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Tumors of the Central Nervous System, Volume 2: Gliomas: Glioblastoma (Part 2)

ISBN-13: 9789400735804 / Angielski / Miękka / 2013 / 458 str.

M. A. Hayat
Tumors of the Central Nervous System, Volume 2: Gliomas: Glioblastoma (Part 2) Hayat, M. A. 9789400735804 Springer - książkaWidoczna okładka, to zdjęcie poglądowe, a rzeczywista szata graficzna może różnić się od prezentowanej.

Tumors of the Central Nervous System, Volume 2: Gliomas: Glioblastoma (Part 2)

ISBN-13: 9789400735804 / Angielski / Miękka / 2013 / 458 str.

M. A. Hayat
cena 803,21
(netto: 764,96 VAT:  5%)

Najniższa cena z 30 dni: 771,08
Termin realizacji zamówienia:
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Dostawa w 2026 r.

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inne wydania

Advantages and limitations of biomarkers in gliomagenesis are described. Molecular subtypes of gliomas are detailed. The role played by TP53 gene mutation in the deadliest brain tumor, glioblastoma multiforme, is pointed out. The role of mutations of IDH1 and IDH2, and isocitrate dehydrogenases in malignant gliomas are presented. Metabolic differences in different regions of the glioma tumor are clarified. Various types of imaging modalities, including PET and SPECT, to diagnose gliomas in general and glioblastoma in particular in patients are explained in detail. Both low-grade and high-grade gliomas are discussed. Conventional as well as fluorescent-guided resection techniques for high-grade, recurrent malignant gliomas are detailed. Impact of resection extent on outcomes in patients with high-grade gliomas is clarified. The advantage of the use of intraoperative low-field MRI in glioma surgery is explained.

Kategorie:
Nauka, Medycyna
Kategorie BISAC:
Medical > Oncology - General
Medical > Neurologia i neurofizjologia kliniczna
Medical > Radiologia
Wydawca:
Springer
Seria wydawnicza:
Tumors of the Central Nervous System
Język:
Angielski
ISBN-13:
9789400735804
Rok wydania:
2013
Numer serii:
000435155
Ilość stron:
458
Waga:
1.00 kg
Wymiary:
26.0 x 19.3
Oprawa:
Miękka
Wolumenów:
01

