Results 1 to 10 of about 23,289 (161)

Multiple endocrine neoplasia type 2 – solving the puzzle [PDF]

open access: yesJournal of Family Medicine and Primary Care, 2023
Multiple endocrine neoplasia (MEN) are tumors that involve two or more endocrine glands. It can also involve other organs and tissues as well. Out of the four types of MEN type 2 is the most common.
Ajay K. Jha   +2 more
doaj   +2 more sources

Simultaneous bilateral laparoscopic cortical-sparing adrenalectomy for bilateral pheochromocytomas in multiple endocrine neoplasia type 2 [PDF]

open access: yesFrontiers in Surgery, 2023
PurposeThis study aimed to assess the feasibility of synchronous bilateral laparoscopic or open cortical-sparing adrenalectomy (SB-LCSA or SB-OCSA) for bilateral pheochromocytomas (bPHEOs) in multiple endocrine neoplasia type 2 (MEN2).MethodsAltogether ...
Xiao-Ping Qi   +8 more
doaj   +2 more sources

Germline RET Leu56Met Variant Is Likely Not Causative of Multiple Endocrine Neoplasia Type 2 [PDF]

open access: yesFrontiers in Endocrinology, 2021
Activating variants in the receptor tyrosine kinase REarranged during Transfection (RET) cause multiple endocrine neoplasia type 2 (MEN 2), an autosomal dominantly inherited cancer-susceptibility syndrome.
Anna Reimer Hansen   +10 more
doaj   +2 more sources

Clinical features and signaling effects of RET D631Y variant multiple endocrine neoplasia type 2 (MEN2) [PDF]

open access: yesThe Korean Journal of Internal Medicine, 2022
Background/Aims Germline mutations of the rearranged during transfection (RET) gene cause multiple endocrine neoplasia type 2 (MEN2). About 85% of RET mutations in MEN2 occur in codon Cys634.
Ji-young Lee   +7 more
doaj   +2 more sources

Endocrine Perspective of Cutaneous Lichen Amyloidosis: RET-C634 Pathogenic Variant in Multiple Endocrine Neoplasia Type 2 [PDF]

open access: yesClinics and Practice
Background: Medullary thyroid carcinoma (MTC), the third most frequent histological type of thyroid malignancy, may be found isolated or as part of multiple endocrine neoplasia type 2 (MEN2).
Alexandru-Florin Florescu   +8 more
doaj   +2 more sources

5P Strategies for Management of Multiple Endocrine Neoplasia Type 2: A Paradigm of Precision Medicine [PDF]

open access: yesFrontiers in Endocrinology, 2020
Multiple endocrine neoplasia type 2 (MEN2) is a neuroendocrine cancer syndrome characterized by medullary thyroid carcinoma, in combination or not with pheochromocytoma, hyperparathyroidism, and extra-endocrine features.
Shu-Yuan Li   +5 more
doaj   +2 more sources

An Analysis of Primary Hyperparathyroidism in Individuals Diagnosed with Multiple Endocrine Neoplasia Type 2 [PDF]

open access: yesDiseases
Background: Primary hyperparathyroidism (PHPT) represents a multi-faced disease with a wide spectrum of manifestations. Familial forms of PHPT (affecting up to 10% of the cases) involve a particular category that encompasses a large range of hereditary ...
Ana-Maria Gheorghe   +3 more
doaj   +2 more sources

Psychosocial Characteristics and Experiences in Patients with Multiple Endocrine Neoplasia Type 2 (MEN2) and Medullary Thyroid Carcinoma (MTC) [PDF]

open access: yesChildren, 2022
Multiple Endocrine Neoplasia type 2 (MEN2) is a genetic cancer syndrome for which there are limited data pertaining to the quality of life and psychosocial experiences of persons affected.
Robin Lockridge   +6 more
doaj   +2 more sources

Spectrum of Germline RET variants identified by targeted sequencing and associated Multiple Endocrine Neoplasia type 2 susceptibility in China [PDF]

open access: yesBMC Cancer, 2021
Background Germline RET mutations and variants are involved in development of multiple endocrine neoplasia type 2 (MEN2). The present study investigated a spectrum of RET variants, analyzed genotype-phenotype relationships, and evaluated their effect on ...
Xiao-Ping Qi   +9 more
doaj   +2 more sources

Molecular mechanisms of RET receptor-mediated oncogenesis in multiple endocrine neoplasia 2

open access: yesClinics, 2012
Multiple endocrine neoplasia type 2 is an inherited cancer syndrome characterized by tumors of thyroid and adrenal tissues. Germline mutations of the REarranged during Transfection (RET) proto-oncogene, leading to its unregulated activation, are the ...
Simona M. Wagner   +3 more
doaj   +3 more sources

Home - About - Disclaimer - Privacy