Abstract. MAIA, Ana Luiza et al. Diagnóstico, tratamento e seguimento do carcinoma medular de tireoide: recomendações do Departamento de Tireoide da . ARTIGO ORIGINAL. Rastreamento genético do carcinoma medular de tireóide: identificação de mutações no proto-oncogene ret. Molecular screening of. Resumo. O Carcinoma medular da tiroide (CMT) é um tumor neuroendócrino raro (% de todos os tumores da tiroide), que surge a partir de células C.
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Carcinoma Medular da Tiroide – perspetiva após as guidelines de 2015 da ATA
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Molecular screening of medullary thyroid carcinoma: idenfication of ret proto-oncogene mutations
J Nucl Med Radiat Ther. How to cite this article. Somatic mutations in the RET proto-oncogene in sporadic medullary thyroid carcinoma. J Clin Endocrinol Metab ; Calcitonin and carcinoembryonic antigen doubling times as prognostic factors in medullary thyroid carcinoma: RET genetic screening in patients with medullary thyroid cancer and their relatives: Value of routine measurement of serum calcitonin concentrations in patients with nodular thyroid disease: Prolonged administration of bisphosphonates is well-tolerated and effective for skeletal-related events in Chinese breast cancer patients with bone metastasis.
Long-term course of patients with persistent hypercalcitoninemia after apparent curative primary surgery for medullary thyroid carcinoma. Rev Esp Med Nuclear ; Guidelines for diagnosis and therapy of MEN type 1 and type 2.
Survival improvement in patients with medullary thyroid carcinoma who undergo pretargeted anti-carcinoembryonic-antigen radioimmunotherapy: Improved diagnostic methods in the follow-up of medullary thyroid carcinoma by highly specific calcitonin measurements.
Tratamento do Carcinoma Medular da Tiroide
It enables web clients to dynamically resolve hostname records. J Natl Cancer Inst. Takahashi M, Cooper GM. Primary hyperparathyroidism in multiple endocrine neoplasia type 2A. Recent advances in genetics, diagnosis, localization and treatment of pheochromocytoma.