Buscar
Mostrando ítems 31-40 de 157
FEOCROMOCITOMA PHEOCHROMOCYTOMA
(Universidad de Costa Rica, 2019)
Feocromocitoma gigante
(Sociedad de Cirugía de Bogotá, Hospital de San José y Fundación Universitaria de Ciencias de la Salud, 2015-06-01)
Germline mutations in TMEM127 confer susceptibility to pheochromocytoma
(NATURE PUBLISHING GROUP, 2010)
Pheochromocytomas, which are catecholamine-secreting tumors of neural crest origin, are frequently hereditary(1). However, the molecular basis of the majority of these tumors is unknown(2). We identified the transmembrane-encoding ...
Overexpression of the Insulin-like growth factor 1 receptor (IGF-1R) is associated with malignancy in familial pheochromocytomas and paragangliomas
(Wiley, 2013-03)
CONTEXT: Pheochromocytomas and paragangliomas (pheo/pgl) are neuroendocrine tumours derived from chromaffin cells. Although mostly benign, up to 26% of pheo/pgl will undergo malignant transformation. Reliable histological ...
Fibroblast deficiency of insulin-like growth factor 1 receptor type 1 (IGF1R) impairs initial steps of murine pheochromocytoma development
(Elsevier France-Editions Scientifiques Medicales Elsevier, 2019-08)
Insulin-like growth factor 1 (IGF1) has a critical role in maintaining tumor phenotype and survival of already transformed murine pheochromocytoma (pheo) cells (MPC4/30) and it is required for the initial establishment of ...
What determines mortality in malignant pheochromocytoma? : report of a case with eighteen-year survival and review of the literature
(Sociedade Brasileira de Endocrinologia e Metabologia, 2018)
Pheochromocytoma (PCC) is a tumor derived from adrenomedullary chromaffin cells. Prognosis of malignant PCC is generally poor due to local recurrence or metastasis. We aim to report a case of malignant PCC with 18-year ...
Association Between Atypical Parathyroid Adenoma And Neurofibromatosis
(SBEM-SOC BRASIL ENDOCRINOLOGIA & METABOLOGIARIO DE JANEIRO, RJ, 2015)
Swelling Of The Hard And Soft Palates
(ELSEVIER SCIENCE INCNEW YORK, 2015)
Feocromocitoma y manejo anestésico perioperatorio: reporte de caso
El feocromocitoma es un tumor originario del tejido cromafin, cuya sintomatología está relacionada con el exceso de catecolaminas. La incidencia en la población general es de 1-8 casos/millón. Presentamos el caso de una ...
Feocromocitoma y manejo anestésico perioperatorio: reporte de caso
El feocromocitoma es un tumor originario del tejido cromafin, cuya sintomatología está relacionada con el exceso de catecolaminas. La incidencia en la población general es de 1-8 casos/millón. Presentamos el caso de una ...