254 related articles for article (PubMed ID: 3457782)
1. [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]
2. [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]
3. [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]
4. [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]
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. Lipoprotein electrophoresis in recessive X-linked ichthyosis.
Ibsen HH; Brandrup F; Blaabjerg O; Lykkesfeldt G
Acta Derm Venereol; 1986; 66(1):59-62. PubMed ID: 2424217
[TBL] [Abstract][Full Text] [Related]
7. Rapid laboratory diagnostic of X-linked ichthyosis.
Meyer JC; Groh V; Giger V; Weiss H; Varbelow H; Schnyder UW
Dermatologica; 1982 Apr; 164(4):249-57. PubMed ID: 6953038
[TBL] [Abstract][Full Text] [Related]
8. [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]
9. [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]
10. A new syndrome of anosmia, ichthyosis, hypogonadism, and various neurological manifestations with deficiency of steroid sulfatase and arylsulfatase C.
Sunohara N; Sakuragawa N; Satoyoshi E; Tanae A; Shapiro LJ
Ann Neurol; 1986 Feb; 19(2):174-81. PubMed ID: 3516063
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. Carrier identification in steroid sulphatase deficiency and recessive X-linked ichthyosis.
Lykkesfeldt G; Lykkesfeldt AE
Acta Derm Venereol; 1986; 66(2):134-8. PubMed ID: 2424236
[TBL] [Abstract][Full Text] [Related]
13. Sulfatase activity of keratinizing tissues in X-linked ichthyosis.
Baden HP; Hooker PA; Kubilus J; Tarascio A
Pediatr Res; 1980 Dec; 14(12):1347-8. PubMed ID: 7208152
[TBL] [Abstract][Full Text] [Related]
14. Look at the genes, see what's in the jeans.
Goldsmith LA
Arch Dermatol; 1990 May; 126(5):585-6. PubMed ID: 2334178
[No Abstract] [Full Text] [Related]
15. Deletion of the distal short arm of the X chromosome (Xp) in a patient with short stature, chondrodysplasia punctata, and X-linked ichthyosis due to steroid sulfatase deficiency.
Ballabio A; Zollo M; Carrozzo R; Caiulo A; Zuffardi O; Cascioli CF; Viggiano D; Strisciuglio P
Am J Med Genet; 1991 Nov; 41(2):184-7. PubMed ID: 1785631
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. Steroid sulphatase deficiency in patients initially diagnosed as ichthyosis vulgaris or recessive X-linked ichthyosis.
Yoshiike T; Matsui T; Ogawa H
Br J Dermatol; 1985 Apr; 112(4):431-3. PubMed ID: 3857937
[TBL] [Abstract][Full Text] [Related]
18. PCR diagnosis of X-linked ichthyosis: identification of a novel mutation (E560P) of the steroid sulfatase gene.
Sugawara T; Shimizu H; Hoshi N; Fujimoto Y; Nakajima A; Fujimoto S
Hum Mutat; 2000 Mar; 15(3):296. PubMed ID: 10679952
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. Familial X-linked ichthyosis, steroid sulfatase deficiency, mental retardation, and nullisomy for Xp223-pter.
Ross JB; Allderdice PW; Shapiro LJ; Aveling J; Eales BA; Simms D
Arch Dermatol; 1985 Dec; 121(12):1524-8. PubMed ID: 3864397
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
