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Alpha7 Nicotinic Acetylcholine Receptor Expression and Activity During Neuronal Differentiation of PC12 Pheochromocytoma Cells
(HUMANA PRESS INC, 2010)
Nicotinic acetylcholine receptors (nAChR) exert pivotal roles in synaptic transmission, neuroprotection and differentiation. Particularly, homomeric alpha 7 receptors participate in neurite outgrowth, presynaptic control ...
Single-stage laparoscopic adrenalectomy and pancreatic cyst excision in a patient with Von Hippel-Lindau disease Resección laparoscópica de feocromocitoma y quiste pancreático en un paciente con enfermedad de Von Hippel-Lindau
(Ene Ediciones S.A., 2007)
Introduction: Von Hippel-Lindau disease is a dominant autosomic hereditary condition, characterized by cerebellar hemangioblastomas, retinal animas and visceral cysts and tumors. We report a case of a patient with Von ...
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 ...
Genetics informs precision practice in the diagnosis and management of pheochromocytoma
(BioScientifica Ltd., 2018)
© 2018 Society for Endocrinology Published by Bioscientifica Ltd. Although the authors of the present review have contributed to genetic discoveries in the field of pheochromocytoma research, we can legitimately ask whether ...
Feocromocitoma: atualização diagnóstica e terapêutica
(Associação Médica Brasileira, 1997-09-01)
Anestesia venosa com fentanil para resseção de feocromocitomas
(Universidade Federal de São Paulo (UNIFESP), 1990)
Molecular analysis of the Von Hippel-Lindau (VHL) gene in a family with non-syndromic pheochromocytoma: the importance of genetic testing
(Sociedade Brasileira de Endocrinologia e Metabologia, 2007-12-01)
Dois pacientes índices da família analisada neste estudo foram submetidos a adrenalectomia bilateral devido a feocromocitoma. Foi, então, realizado o estudo genético dos pacientes e de sete parentes de primeiro grau. Os ...
Multiple paragangliomas associated to a SDHB gene mutation. report of one case Paragangliomas múltiples asociados a mutación del gen SDHB. caso clínico
(2011)
Paragangliomas are tumors arising from sympathetic and parasympathetic tissues. The classic associated syndromes are neurofibromatosis type 1, multiple endocrine neoplasia type 2 and von Hippel-Lindau. Germline mutations ...
Molecular analysis of the Von Hippel-Lindau (VHL) gene in a family with non-syndromic pheochromocytoma: the importance of genetic testing
(Sociedade Brasileira de Endocrinologia e Metabologia, 2014)
Long-term prognosis of patients with pediatric pheochromocytoma
(Bioscientifica, 2014-01)
A third of patients with paraganglial tumors, pheochromocytoma, and paraganglioma, carry germline mutations in one of the susceptibility genes, RET, VHL, NF1, SDHAF2, SDHA, SDHB, SDHC, SDHD, TMEM127, and MAX. Despite ...