BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

221 related articles for article (PubMed ID: 6596909)

  • 41. Antenatal diagnosis of steroid sulphatase deficiency: case report and literature survey.
    Sherwood RA; Rocks BF
    J Clin Pathol; 1982 Nov; 35(11):1236-9. PubMed ID: 6958681
    [TBL] [Abstract][Full Text] [Related]  

  • 42. X chromosome deletions detectable by flow cytometry in some patients with steroid sulphatase deficiency (X-linked ichthyosis).
    Cooke A; Gillard EF; Yates JR; Mitchell MJ; Aitken DA; Weir DM; Affara NA; Ferguson-Smith MA
    Hum Genet; 1988 May; 79(1):49-52. PubMed ID: 3163320
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Deletions of the steroid sulphatase gene in "classical" X-linked ichthyosis and in X-linked ichthyosis associated with Kallmann syndrome.
    Ballabio A; Sebastio G; Carrozzo R; Parenti G; Piccirillo A; Persico MG; Andria G
    Hum Genet; 1987 Dec; 77(4):338-41. PubMed ID: 3480263
    [TBL] [Abstract][Full Text] [Related]  

  • 44. [Ichthyosis X. Clinical review and rapid identification using lipid electrophoresis].
    Febrer MI; Clemente J; Aliaga A; Tuset C; Tuset MT
    Med Cutan Ibero Lat Am; 1985; 13(6):465-70. PubMed ID: 3914597
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Sex specific difference in placental steroid sulphatase activity.
    Lykkesfeldt G; Bock JE; Lykkesfeldt AE
    Lancet; 1981 Aug; 2(8240):255-6. PubMed ID: 6114308
    [No Abstract]   [Full Text] [Related]  

  • 46. Antenatal detection of placental steroid sulphatase deficiency by measurement of urinary 16 alpha-hydroxydehydroepiandrosterone sulphate.
    Wilmot RL; Mawson RJ; Oakey RE
    Ann Clin Biochem; 1988 Mar; 25 ( Pt 2)():155-61. PubMed ID: 2968067
    [TBL] [Abstract][Full Text] [Related]  

  • 47. Lactation in placental steroid sulphatase deficiency.
    Martin RH; Oakey BE
    Br J Obstet Gynaecol; 1985 Oct; 92(10):1073-4. PubMed ID: 3863670
    [No Abstract]   [Full Text] [Related]  

  • 48. [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]  

  • 49. X-linked ichthyosis, due to steroid sulphatase deficiency, associated with Kallmann syndrome (hypogonadotropic hypogonadism and anosmia): linkage relationships with Xg and cloned DNA sequences from the distal short arm of the X chromosome.
    Ballabio A; Parenti G; Tippett P; Mondello C; Di Maio S; Tenore A; Andria G
    Hum Genet; 1986 Mar; 72(3):237-40. PubMed ID: 3007328
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Cholesterol sulphate in the microsomal sulphatase deficient placenta.
    Marinkovic-Ilsen A; Williams ML
    J Inherit Metab Dis; 1984; 7(2):72-6. PubMed ID: 6434831
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Heterozygote detection in steroid sulphatase deficiency.
    Müller CR; Migl B; Ropers HH; Happle R
    Lancet; 1980 Mar; 1(8167):546-7. PubMed ID: 6102271
    [No Abstract]   [Full Text] [Related]  

  • 52. [Case of placental sulfatase deficiency--its relation to x-linked ichthyosis].
    Fukushima Y; Horiguchi M; Ishihara C; Yanaihara T; Hirato K
    Acta Obstet Gynaecol Jpn; 1981 Mar; 33(3):420-3. PubMed ID: 7211229
    [No Abstract]   [Full Text] [Related]  

  • 53. Antenatal detection of placental steroid sulphatase deficiency: use of a dehydroepiandrosterone sulphate loading test.
    Oakey RE
    Br J Obstet Gynaecol; 1984 Apr; 91(4):337-41. PubMed ID: 6231946
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Steroid sulfatase deficiency and the genetics of the short arm of the human X chromosome.
    Shapiro LJ
    Adv Hum Genet; 1985; 14():331-81, 388-9. PubMed ID: 2859745
    [No Abstract]   [Full Text] [Related]  

  • 55. Hair root analysis in X-linked ichthyosis.
    Dancis J; Jansen V; Hutzler J
    J Inherit Metab Dis; 1983; 6(4):173-7. PubMed ID: 6422158
    [TBL] [Abstract][Full Text] [Related]  

  • 56. [Endocrinological and histochemical studies of placental sulfatase deficiency].
    Kawano K; Miyakawa I; Tanaka T; Fujisaki S; Mori N; Ono T; Aikawa E
    Nihon Sanka Fujinka Gakkai Zasshi; 1985 Mar; 37(3):370-6. PubMed ID: 3981046
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Isolation and characterization of a steroid sulfatase cDNA clone: genomic deletions in patients with X-chromosome-linked ichthyosis.
    Ballabio A; Parenti G; Carrozzo R; Sebastio G; Andria G; Buckle V; Fraser N; Craig I; Rocchi M; Romeo G
    Proc Natl Acad Sci U S A; 1987 Jul; 84(13):4519-23. PubMed ID: 3474618
    [TBL] [Abstract][Full Text] [Related]  

  • 58. Absence of testicular steroid sulphatase activity in a boy with recessive X-linked ichthyosis and testicular maldescent.
    Lykkesfeldt G; Müller J; Skakkebaek NE; Bruun E; Lykkesfeldt AE
    Eur J Pediatr; 1985 Sep; 144(3):273-4. PubMed ID: 2865141
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Studies of the biochemical basis of steroid sulphatase deficiency.--II. A finding of decreased phospholipid content in sulphatase deficient placental microsomes.
    McKee JW; Abeysekera R; France JT
    J Steroid Biochem; 1981 Feb; 14(2):195-8. PubMed ID: 6451770
    [No Abstract]   [Full Text] [Related]  

  • 60. Detection of heterozygotes of X-linked ichthyosis by measuring steroid sulphatase activity of lymphocytes. Mode of inheritance in three families.
    Okano M; Kitano Y; Nakamura T; Matsuzawa Y
    Br J Dermatol; 1985 Dec; 113(6):645-9. PubMed ID: 3868422
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 12.