181 related articles for article (PubMed ID: 24862381)
1. Reduced activity of 11β-hydroxylase accounts for elevated 17α-hydroxyprogesterone in preterms.
Kamrath C; Hartmann MF; Boettcher C; Wudy SA
J Pediatr; 2014 Aug; 165(2):280-4. PubMed ID: 24862381
[TBL] [Abstract][Full Text] [Related]
2. Diagnosis of 21-hydroxylase deficiency by urinary metabolite ratios using gas chromatography-mass spectrometry analysis: Reference values for neonates and infants.
Kamrath C; Hartmann MF; Boettcher C; Zimmer KP; Wudy SA
J Steroid Biochem Mol Biol; 2016 Feb; 156():10-6. PubMed ID: 26493852
[TBL] [Abstract][Full Text] [Related]
3. Elevated urine pregnanetriolone definitively establishes the diagnosis of classical 21-hydroxylase deficiency in term and preterm neonates.
Homma K; Hasegawa T; Takeshita E; Watanabe K; Anzo M; Toyoura T; Jinno K; Ohashi T; Hamajima T; Takahashi Y; Takahashi T; Matsuo N
J Clin Endocrinol Metab; 2004 Dec; 89(12):6087-91. PubMed ID: 15579762
[TBL] [Abstract][Full Text] [Related]
4. Serum 21-Deoxycortisol, 17-Hydroxyprogesterone, and 11-deoxycortisol in classic congenital adrenal hyperplasia: clinical and hormonal correlations and identification of patients with 11beta-hydroxylase deficiency among a large group with alleged 21-hydroxylase deficiency.
Tonetto-Fernandes V; Lemos-Marini SH; Kuperman H; Ribeiro-Neto LM; Verreschi IT; Kater CE
J Clin Endocrinol Metab; 2006 Jun; 91(6):2179-84. PubMed ID: 16551734
[TBL] [Abstract][Full Text] [Related]
5. Two-step biochemical differential diagnosis of classic 21-hydroxylase deficiency and cytochrome P450 oxidoreductase deficiency in Japanese infants by GC-MS measurement of urinary pregnanetriolone/ tetrahydroxycortisone ratio and 11β-hydroxyandrosterone.
Koyama Y; Homma K; Fukami M; Miwa M; Ikeda K; Ogata T; Hasegawa T; Murata M
Clin Chem; 2012 Apr; 58(4):741-7. PubMed ID: 22273564
[TBL] [Abstract][Full Text] [Related]
6. [Reevaluation of recalled infants by neonatal mass screening for congenital adrenal hyperplasia due to 21-hydroxylase deficiency. Diagnostic value of pregnanetriolone in a single urine specimen using glass capillary gas chromatography].
Hikita Y
Nihon Naibunpi Gakkai Zasshi; 1985 Mar; 61(3):197-219. PubMed ID: 3874793
[TBL] [Abstract][Full Text] [Related]
7. Congenital Adrenal Hyperplasia: Time to Replace 17OHP with 21-Deoxycortisol.
Miller WL
Horm Res Paediatr; 2019; 91(6):416-420. PubMed ID: 31450227
[TBL] [Abstract][Full Text] [Related]
8. Modified-Release and Conventional Glucocorticoids and Diurnal Androgen Excretion in Congenital Adrenal Hyperplasia.
Jones CM; Mallappa A; Reisch N; Nikolaou N; Krone N; Hughes BA; O'Neil DM; Whitaker MJ; Tomlinson JW; Storbeck KH; Merke DP; Ross RJ; Arlt W
J Clin Endocrinol Metab; 2017 Jun; 102(6):1797-1806. PubMed ID: 27845856
[TBL] [Abstract][Full Text] [Related]
9. Androgen excess is due to elevated 11-oxygenated androgens in treated children with congenital adrenal hyperplasia.
Kamrath C; Wettstaedt L; Boettcher C; Hartmann MF; Wudy SA
J Steroid Biochem Mol Biol; 2018 Apr; 178():221-228. PubMed ID: 29277706
[TBL] [Abstract][Full Text] [Related]
