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Diagnóstico del Proto oncogén RET en una familia tamaulipeca con antecedente positivo de cáncer de tiroides
(2011-06-30)
En este trabajo se presentan los materiales y la metodología utilizada para la búsqueda de la mutación del codón 634 del exón 11 del protooncogén RET del cromosoma 10 en 11 personas, de las cuales 9 son familiares directos ...
Germline mutations of the ret proto-oncogen in chilean patients with hereditary and sporadic medullary thyroid carcinoma
(SOCIEDAD MEDICA DE SANTIAGO, 2001)
Mutaciones de línea germinal del proto-oncogen ret en pacientes chilenos con cáncer medular tiroideo hereditario y esporádico
(Sociedad Médica de Santiago, 2001)
Multiple endocrine neoplasia type 2
(2010)
Multiple endocrine neoplasia type 2 (MEN 2) is an autosomal dominant cancer syndrome with major components of medullary thyroid carcinoma (MTC), pheochromocytoma and hyperparathyroidism. The disease is caused by germline ...
Studies of RET gene expression and acetylcholinesterase activity in a series of sporadic Hirschsprung`s disease
(SPRINGER, 2008)
The purpose is to present the studies of RET gene expression and acetylcholinesterase activity in 23 patients operated for Hirschsprung`s disease (HD). The patients underwent either transanal endorectal pull-through or ...
Association Between Atypical Parathyroid Adenoma And Neurofibromatosis
(SBEM-SOC BRASIL ENDOCRINOLOGIA & METABOLOGIARIO DE JANEIRO, RJ, 2015)
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 ...