Zobrazeno 1 - 10
of 172
pro vyhledávání: '"Multiple endocrine neoplasia type 1 (MEN1)"'
Autor:
Julián C. Riaño-Moreno, Angélica María González-Clavijo, William C. Torres J., Vilma L. Medina B., Alfredo Ernesto Romero-Rojas, Isabella Vieda-Celemin, Jordan A. Avila-Moya, Johan A. Baron-Cardona, Juan P. Bravo-Patiño, Oscar S. Torres-Zambrano, Luis Felipe Fierro Maya
Publikováno v:
Frontiers in Endocrinology, Vol 15 (2024)
BackgroundMultiple Endocrine Neoplasia type 1 (MEN1) is an autosomal dominant disorder marked by pathogenic variants in the MEN1 tumor suppressor gene, leading to tumors in the parathyroid glands, pancreas, and pituitary. The occurrence of ACTH-produ
Externí odkaz:
https://doaj.org/article/8bf651a289424f1a964f118a118b33d9
Autor:
Eline N. M. van Vliembergen, Hidde Eijkelenkamp, Gerlof D. Valk, Menno R. Vriens, Gert J. Meijer, Martijn P. W. Intven, Joanne M. de Laat
Publikováno v:
Frontiers in Endocrinology, Vol 14 (2023)
BackgroundSurgical resection is the standard of care for the treatment of pancreatic neuro-endocrine tumors (pNETs) in patients with Multiple Endocrine Neoplasia Type 1 (MEN1). However, surgery can cause significant short- and long-term morbidity. Ma
Externí odkaz:
https://doaj.org/article/3eb81d2ffca14eb1aa246e4e7613d577
Autor:
Maria Melikyan, Diliara Gubaeva, Anna Shadrina, Anna Bolmasova, Maria Kareva, Anatoly Tiulpakov, Artem Efremenkov, Yuri Sokolov, Klaus Brusgaard, Henrik T. Christesen, Kirstine Andersen, Alexey Stepanov, Julia Averyanova, Sergey Makarov, Larisa Gurevich
Publikováno v:
Frontiers in Endocrinology, Vol 14 (2023)
BackgroundInsulinomas are very rare in childhood with sparse knowledge on the clinical aspects and the presence of Multiple Endocrine Neoplasia type 1 (MEN1).MethodsWe conducted a retrospective review of patients diagnosed with insulinoma between 199
Externí odkaz:
https://doaj.org/article/b221cd46fac44c7eaa51c3bfae4690a0
Publikováno v:
Endocrine Connections, Vol 11, Iss 5, Pp 1-12 (2022)
Multiple endocrine neoplasia type 1 (MEN1) is a rare, inherited cancer syndrome characterized by the development of multiple endocrine and non-endocrine tumors. MEN1 patients show a reduction of bone mass and a higher prevalence of early onset osteop
Externí odkaz:
https://doaj.org/article/0c777d5447254a5f972a5366edc01390
Autor:
Weixi Wang, Rulai Han, Lei Ye, Jing Xie, Bei Tao, Fukang Sun, Ran Zhuo, Xi Chen, Xiaxing Deng, Cong Ye, Hongyan Zhao, Shu Wang
Publikováno v:
Endocrine Connections, Vol 8, Iss 3, Pp 230-238 (2019)
Objective: Up to 40% of multiple endocrine neoplasia type 1 (MEN1) patients may have adrenal cortical tumors. However, adrenocortical carcinoma (ACC) is rare. The clinical manifestations, prevalence, inheritance and prognosis of ACC associated with M
Externí odkaz:
https://doaj.org/article/5d92cdd2ebb640a68edf0acd63b770bb
Autor:
Carmen Biancaniello, Antonia D’Argenio, Deborah Giordano, Serena Dotolo, Bernardina Scafuri, Anna Marabotti, Antonio d’Acierno, Roberto Tagliaferri, Angelo Facchiano
Publikováno v:
Molecules, Vol 27, Iss 5, p 1747 (2022)
Human menin is a nuclear protein that participates in many cellular processes, as transcriptional regulation, DNA damage repair, cell signaling, cell division, proliferation, and migration, by interacting with many other proteins. Mutations of the ge
Externí odkaz:
https://doaj.org/article/f1d231b308c54b6094a90bb1e347c12e
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Publikováno v:
Orphanet Journal of Rare Diseases, Vol 13, Iss 1, Pp 1-18 (2018)
Abstract Background Multiple endocrine neoplasia (MEN1) is a rare inherited multi-tumour syndrome, affecting specific neuroendocrine organs and non-endocrine tissues with a variable spectrum of over 20 possible different combinations, caused by inact
Externí odkaz:
https://doaj.org/article/0d8f76d4b9df4a1896799ef8eb4cfad8
Akademický článek
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