Results 81 to 90 of about 3,490 (181)

Genetics of multiple endocrine neoplasia type 1 syndrome: what's new and what's old [version 1; referees: 3 approved]

F1000Research, 2017
Despite its identification in 1997, the functions of the MEN1 gene—the main gene underlying multiple endocrine neoplasia type 1 syndrome—are not yet fully understood.
Alberto Falchetti
doaj   +1 more source

Sporadic medullary thyroid carcinoma: clinical data from a university hospital

Clinics, 2009
INTRODUCTION: Medullary thyroid carcinoma may occur in a sporadic (s-medullary thyroid carcinoma, 75%) or in a multiple endocrine neoplasia type 2 form (MEN2, 25%).
Joya Emilie M. Correia-Deur, Rodrigo A. Toledo, Alice T. Imazawa, Delmar M. Lourenço Jr., Marilza C. L. Ezabella, Marcos R. Tavares, Sergio P. A. Toledo   +6 more
doaj   +1 more source

Critically evaluated key points on hereditary medullary thyroid carcinoma

Frontiers in Endocrinology
Medullary thyroid carcinoma (MTC) accounts for only 3% of all thyroid carcinomas: 75% as sporadic MTC (sMTC) and 25% as hereditary MTC (hMTC) in the context of multiple endocrine neoplasia type 2 (MEN2).
Daqi Zhang, Nan Liang, Hui Sun, Francesco Frattini, Chengqiu Sui, Mingyu Yang, Hongbo Wang, Gianlorenzo Dionigi, Gianlorenzo Dionigi   +8 more
doaj   +1 more source

Multiple Oral and Eyelid Nodules in a Pediatric Patient

Oral Diseases, Volume 32, Issue 7, Page 1739-1741, July 2026.
Caique Mariano Pedroso, Paulo Victor Mendes Penafort, Patrícia Vitor de Souza, Fernanda M. Pascon, Regina Maria Punppin‐Rontani, Beatriz Frolini Paulo Cherve, Rachel Marinho Robim, Regina Maria Holanda de Mendonça, Marcio Ajudarte Lopes, Pablo Agustin Vargas, Alan Roger Santos‐Silva   +10 more
wiley   +1 more source

Chasing the ubiquitous RET proto-oncogene in South African MEN2 families - Implications for the surgeon [PDF]

, 2010
CITATION: Moore, S. W. & Zaahl, M. G. 2010. Chasing the ubiquitous RET proto-oncogene in South African MEN2 families - Implications for the surgeon. South African Journal of Surgery, 48(4):127-131.The original publication is available at http://sajs ...
Moore, S. W., Zaahl, M. G.
core  

Hereditary pheochromocytoma/paraganglioma and associated syndromes: a clinical and genetic study

陆军军医大学学报
Objective To summarize and analyze the clinical phenotypes, hereditary features and treatment and follow-up strategies of different hereditary pheochromocytoma/paragangliomas (PCC/PGL) and related syndromes.
TANG Peng, LAN Weihua, ZHANG Yao
doaj   +1 more source

Occurrence of paratesticular ganglioneuroma 18 years after concurrent adrenal ganglioneuroma and papillary thyroid carcinoma – a case report

BMC Cancer, 2019
Background Ganglioneuromas (GNs) are composed of mature ganglion cells and Schwann cells with a fibrous stroma; GNs are most often observed in children and young adults.
Chu-Wen Fang, Jyh-Seng Wang, Tony T. Wu, Jen-Tai Lin   +3 more
doaj   +1 more source

Primary Hyperparathyroidism in MEN2 Syndromes

One of the components of the classical form of MEN2 syndromes is primary hyperparathyroidism (PHP). It occurs in 20–30% of the typical MEN2A syndrome.
Saltiki, Katerina, Alevizaki, Maria
core   +1 more source

Sporadic Medullary Thyroid Carcinoma with Paraneoplastic Cushing Syndrome

Case Reports in Endocrinology, 2019
Medullary thyroid cancer (MTC) is a rare form of neoplasm affecting the thyroid gland. This neuroendocrine tumor is capable of releasing active substances causing systemic manifestation in the form of flushing, diarrhea, and uncommonly, Ectopic Cushing’s
Aleksandra I. Pivovarova, Stephanie Patrick, Punuru J. Reddy   +2 more
doaj   +1 more source

Isolating human C cells by FACS for downstream -omics analysis to better understand the development of MTC in MEN2 patients

Background: Multiple endocrine neoplasia type 2 (MEN2) is an inherited condition caused by RET proto-oncogene mutations and is responsible for approximately 20% of medullary thyroid cancer (MTC) cases.
Richardson, Naomi, Brookes, Katie, Desanti, Guillaume E., Read, Martin L.; id_orcid, Dias, Renuka P., McCabe, Christopher J., Fear, Jessica, Thornton, Caitlin E.M., Smith, Vicki E., Zha, Ling   +9 more
core   +1 more source