Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Hamsini Rao"'
Autor:
Vipula Kolli, Hannah Kim, Hamsini Rao, Qizong Lao, Alison Gaynor, Joshua D. Milner, Deborah P. Merke
Publikováno v:
BMC Research Notes, Vol 12, Iss 1, Pp 1-6 (2019)
Abstract Objective Approximately 10% of patients with congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency carry a mutation that disrupts CYP21A2 and the flanking TNXB gene resulting in CAH-X, a contiguous gene deletion syndrome. TNX
Externí odkaz:
https://doaj.org/article/5387be3a568f4f92b26cbdf007538642
Autor:
Ninet Sinaii, Ashwini Mallappa, Aikaterini A. Nella, Deborah P. Merke, Chia Ying Liu, Ashley F. Perritt, Steven J. Soldin, Alexander Ling, Parag Kumar, Hamsini Rao, Verena Gounden
Publikováno v:
Clinical Endocrinology. 89:399-407
Background In a phase 2 short-term (6 months) study of patients with congenital adrenal hyperplasia (CAH), continuous subcutaneous hydrocortisone infusion (CSHI) was found to be a safe, effective and well-tolerated method of replacing cortisol with i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ca6dbcf296c59fe4e34aca149569fc1e
https://doi.org/10.1111/cen.13813
https://doi.org/10.1111/cen.13813
Autor:
James A. Randall, Sonya Malekzadeh, Adnan S. Hussaini, Jessica H. Maxwell, Hamsini Rao, Jamie R. Litvack, Ajay S. Nathan, Sarah M. Dermody
Publikováno v:
American journal of surgery. 220(2)
A gender pay gap has been reported across many professions, including medicine.Surgeons employed at complex Veterans Affairs Medical Centers (VAMC) nationwide in 2016 were identified. Data on salary, gender, years since medical school graduation, pro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e767dac9a82722c057f2b07d55963831
https://pubmed.ncbi.nlm.nih.gov/32354602
https://pubmed.ncbi.nlm.nih.gov/32354602
Autor:
Ashwini Mallappa, Deborah P. Merke, Alexander Tsodikov, Meredith Elman, Hamsini Rao, Jamie Marko, Nilo A. Avila, Richard J. Auchus, Adina F. Turcu
Publikováno v:
The Journal of Clinical Endocrinology and Metabolism
Context: Patients with 21-hydroxylase deficiency (21OHD) have long-term complications, resulting from poor disease control and/or glucocorticoid overtreatment. Lack of optimal biomarkers has made it challenging to tailor therapy and predict long-term
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aa45a937a4fd90cf1fac6b9621c78308
https://pubmed.ncbi.nlm.nih.gov/28472487
https://pubmed.ncbi.nlm.nih.gov/28472487
Autor:
James A. Randall, Sonya Malekzadeh, Sarah M. Dermody, Jamie R. Litvack, Hamsini Rao, Adnan S. Hussaini, Jessica H. Maxwell, Ajay S. Nathan
Publikováno v:
Journal of the American College of Surgeons. 229:e29
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bf8a54050d42cbf1053723960079775b
https://doi.org/10.1016/j.jamcollsurg.2019.08.827
https://doi.org/10.1016/j.jamcollsurg.2019.08.827