about
The rare intracellular RET mutation p.Ser891Ala in an apparently sporadic medullary thyroid carcinoma: a case report and review of the literatureMolecular basis of medullary thyroid carcinoma: the role of RET polymorphismsRole of VEGF-A and its receptors in sporadic and MEN2-associated pheochromocytomaEffect of 3'UTR RET Variants on RET mRNA Secondary Structure and Disease Presentation in Medullary Thyroid Carcinoma.Advanced medullary thyroid cancer: pathophysiology and managementIs there a role for inherited TRβ mutation in human carcinogenesis? [corrected].MEN 2A-related cutaneous lichen amyloidosis: report of three kindred and systematic literature review of clinical, biochemical and molecular characteristics.MAPK and SHH pathways modulate type 3 deiodinase expression in papillary thyroid carcinoma.Role of RET genetic variants in MEN2-associated pheochromocytoma.The RET polymorphic allele S836S is associated with early metastatic disease in patients with hereditary or sporadic medullary thyroid carcinoma.Genotype and phenotype landscape of MEN2 in 554 medullary thyroid cancer patients: the BrasMEN studyGlobal DNA methylation profile in medullary thyroid cancer patientsNatural history, treatment, and long-term follow up of patients with multiple endocrine neoplasia type 2B: an international, multicentre, retrospective studyMedullary thyroid carcinoma beyond surgery: advances, challenges, and perspectives
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description
investigador
@es
researcher
@en
name
Lucieli Ceolin
@en
type
label
Lucieli Ceolin
@en
prefLabel
Lucieli Ceolin
@en
P31
P496
0000-0001-6794-6042