BPG is committed to discovery and dissemination of knowledge
Cited by in F6Publishing
For: Wisniewski AB, Batista RL, Costa EMF, Finlayson C, Sircili MHP, Dénes FT, Domenice S, Mendonca BB. Management of 46,XY Differences/Disorders of Sex Development (DSD) Throughout Life. Endocr Rev 2019;40:1547-72. [PMID: 31365064 DOI: 10.1210/er.2019-00049] [Cited by in Crossref: 16] [Cited by in F6Publishing: 11] [Article Influence: 8.0] [Reference Citation Analysis]
Number Citing Articles
1 Concepción-Zavaleta MJ, García-Villasante EJ, Zavaleta-Gutiérrez FE, Barrantes Ticlla JL, Massucco Revoredo FG. Late Diagnosis of Partial Androgen Insensitivity Syndrome in a Peruvian Child. Cureus 2021;13:e16565. [PMID: 34430167 DOI: 10.7759/cureus.16565] [Reference Citation Analysis]
2 Batista RL, Mendonca BB. Integrative and Analytical Review of the 5-Alpha-Reductase Type 2 Deficiency Worldwide. Appl Clin Genet 2020;13:83-96. [PMID: 32346305 DOI: 10.2147/TACG.S198178] [Cited by in Crossref: 6] [Cited by in F6Publishing: 2] [Article Influence: 3.0] [Reference Citation Analysis]
3 Estermann MA, Smith CA. Applying Single-Cell Analysis to Gonadogenesis and DSDs (Disorders/Differences of Sex Development). Int J Mol Sci 2020;21:E6614. [PMID: 32927658 DOI: 10.3390/ijms21186614] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 2.0] [Reference Citation Analysis]
4 Lee PA, Fuqua JS, Houk CP, Kogan BA, Mazur T, Caldamone A. Individualized care for patients with intersex (disorders/differences of sex development): part I. Journal of Pediatric Urology 2020;16:230-7. [DOI: 10.1016/j.jpurol.2020.02.013] [Cited by in Crossref: 6] [Cited by in F6Publishing: 4] [Article Influence: 3.0] [Reference Citation Analysis]
5 Malliou-becher M, Vogt PH, Capp E, Frank-herrmann P. Varianten der Geschlechtsentwicklung in der Frauenheilkunde. Gynäkologische Endokrinologie 2021;19:2-10. [DOI: 10.1007/s10304-020-00358-3] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
6 Grinspon RP, Bergadá I, Rey RA. Male Hypogonadism and Disorders of Sex Development. Front Endocrinol (Lausanne) 2020;11:211. [PMID: 32351452 DOI: 10.3389/fendo.2020.00211] [Cited by in Crossref: 4] [Cited by in F6Publishing: 3] [Article Influence: 2.0] [Reference Citation Analysis]
7 Shoureshi PS, Rajasegaran A, Kokorowski P, Sparks SS, Seideman CA. Social media engagement, perpetuating selected information, and accuracy regarding CA SB-201: Treatment or intervention on the sex characteristics of a minor. J Pediatr Urol 2021;17:372-7. [PMID: 33663998 DOI: 10.1016/j.jpurol.2021.01.047] [Reference Citation Analysis]
8 Thirumalai A, Anawalt BD. Epidemiology of Male Hypogonadism. Endocrinology and Metabolism Clinics of North America 2022. [DOI: 10.1016/j.ecl.2021.11.016] [Reference Citation Analysis]
9 Chen H, Chen Q, Zhu Y, Yuan K, Li H, Zhang B, Jia Z, Zhou H, Fan M, Qiu Y, Zhuang Q, Lei Z, Li M, Huang W, Liang L, Yan Q, Wang C. MAP3K1 Variant Causes Hyperactivation of Wnt4/β-Catenin/FOXL2 Signaling Contributing to 46,XY Disorders/Differences of Sex Development. Front Genet 2022;13:736988. [DOI: 10.3389/fgene.2022.736988] [Reference Citation Analysis]
10 Montenegro LR, Lerário AM, Nishi MY, Jorge AAL, Mendonca BB. Performance of mutation pathogenicity prediction tools on missense variants associated with 46,XY differences of sex development. Clinics (Sao Paulo) 2021;76:e2052. [PMID: 33503178 DOI: 10.6061/clinics/2021/e2052] [Reference Citation Analysis]
11 Le PTQ, Le TNU, Nguyen TTB, Nguyen MT, Ha TMT, Kita T. An Extremely Rare SRD5A2 Gene c.485A>C Mutation in a Compound Heterozygous Newborn with Disorders of Sex Development First Identified in Vietnam. Case Reports in Endocrinology 2022;2022:1-5. [DOI: 10.1155/2022/6025916] [Reference Citation Analysis]
12 Batista RL, Craveiro FL, Ramos RM, Mendonca BB. Mild androgen insensitivity syndrome: the current landscape. Endocr Pract 2022:S1530-891X(22)00519-5. [PMID: 35660466 DOI: 10.1016/j.eprac.2022.05.009] [Reference Citation Analysis]
13 Rey RA. Recent advancement in the treatment of boys and adolescents with hypogonadism. Ther Adv Endocrinol Metab 2022;13:20420188211065660. [PMID: 35035874 DOI: 10.1177/20420188211065660] [Reference Citation Analysis]
14 Lucas-Herald AK, Rodie ME, Ahmed SF. Update on the management of a newborn with a suspected difference of sex development. Arch Dis Child 2021:archdischild-2020-320872. [PMID: 34772663 DOI: 10.1136/archdischild-2020-320872] [Reference Citation Analysis]
15 Bailez MM, Costanzo M, Guercio G. Role of minimally invasive surgery (MIS) in different sexual development (DSD). Semin Pediatr Surg 2021;30:151078. [PMID: 34412885 DOI: 10.1016/j.sempedsurg.2021.151078] [Reference Citation Analysis]
16 Bever YV, Brüggenwirth HT, Wolffenbuttel KP, Dessens AB, Groenenberg IAL, Knapen MFCM, De Baere E, Cools M, van Ravenswaaij-Arts CMA, Sikkema-Raddatz B, Claahsen-van der Grinten H, Kempers M, Rinne T, Hersmus R, Looijenga L, Hannema SE. Under-reported aspects of diagnosis and treatment addressed in the Dutch-Flemish guideline for comprehensive diagnostics in disorders/differences of sex development. J Med Genet 2020;57:581-9. [PMID: 32303604 DOI: 10.1136/jmedgenet-2019-106354] [Cited by in Crossref: 1] [Article Influence: 0.5] [Reference Citation Analysis]
17 Rey RA, Grinspon RP. Androgen Treatment in Adolescent Males With Hypogonadism. Am J Mens Health 2020;14:1557988320922443. [PMID: 32448030 DOI: 10.1177/1557988320922443] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 3.0] [Reference Citation Analysis]
18 Bertelloni S, Tyutyusheva N, Valiani M, D'Alberton F, Baldinotti F, Caligo MA, Baroncelli GI, Peroni DG. Disorders/Differences of Sex Development Presenting in the Newborn With 46,XY Karyotype. Front Pediatr 2021;9:627281. [PMID: 33968844 DOI: 10.3389/fped.2021.627281] [Reference Citation Analysis]