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 *

147 related articles for article (PubMed ID: 1915976)

  • 21. Prenatal treatment and diagnosis of congenital adrenal hyperplasia owing to steroid 21-hydroxylase deficiency.
    Mercado AB; Wilson RC; Cheng KC; Wei JQ; New MI
    J Clin Endocrinol Metab; 1995 Jul; 80(7):2014-20. PubMed ID: 7608248
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Description and defense of prenatal diagnosis and treatment with low-dose dexamethasone for congenital adrenal hyperplasia.
    New M
    Am J Bioeth; 2010 Sep; 10(9):48-51. PubMed ID: 20818561
    [No Abstract]   [Full Text] [Related]  

  • 23. First trimester prenatal diagnosis of 21-hydroxylase deficiency by linkage analysis to HLA-DNA probes and by 17-hydroxyprogesterone determination.
    Mornet E; Boue J; Raux-Demay M; Couillin P; Oury JF; Dumez Y; Dausset J; Cohen D; Boué A
    Hum Genet; 1986 Aug; 73(4):358-64. PubMed ID: 3017844
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Molecular genetic prenatal diagnosis of congenital adrenal hyperplasia due to 21-hydroxylase deficiency by allele-specific hybridization.
    Speiser PW; White PC; Dupont J; Zhu D; Mercado A; New MI
    Recent Prog Horm Res; 1994; 49():367-71. PubMed ID: 8146433
    [TBL] [Abstract][Full Text] [Related]  

  • 25. RFLPs of 21-hydroxylase and C4 genes: application to pedigree analysis on 21-hydroxylase deficiency.
    Matsumoto T; Kondoh T; Baba T; Yoshimoto M; Niikawa N; Tsuji Y
    Acta Paediatr Jpn; 1988; 30 Suppl():111-6. PubMed ID: 2906201
    [No Abstract]   [Full Text] [Related]  

  • 26. 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]  

  • 27. 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]  

  • 28. [Diagnosis and treatment of fetal congenital adrenal cortex hyperplasia].
    Gustavson KH; Larsson A; Nillius SJ; Gustafsson J; Tuvemo T; Ritzén M; Haglund-Stengler B; Luthman H
    Lakartidningen; 1986 Dec; 83(52):4462-3. PubMed ID: 3821304
    [No Abstract]   [Full Text] [Related]  

  • 29. [Prenatal treatment of congenital adrenal hyperplasia due to 21-hydroxylase deficiency. 9 treated pregnancies].
    Nivelon JL; Chouchane M; Forest MG; Morel Y; Huet F; Nivelon-Chevallier A; François C
    Ann Pediatr (Paris); 1993 Sep; 40(7):421-5. PubMed ID: 7902059
    [TBL] [Abstract][Full Text] [Related]  

  • 30. 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]  

  • 31. 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]  

  • 32. Prenatal diagnosis and management of congenital adrenal hyperplasia due to steroid 21-hydroxylase deficiency.
    Passarge E
    Indian J Pediatr; 1988; 55(4):472-5. PubMed ID: 3262582
    [No Abstract]   [Full Text] [Related]  

  • 33. 21-hydroxylase deficiency congenital adrenal hyperplasia.
    Shaw AM
    Neonatal Netw; 2010; 29(3):191-6. PubMed ID: 20472536
    [No Abstract]   [Full Text] [Related]  

  • 34. Prenatal diagnosis and management of congenital adrenal hyperplasia.
    Speiser PW; New MI
    Clin Perinatol; 1994 Sep; 21(3):631-45. PubMed ID: 7982338
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Fetal sex determination from maternal blood at 6 weeks of gestation when at risk for 21-hydroxylase deficiency.
    Bartha JL; Finning K; Soothill PW
    Obstet Gynecol; 2003 May; 101(5 Pt 2):1135-6. PubMed ID: 12738128
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Congenital adrenal hyperplasia due to steroid 21-hydroxylase deficiency.
    Speiser PW; White PC
    Clin Endocrinol (Oxf); 1998 Oct; 49(4):411-7. PubMed ID: 9876336
    [No Abstract]   [Full Text] [Related]  

  • 37. [Prenatal diagnosis of genetic diseases using chorionic villi].
    Boué J; Deluchat C; Nicolas H; Oury JF; Dumez Y
    J Genet Hum; 1986 Aug; 34(3-4):221-33. PubMed ID: 3760827
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Prenatal treatment of congenital adrenal hyperplasia. The United States experience.
    New MI
    Endocrinol Metab Clin North Am; 2001 Mar; 30(1):1-13. PubMed ID: 11344929
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Prenatal diagnosis of 21-hydroxylase deficiency by RFLP analysis of the 21-hydroxylase, complement C4, and HLA class II genes.
    Keller E; Andreas A; Scholz S; Dörr HC; Knorr D; Albert ED
    Prenat Diagn; 1991 Nov; 11(11):827-40. PubMed ID: 1684434
    [TBL] [Abstract][Full Text] [Related]  

  • 40. [Prenatal diagnosis of congenital adrenal hyperplasia and possibilities of prenatal therapy].
    Snajderová M; Kolousková S
    Cesk Pediatr; 1992 Aug; 47(8):497-9. PubMed ID: 1394557
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.