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Journal Abstract Search

280 related items for PubMed ID: 2743959

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  • 2. [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
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  • 6. [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
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  • 9. 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
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  • 10. 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
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  • 11. 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
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  • 14. Various sulfatase activities in leukocytes and cultured skin fibroblasts from heterozygotes for the multiple sulfatase deficiency (mukosulfatidosis).
    Eto Y, Tahara T, Tokoro T, Maekawa K.
    Pediatr Res; 1983 Feb; 17(2):97-100. PubMed ID: 6572356
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  • 15. A fluorimetric assay of steroid sulphatase in leukocytes: evidence for two genetically different enzymes with arylsulphatase C activity.
    van Diggelen OP, Konstantinidou AE, Bousema MT, Boer M, Bakx T, Jöbsis AC.
    J Inherit Metab Dis; 1989 Feb; 12(3):273-80. PubMed ID: 2533306
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  • 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 Feb; 278(6):491-3. PubMed ID: 3466578
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  • 17. Arylsulfatase C activities in skin preparations of X-linked and autosomal dominant ichthyosis.
    Meyer JC, Grundmann HP.
    Arch Dermatol Res; 1980 Feb; 269(2):213-5. PubMed ID: 6935987
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  • 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
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  • 19. Lipoprotein electrophoresis in recessive X-linked ichthyosis.
    Ibsen HH, Brandrup F, Blaabjerg O, Lykkesfeldt G.
    Acta Derm Venereol; 1986 Mar; 66(1):59-62. PubMed ID: 2424217
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  • 20. [Biochemical diagnostic procedures in X-linked ichthyosis].
    Yoshiike, Takashi, Ogawa, Hideoki.
    Nihon Hifuka Gakkai Zasshi; 1985 Jan; 95(1):7-10. PubMed ID: 3858564
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