Associated Papers
Double mutation for multiple endocrine neoplasia associated with congenital adrenal hyperplasia.
de Oliveira WL et al.
Endocrinology, Diabetes & Metabolism Case Reports, 2025
Multi-locus inherited neoplasia alleles syndromes in cancer: implications for clinical practice.
Yuen J et al.
European Journal of Human Genetics : Ejhg, 2025
39843919 (PubMed )
Supplement: 41431_2025_1785_MOESM5_ESM.pdf
DNA damage response and repair gene mutations predict clinical outcomes in biliary tract cancer.
Tan S et al.
Cancer, 2025
39876053 (PubMed )
Supplement: supplement_1.pdf
GLOBAL ENDOCRINOLOGY: Geographical variation in the profile of RET variants in patients with medullary thyroid cancer: a comprehensive review.
Maciel RMB et al.
European Journal of Endocrinology, 2021
Multigene Panel Testing Increases the Number of Loci Associated with Gastric Cancer Predisposition.
Tedaldi G et al.
Cancers, 2019
31514334 (PubMed )
Supplement: cancers-11-01340-s001.pdf
Integrated Somatic and Germline Whole-Exome Sequencing Analysis in Women with Lung Cancer after a Previous Breast Cancer.
Coco S et al.
Cancers, 2019
30925779 (PubMed )
Supplement: cancers-11-00441-s001.zip › cancers-452240-Supplementary › Table_S5.xlsx › Table_S5
A Homozygous RET K666N Genotype With an MEN2A Phenotype.
Jaber T et al.
The Journal of Clinical Endocrinology and Metabolism, 2018
A pioneering RET genetic screening study in the State of Ceará, Brazil, evaluating patients with medullary thyroid cancer and at-risk relatives: experience with 247 individuals.
Martins-Costa MC et al.
Archives of Endocrinology and Metabolism, 2018
Medullary Thyroid Carcinoma Associated with Germline RETK666N Mutation.
Xu JY et al.
Thyroid : Official Journal of the American Thyroid Association, 2016
A patient with MEN1 typical features and MEN2-like features.
El-Maouche D et al.
International Journal of Endocrine Oncology, 2016
A newly identified missense mutation in RET codon 666 is associated with the development of medullary thyroid carcinoma.
Yamazaki M et al.
Endocrine Journal, 2014
The involvement of the RET variant G691S in medullary thyroid carcinoma enlightened by a meta-analysis study.
Lantieri F et al.
International Journal of Cancer, 2013
Coexistence of multiple endocrine neoplasia type 1 and type 2 in a large Italian family.
Mastroianno S et al.
Endocrine, 2011
Multiple endocrine neoplasia type 2 syndromes (MEN 2): results from the ItaMEN network analysis on the prevalence of different genotypes and phenotypes.
Romei C et al.
European Journal of Endocrinology, 2010
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