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.
43. 15 beta-hydroxylated steroids may be diagnostically misleading in confirming congenital adrenal hyperplasia suspected by a newborn screening programme. Lange-Kubini K; Zachmann M; Kempken B; Torresani T Eur J Pediatr; 1996 Nov; 155(11):928-31. PubMed ID: 8911890 [TBL] [Abstract][Full Text] [Related]
44. Steroid excretion in urine during suppression and stimulation of adrenals in the 17 alpha-hydroxylase deficiency syndrome. Honour J; Millar G; Roitman E; Shackleton C J Clin Endocrinol Metab; 1981 May; 52(5):1039-42. PubMed ID: 6262355 [TBL] [Abstract][Full Text] [Related]
45. Detection of 3 beta-hydroxysteroid dehydrogenase deficiency in a newborn by means of urinary steroid analysis. Wolthers BG; de Vries IJ; Volmer M; Nagel GT Clin Chim Acta; 1987 Oct; 169(1):109-16. PubMed ID: 3479282 [TBL] [Abstract][Full Text] [Related]
46. [Diagnosis of the adrenogenital syndrome caused by 11beta-hydroxylase deficiency using gas chromatographic-mass spectrometric analysis of the urinary steroid profile]. Wudy SA; Homoki J; Wachter UA; Teller WM Dtsch Med Wochenschr; 1997 Jan; 122(1-2):3-10; discussion 11. PubMed ID: 9064231 [TBL] [Abstract][Full Text] [Related]
47. A new marker for early diagnosis of 21-hydroxylase deficiency: 3beta,16alpha,17alpha-trihydroxy-5alpha-pregnane-7,20-dione. Christakoudi S; Cowan DA; Taylor NF J Steroid Biochem Mol Biol; 2010 Aug; 121(3-5):574-81. PubMed ID: 20302934 [TBL] [Abstract][Full Text] [Related]
48. Genetic and hormonal characterization of cryptic 21-hydroxylase deficiency. Levine LS; Dupont B; Lorenzen F; Pang S; Pollack M; Oberfield SE; Kohn B; Lerner A; Cacciari E; Mantero F; Cassio A; Scaroni C; Chiumello G; Rondanini GF; Gargantini L; Giovannelli G; Virdis R; Bartolotta E; Migliori C; Pintor C; Tato L; Barboni F; New MI J Clin Endocrinol Metab; 1981 Dec; 53(6):1193-8. PubMed ID: 6271801 [TBL] [Abstract][Full Text] [Related]
50. Hormonal diagnosis of 21-hydroxylase deficiency in plasma and urine of neonates using benchtop gas chromatography-mass spectrometry. Wudy SA; Hartmann M; Homoki J J Endocrinol; 2000 Jun; 165(3):679-83. PubMed ID: 10828852 [TBL] [Abstract][Full Text] [Related]
51. The urinary steroidome of treated children with classic 21-hydroxylase deficiency. Kamrath C; Wettstaedt L; Boettcher C; Hartmann MF; Wudy SA J Steroid Biochem Mol Biol; 2017 Jan; 165(Pt B):396-406. PubMed ID: 27544322 [TBL] [Abstract][Full Text] [Related]
52. A pilot study for neonatal screening of congenital adrenal hyperplasia due to 21-hydroxylase and 11-beta-hydroxylase deficiency in Campania region. Valentino R; Tommaselli AP; Rossi R; Lombardi G; Varrone S J Endocrinol Invest; 1990 Mar; 13(3):221-5. PubMed ID: 2365957 [TBL] [Abstract][Full Text] [Related]
53. Prenatal diagnosis of congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency by steroid analysis in the amniotic fluid of mid-pregnancy: comparison with HLA typing in 17 pregnancies at risk for CAH. Forest MG; Bétuel H; Couillin P; Boué A Prenat Diagn; 1981 Jul; 1(3):197-207. PubMed ID: 6981108 [TBL] [Abstract][Full Text] [Related]
55. Selective LC-MRM/SIM-MS based profiling of adrenal steroids reveals metabolic signatures of 17α-hydroxylase deficiency. Lee C; Kim JH; Moon SJ; Shim J; Kim HI; Choi MH J Steroid Biochem Mol Biol; 2020 Apr; 198():105615. PubMed ID: 32014605 [TBL] [Abstract][Full Text] [Related]
56. Urinary steroid profiling in the diagnosis of congenital adrenal hyperplasia and disorders of sex development: experience of a urinary steroid referral centre in Hong Kong. Chan AO; Shek CC Clin Biochem; 2013 Mar; 46(4-5):327-34. PubMed ID: 23261836 [TBL] [Abstract][Full Text] [Related]
57. Pitfalls of prenatal diagnosis of 21-hydroxylase deficiency congenital adrenal hyperplasia. Pang S; Pollack MS; Loo M; Green O; Nussbaum R; Clayton G; Dupont B; New MI J Clin Endocrinol Metab; 1985 Jul; 61(1):89-97. PubMed ID: 3873469 [TBL] [Abstract][Full Text] [Related]
58. [Neonatal screening for congenital adrenal hyperplasia due to 21-hydroxylase deficiency. 1. Enzyme immunoassay of dried blood 17 alpha-hydroxyprogesterone and its application to neonatal screening for congenital adrenal hyperplasia]. Fukushi M; Arai O; Mizushima Y; Takasugi N; Fujieda K; Matsuura N Nihon Naibunpi Gakkai Zasshi; 1986 Jun; 62(6):683-96. PubMed ID: 3530828 [TBL] [Abstract][Full Text] [Related]
59. Diagnosis of congenital adrenal hyperplasia with 11-hydroxylase deficiency by determination of tetrahydro-11-desoxycortisol in urine. Knorr D; Bidlingmaier F Helv Paediatr Acta; 1974; Suppl 34():119-25. PubMed ID: 4452634 [No Abstract] [Full Text] [Related]
60. Urinary excretion of pregnanetriol and 5 -pregnenetriol in two forms of congenital adrenal hyperplasia. Bongiovanni AM; Eberlein WR; Moshang T J Clin Invest; 1971 Dec; 50(12):2751-4. PubMed ID: 5129323 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]