Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Natalie Nokoff"'
Autor:
Matthew S. Minturn, Erica I. Martinez, Thien Le, Natalie Nokoff, Louis Fitch, Carley E. Little, Rita S. Lee
Publikováno v:
MedEdPORTAL, Vol 17 (2021)
Introduction Individuals who identify as lesbian, gay, bisexual, transgender, or queer (LGBTQ) face significant health disparities and barriers to accessing care. Patients have reported provider lack of knowledge as one of the key barriers to cultura
Externí odkaz:
https://doaj.org/article/fac96d1e399a455fb2c5ed21202561b7
Autor:
David Harrison, Francisco Prada, Natalie Nokoff, Sean Iwamoto, Tony Pastor, Elizabeth Yeung, Roni M. Jacobsen
Publikováno v:
Journal of the American College of Cardiology. 81:1597
Autor:
Danielle M Kline, Sean J Iwamoto, Lindsey Warner, Micol S Rothman, Danielle Loeb, Lisa M Schilling, Mary P Mancuso, Natalie Nokoff
Publikováno v:
Journal of the Endocrine Society. 6:A705-A706
Background There is a growing awareness surrounding gender diversity and the critical need for more robust research and evidence to guide gender-affirming healthcare, including gender-affirming hormone therapy (GAHT). Research priorities are often de
Publikováno v:
Journal of the Endocrine Society. 6:A192-A193
Background 2% of youth identify as transgender. Many have puberty blocked with gonadotropin-releasing hormone analogues (GnRHa), followed by testosterone (T) or estradiol (E2). Bone mineral density (BMD) effects of these therapies are understudied. O
Autor:
Anna Valentine, Shanlee Davis, Anna Furniss, Nadia Dowshen, Anne E Kazak, Christopher Lewis, Danielle F Loeb, Leena Nahata, Laura Pyle, Lisa M Schilling, Gina M Sequeira, Natalie Nokoff
Publikováno v:
The Journal of clinical endocrinology and metabolism. 107(10)
Context Studies on cardiometabolic health in transgender and gender-diverse youth (TGDY) are limited to small cohorts. Objective This work aimed to determine the odds of cardiometabolic-related diagnoses in TGDY compared to matched controls in a cros
Autor:
Richard Auchus, Jean Chan, Robert Farber, Patricia Fechner, Nagdeep Giri, Natalie Nokoff, Eiry Roberts, Kyriakie Sarafoglou, Julia Sturgeon, Maria Vogiatzi, Ron Newfield
Publikováno v:
Journal of the Endocrine Society. 6:A618-A618
Introduction Classic congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency (21OHD) is a rare autosomal recessive disease characterized by deficiency of cortisol and oftentimes aldosterone, with elevated adrenocorticotropic hormone (AC
Publikováno v:
Journal of the Endocrine Society. 6:A593-A593
Background About 2% of youth in the United States identify as transgender, meaning their gender identity differs from sex at birth. The Endocrine Society recommends gonadotropin-releasing hormone agonist (GnRHa) therapy for eligible individuals start
Autor:
Rachel L. Sewell, Marissa Nunes-Moreno, Abby Simon, null LCSW, Syd Staggs, Brittan Sutphin, Daniel Reirden, Natalie Nokoff
Publikováno v:
Pediatrics. 146:305-306