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5. X-linked recessive ichthyosis. Enzymatic diagnosis of affected males and female carriers. Piraud M; Maire I; Zabot MT Enzyme; 1989; 41(4):227-34. PubMed ID: 2743959 [TBL] [Abstract][Full Text] [Related]
6. [The enzyme arylsulfatase C and steroid sulfatase as biochemical markers and pathogenetic factors in X-chromosome recessively inherited ichthyosis]. Schlenzka K Dermatol Monatsschr; 1983; 169(10):621-4. PubMed ID: 6580240 [No Abstract] [Full Text] [Related]
7. [Ichthyosis and steroid sulfatase: study of enzymatic activity in leukocytes and fibroblasts according to the sex and type of ichthyosis]. Piraud M; Cambazard F; Barrut D Pediatrie; 1990; 45(2):133-40. PubMed ID: 2158060 [TBL] [Abstract][Full Text] [Related]
8. [Arylsulfatase C deficiency in leukocytes in patients and carrier of X-chromosome recessive ichthyosis]. Hadlich J; Herrmann FH; Grimm U Dermatol Monatsschr; 1986; 172(10):624-6. PubMed ID: 3468016 [No Abstract] [Full Text] [Related]
9. Autosomal dominant and X-linked ichthyosis in the same family. Biochemical analysis of steroid sulfatase activity. Migl B; Mevorah B; Müller CR; Wolff G; Frenk E Clin Genet; 1980 Jul; 18(1):48-50. PubMed ID: 6932268 [No Abstract] [Full Text] [Related]
10. 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 [TBL] [Abstract][Full Text] [Related]
11. Steroid sulfatase = aryl sulfatase C? Chromatographic and electrophoretic properties in extracts from placental microsomes and skin fibroblasts. Meyer JC; Grundmann H; Weiss H Dermatologica; 1984; 169(5):305-10. PubMed ID: 6594286 [TBL] [Abstract][Full Text] [Related]
12. 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 [TBL] [Abstract][Full Text] [Related]
13. [X-chromosomal recessive ichthyosis. Detection of heterozygote status in genetically possible carriers by determination of arylsulfatase C activity]. Hadlich J; Herrmann FH; Grimm U Dermatol Monatsschr; 1986; 172(12):734-6. PubMed ID: 3470217 [No Abstract] [Full Text] [Related]
14. [Biochemical diagnosis of X chromosomal ichthyosis]. Meyer JC; Gilardi S Hautarzt; 1986 Apr; 37(4):205-9. PubMed ID: 3457782 [TBL] [Abstract][Full Text] [Related]
15. X-linked recessive ichthyosis. Reinvestigation of a family first described in 1928. Schlammadinger J; Meyer JC; Vajda I; Szabó G Dermatologica; 1987; 175(5):217-23. PubMed ID: 3479355 [TBL] [Abstract][Full Text] [Related]
16. Intermediate levels of aryl sulfatase C in human leukocytes of female carriers for X-linked recessive ichthyosis. Meyer JC; Gilardi S; Sigg C; Bruckner-Tudermann L Arch Dermatol Res; 1986; 278(6):491-3. PubMed ID: 3466578 [No Abstract] [Full Text] [Related]
17. Steroid sulfatase of human leukocytes and epidermis and the diagnosis of recessive X-linked ichthyosis. Epstein EH; Leventhal ME J Clin Invest; 1981 May; 67(5):1257-62. PubMed ID: 6939689 [TBL] [Abstract][Full Text] [Related]
18. Biochemical characterization of arylsulfatase-C isozymes in human fibroblasts. Simard JP; Ameen M; Chang PL Biochem Biophys Res Commun; 1985 May; 128(3):1388-94. PubMed ID: 3859293 [TBL] [Abstract][Full Text] [Related]
19. Arylsulphatase C activity in leukocytes of patients and carriers of X-linked ichthyosis. Herrmann FH; Grimm U; Hadlich J J Inherit Metab Dis; 1987; 10(1):89-94. PubMed ID: 3106720 [TBL] [Abstract][Full Text] [Related]
20. Steroid sulphatase deficiency. Steroid sulphatase and arylsulphatase C determination in normal and affected fibroblasts. Piraud M; Zabot MT; Maire I J Inherit Metab Dis; 1984; 7 Suppl 2():157-8. PubMed ID: 6434877 [No Abstract] [Full Text] [Related] [Next] [New Search]