000 | 03161nam a22005175i 4500 | ||
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001 | 978-1-4020-3998-0 | ||
003 | DE-He213 | ||
005 | 20161121230658.0 | ||
007 | cr nn 008mamaa | ||
008 | 100301s2006 ne | s |||| 0|eng d | ||
020 |
_a9781402039980 _9978-1-4020-3998-0 |
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024 | 7 |
_a10.1007/1-4020-3998-0 _2doi |
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050 | 4 | _aRC261-271 | |
072 | 7 |
_aMJCL _2bicssc |
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072 | 7 |
_aMED062000 _2bisacsh |
|
082 | 0 | 4 |
_a614.5999 _223 |
100 | 1 |
_aSchiffer, Davide. _eauthor. |
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245 | 1 | 0 |
_aBrain Tumor Pathology: Current Diagnostic Hotspots and Pitfalls _h[electronic resource] / _cby Davide Schiffer. |
264 | 1 |
_aDordrecht : _bSpringer Netherlands, _c2006. |
|
300 |
_aVI, 272 p. _bonline resource. |
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336 |
_atext _btxt _2rdacontent |
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337 |
_acomputer _bc _2rdamedia |
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338 |
_aonline resource _bcr _2rdacarrier |
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347 |
_atext file _bPDF _2rda |
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505 | 0 | _aThe Origin of Gliomas in Relation to the Histological Diagnosis -- Molecular Genetics Outline of Brain Tumors -- General Remarks -- Astrocytic Tumors I -- Astrocytic Tumors II -- Oligodendroglial Tumors -- Ependymal Tumors -- Neuronal and Mixed Glio-Neural Tumors I -- Neuronal and Mixed Glio-Neural Tumors II -- Peculiar Tumors -- Cell Migration and Invasion -- Apoptosis -- The Ubiquitin-Proteasome System -- Angiogenesis -- Meningiomas. | |
520 | _aSince Bailey and Cushing (1926), all brain tumor classifications have been called histogenetic. The nosographic position that the tumor types progressively acquired in the classification systems derived from the resemblance of tumor cells to those of the cytogenesis, modified whenever new information became available from different biological research fields and especially from molecular genetics. Classically, on the basis of the rough correspondence between the mature/immature aspect of tumor cells and the benign/malignant biological behavior of the tumors, the histological labels contained a prognostic significance. The supposed origin of the tumors was thus a factor for prognosis. Later on, with the concept of anaplasia (Cox, 1933; Kernohan et al., 1949) new criteria were introduced for establishing the malignancy grades of tumors. Immunohistochemistry and later molecular genetics further refined the prognostic diagnoses, substantially increasing the opportunities to recognize the cell origin of tumors, beside revealing the pathogenetic mechanisms. Prognoses became more accurate, as required by the greater and more targeted possibilities of therapy. | ||
650 | 0 | _aMedicine. | |
650 | 0 | _aCancer research. | |
650 | 0 | _aNeurosciences. | |
650 | 0 | _aNeurology. | |
650 | 0 | _aNeurosurgery. | |
650 | 0 | _aPathology. | |
650 | 1 | 4 | _aBiomedicine. |
650 | 2 | 4 | _aCancer Research. |
650 | 2 | 4 | _aNeurosciences. |
650 | 2 | 4 | _aPathology. |
650 | 2 | 4 | _aNeurosurgery. |
650 | 2 | 4 | _aNeurology. |
650 | 2 | 4 | _aBiomedicine general. |
710 | 2 | _aSpringerLink (Online service) | |
773 | 0 | _tSpringer eBooks | |
776 | 0 | 8 |
_iPrinted edition: _z9781402039973 |
856 | 4 | 0 | _uhttp://dx.doi.org/10.1007/1-4020-3998-0 |
912 | _aZDB-2-SBL | ||
950 | _aBiomedical and Life Sciences (Springer-11642) | ||
999 |
_c502332 _d502332 |