Chapter 1. INTRODUCTION. I. BIOMARKERS AND DIAGNOSIS. Chapter  2. GLIOMAGENESIS: ADVANTAGES AND LIMITATIONS OF BIOMARKERS. Chapter  3. MOLECULAR SUBTYPES OF GLIOMAS. Chapter  4. GLIOBLASTOMA: GERMLINE MUTATION OF TP53. Chapter  5. GLIOMAS: ROLE OF THE TP53 GENE. Chapter  6. THE ROLE OF IDH1 AND IDH2 MUTATIONS IN MALIGNANT GLIOMAS. Chapter  7. MALIGNANT GLIOMA: ISOCITRATE DEHYDROGENASES 1 AND 2  MUTATIONS. Chapter  8. METABOLIC DIFFERNCES IN DIFFERENT REGIONS OF GLIOMA SAMPLES. Chapter  9. GLIOBLASTOMA PATIENTS: ROLE OF METHYLATED MGMT. Chapter  10. BRAIN TUMOR ANGIOGENESIS AND GLIOMA GRADING: ROLE OF TUMOR BLOOD VOLUME AND PERMEABILITY ESTIMATES USING PERFUSION CT. Chapter 11.  VASCULOGENIC MIMICRY IN GLIOMA. Chapter 12. NEWLY DIAGNOSED GLIOMA: DIAGNOSIS USING POSITRON EMISSION TOMOGRAPHY WITH METHIONINE AND FLUOROTHYMIDINE. Chapter  13. ROLE OF DIFFUSION TENSOR IMAGING IN DIFFERENTIATION OF GLIOBLASTOMAS FROM  SOLITARY BRAIN METASTASES. Chapter  14. I-TM-601 SPECT IMAGING OF HUMAN GLIOMA. Chapter  15. ASSESSMENT OF BIOLOGICAL TARGET VOLUME USING POSITRON EMISSION TOMOGRAPHY IN HIGH-GRADE GLIOMA PATIENTS. Chapter  16. SKIN METASTASES OF GLIOBLASTOMA. II. THERAPY. Chapter 17. DIFFUSE LOW-GRADE GLIOMAS. WHAT DOES “COMPLETE RESECTION” MEAN? Chapter 18. QUANTITATIVE APPROACH OF THE NATURAL COURSE OF DIFFUSE LOW-GRADE GLIOMAS. Chapter  19. IMPACT OF RESECTION EXTENT ON OUTCOMES IN PATIENTS WITH HIGH-GRADE GLIOMAS. Chapter 20. RECURRENT MALIGNANT GLIOMAS: 5-AMINOLEVULINIC ACID FLUORESCENCE-GUIDED RESECTION. Chapter 21. GLIOMA SURGERY: INTRAOPERATIVE LOW FIELD MAGNETIC RESONANCE IMAGING. Chapter  22. LOW-GRADE GLIOMAS: INTRAOPERATIVE ELECTRICAL STIMULATIONS. Chapter  23. MALIGNANT GLIOMAS: PRESENT AND FUTURE THERAPEUTIC DRUGS. Chapter 24. RECURRENT MALIGNANT GLIOMA PATIENTS: TREATMENT WITH CONFORMAL RADIOTHERAPY AND SYSTEMIC THERAPY. Chapter  25. GLIOBLASTOMA: BORON NEUTRON CAPTURE THERAPY. Chapter  26. GLIOBLASTOMA: ANTI-TUMOR ACTION OF CYCLOSPORINE A AND FUCTIONALLY RELATED DRUGS.Chapter 27. GLIOBLASTOMA PATIENTS: CHEMOTHERAPY WITH CISPLATIN, TEMOZOLOMIDE AND THALIDOMIDE. Chapter  28. GLIOBLASTOMA : ROLE OF GALECTIN- 1 IN CHEMORESISTANCE. Chapter  29. GLIOMA-INITIATING CELLS: INTERFERON TREATMENT. Chapter  30. GLIOBLASTOMA : ANTITUMOR ACTION OF NATURAL AND SYNTHETIC  CANNABINOIDS. Chapter  31. PATIENTS WITH RECURRENT HIGH-GRADE GLIOMA: THERAPY WITH COMBINATION OF BEVACIZUMAB AND IRINOTECAN. Chapter 32. MONITORING GLIOMAS IN VIVO USING DIFFUSION- WEIGHTED MRI DURING GENE THREAPY –INDUCED APOPTOSIS. Chapter 33. HIGH-GRADE GLIOMAS: DENDRITIC CELL THERAPY. Chapter 34. GLIOBLASTOMA MULTIFORME: USE OF ADENOVIRAL VECTORS. Chapter 35. FISCHER-F98 GLIOMA MODEL: METHODOLOGY. Chapter  36. CELLULAR CHARACTERIZATION OF ANTI-VEGF AND IL-6 THERAPY IN EXPERIMENTAL  GLIOMA. Chapter  37. ADULT BRAINSTEM GLIOMAS: DIAGNOSIS AND TREATMENT . Chapter  38. USE OF LOW MOLECULAR WEIGHT HEPARIN IN THE TREATMENT AND PREVENTION OF THROMBOEMBOLIC DISEASE IN GLIOMA PATIENTS. III. PROGNOSIS. Chapter 39. BRAINSTEM GLIOMAS: AN OVERVIEW. Chapter  40. TUMOR-ASSOCIATED EPILEPSY IN PATIENTS WITH GLIOMA. Chapter 41. CHRONIC EPILEPSY ASSOCIATED WITH BRAIN TUMORS: SURGICAL NEUROPATHOLOGY. Chapter 42. LOW-GRADE GLIOMAS: ROLE OF RELATIVE CEREBRAL BLOOD VOLUME IN MALIGNANT TRANSFORMATION. Chapter 43. ANGIOCENTRIC GLIOMA- INDUCED SEIZURES: LESIONECTOMY.

Advantages and limitations of biomarkers in gliomagenesis are described. Molecular subtypes of gliomas are detailed. The role played by TP53 gene mutation in the deadliest brain tumor, glioblastoma multiforme, is pointed out. The role of mutations of IDH1 and IDH2, and isocitrate dehydrogenases in malignant gliomas are presented. Metabolic differences in different regions of the glioma tumor are clarified. Various types of imaging modalities, including PET and SPECT, to diagnose gliomas in general and glioblastoma in particular in patients are explained in detail. Both low-grade and high-grade gliomas are discussed. Conventional as well as fluorescent-guided resection techniques for high-grade, recurrent malignant gliomas are detailed. Impact of resection extent on outcomes in patients with high-grade gliomas is clarified. The advantage of the use of intraoperative low-field MRI in glioma surgery is explained.



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