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2. Growth inhibition by glucocorticoid treatment in salt wasting 21-hydroxylase deficiency: in early infancy and (pre)puberty. Stikkelbroeck NM; Van't Hof-Grootenboer BA; Hermus AR; Otten BJ; Van't Hof MA J Clin Endocrinol Metab; 2003 Aug; 88(8):3525-30. PubMed ID: 12915631 [TBL] [Abstract][Full Text] [Related]
3. Growth patterns and final height in congenital adrenal hyperplasia due to classical 21-hydroxylase deficiency. Results of a multicenter study. Hargitai G; Sólyom J; Battelino T; Lebl J; Pribilincová Z; Hauspie R; Kovács J; Waldhauser F; Frisch H; Horm Res; 2001; 55(4):161-71. PubMed ID: 11598369 [TBL] [Abstract][Full Text] [Related]
4. Glucocorticoid replacement regimens for treating congenital adrenal hyperplasia. Ng SM; Stepien KM; Krishan A Cochrane Database Syst Rev; 2020 Mar; 3(3):CD012517. PubMed ID: 32190901 [TBL] [Abstract][Full Text] [Related]
5. [Congenital adrenal hyperplasia due to 21-hydroxylase deficiency: final height in 27 patients with the classical form]. Lemos-Marini SH; Guerra-Júnior G; Morcillo AM; Baptista MT; Silva LO; Maciel-Guerra AT Arq Bras Endocrinol Metabol; 2005 Dec; 49(6):902-7. PubMed ID: 16544012 [TBL] [Abstract][Full Text] [Related]
6. Non-classical 21-hydroxylase deficiency in infancy and childhood: the effect of time of initiation of therapy on puberty and final height. Weintrob N; Dickerman Z; Sprecher E; Galatzer A; Pertzelan A Eur J Endocrinol; 1997 Feb; 136(2):188-95. PubMed ID: 9116914 [TBL] [Abstract][Full Text] [Related]
7. Growth pattern of untreated boys with simple virilizing congenital adrenal hyperplasia indicates relative androgen insensitivity during the first six months of life. Bonfig W; Schwarz HP Horm Res Paediatr; 2011; 75(4):264-8. PubMed ID: 21196707 [TBL] [Abstract][Full Text] [Related]
8. Obesity among children and adolescents with classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency. Völkl TM; Simm D; Beier C; Dörr HG Pediatrics; 2006 Jan; 117(1):e98-105. PubMed ID: 16396852 [TBL] [Abstract][Full Text] [Related]
9. [Identification of congenital adrenal hyperplasia by measurement of blood-spot 17-hydroxyprogesterone]. Sólyom J; Eckhardt G; Török D Orv Hetil; 2004 Oct; 145(40):2051-6. PubMed ID: 15559532 [TBL] [Abstract][Full Text] [Related]
10. Recent advances in the diagnosis and management of congenital adrenal hyperplasia due to 21-hydroxylase deficiency. Forest MG Hum Reprod Update; 2004; 10(6):469-85. PubMed ID: 15514016 [TBL] [Abstract][Full Text] [Related]
11. Longer term outcome in females with congenital adrenal hyperplasia (CAH): the Cardiff experience. Premawardhana LD; Hughes IA; Read GF; Scanlon MF Clin Endocrinol (Oxf); 1997 Mar; 46(3):327-32. PubMed ID: 9156043 [TBL] [Abstract][Full Text] [Related]
12. Treatment and disease effects on short-term growth and adult height in children and adolescents with 21-hydroxylase deficiency. Hauffa BP; Winter A; Stolecke H Klin Padiatr; 1997; 209(2):71-7. PubMed ID: 9113619 [TBL] [Abstract][Full Text] [Related]
13. Reduced final height outcome in congenital adrenal hyperplasia under prednisone treatment: deceleration of growth velocity during puberty. Bonfig W; Bechtold S; Schmidt H; Knorr D; Schwarz HP J Clin Endocrinol Metab; 2007 May; 92(5):1635-9. PubMed ID: 17299071 [TBL] [Abstract][Full Text] [Related]
14. Growth pattern during the first 36 months of life in congenital adrenal hyperplasia (21-hydroxylase deficiency). Gasparini N; Di Maio S; Salerno M; Argenziano A; Franzese A; Tenore A Horm Res; 1997; 47(1):17-22. PubMed ID: 9010713 [TBL] [Abstract][Full Text] [Related]
15. Near-final height in 82 Chinese patients with congenital adrenal hyperplasia due to classic 21-hydroxylase deficiency: a single-center study from China. Juan L; Huamei M; Zhe S; Yanhong L; Hongshan C; Qiuli C; Jun Z; Song G; Minlian D J Pediatr Endocrinol Metab; 2016 Jul; 29(7):841-8. PubMed ID: 27054598 [TBL] [Abstract][Full Text] [Related]
16. Adiponectin levels are high in children with classic congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency. Völkl TM; Simm D; Körner A; Kiess W; Kratzsch J; Dörr HG Acta Paediatr; 2009 May; 98(5):885-91. PubMed ID: 19236311 [TBL] [Abstract][Full Text] [Related]
17. Molecular testing in congenital adrenal hyperplasia due to 21α-hydroxylase deficiency in the era of newborn screening. Sarafoglou K; Lorentz CP; Otten N; Oetting WS; Grebe SK Clin Genet; 2012 Jul; 82(1):64-70. PubMed ID: 21534945 [TBL] [Abstract][Full Text] [Related]
18. The relation of peripubertal and pubertal growth to final adult height in children with classic congenital adrenal hyperplasia. Bomberg EM; Addo OY; Kyllo J; Gonzalez-Bolanos MT; Ltief AM; Pittock S; Himes JH; Miller BS; Sarafoglou K J Pediatr; 2015 Mar; 166(3):743-50. PubMed ID: 25557963 [TBL] [Abstract][Full Text] [Related]
19. Long-term follow-up of children with classic congenital adrenal hyperplasia: suggestions for age dependent treatment in childhood and puberty. Pijnenburg-Kleizen KJ; Thomas CMG; Otten BJ; Roeleveld N; Claahsen-van der Grinten HL J Pediatr Endocrinol Metab; 2019 Oct; 32(10):1055-1063. PubMed ID: 31573958 [TBL] [Abstract][Full Text] [Related]
20. Adult height of subjects with nonclassical 21-hydroxylase deficiency. Eyal O; Tenenbaum-Rakover Y; Shalitin S; Israel S; Weintrob N Acta Paediatr; 2013 Apr; 102(4):419-23. PubMed ID: 23298233 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]