Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Sakshi Jhawar"'
Autor:
Sakshi Jhawar, Rahul Lakhotia, Mari Suzuki, James Welch, Sunita K Agarwal, John Sharretts, Maria Merino, Mark Ahlman, Jenny E Blau, William F Simonds, Jaydira Del Rivero
Publikováno v:
Endocrinology, Diabetes & Metabolism Case Reports, Vol 1, Iss 1, Pp 1-7 (2019)
Externí odkaz:
https://doaj.org/article/256a85b25ba84b84963ad8250aa3054b
Autor:
Jovan Milosavljevic, Navya Reddy Perkit, Sakshi Jhawar, Melbin Thomas, Justin Ling, Samuel Amankwah, Asha Mary Thomas
Publikováno v:
Journal of Community Hospital Internal Medicine Perspectives. 12:27-34
Autor:
Cristiane J Gomes-Lima, Sanjita Chittimoju, Leen Wehbeh, Sunita Dia, Prathyusha Pagadala, Mohammad Al-Jundi, Sakshi Jhawar, Eshetu Tefera, Mihriye Mete, Joanna Klubo-Gwiezdzinska, Douglas Van Nostrand, Jacqueline Jonklaas, Leonard Wartofsky, Kenneth D Burman
Publikováno v:
Journal of the Endocrine Society. 7
Autor:
Cristiane J Gomes-Lima, Sanjita Chittimoju, Leen Wehbeh, Sunita Dia, Prathyusha Pagadala, Mohammad Al-Jundi, Sakshi Jhawar, Eshetu Tefera, Mihriye Mete, Joanna Klubo-Gwiezdzinska, Douglas Van Nostrand, Jacqueline Jonklaas, Leonard Wartofsky, Kenneth D Burman
Publikováno v:
Journal of the Endocrine Society. 6
Context Recombinant human thyrotropin (rhTSH) is currently not Food and Drug Administration approved for the treatment of high-risk patients with differentiated thyroid cancer (DTC). Objective The goal of our study was to compare the outcomes in high
Autor:
Sakshi Jhawar, Yasuhiro Arakawa, Suresh Kumar, Diana Varghese, Yoo Sun Kim, Nitin Roper, Fathi Elloumi, Yves Pommier, Karel Pacak, Jaydira Del Rivero
Publikováno v:
Cancers, Vol 14, Iss 594, p 594 (2022)
Pheochromocytomas (PHEOs) and paragangliomas (PGLs) are rare neuroendocrine tumors that arise from chromaffin cells. PHEOs arise from the adrenal medulla, whereas PGLs arise from the neural crest localized outside the adrenal gland. Approximately 40%
Autor:
Cristiane J, Gomes-Lima, Sanjita, Chittimoju, Leen, Wehbeh, Sunita, Dia, Prathyusha, Pagadala, Mohammad, Al-Jundi, Sakshi, Jhawar, Eshetu, Tefera, Mihriye, Mete, Joanna, Klubo-Gwiezdzinska, Douglas, Van Nostrand, Jacqueline, Jonklaas, Leonard, Wartofsky, Kenneth D, Burman
Publikováno v:
Journal of the Endocrine Society. 6(5)
Recombinant human thyrotropin (rhTSH) is currently not Food and Drug Administration approved for the treatment of high-risk patients with differentiated thyroid cancer (DTC).The goal of our study was to compare the outcomes in higher-risk patients wi
Autor:
James Welch, Jaydira Del Rivero, Sakshi Jhawar, Mark A. Ahlman, William F. Simonds, Jenny E Blau, Rahul Lakhotia, John Sharretts, Sunita K. Agarwal, Mari Suzuki, Maria J. Merino
Publikováno v:
Endocrinology, Diabetes & Metabolism Case Reports
Endocrinology, Diabetes & Metabolism Case Reports, Vol 1, Iss 1, Pp 1-7 (2019)
Endocrinology, Diabetes & Metabolism Case Reports, Vol 1, Iss 1, Pp 1-7 (2019)
Multiple endocrine neoplasia type 1 (MEN1) is an autosomal dominant condition characterized by parathyroid, anterior pituitary and enteropancreatic endocrine cell tumors. Neuroendocrine tumors occur in approximately in 5–15% of MEN1 patients. Very
SAT-LB059 NET or NOT: Physiological Uptake in Pancreatic Head on Somatostatin Receptor Based Imaging
Publikováno v:
Journal of the Endocrine Society
Introduction Neuroendocrine tumors (NETs) are neoplasms that can arise from the neuroendocrine cells distributed widely throughout the body. Majority of NETs overexpress somatostatin receptors (SSTR) on their cell surface. This biologic characteristi
Autor:
Sakshi Jhawar, Jenny E Blau, William F. Simonds, James Welch, Maria J. Merino, Sunita K. Agarwal, Jaydira Del Rivero, Mari Suzuki, Ahlman Mark, John Sharretts, Rahul Lakhotia
Publikováno v:
Journal of the Endocrine Society
Introduction MEN1 is an autosomal dominant condition characterized by parathyroid, anterior pituitary and enteropancreatic endocrine cell tumors. Carcinoids occur in 5-15% patients, majority of which are of foregut origin (thymus, bronchus, stomach a
Autor:
Rahul Lakhotia, Corina Millo, Ashkan A. Malayeri, Jaydira Del Rivero, Mark A. Ahlman, Sakshi Jhawar
Publikováno v:
Medicine. 99:e20197
RATIONALE Neuroendocrine tumors (NETs) are neoplasms that can arise from the neuroendocrine cells distributed widely throughout the body. Majority of NETs overexpress somatostatin receptors (SSTR) on their cell surface. This biologic characteristic i