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Detection of Cerebral Vasculopathy by Transcranial Doppler in Children With Neurofibromatosis Type 1
(Sage Publications Inc, 2016)
Neurofibromatosis type 1 is characterized by nerve sheath neurofibromas associated with a number of additional clinical features, including cerebrovascular disease. The aim of this study was to use transcranial Doppler as ...
Neurinoma del acústico bilateral como diagnóstico de neurofibromatosis tipo 2: reporte de caso clínico
(Ediciones Doyma, S.L., 2017-06)
Neurofibromatosis type 2 (NF2) is an autosomal dominant genetic disease that is characterized by the presence of bilateral schwannomas, meningiomas and gliomas. This is a case report of a woman of 34 years who has bilateral ...
How the Perception of Being a Neurofibromatosis Carrier Affects Nursing Care
(Aquichan, 2009)
La neurofibromatosis 1 es un síndrome genético autosómico muy frecuente en el ser humano. Se caracteriza por el crecimiento de tumores benignos de los nervios; puede presentarse en cualquier parte del cuerpo. Objetivos: ...
Implicaciones psicológicas en paciente con diagnóstico de neurofibromatosis tipo II
(Universidad del NorteMaestría en PsicologíaDepartamento de psicologíaBarranquilla, Colombia, 2022)
High frequencies of plexiform neurofibromas, mental retardation, learning difficulties, and scoliosis in Brazilian patients with neurofibromatosis type 1
(Associação Brasileira de Divulgação Científica (ABRADIC), 2014)
Neurofibromin: a general outlook
(Blackwell Publishing, 2006-07-01)
Neurofibromin is a cytoplasmic protein that is predominantly expressed in neurons, Schwann cells, oligodendrocytes, astrocytes and leukocytes. It is encoded by the gene NF1, located on chromosome 17, at q11.2, and has ...
Neurofibromin: a general outlook
(Blackwell Publishing, 2006-07-01)
Neurofibromin is a cytoplasmic protein that is predominantly expressed in neurons, Schwann cells, oligodendrocytes, astrocytes and leukocytes. It is encoded by the gene NF1, located on chromosome 17, at q11.2, and has ...
Giant intrathoracic meningoceles associated with cutaneous neurofibromatosis type I: case report
(Academia Brasileira de Neurologia - ABNEURO, 2003-09-01)
BACKGROUND: Intrathoracic meningocele is a rare pathology, almost always associated with neurofibromatosis type I and with a few cases related in the literature. In the majority of cases cysts are small or asymptomatic, ...
Neurofibromin: a general outlook
(Blackwell Publishing, 2014)