Zobrazeno 1 - 10
of 44
pro vyhledávání: '"Oksana Hamidi"'
Autor:
Vivian A Fonseca, John B Buse, Julio Rosenstock, Richard E Pratley, Lawrence Blonde, Irina Bancos, Iulia Cristina Tudor, Ralph A DeFronzo, Richard J Auchus, Robert S Busch, James W Findling, Juan P Frias, Oksana Hamidi, Yehuda Handelsman, Andreas G Moraitis, Daniel Einhorn
Publikováno v:
BMJ Open, Vol 14, Iss 7 (2024)
Introduction Even with recent treatment advances, type 2 diabetes (T2D) remains poorly controlled for many patients, despite the best efforts to adhere to therapies and lifestyle modifications. Although estimates vary, studies indicate that in >10% o
Externí odkaz:
https://doaj.org/article/519af66c56274a5fb81b50cbc366808d
Autor:
Elise R. Venable, Sarah E. Kerr, M. Beatriz S. Lopes, Karra A. Jones, Andrew M. Bellizzi, Taofic Mounajjed, Aditya Raghunathan, Oksana Hamidi, Thorvardur R. Halfdanarson, Mabel Ryder, Rondell P. Graham
Publikováno v:
Diagnostic Pathology, Vol 15, Iss 1, Pp 1-7 (2020)
Abstract Background Pathologists frequently encounter neuroendocrine tumors (NETs) presenting as multiple liver masses in routine practice. Most often, these are well-differentiated tumors with characteristic histologic features. In contrast, pituita
Externí odkaz:
https://doaj.org/article/6763d164554d484295728dbca621424e
Autor:
Sasan Mirfakhraee MD, Maria Rodriguez BS, Niloofar Ganji BS, Richard J. Auchus MD, PhD, Oksana Hamidi DO
Publikováno v:
Journal of Investigative Medicine High Impact Case Reports, Vol 9 (2021)
Primary aldosteronism (PA) is the most common cause of secondary hypertension but remains largely undiagnosed. Chronic kidney disease (CKD) complicates the diagnosis of PA by affecting the biochemical screening evaluation and confirmatory testing, an
Externí odkaz:
https://doaj.org/article/014bde24a7dc4c3c8b122630ce13ce35
Autor:
Raffaele Rocco, Brittany L. Murphy, Vatsal P. Patel, Oksana Hamidi, Alice Y. Chang, Melanie L. Lyden
Publikováno v:
Human Pathology: Case Reports, Vol 19, Iss , Pp - (2020)
Paragangliomas (PGLs) originate from neuroendocrine cells of the autonomic paraganglia and are classically found in the neck and skull base region, chest cavity, abdomen, pelvis, and bladder. We report a rare case of a mesenteric PGL in a 65-year-old
Externí odkaz:
https://doaj.org/article/4931ba7a26794a498131ab4b4c1004c6
Autor:
Lindsay E. Carafone, Catherine D. Zhang, Dingfeng Li, Natalia Lazik, Oksana Hamidi, Maria Daniela Hurtado, William F. Young, Melinda A. Thomas, Benzon M. Dy, Melanie L. Lyden, Trenton R. Foster, Travis J. McKenzie, Irina Bancos
Publikováno v:
Biomedicines, Vol 9, Iss 7, p 741 (2021)
Autonomous cortisol secretion (ACS) affects up to 50% of patients with adrenal adenomas. Despite the limited evidence, clinical guidelines recommend measurement of serum concentrations of dehydroepiandrosterone-sulfate (DHEA-S) and corticotropin (ACT
Externí odkaz:
https://doaj.org/article/406c1d7121434e9d8add04cab196ef9e
Publikováno v:
International journal of surgical pathology.
Birt-Hogg-Dubé (BHD) syndrome is a rare autosomal dominant disorder caused by germline alterations in the FLCN gene. We report a 38-year-old man with BHD syndrome presenting with multiple rare pathologic findings involving various organs, including
Autor:
Gayane Tumyan, Oksana Hamidi, Alana Christie, Sasan Mifrakhraee, Michael Dohopolski, Sujana Gottumukkala, Raquibul Hannan
Publikováno v:
Journal of the Endocrine Society. 6:A126-A127
Introduction Adrenal metastases are the second most common neoplasms of the adrenal cortex. Adrenal insufficiency (AI) develops when more than 90% of the cortex is destroyed. In patients with adrenal metastases requiring local treatment, stereotactic
Publikováno v:
Journal of the Endocrine Society. 6:A105-A106
Cushing syndrome (CS) secondary to ectopic ACTH secretion (EAS) is rare and accounts for 10% of CS with majority being bronchial or gut neuroendocrine tumors (NETs) and squamous cell lung cancer. There are only a few case reports of EAS due to append
Autor:
Natia Murvelashvili, Patricio Polanco, Sarah Khorsand, Jorge Marrero, Liwei Jia, Sasan Mirfakhraee, Tobias Else, Mouhammed Habra, Suzanne Cole, Oksana Hamidi
Publikováno v:
Journal of the Endocrine Society. 6:A90-A91
Introduction Adrenocortical Carcinoma (ACC) is a rare and often aggressive malignancy arising from the adrenal cortex. Rarely, ACC can be associated with a paraneoplastic syndrome, such as tumor-associated hypoglycemia due to insulin-like growth fact
Autor:
Tobias Else, Mouhammed Habra, Oksana Hamidi, Gary D Hammer, Natia Murvelashvili, Jenae Osborne, Katherine Wolf
Publikováno v:
Journal of the Endocrine Society. 6:A134-A135
Adrenocortical carcinoma (ACC) can occur as part of hereditary cancer syndromes, particularly Lynch syndrome and Li-Fraumeni syndrome. Here we describe 5 patients (3 women) with adrenal tumors and Birt-Hogg-Dubé syndrome (BHDS). BHDS is a hereditary