Zobrazeno 1 - 10
of 70
pro vyhledávání: '"Courtney, Finlayson"'
Autor:
Soojin Kim, Esther L. Finney, Ushasi Naha, Ilina Rosoklija, Kyle S. Honegger, Allison Goetsch Weisman, Jane L. Holl, Courtney Finlayson, Diane Chen, Emilie K. Johnson
Publikováno v:
Frontiers in Urology, Vol 3 (2023)
ObjectiveCell-free DNA (cfDNA) prenatal screening is a commercially available noninvasive test that detects fetal genetic material in maternal blood. While expectant parents often use it for “gender” determination, there is little information abo
Externí odkaz:
https://doaj.org/article/499d0cb9a2f94a3d804dbe3816783e7d
Autor:
Aisha L. Siebert, Veronica Gomez-Lobo, Emilie K. Johnson, Leena Nahata, Kyle E. Orwig, Louise C. Pyle, Selma F. Witchel, Courtney Finlayson, Monica M. Laronda
Publikováno v:
Frontiers in Endocrinology, Vol 13 (2023)
ObjectiveSome individuals with differences of sex development (DSD) conditions undergo medically indicated prophylactic gonadectomy. Gonads of individuals with DSD can contain germ cells and precursors and patients interested in future fertility pres
Externí odkaz:
https://doaj.org/article/c418e05e6c944e369b743d60169f254c
Autor:
Courtney Finlayson, Diane Chen, Jaclyn Lennon Papadakis, Emilie K. Johnson, Jonathan L. Poquiz
Publikováno v:
Clinical Practice in Pediatric Psychology. 10:241-250
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ab820915adb45c3a1264aa9fee2aa4ca
https://doi.org/10.1037/cpp0000409
https://doi.org/10.1037/cpp0000409
Autor:
Afiya Sajwani, Moira A. Kyweluk, Elisa J. Gordon, Emilie K. Johnson, Courtney Finlayson, Diane Chen
Publikováno v:
LGBTQ+ Family: An Interdisciplinary Journal. 18:386-402
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dec289edd4875990d742bc35de1b6df5
https://doi.org/10.1080/27703371.2022.2113947
https://doi.org/10.1080/27703371.2022.2113947
Publikováno v:
Seminars in Reproductive Medicine. 40:016-022
Primary amenorrhea may be a feature or a presenting sign of a difference of sex development, most often due to a congenital anatomic difference or hypergonadotropic hypogonadism. History and physical exam are very important, including whether any var
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dfaa20d142b2d0790f0ea9f6daa238ab
https://doi.org/10.1055/s-0042-1753551
https://doi.org/10.1055/s-0042-1753551
Autor:
Phyllis W. Speiser, Reeti Chawla, Ming Chen, Alicia Diaz-Thomas, Courtney Finlayson, Meilan M. Rutter, David E. Sandberg, Kim Shimy, Rashida Talib, Jane Cerise, Eric Vilain, Emmanuèle C. Délot
Publikováno v:
International Journal of Neonatal Screening, Vol 6, Iss 2, p 37 (2020)
Newborn screening for congenital adrenal hyperplasia (CAH) caused by 21-hydroxylase deficiency is mandated throughout the US. Filter paper blood specimens are assayed for 17-hydroxyprogesterone (17OHP). Prematurity, low birth weight, or critical illn
Externí odkaz:
https://doaj.org/article/c05350091ccc401a86323a0add4d4ff3
Autor:
DSD-TRN Endocrine & Genetics Working Groups, Courtney Finlayson, Catherine Keegan, Lauren Mohnach, Phyllis Speiser, Deepa Mathew, Meilan Rutter, Tara Schafer-Kalkhoff, Alicia Diaz-Thomas, J Whitehead
Publikováno v:
Journal of the Endocrine Society. 6:A617-A618
Objectives The 17β-hydroxysteroid dehydrogenase type 3 (17βHSD3) enzyme, expressed in the testes, converts androstenedione to testosterone. Deficiency of 17βHSD3 causes a 46,XY difference of sex development (DSD). Until recently, just 12 cases of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a62462a5f1a4739a0c169492034aa3b9
https://doi.org/10.1210/jendso/bvac150.1280
https://doi.org/10.1210/jendso/bvac150.1280
Autor:
J Whitehead, Josephine Hirsch, Ilina Rosoklija, Allison Goetsch Weisman, Jeffrey Dungan, Courtney Finlayson, Diane Chen, Emilie K. Johnson
Publikováno v:
Prenatal diagnosis. 42(10)
Prenatal diagnoses of differences of sex development (DSD) are increasing due to availability of cell-free DNA screening (cell-free DNA screening (cfDNA)). This study explores first-hand experiences of parents whose children had prenatal findings of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e2ee45315ea6603c6fc78a3e6f8085f0
https://pubmed.ncbi.nlm.nih.gov/35670269
https://pubmed.ncbi.nlm.nih.gov/35670269
Autor:
Emilie K. Johnson, Kristine S. Corkum, Earl Y. Cheng, Courtney Finlayson, Erin E. Rowell, Monica M. Laronda, Elizabeth B. Yerkes, Molly B. Reimann, Courtney J. Harris
Publikováno v:
Journal of Urology. 204:1054-1061
Many individuals with differences of sex development experience subfertility. We describe a novel gonadal tissue cryopreservation protocol for those individuals.Before 2018 patients with differences of sex development electing gonadal tissue cryopres
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b4355901370e05f3081c449c1bf157a5
https://doi.org/10.1097/ju.0000000000001128
https://doi.org/10.1097/ju.0000000000001128
Autor:
Paul F. Austin, Elizabeth B. Yerkes, Ilina Rosoklija, Lefkothea P. Karaviti, Deborah L. Jacobson, Anthony D'Oro, Sheila Gunn, Paul Kokorowski, Earl Y. Cheng, Hillary M. Kapa, Diane Chen, Duong Tu, Alyssa C. Messina, Courtney Finlayson, Mimi S. Kim, Leena Nahata, Thomas F. Kolon, Emilie K. Johnson
Publikováno v:
Journal of Urology. 204:835-842
The medical terminology applied to differences/disorders of sex development has been viewed negatively by some affected individuals. A clinical population of patients with differences/disorders of sex development and their caregivers were surveyed re
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2bed357ff03b07c833dcd9ec31fe0065
https://doi.org/10.1097/ju.0000000000001076
https://doi.org/10.1097/ju.0000000000001076