Multiple endocrine neoplasia type 2: From molecular genetics to precision therapy
- 8 June 2026
- journal article
- review article
- Published by Elsevier in Best Practice & Research Clinical Endocrinology & Metabolism
- p. 102135
Abstract
No abstract availableKeywords
This publication has 99 references indexed in Scilit:
- Temporal trends in referrals of RET gene carriers for neck surgery to a tertiary surgical center in the era of international management guidelinesEndocrine, 2022
- MEN2-related pheochromocytoma: current state of knowledge, specific characteristics in MEN2B, and perspectivesEndocrine, 2020
- Clinical utility of 177Lu‐DOTATATE PRRT in somatostatin receptor‐positive metastatic medullary carcinoma of thyroid patients with assessment of efficacy, survival analysis, prognostic variables, and toxicityHead & Neck, 2019
- EANM practice guideline for PET/CT imaging in medullary thyroid carcinomaEuropean Journal of Nuclear Medicine and Molecular Imaging, 2019
- Genotype-specific progression of hereditary medullary thyroid cancerHuman Mutation, 2018
- Treatment for Malignant Pheochromocytomas and Paragangliomas: 5 Years of ProgressCurrent Oncology Reports, 2017
- Pheochromocytoma in an 8‐year‐old patient with multiple endocrine neoplasia type 2A: Implications for screeningJournal of Surgical Oncology, 2013
- Risk profiles and penetrance estimations in multiple endocrine neoplasia type 2A caused by germline RET mutations located in exon 10Human Mutation, 2010
- The Relationship Between Specific RET Proto-oncogene Mutations and Disease Phenotype in Multiple Endocrine Neoplasia Type 2JAMA, 1996
- Multiple mucosal neuromata with endocrine tumours: A syndrome allied to von Recklinghausen's diseaseThe Journal of Pathology and Bacteriology, 1966