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Management Of Ossifying Fibroma In A Suspicious Case Of Hyperparathyroid-jaw Tumor Syndrome
(THIEME MEDICAL PUBL INCNEW YORK, 2015)
Novel intronic mutation of MEN1 gene causing familial isolated primary hyperparathyroidism
(ENDOCRINE SOC, 2004-08)
Primary hyperparathyroidism may occur as part of hereditary syndromes, including multiple endocrine neoplasia types 1 and 2A (MEN1 and MEN2A), hyperparathyroidism-jaw tumor syndrome, and the familial isolated hyperparathyroidism ...
Novel intronic mutation of MEN1 gene causing familial isolated primary hyperparathyroidism
(ENDOCRINE SOC, 2004)
Primary hyperparathyroidism may occur as part of hereditary syndromes, including multiple endocrine neoplasia types 1 and 2A (MEN1 and MEN2A), hyperparathyroidism-jaw tumor syndrome, and the familial isolated hyperparathyroidism ...
Análise comparativa do perfil metabólico e funcional das variantes patogênicas G533c, C634y, M918v e M918t no gene Ret associadas à síndrome de neoplasia endócrina múltipla do tipo 2
(Universidade Federal de São Paulo (UNIFESP), 2021)
Medullary thyroid carcinoma (MTC) is a tumor that originates from thyroid C cells, which can occur in sporadic or hereditary form. In the hereditary form, MTC is an integral part of multiple endocrine neoplasia type 2 (MEN ...
Long-term follow-up of an 8-year-old boy with insulinoma as the first manifestation of a familial form of multiple endocrine neoplasia type 1Seguimento de longo prazo em um menino de 8 anos de idade com insulinoma como primeira manifestação de neoplasia endócrina múltipla tipo 1
(Sociedade Brasileira de Endocrinologia e Metabologia, 2010)
Carcinoma medular da tireoide e feocromocitoma esporádico e hereditário: investigação de eventos genéticos somáticos no gene ret
(Universidade Federal de São Paulo (UNIFESP), 2014-12-18)
Introduction: Mutations in the RET gene are associated with MEN 2 syndrome (multiple endocrine neoplasia type 2), which includes three types: familial medullary carcinoma (FMTC), characterized by medullary thyroid carcinoma ...
Estudo de familias com neopastia endocrina multipla tipo 2A, 2B e carcinoma medular familiar: correlação genotipo, fenótipo e isoformas da proteína RET (RET 9 e RET 51)
(Universidade Federal de Minas GeraisUFMG, 2010-03-12)
The multiple endocrine neoplasia Type 2 (MEN-2) is a hereditary syndrome comprising: medullary thyroid carcinoma (MTC), primary hyperparathyroidism, pheochromocytoma and other non-endocrine diseases. Is subdivided into ...