Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Selma Witchel"'
Autor:
H.J. Teede, M. Gibson, J. Laven, A. Dokras, L.J. Moran, T. Piltonin, M. Costello, A. Mousa, A.E. Joham, C.T. Tay, Wiebke Arlt, Ricardo Azziz, Adam Balen, Lisa Bedson, Lorna Berry, Jacky Boivin, Jacqueline Boyle, Leah Brennan, Wendy Brown, Tania Burgert, Maureen Busby, Carolyn Ee, Rhonda M. Garad, Cheryce Harrison, Roger Hart, Marie Misso, Rachel Morman, Angelica Lindén Hirschberg, Tuong Ho, Kathleen Hoeger, Sonia Jitpiriyaroj, Cailin Jordan, Richard S. Legro, Rong Li, Marla Lujan, Ronald C. Ma, Darren Mansfield, Kate Marsh, Edgar Mocanu, Robert J. Norman, Sharon Oberfield, Dawn Kimberly Hopkins, Malika Patel, Alexia Peña, Leanne Redman, Luk Rombauts, Daniela Romualdi, Duru Shah, Poli Mara Spritzer, Elisabet Stener-Victorin, Fahimeh Ramezani Tehrani, Shakila Thangaratinam, Mala Thondan, Eszter Vanky, Bassel H. Al Wattar, Chandrika Wijeyaratne, Selma Witchel, Dongzi Yang, Bulent O. Yildiz
Publikováno v:
EClinicalMedicine, Vol 78, Iss , Pp 102927- (2024)
Summary: Background: Polycystic ovary syndrome (PCOS) is a common endocrinopathy with significant reproductive, metabolic, and psychological complications. Consensus on PCOS clinical research priorities across end-users is fundamental and necessitate
Externí odkaz:
https://doaj.org/article/1ec515db305646dabe59d1d617e97d5f
Publikováno v:
Diagnostics, Vol 12, Iss 8, p 1931 (2022)
Polycystic ovary syndrome (PCOS) is one of the most common endocrine conditions in women. PCOS may be more challenging to diagnose during adolescence due to an overlap with the physiological events of puberty, which are part of the diagnostic criteri
Externí odkaz:
https://doaj.org/article/56e5198d56104cebaa90c704a5d231e9
Autor:
Maria Forslund, Johanna Melin, Simon Alesi, Terhi Piltonen, Daniela Romualdi, Chau Thien Tay, Selma Witchel, Alexia Pena, Aya Mousa, Helena Teede
Publikováno v:
Clinical Endocrinology.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2ba9aef6eadd8117fc80046530615f6f
https://doi.org/10.1111/cen.14913
https://doi.org/10.1111/cen.14913
Publikováno v:
Journal of the Endocrine Society. 6:A611-A612
Objective GnRH agonists (GnRHa), used to prevent development of undesired secondary sex characteristics for gender diverse youth (GDY), may impede pubertal bone mineral accrual increasing the risk for osteopenia/osteoporosis during adulthood. Based o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::71a8a56e989411d719b02288a87917bd
https://doi.org/10.1210/jendso/bvac150.1269
https://doi.org/10.1210/jendso/bvac150.1269
Autor:
Angelina Bernier, Tania Burgert, Melanie Cree-Green, Vanessa Davis, David Geller, Emily Paprocki, Camila Pereira-Eshraghi, Rachana S Shah, Aviva Sopher, Laura Torchen, Selma Witchel, Angie Chen
Publikováno v:
Journal of the Endocrine Society. 6:A681-A681
Objective Adolescent polycystic ovary syndrome (PCOS) is a heterogenous clinical syndrome characterized by hyperandrogenism and irregular menses. Heterogeneous features of the syndrome include the presence/absence of obesity, degree of insulin resist
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b75bd4ffa16484455f19f4607586d615
https://doi.org/10.1210/jendso/bvac150.1407
https://doi.org/10.1210/jendso/bvac150.1407
Autor:
Caroline, Eozenou, Nitzan, Gonen, Maria Sol, Touzon, Anne, Jorgensen, Svetlana A, Yatsenko, Leila, Fusee, Alaa K, Kamel, Balazs, Gellen, Gabriela, Guercio, Priti, Singh, Selma, Witchel, Andrea J, Berman, Rana, Mainpal, Mehdi, Totonchi, Anahita, Mohseni Meybodi, Masomeh, Askari, Tiphanie, Merel-Chali, Joelle, Bignon-Topalovic, Roberta, Migale, Mariana, Costanzo, Roxana, Marino, Pablo, Ramirez, Natalia, Perez Garrido, Esperanza, Berensztein, Mona K, Mekkawy, John C, Schimenti, Rita, Bertalan, Inas, Mazen, Ken, McElreavey, Alicia, Belgorosky, Robin, Lovell-Badge, Aleksandar, Rajkovic, Anu, Bashamboo
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America
Significance Sex development involves a precise spatiotemporal expression and interactions of numerous genetic factors, including the WT1 (Wilms tumor 1) gene. Complete and partial loss-of-function WT1 variants are associated with 46,XY disorders/dif
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::494cb668f23b408c21730411a68e42f5
https://pubmed.ncbi.nlm.nih.gov/32493750
https://pubmed.ncbi.nlm.nih.gov/32493750
Autor:
Selma Witchel
Publikováno v:
Jornal de Pediatria (Versão em Português). 95:257-259
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9f19a340294a446159b31d6b91662a3f
https://doi.org/10.1016/j.jpedp.2018.08.001
https://doi.org/10.1016/j.jpedp.2018.08.001
Publikováno v:
Journal of Adolescent Health. 64:S46
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7005701d4a03a1ec4d73c3225a7178f8
https://doi.org/10.1016/j.jadohealth.2018.10.101
https://doi.org/10.1016/j.jadohealth.2018.10.101
Publikováno v:
Journal of Gay & Lesbian Mental Health. 10:57-75
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::55f5a8609b5f928b700a52c73085a0ef
https://doi.org/10.1080/19359705.2006.9962437
https://doi.org/10.1080/19359705.2006.9962437
