Neurofibromatosis
Neurofibromatosis, 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,...
Đã lưu trong:
| Định dạng: | Online |
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| Ngôn ngữ: | Tiếng Anh |
| Được phát hành: |
IntechOpen
2021
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| Những chủ đề: | |
| Truy cập trực tuyến: | ONIX_20210420_9781789855302_2855 |
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| _version_ | 1869523179188256768 |
|---|---|
| collection | Directory of Open Access Books |
| description | Neurofibromatosis, 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. |
| format | Online |
| id | doab-20.500.12854ir-67495 |
| institution | Directory of Open Access Books |
| language | eng |
| publishDate | 2021 |
| publishDateRange | 2021 |
| publishDateSort | 2021 |
| publisher | IntechOpen |
| publisherStr | IntechOpen |
| record_format | ojs |
| spelling | doab-20.500.12854ir-674952024-03-31T22:43:30Z Neurofibromatosis Signorelli, Francesco Messina, Raffaella Oncology thema EDItEUR::M Medicine and Nursing::MJ Clinical and internal medicine::MJC Diseases and disorders::MJCL Oncology Neurofibromatosis, 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. 2021-04-20T16:15:59Z 2021-04-20T16:15:59Z 2020 book ONIX_20210420_9781789855302_2855 9781789855302 9781789855296 9781838805760 https://directory.doabooks.org/handle/20.500.12854/67495 eng image/jpeg n/a https://www.intechopen.com/books https://mts.intechopen.com/storage/books/8729/authors_book/authors_book.pdf IntechOpen IntechOpen 10.5772/intechopen.80146 10.5772/intechopen.80146 78a36484-2c0c-47cb-ad67-2b9f5cd4a8f6 9781789855302 9781789855296 9781838805760 IntechOpen 120 open access |
| spellingShingle | Oncology thema EDItEUR::M Medicine and Nursing::MJ Clinical and internal medicine::MJC Diseases and disorders::MJCL Oncology Neurofibromatosis |
| title | Neurofibromatosis |
| title_full | Neurofibromatosis |
| title_fullStr | Neurofibromatosis |
| title_full_unstemmed | Neurofibromatosis |
| title_short | Neurofibromatosis |
| title_sort | neurofibromatosis |
| topic | Oncology thema EDItEUR::M Medicine and Nursing::MJ Clinical and internal medicine::MJC Diseases and disorders::MJCL Oncology |
| topic_facet | Oncology thema EDItEUR::M Medicine and Nursing::MJ Clinical and internal medicine::MJC Diseases and disorders::MJCL Oncology |
| url | ONIX_20210420_9781789855302_2855 |