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25. Clinical characteristics of Taiwanese children with congenital adrenal hyperplasia due to 21-hydroxylase deficiency detected by neonatal screening. Liu SY; Lee CT; Tung YC; Chien YH; Hwu WL; Tsai WY J Formos Med Assoc; 2018 Feb; 117(2):126-131. PubMed ID: 28392195 [TBL] [Abstract][Full Text] [Related]
26. 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]
27. Mutations in steroid 21-hydroxylase (CYP21). White PC; Tusie-Luna MT; New MI; Speiser PW Hum Mutat; 1994; 3(4):373-8. PubMed ID: 8081391 [TBL] [Abstract][Full Text] [Related]
28. Comments to “A rational, non-radioactive strategy for the molecular diagnosis of congenital adrenal hyperplasia due to 21-hydroxylase deficiency”. Concolino P; Mello E; Rossodivita A; Giardina B; Capoluongo E Gene; 2014 Jan; 534(2):449-450. PubMed ID: 24501745 [No Abstract] [Full Text] [Related]
29. Comments to "a rational, non-radioactive strategy for the molecular diagnosis of congenital adrenal hyperplasia due to 21-hydroxylase deficiency". Coeli-Lacchini FB; Turatti W; Elias PC; Elias LL; Martinelli CE; Moreira AC; Antonini SR; de Castro M Gene; 2014 Jan; 534(2):451-2. PubMed ID: 24100083 [No Abstract] [Full Text] [Related]
30. [Characterization of new splicing mutation in steroid 21-hydroxylase gene]. Rubtsov PM; Igudin EL; Pichugina MIu; Spirin PV; Prasolov VS; Tul'pakov AN Bioorg Khim; 2011; 37(6):815-20. PubMed ID: 22497080 [TBL] [Abstract][Full Text] [Related]
31. Congenital adrenal hyperplasia: focus on the molecular basis of 21-hydroxylase deficiency. Gonçalves J; Friães A; Moura L Expert Rev Mol Med; 2007 Apr; 9(11):1-23. PubMed ID: 17466088 [TBL] [Abstract][Full Text] [Related]
32. Genetics of congenital adrenal hyperplasia and genotype-phenotype correlation. Narasimhan ML; Khattab A Fertil Steril; 2019 Jan; 111(1):24-29. PubMed ID: 30611409 [TBL] [Abstract][Full Text] [Related]
33. Non-classic congenital adrenal hyperplasia due to 21-hydoxylase deficiency as a cause of infertility and miscarriages. Falhammar H N Z Med J; 2010 Apr; 123(1312):77-80. PubMed ID: 20389322 [TBL] [Abstract][Full Text] [Related]
34. An X-traordinary stroke. Verma S; Lewis D; Warne G; Grossmann M Lancet; 2011 Apr; 377(9773):1288. PubMed ID: 21481709 [No Abstract] [Full Text] [Related]
35. A male case of nonclassical 21-hydroxylase deficiency first manifested in his sixties with adrenocortical incidentaloma. Nigawara T; Kageyama K; Sakihara S; Takayasu S; Kawahara M; Imai A; Ohyama C; Usui T; Sasano H; Suda T Endocr J; 2008 May; 55(2):291-7. PubMed ID: 18323673 [TBL] [Abstract][Full Text] [Related]
36. Diagnosis and management of congenital adrenal hyperplasia. New MI Annu Rev Med; 1998; 49():311-28. PubMed ID: 9509266 [TBL] [Abstract][Full Text] [Related]
38. NIH conference. Future directions in the study and management of congenital adrenal hyperplasia due to 21-hydroxylase deficiency. Merke DP; Bornstein SR; Avila NA; Chrousos GP Ann Intern Med; 2002 Feb; 136(4):320-34. PubMed ID: 11848730 [TBL] [Abstract][Full Text] [Related]
39. Macronodular congenital adrenal hyperplasia in an adult with female pseudohermaphroditism. Norris AM; O'Driscoll JB; Mamtora H Eur Radiol; 1996; 6(4):470-2. PubMed ID: 8798026 [TBL] [Abstract][Full Text] [Related]
40. The prevalence of 21-hydroxylase deficiency in adrenal incidentalomas - hormonal and mutation screening. Wagnerova H; Lazúrová I; Habalová V; Dudásová D; Vrzgula A Exp Clin Endocrinol Diabetes; 2008 May; 116(5):272-5. PubMed ID: 18589890 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]