Publications by authors named "Aisha A Tepede"
Article Synopsis
- * The loss of the menin protein, caused by MEN1 mutations, is a significant factor in the development of these tumors and leads to an increase in the oncogenic receptor c-MET.
- * The review discusses clinical features, treatment options, and outcomes of GEP NETs, and highlights research on c-MET expression and potential treatments targeting c-MET as a precision-medicine strategy.
18F-FDOPA PET/CT accurately identifies MEN1-associated pheochromocytoma.
Endocrinol Diabetes Metab Case Rep
March 2020
Summary: Pheochromocytoma (PHEO) in multiple endocrine neoplasia type 1 (MEN1) is extremely rare. The incidence is reported as less than 2%. We report a case of a 76-year-old male with familial MEN1 who was found to have unilateral PHEO.
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