10. Profiles of 21-Carbon Steroids in 21-hydroxylase Deficiency.
Turcu AF; Rege J; Chomic R; Liu J; Nishimoto HK; Else T; Moraitis AG; Palapattu GS; Rainey WE; Auchus RJ
J Clin Endocrinol Metab; 2015 Jun; 100(6):2283-90. PubMed ID: 25850025
[TBL] [Abstract][Full Text] [Related]
11. Urinary GC-MS steroid metabotyping in treated children with congenital adrenal hyperplasia.
Kamrath C; Hartmann MF; Pons-Kühnemann J; Wudy SA
Metabolism; 2020 Nov; 112():154354. PubMed ID: 32916150
[TBL] [Abstract][Full Text] [Related]
12. Neonatal screening: identification of children with 11β-hydroxylase deficiency by second-tier testing.
Janzen N; Riepe FG; Peter M; Sander S; Steuerwald U; Korsch E; Krull F; Müller HL; Heger S; Brack C; Sander J
Horm Res Paediatr; 2012; 77(3):195-9. PubMed ID: 22508345
[TBL] [Abstract][Full Text] [Related]
13. Newborn screening for congenital adrenal hyperplasia: additional steroid profile using liquid chromatography-tandem mass spectrometry.
Janzen N; Peter M; Sander S; Steuerwald U; Terhardt M; Holtkamp U; Sander J
J Clin Endocrinol Metab; 2007 Jul; 92(7):2581-9. PubMed ID: 17456574
[TBL] [Abstract][Full Text] [Related]
14. Early diagnosis of 11 beta-hydroxylase deficiency in two siblings confirmed by analysis of a novel steroid metabolite in newborn urine.
Hughes IA; Arisaka O; Perry LA; Honour JW
Acta Endocrinol (Copenh); 1986 Mar; 111(3):349-54. PubMed ID: 3515819
[TBL] [Abstract][Full Text] [Related]
15. Steroid profile in dried blood spots by liquid chromatography tandem mass spectrometry: Application to newborn screening for congenital adrenal hyperplasia in China.
Zhan X; Han L; Qiu W; Gu X; Guo J; Chang S; Wang Y; Zhang H
Steroids; 2022 Sep; 185():109056. PubMed ID: 35660382
[TBL] [Abstract][Full Text] [Related]
16. 11 Beta-hydroxylase deficiency congenital adrenal hyperplasia: update of prenatal diagnosis.
Rösler A; Weshler N; Leiberman E; Hochberg Z; Weidenfeld J; Sack J; Chemke J
J Clin Endocrinol Metab; 1988 Apr; 66(4):830-8. PubMed ID: 3346360
[TBL] [Abstract][Full Text] [Related]
17. Utility of a precursor-to-product ratio in the evaluation of presumptive positives in newborn screening of congenital adrenal hyperplasia.
Tieh PY; Yee JK; Hicks RA; Mao CS; Lee WN
J Perinatol; 2017 Mar; 37(3):283-287. PubMed ID: 27929529
[TBL] [Abstract][Full Text] [Related]
18. The balance of cortisol-cortisone interconversion is shifted towards cortisol in neonates with congenital adrenal hyperplasia due to 21-hydroxylase deficiency.
Kamrath C; Hartmann MF; Wudy SA
J Steroid Biochem Mol Biol; 2014 Sep; 143():386-91. PubMed ID: 24861266
[TBL] [Abstract][Full Text] [Related]
19. Combined 21- and 11 beta-hydroxylase deficiency in familial congenital adrenal hyperplasia.
Hurwitz A; Brautbar C; Milwidsky A; Vecsei P; Milewicz A; Navot D; Rösler A
J Clin Endocrinol Metab; 1985 Apr; 60(4):631-8. PubMed ID: 2982904
[TBL] [Abstract][Full Text] [Related]
20. The High Relevance of 21-Deoxycortisol, (Androstenedione + 17α-Hydroxyprogesterone)/Cortisol, and 11-Deoxycortisol/17α-Hydroxyprogesterone for Newborn Screening of 21-Hydroxylase Deficiency.
Watanabe K; Tsuji-Hosokawa A; Hashimoto A; Konishi K; Ishige N; Yajima H; Sutani A; Nakatani H; Gau M; Takasawa K; Tajima T; Hasegawa T; Morio T; Kashimada K
J Clin Endocrinol Metab; 2022 Nov; 107(12):3341-3352. PubMed ID: 36071550
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]