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Von Hippel-Lindau disease with extramedullary and pancreatic involvement
(Elsevier B.V., 2020-01-01)
We report a patient with Von Hippel-Lindau disease who presented with an intradural extramedullary hemangioblastoma as a primary manifestation.
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 ...
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 ...
Importância do exame oftalmológico na doença de von Hippel-Lindau
(Sociedade Brasileira de Oftalmologia, 2009-08-01)
Von Hippel-Lindau (VHL) disease is an autossomical, dominant inherited tumour syndrom. These tumours may include haemangioblastoma in the retina and central nervous system (CNS), renal cell carcinoma, phaeochromocytoma, ...
Extra and intradural spinal HemangioblastomaHemangioblastoma espinhal extra e intraduralHemangioblastoma espinal extra e intradural
(Sociedade Brasileira de Coluna, 2012)
Hemangioblastomas of the central nervous system (CNS) are low-grade highly vascularized tumors that may be sporadic or associated with Von Hippel-Lindau disease. Extradural hemangioblastomas are uncommon and those located ...
Preventive medicine of von Hippel-Lindau disease-associated pancreatic neuroendocrine tumors
(BioScientifica Ltd., 2018)
© 2018 Society for Endocrinology Published by Bioscientifica Ltd. Printed in Great Britain. Pancreatic neuroendocrine tumors (PanNETs) are rare in von Hippel-Lindau disease (VHL) but cause serious morbidity and mortality. ...
Clinical and molecular characterization of Brazilian families with von Hippel-Lindau disease: a need for delineating genotype-phenotype correlation
(SPRINGER, 2010)
von Hippel-Lindau (VHL) disease is an autosomal dominant hereditary cancer syndrome that predisposes to the development of a variety of benign and malignant tumours, especially cerebellar haemangioblastomas, retinal angiomas ...
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)
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 ...
von Hippel-Lindau mutants in renal cell carcinoma are regulated by increased expression of RSUME
(Nature Publishing Group, 2019-04)
Renal cell carcinoma (RCC) is the major cause of death among patients with von Hippel-Lindau (VHL) disease. Resistance to therapies targeting tumor angiogenesis opens the question about the underlying mechanisms. Previously ...