genet; 1977 Mar 02; 29(2):191-4. PubMed ID: 15452
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  • 16. Placental steroid sulfatase deficiency.
    Marinkovic-Ilsen A, deGroot WP, Treffers PE.
    Obstet Gynecol; 1985 Nov 02; 66(5):747-8. PubMed ID: 3864079
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  • 17. X-linked recessive ichthyosis. Reinvestigation of a family first described in 1928.
    Schlammadinger J, Meyer JC, Vajda I, Szabó G.
    Dermatologica; 1987 Nov 02; 175(5):217-23. PubMed ID: 3479355
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  • 18. Impaired cerebroside sulfate hydrolysis in fibroblasts of sibs with "pseudo" arylsulfatase A deficiency without metachromatic leukodystrophy.
    Hreidarsson SJ, Thomas GH, Kihara H, Fluharty AL, Kolodny EH, Moser HW, Reynolds LW.
    Pediatr Res; 1983 Sep 02; 17(9):701-4. PubMed ID: 6137805
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  • 19. Genetic heterogeneity of steroid sulfatase deficiency revealed with cDNA for human steroid sulfatase.
    Conary JT, Lorkowski G, Schmidt B, Pohlmann R, Nagel G, Meyer HE, Krentler C, Cully J, Hasilik A, von Figura K.
    Biochem Biophys Res Commun; 1987 Apr 29; 144(2):1010-7. PubMed ID: 3034252
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