BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

656 related articles for article (PubMed ID: 10487675)

  • 1. Prenatal diagnosis and treatment of 11beta-hydroxylase deficiency congenital adrenal hyperplasia resulting in normal female genitalia.
    Cerame BI; Newfield RS; Pascoe L; Curnow KM; Nimkarn S; Roe TF; New MI; Wilson RC
    J Clin Endocrinol Metab; 1999 Sep; 84(9):3129-34. PubMed ID: 10487675
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Update on the prenatal diagnosis and treatment of congenital adrenal hyperplasia due to 11beta-hydroxylase deficiency.
    Motaghedi R; Betensky BP; Slowinska B; Cerame B; Cabrer M; New MI; Wilson RC
    J Pediatr Endocrinol Metab; 2005 Feb; 18(2):133-42. PubMed ID: 15751602
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Congenital adrenal hyperplasia: update on prenatal diagnosis and treatment.
    Carlson AD; Obeid JS; Kanellopoulou N; Wilson RC; New MI
    J Steroid Biochem Mol Biol; 1999; 69(1-6):19-29. PubMed ID: 10418977
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [Prenatal diagnosis and treatment of adrenogenital syndrome. Prevent virilization of female fetuses].
    Lajic S; Bui TH; Holst M; Ritzén M; Wedell A
    Lakartidningen; 1997 Dec; 94(50):4781-6. PubMed ID: 9445959
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Prenatal diagnosis for congenital adrenal hyperplasia in 532 pregnancies.
    New MI; Carlson A; Obeid J; Marshall I; Cabrera MS; Goseco A; Lin-Su K; Putnam AS; Wei JQ; Wilson RC
    J Clin Endocrinol Metab; 2001 Dec; 86(12):5651-7. PubMed ID: 11739415
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Two novel CYP11B1 mutations in congenital adrenal hyperplasia due to steroid 11β hydroxylase deficiency in a Tunisian family.
    Ben Charfeddine I; Riepe FG; Kahloul N; Kulle AE; Adala L; Mamaï O; Amara A; Mili A; Amri F; Saad A; Holterhus PM; Gribaa M
    Gen Comp Endocrinol; 2012 Feb; 175(3):514-8. PubMed ID: 22210247
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Normal external genitalia in a female with classical congenital adrenal hyperplasia who was not treated during embryogenesis.
    Quercia N; Chitayat D; Babul-Hirji R; New MI; Daneman D
    Prenat Diagn; 1998 Jan; 18(1):83-5. PubMed ID: 9483646
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A novel missense mutation, GGC(Arg454) --> TGC(Cys), of CYP11B1 gene identified in a Chinese family with steroid 11beta-hydroxylase deficiency.
    Ye ZQ; Zhang MN; Zhang HJ; Jiang JJ; Li XY; Zhang KQ
    Chin Med J (Engl); 2010 May; 123(10):1264-8. PubMed ID: 20529578
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Prenatal diagnosis and successful intrauterine treatment of a female fetus with 21-hydroxylase deficiency.
    Haan EA; Serjeantson SW; Norman R; Rollond AK; Antonis P; Richards RI; Penfold JL
    Med J Aust; 1992 Jan; 156(2):132-5. PubMed ID: 1736054
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [The effect of maternal dexamethasone treatment after the 12th week of pregnancy on fetal genital development in adrenogenital syndrome with 21-hydroxylase deficiency].
    Schwab KO; Kruse K; Dörr HG; Horwitz AE; Spingler H
    Monatsschr Kinderheilkd; 1989 May; 137(5):293-6. PubMed ID: 2786992
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Dexamethasone treatment of congenital adrenal hyperplasia in utero: an experimental therapy of unproven safety.
    Miller WL
    J Urol; 1999 Aug; 162(2):537-40. PubMed ID: 10411085
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Prenatal diagnosis and treatment of congenital adrenal hyperplasia owing to 21-hydroxylase deficiency.
    Nimkarn S; New MI
    Nat Clin Pract Endocrinol Metab; 2007 May; 3(5):405-13. PubMed ID: 17452967
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Prenatal treatment of congenital adrenal hyperplasia due to 21-hydroxylase deficiency.
    Pang SY; Pollack MS; Marshall RN; Immken L
    N Engl J Med; 1990 Jan; 322(2):111-5. PubMed ID: 2403652
    [No Abstract]   [Full Text] [Related]  

  • 14. New developments in prenatal diagnosis of congenital adrenal hyperplasia.
    Kazmi D; Bailey J; Yau M; Abu-Amer W; Kumar A; Low M; Yuen T
    J Steroid Biochem Mol Biol; 2017 Jan; 165(Pt A):121-123. PubMed ID: 27378492
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Prenatal molecular genetic diagnosis and treatment of congenital adrenal hyperplasia due to 21-hydroxylase deficiency].
    Rodríguez A; Ezquieta B; Varela JM; Moreno M; Dulín E; Rodríguez Arnao MD
    Med Clin (Barc); 1997 Nov; 109(17):669-72. PubMed ID: 9488957
    [TBL] [Abstract][Full Text] [Related]  

  • 16. First trimester prenatal treatment and molecular genetic diagnosis of congenital adrenal hyperplasia (21-hydroxylase deficiency).
    Speiser PW; Laforgia N; Kato K; Pareira J; Khan R; Yang SY; Whorwood C; White PC; Elias S; Schriock E
    J Clin Endocrinol Metab; 1990 Apr; 70(4):838-48. PubMed ID: 1969421
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Prenatal treatment of congenital adrenal hyperplasia: report of a new case.
    Loeuille GA; David M; Forest MG
    Eur J Pediatr; 1990 Jan; 149(4):237-40. PubMed ID: 2406146
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Prenatal fetal adrenal suppression following in utero diagnosis of congenital adrenal hyperplasia.
    Shapiro E; Santiago JV; Crane JP
    J Urol; 1989 Aug; 142(2 Pt 2):663-6; discussion 667-8. PubMed ID: 2746796
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Prenatal diagnosis of steroid 21-hydroxylase deficiency by allele-specific amplification.
    Theodoropoulou M; Barta C; Szoke M; Guttman A; Staub M; Niederland T; Sólyom J; Fekete G; Sasvari-Szekely M
    Fetal Diagn Ther; 2001; 16(4):237-40. PubMed ID: 11399887
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Prenatal diagnosis and treatment of adrenogenital syndrome (steroid 21-hydroxylase deficiency).
    New MI
    Dev Pharmacol Ther; 1990; 15(3-4):200-10. PubMed ID: 2099900
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 33.