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For: Miller WL. MECHANISMS IN ENDOCRINOLOGY: Rare defects in adrenal steroidogenesis. European Journal of Endocrinology 2018;179:R125-41. [DOI: 10.1530/eje-18-0279] [Cited by in Crossref: 31] [Cited by in F6Publishing: 11] [Article Influence: 7.8] [Reference Citation Analysis]
Number Citing Articles
1 Raygorodskaya NY, Novikova EP, Tyulpakov AN, Kareva MA, Nikolaeva NA, Bolotova NV. [Congenital adrenal hyperplasia due to 11β-hydroxylase deficiency: late diagnosis and gender reassignment in a two-year-old child]. Probl Endokrinol (Mosk) 2021;67:53-7. [PMID: 34766491 DOI: 10.14341/probl12749] [Reference Citation Analysis]
2 Arriba M, Ezquieta B. Molecular Diagnosis of Steroid 21-Hydroxylase Deficiency: A Practical Approach. Front Endocrinol 2022;13:834549. [DOI: 10.3389/fendo.2022.834549] [Reference Citation Analysis]
3 Aherrahrou R, Kulle AE, Alenina N, Werner R, Vens-Cappell S, Bader M, Schunkert H, Erdmann J, Aherrahrou Z. CYP17A1 deficient XY mice display susceptibility to atherosclerosis, altered lipidomic profile and atypical sex development. Sci Rep 2020;10:8792. [PMID: 32472014 DOI: 10.1038/s41598-020-65601-0] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 1.5] [Reference Citation Analysis]
4 Liu Y, Zheng J, Liu N, Xu X, Zhang X, Zhang Y, Li G, Liu G, Cai C, Shu J. The spectrum of CYP21A2 gene mutations in patients with classic salt wasting form of 2l-hydroxylase deficiency in a Chinese cohort. Mol Genet Genomic Med 2020;8:e1501. [PMID: 32959514 DOI: 10.1002/mgg3.1501] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 0.5] [Reference Citation Analysis]
5 Grinspon RP, Castro S, Rey RA. Up-to-Date Clinical and Biochemical Workup of the Child and the Adolescent with a Suspected Disorder of Sex Development. Horm Res Paediatr 2021;:1-12. [PMID: 34781296 DOI: 10.1159/000519895] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
6 Lee HI, Kwon A, Suh JH, Choi HS, Song KC, Chae HW, Kim HS. Two cases of 17α-hydroxylase/17,20-lyase deficiency caused by the CYP17A1 mutation. Ann Pediatr Endocrinol Metab 2021;26:66-70. [PMID: 33819959 DOI: 10.6065/apem.2040184.092] [Reference Citation Analysis]
7 Heintze T, Wilhelm D, Schmidlin T, Hofmann U, Zanger UM, Schwab M, Klein K. Effects of Diminished NADPH:cytochrome P450 Reductase in Human Hepatocytes on Lipid and Bile Acid Homeostasis. Front Pharmacol 2021;12:769703. [PMID: 34867397 DOI: 10.3389/fphar.2021.769703] [Reference Citation Analysis]
8 Pan P, Zheng L, Chen X, Huang J, Yang D, Li Y. Successful live birth in a Chinese woman with P450 oxidoreductase deficiency through frozen-thawed embryo transfer: a case report with review of the literature. J Ovarian Res 2021;14:22. [PMID: 33526062 DOI: 10.1186/s13048-021-00778-0] [Reference Citation Analysis]
9 Hathi D, Goswami S, Sengupta N, Acharya S, Kumar S, Talwar D. Myriad Manifestations of 3-Beta-Hydroxysteroid Dehydrogenase 2 Deficiency—A Tale of Two Infants. Cureus. [DOI: 10.7759/cureus.21779] [Reference Citation Analysis]
10 Josso N, Rey RA. What Does AMH Tell Us in Pediatric Disorders of Sex Development? Front Endocrinol (Lausanne) 2020;11:619. [PMID: 33013698 DOI: 10.3389/fendo.2020.00619] [Cited by in Crossref: 2] [Cited by in F6Publishing: 3] [Article Influence: 1.0] [Reference Citation Analysis]
11 Jha S, Turcu AF. Nonclassic Congenital Adrenal Hyperplasia: What Do Endocrinologists Need to Know? Endocrinol Metab Clin North Am 2021;50:151-65. [PMID: 33518183 DOI: 10.1016/j.ecl.2020.10.008] [Reference Citation Analysis]
12 Lee BR, Strobel KM, Chu A. The Neonate with Ambiguous Genitalia. Neoreviews 2021;22:e241-9. [PMID: 33795399 DOI: 10.1542/neo.22-4-e241] [Reference Citation Analysis]
13 Al Alawi AM, Nordenström A, Falhammar H. Clinical perspectives in congenital adrenal hyperplasia due to 3β-hydroxysteroid dehydrogenase type 2 deficiency. Endocrine 2019;63:407-21. [PMID: 30719691 DOI: 10.1007/s12020-018-01835-3] [Cited by in Crossref: 25] [Cited by in F6Publishing: 19] [Article Influence: 8.3] [Reference Citation Analysis]
14 Baronio F, Ortolano R, Menabò S, Cassio A, Baldazzi L, Di Natale V, Tonti G, Vestrucci B, Balsamo A. 46,XX DSD due to Androgen Excess in Monogenic Disorders of Steroidogenesis: Genetic, Biochemical, and Clinical Features. Int J Mol Sci 2019;20:E4605. [PMID: 31533357 DOI: 10.3390/ijms20184605] [Cited by in Crossref: 11] [Cited by in F6Publishing: 7] [Article Influence: 3.7] [Reference Citation Analysis]
15 Balsamo A, Baronio F, Ortolano R, Menabo S, Baldazzi L, Di Natale V, Vissani S, Cassio A. Congenital Adrenal Hyperplasias Presenting in the Newborn and Young Infant. Front Pediatr 2020;8:593315. [PMID: 33415088 DOI: 10.3389/fped.2020.593315] [Reference Citation Analysis]
16 Nan MN, Roig R, Martínez S, Rives J, Urgell E, Espinós JJ, Tirado M, Carreras G, Aulinas A, Webb SM, Corcoy R, Blanco-Vaca F, Tondo M. Comprehensive Genetic Testing of CYP21A2: A Retrospective Analysis in Patients with Suspected Congenital Adrenal Hyperplasia. J Clin Med 2021;10:1183. [PMID: 33809035 DOI: 10.3390/jcm10061183] [Reference Citation Analysis]
17 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]
18 Huneif MA, Al Mutairi M, AlHazmy ZH, AlOsaimi FK, AlShoomi AM, AlGhofely MA, AlSaheel A. Screening for testicular adrenal rest tumors among children with congenital adrenal hyperplasia at King Fahad Medical City, Saudi Arabia. J Pediatr Endocrinol Metab 2021. [PMID: 34757702 DOI: 10.1515/jpem-2021-0291] [Reference Citation Analysis]