139 related items for PubMed ID: 36990162
1. Metabotypes of congenital adrenal hyperplasia in infants determined by gas chromatography-mass spectrometry in spot urine.
Kamrath C, Friedrich C, Hartmann MF, Wudy SA.
J Steroid Biochem Mol Biol; 2023 Jul; 231():106304. PubMed ID: 36990162
[Abstract] [Full Text] [Related]
2. 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
[Abstract] [Full Text] [Related]
3. 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
[Abstract] [Full Text] [Related]
4. 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
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5. 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 01; 102(6):1797-1806. PubMed ID: 27845856
[Abstract] [Full Text] [Related]
6. Urinary steroidomic profiles by LC-MS/MS to monitor classic 21-Hydroxylase deficiency.
Pussard E, Travers S, Bouvattier C, Xue QY, Cosson C, Viengchareun S, Martinerie L, Lombès M.
J Steroid Biochem Mol Biol; 2020 Apr 01; 198():105553. PubMed ID: 31778802
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7. Correlation of blood-spot 17-hydroxyprogesterone daily profiles and urinary steroid profiles in congenital adrenal hyperplasia.
Erhardt E, Sólyom J, Homoki J, Juricskay S, Soltész G.
J Pediatr Endocrinol Metab; 2000 Feb 01; 13(2):205-10. PubMed ID: 10711668
[Abstract] [Full Text] [Related]
8. Delineating endogenous Cushing's syndrome by GC-MS urinary steroid metabotyping.
Braun LT, Osswald A, Zopp S, Rubinstein G, Vogel F, Riester A, Honegger J, Eisenhofer G, Constantinescu G, Deutschbein T, Quinkler M, Elbelt U, Künzel H, Nowotny HF, Reisch N, Hartmann MF, Beuschlein F, Pons-Kühnemann J, Reincke M, Wudy SA.
EBioMedicine; 2024 Jan 01; 99():104907. PubMed ID: 38128413
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9. A possible defect in the inter-conversion between cortisone and cortisol in prepubertal patients with congenital adrenal hyperplasia receiving cortisone acetate therapy.
Whorwood CB, Warne GL.
J Steroid Biochem Mol Biol; 1991 Oct 01; 39(4A):461-70. PubMed ID: 1911435
[Abstract] [Full Text] [Related]
10. 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 01; 58(4):741-7. PubMed ID: 22273564
[Abstract] [Full Text] [Related]
11. Sodium Chloride Supplementation Is Not Routinely Performed in the Majority of German and Austrian Infants with Classic Salt-Wasting Congenital Adrenal Hyperplasia and Has No Effect on Linear Growth and Hydrocortisone or Fludrocortisone Dose.
Bonfig W, Roehl F, Riedl S, Brämswig J, Richter-Unruh A, Fricke-Otto S, Hübner A, Bettendorf M, Schönau E, Dörr H, Holl RW, Mohnike K.
Horm Res Paediatr; 2018 Apr 01; 89(1):7-12. PubMed ID: 29073619
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12. Effect of carbenoxolone on the plasma renin activity and hypothalamic-pituitary-adrenal axis in congenital adrenal hyperplasia due to 21-hydroxylase deficiency.
Irony I, Cutler GB.
Clin Endocrinol (Oxf); 1999 Sep 01; 51(3):285-91. PubMed ID: 10469007
[Abstract] [Full Text] [Related]
13. Interaction between accumulated 21-deoxysteroids and mineralocorticoid signaling in 21-hydroxylase deficiency.
Travers S, Bouvattier C, Fagart J, Martinerie L, Viengchareun S, Pussard E, Lombès M.
Am J Physiol Endocrinol Metab; 2020 Feb 01; 318(2):E102-E110. PubMed ID: 31821037
[Abstract] [Full Text] [Related]
14. Serum cortisol and 17-hydroxyprogesterone interrelation in classic 21-hydroxylase deficiency: is current replacement therapy satisfactory?
Charmandari E, Matthews DR, Johnston A, Brook CG, Hindmarsh PC.
J Clin Endocrinol Metab; 2001 Oct 01; 86(10):4679-85. PubMed ID: 11600525
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15. Steroid 17-Hydroxyprogesterone in Hair Is a Potential Long-Term Biomarker of Androgen Control in Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency.
Auer MK, Krumbholz A, Bidlingmaier M, Thieme D, Reisch N.
Neuroendocrinology; 2020 Oct 01; 110(11-12):938-949. PubMed ID: 31711056
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16. Height Velocity Defined Metabolic Control in Children With Congenital Adrenal Hyperplasia Using Urinary Steroid GC-MS Analysis.
Kamrath C, Wettstaedt L, Hartmann MF, Wudy SA.
J Clin Endocrinol Metab; 2019 Sep 01; 104(9):4214-4224. PubMed ID: 31112272
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17. Glucocorticoid replacement regimens for treating congenital adrenal hyperplasia.
Ng SM, Stepien KM, Krishan A.
Cochrane Database Syst Rev; 2020 Mar 19; 3(3):CD012517. PubMed ID: 32190901
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18. Reduced activity of 11β-hydroxylase accounts for elevated 17α-hydroxyprogesterone in preterms.
Kamrath C, Hartmann MF, Boettcher C, Wudy SA.
J Pediatr; 2014 Aug 19; 165(2):280-4. PubMed ID: 24862381
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19. 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 19; 156():10-6. PubMed ID: 26493852
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20. Congenital adrenal hyperplasia: issues in diagnosis and treatment in children.
Sharma R, Seth A.
Indian J Pediatr; 2014 Feb 19; 81(2):178-85. PubMed ID: 24254335
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