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1
Published in 2022 at "Journal of Hypertension"
DOI: 10.1097/01.hjh.0000837464.81691.1f
Abstract: Objective: In recent years, there has been a lot of controversy about the factors affecting the penetrance of multiple endocrine neoplasia type 2A(MEN2A). Some studies considered it may be related to gene mutations. In the…
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Keywords:
men2a;
ret 1901g;
novel slc12a3;
multiple endocrine ... See more keywords
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0
Published in 2025 at "Annals of Medicine and Surgery"
DOI: 10.1097/ms9.0000000000002923
Abstract: Introduction and importance: Multiple endocrine neoplasia type 2A (MEN2A) is a rare hereditary cancer syndrome marked by medullary thyroid carcinoma (MTC), pheochromocytoma, and primary hyperparathyroidism. The RET proto-oncogene mutation, particularly the C634R variant, significantly increases…
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Keywords:
history;
men2a;
mutation;
case ... See more keywords
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Published in 2025 at "Journal of the Endocrine Society"
DOI: 10.1210/jendso/bvaf149.2488
Abstract: Abstract Disclosure: M. Trieu: None. J.O. Culver: None. Y. Cardona: None. A.N. Lim: None. M.S. Swanson: None. T.E. Angell: None. Background: Multiple endocrine neoplasia 2A (MEN2A) is a hereditary syndrome associated with an increased risk…
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Keywords:
men2a;
ret;
none;
ret k666n ... See more keywords
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2
Published in 2022 at "Frontiers in Endocrinology"
DOI: 10.3389/fendo.2022.905963
Abstract: Background Multiple endocrine neoplasia type 2A (MEN2A) is a rare syndrome that presents as medullary thyroid carcinoma, pheochromocytoma, and hyperparathyroidism. Experience is lacking in the anesthetic management of patients with this syndrome, particularly in those…
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Keywords:
men2a;
multiple endocrine;
pheochromocytoma;
resection ... See more keywords