203 related articles for article (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
[TBL] [Abstract][Full Text] [Related]
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
[TBL] [Abstract][Full Text] [Related]
3. [Microsomal sulfatase deficiency in X chromosome-linked ichthyosis].
Meyer JC; Schnyder UW
Hautarzt; 1982 Feb; 33(2):82-8. PubMed ID: 6951821
[TBL] [Abstract][Full Text] [Related]
4. Placental sulfatase deficiency: maternal and fetal expression of steroid sulfatase deficiency and X-linked ichthyosis.
Bradshaw KD; Carr BR
Obstet Gynecol Surv; 1986 Jul; 41(7):401-13. PubMed ID: 3531932
[TBL] [Abstract][Full Text] [Related]
5. Steroid sulfatase deficiency: enzymatic studies using placenta and leucocytes in one family.
Sakai S; Honda H; Kawai N; Sakuragawa N; Arimoto K
Asia Oceania J Obstet Gynaecol; 1986 Dec; 12(4):555-61. PubMed ID: 3469950
[No Abstract] [Full Text] [Related]
6. Placental steroid sulphatase deficiency.
Attenburrow AA; Heslip M; Henderson MJ; Holton JB; Scott IV; Arthur LJ
Arch Dis Child; 1984 Dec; 59(12):1187-9. PubMed ID: 6596909
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. Recognising placental steroid sulphatase deficiency.
Harkness RA; Taylor NF; Crawfurd MA; Rose FA
Br Med J (Clin Res Ed); 1983 Jul; 287(6384):2-3. PubMed ID: 6407677
[No Abstract] [Full Text] [Related]
9. [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]
10. Steroid sulfatase deficiency and X-linked ichthyosis.
Shapiro LJ
Clin Biochem; 1979 Dec; 12(6):205. PubMed ID: 294955
[No Abstract] [Full Text] [Related]
11. Current clinical problems in placental steroid or aryl sulphatase C deficiency and the related 'cervical dystocia' and X-linked ichthyosis.
Harkness RA
J Inherit Metab Dis; 1982; 5(3):142-4. PubMed ID: 6820435
[No Abstract] [Full Text] [Related]
12. Foetal steroid sulphatase deficiency. A case report.
Follett GF; Finn OA; Stewart K
Scott Med J; 1984 Jul; 29(3):193-5. PubMed ID: 6598228
[TBL] [Abstract][Full Text] [Related]
13. [Steroid sulfatase and placental deficiency. Current data as instigators of new research].
Bedin M; Pointis G
Ann Endocrinol (Paris); 1987; 48(4):323-33. PubMed ID: 3477995
[TBL] [Abstract][Full Text] [Related]
14. 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]
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; 29(2):191-4. PubMed ID: 15452
[TBL] [Abstract][Full Text] [Related]
16. Placental steroid sulfatase deficiency.
Marinkovic-Ilsen A; deGroot WP; Treffers PE
Obstet Gynecol; 1985 Nov; 66(5):747-8. PubMed ID: 3864079
[No Abstract] [Full Text] [Related]
17. 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]
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; 17(9):701-4. PubMed ID: 6137805
[TBL] [Abstract][Full Text] [Related]
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; 144(2):1010-7. PubMed ID: 3034252
[TBL] [Abstract][Full Text] [Related]
20. Clinical spectrum of steroid sulfatase deficiency: X-linked recessive ichthyosis, birth complications and cryptorchidism.
Traupe H; Happle R
Eur J Pediatr; 1983 Mar; 140(1):19-21. PubMed ID: 6135610
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
