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Disorders of sex development (DSD): Clinical service delivery in the United States.
Rolston AM, Gardner M, van Leeuwen K, Mohnach L, Keegan C, Délot E, Vilain E, Sandberg DE; members of the DSD-TRN Advocacy; Advisory Network Accord Alliance. Rolston AM, et al. Among authors: sandberg de. Am J Med Genet C Semin Med Genet. 2017 Jun;175(2):268-278. doi: 10.1002/ajmg.c.31558. Epub 2017 May 30. Am J Med Genet C Semin Med Genet. 2017. PMID: 28557237 Free PMC article.
Defining successful outcomes and preferences for clinical management in differences/disorders of sex development: Protocol overview and a qualitative phenomenological study of stakeholders' perspectives.
Suorsa-Johnson KI, Gardner MD, Baskin A, Gruppen LD, Rose A, Rutter MM, Schafer-Kalkhoff T, Stacey D, van Leeuwen KD, Weidler EM, Sandberg DE. Suorsa-Johnson KI, et al. Among authors: sandberg de. J Pediatr Urol. 2022 Feb;18(1):36.e1-36.e17. doi: 10.1016/j.jpurol.2021.10.020. Epub 2021 Oct 30. J Pediatr Urol. 2022. PMID: 34876378 Free PMC article.
Psychosocial Screening in Disorders/Differences of Sex Development: Psychometric Evaluation of the Psychosocial Assessment Tool.
Ernst MM, Gardner M, Mara CA, Délot EC, Fechner PY, Fox M, Rutter MM, Speiser PW, Vilain E, Weidler EM, Sandberg DE; The DSD-Translational Research Network Leadership Group and Psychosocial Workgroup. Ernst MM, et al. Among authors: sandberg de. Horm Res Paediatr. 2018;90(6):368-380. doi: 10.1159/000496114. Epub 2019 Feb 15. Horm Res Paediatr. 2018. PMID: 30783028 Free PMC article.
Creation of an Electronic Resource Repository for Differences of Sex Development (DSD): Collaboration Between Advocates and Clinicians in the DSD-Translational Research Network.
Rutter MM, Muscarella M, Green J, Indig G, von Klan A, Kennedy K, Weidler EM, Barrett M, Sandberg DE; DSD-Translational Research Network. Rutter MM, et al. Among authors: sandberg de. Sex Dev. 2022;16(4):227-235. doi: 10.1159/000524629. Epub 2022 May 30. Sex Dev. 2022. PMID: 35636406 Free PMC article.
Unexpected ethical dilemmas in sex assignment in 46,XY DSD due to 5-alpha reductase type 2 deficiency.
Byers HM, Mohnach LH, Fechner PY, Chen M, Thomas IH, Ramsdell LA, Shnorhavorian M, McCauley EA, Amies Oelschlager AE, Park JM, Sandberg DE, Adam MP, Keegan CE. Byers HM, et al. Among authors: sandberg de. Am J Med Genet C Semin Med Genet. 2017 Jun;175(2):260-267. doi: 10.1002/ajmg.c.31560. Epub 2017 May 25. Am J Med Genet C Semin Med Genet. 2017. PMID: 28544750 Free PMC article.
120 results