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008			190812s2020 gw a o |||| 0|eng d
020			_a9783030183967
024	7		_a10.1007/978-3-030-18396-7 _2doi
040			_aES-MaUEC _bspa _cES-MaUEC _dES-VaUE
050		4	_aRC280 _b.N48 2020 EB
245	0	0	_aNeuroblastoma : _bClinical and Surgical Management _cedited by Sabine Sarnacki, Luca Pio.
250			_a1st ed. 2020.
264		1	_aCham _bSpringer International Publishing : _bImprint: Springer _c2020.
300			_a1 recurso en línea (VIII, 383 páginas) _b 104 ilustraciones, 59 ilustraciones a color.
336			_2rdacontent _aTexto _btxt
337			_2rdamedia _aelectrónico _bc
338			_2rdacarrier _arecurso electrónico _bcr
347			_atext file _bPDF
490	0		_aMedicine (Springer-11650)
505	0		_aChapter 1. Epidemiology -- Chapter 2. Biology of neuroblastoma -- Chapter 3. Neuroblastoma pathogenesis -- Chapter 4. Neuroblastoma Pathology -- Chapter 5. Radiology -- Chapter 6. Image Defined Risk Factors -- Chapter 7. Nuclear Medicine procedures in Neuroblastoma -- Chapter 8. Radiotherapy for neuroblastoma -- Chapter 9. Spinal canal involvement in peripheral neuroblastic tumors -- Chapter 10. Neonatal Neuroblastoma -- Chapter 11. Low and intermediate risk Neuroblastoma -- Chapter 12. High risk Neuroblastoma and current Protocols -- Chapter 13. Immunotherapy -- Chapter 14. Prognostic Factors and Risk Stratification -- Chapter 15. BIOPSY OF NEUROBLASTOMA -- Chapter 16. Surgical Techniques -- Chapter 17. Surgical strategies for high risk neuroblastoma -- Chapter 18. Surgical strategies for Neuroblastoma with spinal canal involvement -- Chapter 19. Neuroblastoma - Minimally invasive surgery -- Chapter 20. Robotic Surgery for Neuroblastoma -- Chapter 21. Complications of the surgical management of children with neuroblastoma -- Chapter 22. Palliative Care.
520	3		_aThis book addresses neuroblastoma, a type of embryonic tumor derived from neural crest cells and one of the most frequent extra-cranial solid tumors in children. However, the term also describes a heterogeneous group of tumors, the prognosis of which can differ greatly according to age, stage and biology. Some forms undergo spontaneous regression, and some are cured by surgery alone or after chemo-reduction, while others exhibit extremely aggressive behavior. Their successful treatment is one of the best examples of tailored medicine, which involves close collaboration between pediatric surgeons, pediatric oncologists, radiologists, nuclear medicine specialists, biologists, oncogeneticists and radiotherapists. The book pursues a unique approach, as it combines most essential insights from all of these fields, together with key information regarding epidemiology, physiopathology and palliative care. The respective chapters were written by the leading international experts on neuroblastoma, and present the latest advances in terms of research, surgical approaches and medical treatments. The book offers an invaluable resource to all pediatric surgeons, pediatricians, oncologists, students, researchers and all others involved in neuroblastoma management who want to benefit from their colleagues' expertise.
988			_aSegundosemestre_2019_Medicine
650		7	_2embne _9671439 _aNeuroblastoma
700	1		_aSarnacki, Sabine _eeditor _4edt _4http://id.loc.gov/vocabulary/relators/edt
700	1		_aPio, Luca _eeditor _4edt _4http://id.loc.gov/vocabulary/relators/edt
710	2		_aSpringerLink (Online service) _9106937
773	0		_tSpringer eBooks
776	0	8	_iPrinted edition: _z9783030183950
776	0	8	_iPrinted edition: _z9783030183974
776	0	8	_iPrinted edition: _z9783030183981
856	4	0	_uhttps://go.openathens.net/redirector/universidadeuropea.es?url=https://doi.org/10.1007/978-3-030-18396-7 _zAcceso a este recurso digital (usuarios Universidad Europea de Valencia)
942			_2lcc _cLE
998			_db _feng _ggw _h0 _ea _zSI