Zobrazeno 1 - 10
of 21
pro vyhledávání: '"Özgür Mete"'
Autor:
Hande Turan, Gürkan Tarçın, Özgür Mete, Ada Bulut Sinoplu, Saadet Olcay Evliyaoğlu, Büge Öz, Oya Ercan
Publikováno v:
JCRPE, Vol 14, Iss 1, Pp 126-130 (2022)
Silent corticotroph tumors are composed of corticotroph cells, but do not manifest any biochemical or clinical evidence of hypercortisolism. A choristoma is a benign, congenital proliferation of histologically mature tissue elements normally not pres
Externí odkaz:
https://doaj.org/article/0f2dc468a88546eba3f2cdda78669d3a
Publikováno v:
Turkish Archives of Otorhinolaryngology, Vol 50, Iss 2, Pp 26-27 (2012)
Myxoma is a rare benign mesenchymal tumor, and occurs most commonly in the mandible and maxilla in the head and neck region. Myxoma of the larynx is extremely rare and is frequently misdiagnosed as a vocal polyp. We report a myxoma arising from the r
Externí odkaz:
https://doaj.org/article/045e7f4a050b4cd98cba8d656b0321cb
Publikováno v:
Türk Patoloji Dergisi, Vol 40, Iss 3, Pp 190-195 (2024)
Objective: The association between autoimmunity-related tissue injury and thyroid cancer development remains an area of interest. Evidence suggests that patients with Graves disease (GD) may have an elevated risk for differentiated thyroid cancer. Mu
Externí odkaz:
https://doaj.org/article/b7d4569fd9374830a331d0291306f128
Autor:
C. Christofer JUHLIN, Ozgur METE
Publikováno v:
Türk Patoloji Dergisi, Vol 40, Iss 3, Pp 143-148 (2024)
Pheochromocytoma and abdominal paraganglioma (PPGL) are rare catecholamine-producing, keratin-negative, non-epithelial neuroendocrine neoplasms characterized by a unique association with syndromic diseases caused by constitutional mutations in a wide
Externí odkaz:
https://doaj.org/article/177865bb7b814dfba17cc4cf06fbf6d2
Autor:
Shereen Ezzat, Jesse D. Pasternak, Murali Rajaraman, Omar Abdel-Rahman, Andrée Boucher, Nicole G. Chau, Shirley Chen, Sabrina Gill, Martin D. Hyrcza, Nathan Lamond, Marie-Hélène Massicotte, Eric Winquist, Ozgur Mete
Publikováno v:
Frontiers in Oncology, Vol 14 (2024)
Most follicular cell-derived differentiated thyroid carcinomas are regarded as low-risk neoplasms prompting conservative therapeutic management. Here, we provide consensus recommendations reached by a multidisciplinary group of endocrinologists, medi
Externí odkaz:
https://doaj.org/article/12b7c128e73d4d7994494caa12b0c5d4
Autor:
Leslie E. Oldfield, Jessica Grzybowski, Sylvie Grenier, Elizabeth Chao, Gregory S. Downs, Kirsten M. Farncombe, Tracy L. Stockley, Ozgur Mete, Raymond H. Kim
Publikováno v:
npj Genomic Medicine, Vol 7, Iss 1, Pp 1-5 (2022)
Abstract Von Hippel-Lindau disease (VHL) is an autosomal dominant, inherited syndrome with variants in the VHL gene causing predisposition to multi-organ benign and malignant neoplasms. A germline VHL variant is identified in 95–100% of individuals
Externí odkaz:
https://doaj.org/article/cdf9e2fa2df24b4ab8df4e80fa08a011
Autor:
Jelena Lukovic, Irina Petrovic, Zijin Liu, Susan M. Armstrong, James D. Brierley, Richard Tsang, Jesse D. Pasternak, Karen Gomez-Hernandez, Amy Liu, Sylvia L. Asa, Ozgur Mete
Publikováno v:
Frontiers in Endocrinology, Vol 12 (2021)
ObjectiveThe main objective of this study was to review the clinicopathologic characteristics and outcome of patients with oncocytic papillary thyroid carcinoma (PTC) and oncocytic poorly differentiated thyroid carcinoma (PDTC). The secondary objecti
Externí odkaz:
https://doaj.org/article/1c0d7cf23a2d4ddfa6bcd757e9b12a66
Autor:
Matthias Millesi, Carolyn Lai, Ruth Lau, Vincent Chen Ye, Kaiyun Yang, Matheus Leite, Nilesh Mohan, Ozgur Mete, Shereen Ezzat, Fred Gentili, Gelareh Zadeh, Aristotelis Kalyvas
Publikováno v:
Brain Sciences, Vol 12, Iss 11, p 1482 (2022)
Background: Rathke’s cleft cysts (RCC) arise from the pars intermedia because of incomplete regression of the embryologic Rathke pouch. A subset of RCC becomes symptomatic causing headaches, visual and endocrinological disturbances such that surgic
Externí odkaz:
https://doaj.org/article/f3da4e923dd94e5c85cf35f1bc16a98b
Autor:
Sylvia L. Asa, Ozgur Mete
Publikováno v:
Frontiers in Endocrinology, Vol 12 (2021)
Oncocytes are cells that have abundant eosinophilic cytoplasm due to the accumulation of mitochondria; they are also known as oxyphils. In the thyroid they have been called Hürthle cells but this is a misnomer, since Hürthle described C cells; for
Externí odkaz:
https://doaj.org/article/135b7ee6adb2463980489d9fed9fd7ae
Autor:
Amit Akirov, Vincent Larouche, Ilan Shimon, Sylvia L. Asa, Ozgur Mete, Anna M. Sawka, Fred Gentili, Shereen Ezzat
Publikováno v:
Frontiers in Endocrinology, Vol 12 (2021)
BackgroundGlucocorticoid excess in Cushing disease (CD) leads to negative feedback suppression, resulting in Crooke's hyaline change (CC) of nontumorous pituitary corticotrophs. We aimed to determine the predictive value of CC of nontumorous corticot
Externí odkaz:
https://doaj.org/article/9dc3a340ba1d45ad9d58980bc45bddbd