Zobrazeno 1 - 10
of 24
pro vyhledávání: '"Maja, Marinkovic"'
Publikováno v:
Transgender health, vol 8, iss 3
PurposeHistrelin implant (HI) is a gonadotropin-releasing hormone agonist (GnRHa) used in pediatrics to treat central precocious puberty (CPP) and for pubertal suppression in transgender/non-binary (TG/NB) youth with gender dysphoria. HI is designed
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c00e0f835924bb94e145b7f44cb4e27d
https://escholarship.org/uc/item/01n401mq
https://escholarship.org/uc/item/01n401mq
Publikováno v:
Transgender Health
Purpose: To describe our Center's 8-year experience with subcutaneous testosterone (SC-T) as gender-affirming hormone therapy (GAHT) in transmasculine and gender-diverse (TM/GD) youth. Methods: An Institutional Review Board (IRB)-approved retrospecti
Autor:
David Inwards-Breland, Debra Yeh, T Richardson, Maja Marinkovic, Bixby Marino-Kibbee, Kay Rhee
Publikováno v:
Journal of the Endocrine Society. 6:A635-A636
Background Multi-disciplinary gender-affirming care centers (GACC) are seeing increasing numbers of transgender and non-binary (TNB) youth seeking medical care. In the wake of the COVID pandemic, telemedicine use in clinical settings, including GACC,
Publikováno v:
Journal of the Endocrine Society. 6:A621-A621
While evidence supports the need for increased provider education on gender-affirming care, few medical curricula address the healthcare needs of transgender and non-binary (TGNB) patients. To bridge this knowledge gap, we developed an online learnin
Autor:
Erin Fisher, Lauren Gist, David Inwards-Breland, Maja Marinkovic, Bixby Marino-Kibbee, Aarti Patel, Kay Rhee, Tay Richardson, Debra Yeh
Publikováno v:
Journal of the Endocrine Society. 6:A612-A612
Background Studies have shown transgender and non-binary individuals encounter discrimination and harassment in medical settings leading to delays in seeking care and worse physical and mental health outcomes. Organizations, including the American Ac
Autor:
Bethany Gottesman, Maja Marinkovic
Publikováno v:
Journal of the Endocrine Society
Background: Aromatase deficiency (AD) is a rare autosomal recessive genetic disorder caused by loss of function mutation in CYP19A1 leading to normal androgen but low estrogen levels. As a result men with this condition have increased linear bone gro
Autor:
Jeremi M. Carswell, Diane Chen, Erica Eugster, Joel E. Frader, Anisha Gohil, Rebecca M. Harris, Marco A. Hidalgo, Janet Y. Lee, Maja Marinkovic, Leena Nahata, Liat Perl, Stephanie A. Roberts, Stephen M. Rosenthal, Loren S. Schechter, Rebecca B. Schechter, Daniel Evan Shumer, Lisa Simons, Norman Spack, Dennis M. Styne, Amy C. Tishelman, Anna Valentine, J. Whitehead
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5c16de88595282b1b4ee59f27bfc1935
https://doi.org/10.1016/b978-0-323-56963-7.01002-4
https://doi.org/10.1016/b978-0-323-56963-7.01002-4
Publikováno v:
Pubertal Suppression in Transgender Youth
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8fa5247e3d0d8e848b46c9f1426c1fbf
https://doi.org/10.1016/b978-0-323-56963-7.00012-0
https://doi.org/10.1016/b978-0-323-56963-7.00012-0
Publikováno v:
Journal of the Endocrine Society
Introduction: Aromatase deficiency (AD), an exceedingly rare autosomal recessive condition, causes virilization in females and tall stature with metabolic derangements in males. Clinical manifestations result from decreased estrogen production and an