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dc.contributor.editorSignorelli, Francesco
dc.contributor.editorMessina, Raffaella
dc.date.accessioned2021-04-20T16:15:59Z
dc.date.available2021-04-20T16:15:59Z
dc.date.issued2020
dc.identifierONIX_20210420_9781789855302_2855
dc.identifier.urihttps://directory.doabooks.org/handle/20.500.12854/67495
dc.description.abstractNeurofibromatosis, one of the most common genetic disorders, is a group of three conditions—Neurofibromatosis 1, Neurofibromatosis 2 and Schwannomatosis—that share some clinical features, such as the presence of cranial and spinal nerve sheet tumors. However, they differ in type of genetic disorder, age of clinical onset, manifestations, management and prognosis. Due to multisystem involvement, a multidisciplinary treatment approach that includes research is ideal. This book provides a systematic, comprehensive and updated outline of Neurofibromatosis. It is a useful reference for clinicians, researchers and students.
dc.languageEnglish
dc.subject.classificationthema EDItEUR::M Medicine and Nursing::MJ Clinical and internal medicine::MJC Diseases and disorders::MJCL Oncologyen_US
dc.subject.otherOncology
dc.titleNeurofibromatosis
dc.title.alternativeCurrent Trends and Future Directions
dc.typebook
oapen.identifier.doi10.5772/intechopen.80146
oapen.relation.isPublishedBy78a36484-2c0c-47cb-ad67-2b9f5cd4a8f6
oapen.relation.isbn9781789855302
oapen.relation.isbn9781789855296
oapen.relation.isbn9781838805760
oapen.imprintIntechOpen
oapen.pages120


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