Results 51 to 60 of about 38,029,237 (226)

A Rare Combination: Multiple Endocrine Neoplasia Type 1 and Follicular Thyroid Carcinoma

Endocrinology Research and Practice, 2020
Multiple endocrine neoplasia Type 1 (MEN-1) is an inherited syndrome characterized by the development of endocrine tumors of the pancreas, parathyroid, and pituitary glands.
Ahmet GÖRGEL, Sacit Nuri GÖRGEL, Mustafa DEMİRPENÇE, Mitat BAHÇECİ   +3 more
doaj   +1 more source

A multilevel perspective on MSH6‐associated Lynch syndrome: Integrating molecular, biological, and clinical insights

International Journal of Cancer, EarlyView.
Abstract Lynch syndrome (LS) is the most common hereditary colorectal cancer syndrome, caused by a germline pathogenic variant in one of the mismatch repair (MMR) genes. Among these, MSH6‐associated LS represents a distinct subtype with unique molecular and clinical characteristics.
Salwa Ben Yahia, Anne‐Sophie van der Werf‐'t Lam, Madalina Cabuta, Maartje Nielsen, Noah C. Helderman   +4 more
wiley   +1 more source

Multiple Endocrine Neoplasia Type 1

, 2022
Multiple endocrine neoplasia type 1 (MEN1) is characterized by the combined occurrence of parathyroid, duodenopancreatic neuroendocrine tumors, and anterior pituitary adenomas. In addition, some patients develop thymic and bronchopulmonary carcinoids, as
Thakker, Rajesh V., Newey, Paul J.
core   +1 more source

Total parathyroidectomy in a large cohort of cases with hyperparathyroidism associated with multiple endocrine neoplasia type 1: experience from a single academic center

Clinics, 2012
Most cases of sporadic primary hyperparathyroidism present disturbances in a single parathyroid gland and the surgery of choice is adenomectomy. Conversely, hyperparathyroidism associated with multiple endocrine neoplasia type 1 (hyperparathyroidism ...
Fabio Luiz de Menezes Montenegro, Delmar Muniz Lourenço Junior, Marcos Roberto Tavares, Sergio Samir Arap, Climerio Pereira Nascimento Junior, Ledo Mazzei Massoni Neto, André D'Alessandro, Rodrigo Almeida Toledo, Flávia Lima Coutinho, Lenine Garcia Brandão, Gilberto de Britto e Silva Filho, Anói Castro Cordeiro, Sergio Pereira Almeida Toledo   +12 more
doaj   +1 more source

Preoperative and postoperative pathology concordance in endometrial intraepithelial neoplasia: A retrospective cohort study

International Journal of Gynecology &Obstetrics, EarlyView.
Abstract Objective To assess the concordance between pre‐ and postoperative pathology in patients with endometrial intraepithelial neoplasia (EIN) undergoing hysterectomy, and identify predictors of malignancy, including sampling method, progestin therapy, and surgical timing.
Jenny Dimakos, Dong Bach Nguyen, Xing Zeng, Jessica Papillon Smith, Fady W. Mansour, Srinivasan Krishnamurthy, Andrew Zakhari   +6 more
wiley   +1 more source

Multiple endocrine neoplasia syndroms. Type 1 [PDF]

, 2004
Multiple endocrine neoplasia (MEN) type 1 syndrome or Wermer syndrome is a classical malignant neoplasia syndrome, inherited in the autosomal dominant pattern, when hyperplastic and/or neoplastic injury develops synchronously or metachronously in the ...
Juodelė, Linas, Pundzius, Juozas, Žindžius, Algimantas Stanislovas, Juozaitytė, Elona   +3 more
core  

Multiple endocrine neoplasia type 4: a new member of the MEN family. [PDF]

, 2023
OBJECTIVE Multiple endocrine neoplasia type 4 (MEN4) is caused by a CDKN1B germline mutation first described in 2006. Its estimated prevalence is less than 1/million. The aim of this study was to define the disease characteristics.
Probst, Pascal, Adamczyk, Magdalene, Weber, Achim; https://orcid.org/, Singeisen, Hélène, Hauswirth, Fabian, Kaderli, Reto Martin, Muller, Markus K; https://orcid.org/, Weber, Achim, Muller, Markus K, Renzulli, Pietro, Pavlicek, Vojtech, Renzulli, Mariko Melanie   +11 more
core   +2 more sources

Post-surgical follow-up of primary hyperparathyroidism associated with multiple endocrine neoplasia type 1

Clinics, 2012
The bone mineral density increments in patients with sporadic primary hyperparathyroidism after parathyroidectomy have been studied by several investigators, but few have investigated this topic in primary hyperparathyroidism associated with multiple ...
Flavia L. Coutinho, Delmar M. Lourenco Jr., Rodrigo A. Toledo, Fabio L. M. Montenegro, Sergio P. A. Toledo   +4 more
doaj   +1 more source

Analysis of 55 patients with multiple endocrine neoplasia type 1-associated insulinoma from a single center in China

Orphanet Journal of Rare Diseases, 2022
Objective To investigate the clinical characteristics of patients with multiple endocrine neoplasia type 1 (MEN1)-related insulinoma and their relationship with specific biochemical changes and to summarize the features of treatment options for the ...
Yuan Zhao, Jie Yu, Yiwen Liu, Lu Lyu, Fan Ping, Lingling Xu, Wei Li, Ou Wang, Qiang Xu, Wenming Wu, Huabing Zhang, Yuxiu Li   +11 more
doaj   +1 more source

From prevalence to precision: Integrating phenotype, symptoms, reproductive goals, and treatment in leiomyoma care

International Journal of Gynecology &Obstetrics, EarlyView.
Abstract Uterine fibroids (leiomyomas) are present in most women during their reproductive years, yet only a subset becomes clinically meaningful. This disparity poses a central clinical challenge: distinguishing symptoms caused by fibroids from those unrelated to them.
Malcolm G. Munro
wiley   +1 more source