Soft Tissue and Bone Sarcoma
Soft tissue and bone sarcomas disproportionately affect children, adolescents, and young adults. Although considered a rare disease, sarcomas continue to have a devastating effect on these patients and their loved ones, and their impact on our society far exceed their relatively low prevalence. Beca...
- Autores:
- Tipo de recurso:
- Book
- Fecha de publicación:
- 2014
- Institución:
- Universidad de Bogotá Jorge Tadeo Lozano
- Repositorio:
- Expeditio: repositorio UTadeo
- Idioma:
- eng
- OAI Identifier:
- oai:expeditiorepositorio.utadeo.edu.co:20.500.12010/14470
- Acceso en línea:
- https://www.mdpi.com/books/pdfview/book/65
http://hdl.handle.net/20.500.12010/14470
https://doi.org/10.3390/books978-3-906980-58-4
- Palabra clave:
- Medicina
Tumor óseo
Oncología del tejido conectivo
- Rights
- License
- Abierto (Texto Completo)
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| dc.title.spa.fl_str_mv |
Soft Tissue and Bone Sarcoma |
| title |
Soft Tissue and Bone Sarcoma |
| spellingShingle |
Soft Tissue and Bone Sarcoma Medicina Tumor óseo Oncología del tejido conectivo |
| title_short |
Soft Tissue and Bone Sarcoma |
| title_full |
Soft Tissue and Bone Sarcoma |
| title_fullStr |
Soft Tissue and Bone Sarcoma |
| title_full_unstemmed |
Soft Tissue and Bone Sarcoma |
| title_sort |
Soft Tissue and Bone Sarcoma |
| dc.subject.spa.fl_str_mv |
Medicina |
| topic |
Medicina Tumor óseo Oncología del tejido conectivo |
| dc.subject.lemb.spa.fl_str_mv |
Tumor óseo Oncología del tejido conectivo |
| description |
Soft tissue and bone sarcomas disproportionately affect children, adolescents, and young adults. Although considered a rare disease, sarcomas continue to have a devastating effect on these patients and their loved ones, and their impact on our society far exceed their relatively low prevalence. Because of its rarity and heterogeneity, clinical decision making on management of sarcomas are often individualized and without a consensus treatment strategy. Furthermore, research to improve clinical outcomes are particularly challenging as sizeable studies are hard to produce. By improving our knowledge about the molecular biology of sarcomas, we hope to identify new treatment strategies and targets for further drug development. [...] |
| publishDate |
2014 |
| dc.date.created.none.fl_str_mv |
2014 |
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2020-10-14T22:26:34Z |
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2020-10-14T22:26:34Z |
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Libro |
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http://purl.org/coar/resource_type/c_2f33 |
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978-3-906-98046-1 978-3-906-98058-4 |
| dc.identifier.other.none.fl_str_mv |
https://www.mdpi.com/books/pdfview/book/65 |
| dc.identifier.uri.none.fl_str_mv |
http://hdl.handle.net/20.500.12010/14470 |
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https://doi.org/10.3390/books978-3-906980-58-4 |
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978-3-906-98046-1 978-3-906-98058-4 |
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https://www.mdpi.com/books/pdfview/book/65 http://hdl.handle.net/20.500.12010/14470 https://doi.org/10.3390/books978-3-906980-58-4 |
| dc.language.iso.spa.fl_str_mv |
eng |
| language |
eng |
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Abierto (Texto Completo) |
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https://creativecommons.org/licenses/by/4.0/legalcode |
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Abierto (Texto Completo) https://creativecommons.org/licenses/by/4.0/legalcode http://purl.org/coar/access_right/c_abf2 |
| dc.format.extent.spa.fl_str_mv |
158 páginas |
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application/pdf |
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MDPI - Multidisciplinary Digital Publishing Institute |
| institution |
Universidad de Bogotá Jorge Tadeo Lozano |
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2020-10-14T22:26:34Z2020-10-14T22:26:34Z2014978-3-906-98046-1978-3-906-98058-4https://www.mdpi.com/books/pdfview/book/65http://hdl.handle.net/20.500.12010/14470https://doi.org/10.3390/books978-3-906980-58-4158 páginasapplication/pdfengMDPI - Multidisciplinary Digital Publishing InstituteMedicinaTumor óseoOncología del tejido conectivoSoft Tissue and Bone SarcomaLibrohttp://purl.org/coar/resource_type/c_2f33Abierto (Texto Completo)https://creativecommons.org/licenses/by/4.0/legalcodehttp://purl.org/coar/access_right/c_abf2Soft tissue and bone sarcomas disproportionately affect children, adolescents, and young adults. Although considered a rare disease, sarcomas continue to have a devastating effect on these patients and their loved ones, and their impact on our society far exceed their relatively low prevalence. Because of its rarity and heterogeneity, clinical decision making on management of sarcomas are often individualized and without a consensus treatment strategy. Furthermore, research to improve clinical outcomes are particularly challenging as sizeable studies are hard to produce. By improving our knowledge about the molecular biology of sarcomas, we hope to identify new treatment strategies and targets for further drug development. 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