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Mostrando ítems 41-50 de 133
Hemifacial spasm in a patient with neurofibromatosis and Arnold-Chiari malformation: a unique case association
(Academia Brasileira de Neurologia - ABNEURO, 2007-09-01)
BACKGROUND: The association of hemifacial spasm (HFS), Chiari type I malformation (CIM) and neurofibromatosis type 1 (NF1) has not been described yet. CASE REPORT: We report the case of a 31-year-old woman with NF1 who ...
Spontaneous hip dislocation secondary to intraarticular neurofibroma: a case report
(Springer, 2014-07-01)
Spontaneous hip dislocation due to intraarticular neurofibroma in patients with neurofibromatosis type 1 is extremely rare. We describe the imaging features of spontaneous dislocation of hip due to histologically proven ...
Tradução e adaptação transcultural do questionário PEDSQL "Neurofibromatosis type 1 module 3.0" para pacientes com neurofibromatose tipo 1
(Universidade Federal de São Paulo, 2023-02-17)
Introdução: A neurofibromatose tipo1 (NF1) é uma doença genética que compromete 1: 3000 nascidos vivos, não tem tratamento medicamentoso, e a qualidade de vida dos pacientes depende do quadro clínico, psíquico e social. ...
Avaliação da cefaleia em pacientes com diagnóstico de neurofibromatose tipo 1
(Universidade Federal de São Paulo (UNIFESP), 2015-07-29)
Objetivo: avaliar a presença da queixa de cefaleia em pacientes com Neurofibromatose tipo 1 (NF1) e em grupos controles, comparando as características da cefaleia entre os grupos e, quando possível, estabelecendo o diagnóstico ...
The Sword of Damocles: Living with Neurofibromatosis Type 1.
Both as a physician and as a patient, having neurofibromatosis type 1 has been an important part of my life. In my practice as a physician and as a professor, I have tried to reflect on the reality of living with a genetic ...
The Sword of Damocles: Living with Neurofibromatosis Type 1
Both as a physician and as a patient, having neurofibromatosis type 1 has been an important part of my life. In my practice as a physician and as a professor, I have tried to reflect on the reality of living with a genetic ...
Neurofibroma cervicodorsal en una niña con Neurofibromatosis Tipo 1
(Udelar. FM, 2018)
La neurofibromatosis es el síndrome neurocutáneo más frecuente, una enfermedad hereditaria con afectación multisistémica. Se distinguen tres formas clínicas de la enfermedad; la neurofibromatosis tipo 1 (NF-1) es la más ...
Aneurisma da artéria vertebral extracraniana em puérpera portadora de neurofibromatose clássicaExtracranial vertebral artery aneurysm during the puerperium in women with neurofibromatosis type 1
(Sociedade Brasileira de Angiologia e de Cirurgia Vascular (SBACV), 2005)