These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

84 related articles for article (PubMed ID: 2530495)

  • 21. 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]  

  • 22. [Biochemical diagnostic procedures in X-linked ichthyosis].
    Yoshiike ; Takashi ; Ogawa ; Hideoki
    Nihon Hifuka Gakkai Zasshi; 1985 Jan; 95(1):7-10. PubMed ID: 3858564
    [No Abstract]   [Full Text] [Related]  

  • 23. Prenatal diagnosis of X-linked ichthyosis.
    Hähnel R; Hähnel E; Wysocki SJ; Wilkinson SP; Hockey A
    Clin Chim Acta; 1982 Mar; 120(1):143-52. PubMed ID: 6461439
    [TBL] [Abstract][Full Text] [Related]  

  • 24. X-linked ichthyosis without STS deficiency: clinical, genetical, and molecular studies.
    Robledo R; Melis P; Schillinger E; Casciano I; Balazs I; Rinaldi A; Siniscalco M; Filippi G
    Am J Med Genet; 1995 Nov; 59(2):143-8. PubMed ID: 8588575
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Non-inactivation of an x-chromosome locus in man.
    Shapiro LJ; Mohandas T; Weiss R; Romeo G
    Science; 1979 Jun; 204(4398):1224-6. PubMed ID: 156396
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Placental sulfatase deficiency. Biochemical and clinical aspects.
    Nakayama T; Yanaihara T
    Contrib Gynecol Obstet; 1982; 9():145-56. PubMed ID: 6216072
    [No Abstract]   [Full Text] [Related]  

  • 27. X-linked ichthyosis. Five families in southern Kyushu.
    Saita B; Kikuchi I; Hiejima M; Inoue S; Fukuzaki M
    J Dermatol; 1980 Aug; 7(4):273-6. PubMed ID: 6999054
    [No Abstract]   [Full Text] [Related]  

  • 28. [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]  

  • 29. Molecular genetics of the X chromosome and X-linked diseases.
    Craig IW; Goodfellow PN
    Lab Invest; 1986 Mar; 54(3):241-53. PubMed ID: 3512907
    [No Abstract]   [Full Text] [Related]  

  • 30. X-linked recessive ichthyosis in three sisters: evidence for homozygosity.
    Mevorah B; Frenk E; Müller CR; Ropers HH
    Br J Dermatol; 1981 Dec; 105(6):711-7. PubMed ID: 6947821
    [TBL] [Abstract][Full Text] [Related]  

  • 31. [Should we still explore placental sulfatase deficiencies? Reflections apropos of a case report].
    Giovangrandi Y; Magnin G; Sauvanet E; Soutoul JH; Cedard L; Bedin M; Moraine C; Nottin P; Hamard G
    Rev Fr Gynecol Obstet; 1984 Oct; 79(10):653-7. PubMed ID: 6528160
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Association in the same patient of autosomal dominant progressive external ophthalmoplegia with multiple mtDNA deletions and X-linked ichthyosis: clinical, biochemical, histological, submicroscopic and molecular genetic study.
    Federico A; Dotti MT; Cardaioli E; Grieco G; Malandrini A; Manneschi L; Plewnia K; Rufa A; Renieri A; Bruttini M; Perticoni GF
    J Submicrosc Cytol Pathol; 1998 Oct; 30(4):521-6. PubMed ID: 9851061
    [TBL] [Abstract][Full Text] [Related]  

  • 33. 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]  

  • 34. Placental steroid sulfatase deficiency: biochemical diagnosis and clinical review.
    Lykkesfeldt G; Nielsen MD; Lykkesfeldt AE
    Obstet Gynecol; 1984 Jul; 64(1):49-54. PubMed ID: 6234482
    [TBL] [Abstract][Full Text] [Related]  

  • 35. The biochemical identification of carrier state in mothers of sporadic cases of X-linked recessive ichthyosis.
    Cuevas-Covarrubias SA; Kofman-Alfaro S; Orozco Orozco E; Diaz-Zagoya JC
    Genet Couns; 1995; 6(2):103-7. PubMed ID: 7546451
    [TBL] [Abstract][Full Text] [Related]  

  • 36. [Clinical picture of X chromosome recessive ichthyosis].
    Voss M
    Dermatol Monatsschr; 1985; 171(1):25-37. PubMed ID: 4038949
    [No Abstract]   [Full Text] [Related]  

  • 37. Steroid-sulfatase deficiency in sex-linked ichthyosis.
    Kubilus J; Tarascio AJ; Baden HP
    Am J Hum Genet; 1979 Jan; 31(1):50-3. PubMed ID: 155398
    [TBL] [Abstract][Full Text] [Related]  

  • 38. 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]  

  • 39. A family with X-linked ichthyosis and hypogonadism.
    Pike MG; Hammerton M; Edge J; Atherton DJ; Grant DB
    Eur J Pediatr; 1989 Feb; 148(5):442-4. PubMed ID: 2493379
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Recurrent bilateral corneal erosions due to an association of epidermolysis bullosa simplex Köbner and X-linked ichthyosis with steroid sulfatase deficiency.
    Steuhl KP; Anton-Lamprecht I; Arnold ML; Thiel HJ
    Graefes Arch Clin Exp Ophthalmol; 1988; 226(3):216-23. PubMed ID: 3165358
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 5.