BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

167 related articles for article (PubMed ID: 7704955)

  • 21. Nephrotic syndrome with X-linked ichthyosis, Kallmann Syndrome and unilateral renal agenesis.
    Krishnamurthy S; Kapoor S; Yadav S
    Indian Pediatr; 2007 Apr; 44(4):301-3. PubMed ID: 17468528
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Molecular heterogeneity of steroid sulfatase deficiency: a multicenter study on 57 unrelated patients, at DNA and protein levels.
    Ballabio A; Carrozzo R; Parenti G; Gil A; Zollo M; Persico MG; Gillard E; Affara N; Yates J; Ferguson-Smith MA
    Genomics; 1989 Jan; 4(1):36-40. PubMed ID: 2644167
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Somatic and germinal mosaicism for the steroid sulfatase gene deletion in a steroid sulfatase deficiency carrier.
    Cuevas-Covarrubias SA; Jiménez-Vaca AL; González-Huerta LM; Valdes-Flores M; Del Refugio Rivera-Vega M; Maya-Nunez G; Kofman-Alfaro SH
    J Invest Dermatol; 2002 Oct; 119(4):972-5. PubMed ID: 12406347
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Deletion pattern of the steroid sulphatase gene in Japanese patients with X-linked ichthyosis.
    Saeki H; Kuwata S; Nakagawa H; Shimada S; Tamaki K; Ishibashi Y
    Br J Dermatol; 1998 Jul; 139(1):96-8. PubMed ID: 9764155
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Male infant with ichthyosis, Kallmann syndrome, chondrodysplasia punctata, and an Xp chromosome deletion.
    Bick D; Curry CJ; McGill JR; Schorderet DF; Bux RC; Moore CM
    Am J Med Genet; 1989 May; 33(1):100-7. PubMed ID: 2750777
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Analysis of an interstitial deletion in a patient with Kallmann syndrome, X-linked ichthyosis and mental retardation.
    Weissörtel R; Strom TM; Dörr HG; Rauch A; Meitinger T
    Clin Genet; 1998 Jul; 54(1):45-51. PubMed ID: 9727739
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Deletion analysis maps ocular albinism proximal to the steroid sulphatase locus.
    Bouloux PM; Kirk J; Munroe P; Duke V; Meindl A; Hilson A; Grant D; Carter N; Betts D; Meitinger T
    Clin Genet; 1993 Apr; 43(4):169-73. PubMed ID: 8330450
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Xp22.3 interstitial deletion: a recognizable chromosomal abnormality encompassing VCX3A and STS genes in a patient with X-linked ichthyosis and mental retardation.
    Ben Khelifa H; Soyah N; Ben-Abdallah-Bouhjar I; Gritly R; Sanlaville D; Elghezal H; Saad A; Mougou-Zerelli S
    Gene; 2013 Sep; 527(2):578-83. PubMed ID: 23791652
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Clinical evaluation in isolated hypogonadotrophic hypogonadism (Kallmann syndrome).
    Dissaneevate P; Warne GL; Zacharin MR
    J Pediatr Endocrinol Metab; 1998; 11(5):631-8. PubMed ID: 9829214
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Failure to induce puberty in a man with X-linked congenital adrenal hypoplasia and hypogonadotropic hypogonadism by pulsatile administration of low-dose gonadotropin-releasing hormone.
    Kikuchi K; Kaji M; Momoi T; Mikawa H; Shigematsu Y; Sudo M
    Acta Endocrinol (Copenh); 1987 Jan; 114(1):153-60. PubMed ID: 3101337
    [TBL] [Abstract][Full Text] [Related]  

  • 31. X-linked ichthyosis: an update.
    Hernández-Martín A; González-Sarmiento R; De Unamuno P
    Br J Dermatol; 1999 Oct; 141(4):617-27. PubMed ID: 10583107
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Prenatal diagnosis of X-linked ichthyosis using molecular cytogenetics.
    Santolaya-Forgas J; Cohen L; Vengalil S; Field F; Rodriguez A; McCorquadale M; McCorquadale DJ
    Fetal Diagn Ther; 1997; 12(1):36-9. PubMed ID: 9101220
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Steroid sulphatase deficiency is present in patients with the syndrome 'ichthyosis and male hypogonadism' and with 'Rud syndrome'.
    Andria G; Ballabio A; Parenti G; Di Maio S; Piccirillo A
    J Inherit Metab Dis; 1984; 7 Suppl 2():159-60. PubMed ID: 6434878
    [No Abstract]   [Full Text] [Related]  

  • 34. Prenatal diagnosis and investigation of a fetus with chondrodysplasia punctata, ichthyosis, and Kallmann syndrome due to an Xp deletion.
    Bick DP; Schorderet DF; Price PA; Campbell L; Huff RW; Shapiro LJ; Moore CM
    Prenat Diagn; 1992 Jan; 12(1):19-29. PubMed ID: 1557308
    [TBL] [Abstract][Full Text] [Related]  

  • 35. More on X-linked ichthyosis, steroid sulfatase deficiency, and hypogonadism and anosmia.
    Andria G; Ballabio A; Parenti G
    Ann Neurol; 1988 Jan; 23(1):103. PubMed ID: 3422798
    [No Abstract]   [Full Text] [Related]  

  • 36. Ichthyosis vulgaris with hypogenitalism and hypogonadism: evidence for different genotypes by lipoprotein electrophoresis and steroid sulfatase testing.
    Traupe H; Müller-Migl CR; Kolde G; Happle R; Kövary PM; Hameister H; Ropers HH
    Clin Genet; 1984 Jan; 25(1):42-51. PubMed ID: 6584254
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Magnetic resonance imaging of the brain in patients with anosmia and hypothalamic hypogonadism (Kallmann's syndrome).
    Klingmüller D; Dewes W; Krahe T; Brecht G; Schweikert HU
    J Clin Endocrinol Metab; 1987 Sep; 65(3):581-4. PubMed ID: 3114308
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Isolated hypogonadotrophic hypogonadism: a family with autosomal dominant inheritance.
    Dean JC; Johnston AW; Klopper AI
    Clin Endocrinol (Oxf); 1990 Mar; 32(3):341-7. PubMed ID: 2111748
    [TBL] [Abstract][Full Text] [Related]  

  • 39. [Effect of clomiphene citrate on FSH and LH levels in 4 cases of hypogonadism with hyposmia or anosmia].
    Bricaire H; Franchimont P; Luton JP; Valcke JC; Charbonnel B
    Ann Endocrinol (Paris); 1972; 33(6):622-8. PubMed ID: 4665420
    [No Abstract]   [Full Text] [Related]  

  • 40. [Gene deletion of X-linked ichthyosis].
    Li M
    Zhonghua Yi Xue Za Zhi; 1992 Apr; 72(4):210-2, 254. PubMed ID: 1327447
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 9.