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For: White PC. Update on diagnosis and management of congenital adrenal hyperplasia due to 21-hydroxylase deficiency. Curr Opin Endocrinol Diabetes Obes 2018;25:178-84. [PMID: 29718004 DOI: 10.1097/MED.0000000000000402] [Cited by in Crossref: 16] [Cited by in F6Publishing: 6] [Article Influence: 5.3] [Reference Citation Analysis]
Number Citing Articles
1 Cheuiche AV, da Silveira LG, de Paula LCP, Lucena IRS, Silveiro SP. Diagnosis and management of precocious sexual maturation: an updated review. Eur J Pediatr 2021. [PMID: 33745030 DOI: 10.1007/s00431-021-04022-1] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
2 Hamed SA, Metwalley KA, Farghaly HS. Cognitive function in children with classic congenital adrenal hyperplasia. Eur J Pediatr 2018;177:1633-40. [PMID: 30088136 DOI: 10.1007/s00431-018-3226-7] [Cited by in Crossref: 11] [Cited by in F6Publishing: 8] [Article Influence: 2.8] [Reference Citation Analysis]
3 Elfekih H, Ben Abdelkrim A, Marzouk H, Saad G, Gasmi A, Gribaa M, Zaghouani H, Hasni Y, Maaroufi A. Prostatic tissue in 46XX congenital adrenal hyperplasia: Case report and literature review. Clin Case Rep 2021;9:1655-62. [PMID: 33768909 DOI: 10.1002/ccr3.3868] [Reference Citation Analysis]
4 Fouques C, Fatfouta I, Hieronimus S, Sadoul JL, Bongain A. Two cases of male patients followed for a classical form of congenital adrenal hyperplasia (CAH), presenting an azoospermia: analysis and review of the literature. Basic Clin Androl 2019;29:10. [PMID: 31143447 DOI: 10.1186/s12610-019-0084-8] [Reference Citation Analysis]
5 Mazzilli R, Stigliano A, Delfino M, Olana S, Zamponi V, Iorio C, Defeudis G, Cimadomo D, Toscano V, Mazzilli F. The High Prevalence of Testicular Adrenal Rest Tumors in Adult Men With Congenital Adrenal Hyperplasia Is Correlated With ACTH Levels. Front Endocrinol (Lausanne) 2019;10:335. [PMID: 31214118 DOI: 10.3389/fendo.2019.00335] [Cited by in Crossref: 10] [Cited by in F6Publishing: 6] [Article Influence: 3.3] [Reference Citation Analysis]
6 Kocova M, Anastasovska V, Falhammar H. Clinical outcomes and characteristics of P30L mutations in congenital adrenal hyperplasia due to 21-hydroxylase deficiency. Endocrine 2020;69:262-77. [PMID: 32367336 DOI: 10.1007/s12020-020-02323-3] [Cited by in Crossref: 5] [Cited by in F6Publishing: 3] [Article Influence: 2.5] [Reference Citation Analysis]
7 Held PK, Bialk ER, Lasarev MR, Allen DB. 21-Deoxycortisol is a Key Screening Marker for 21-Hydroxylase Deficiency. J Pediatr 2021:S0022-3476(21)01063-5. [PMID: 34780778 DOI: 10.1016/j.jpeds.2021.10.063] [Reference Citation Analysis]
8 Held PK, Bird IM, Heather NL. Newborn Screening for Congenital Adrenal Hyperplasia: Review of Factors Affecting Screening Accuracy. Int J Neonatal Screen 2020;6:67. [PMID: 33117906 DOI: 10.3390/ijns6030067] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 2.0] [Reference Citation Analysis]
9 Krysiak R, Kowalcze K, Marek B, Okopień B. Cardiometabolic risk factors in women with non-classic congenital adrenal hyperplasia. Acta Cardiol 2020;75:705-10. [PMID: 31538536 DOI: 10.1080/00015385.2019.1666964] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]