Download Advances and Technical Standards in Neurosurgery Volume 33 by John D. Pickard, Nejat Akalan, C. Di Rocco, Vinko V. Dolenc, PDF

By John D. Pickard, Nejat Akalan, C. Di Rocco, Vinko V. Dolenc, J. Lobo Antunes, J. J. A. Mooij, J. Schramm, Marc Sindou

This sequence has already develop into a vintage. as a rule, one quantity is released consistent with 12 months. The advances part provides fields of neurosurgery and comparable parts during which very important fresh development has been made. The technical criteria part gains distinctive descriptions of ordinary systems to aid younger neurosurgeons of their post-graduate education. The contributions are written by way of skilled clinicians and are reviewed through all individuals of the editorial board.

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Ivanco TL, Greenough WT (2000) Physiological consequences of morphologically detectable synaptic plasticity: potential uses for examining recovery following damage. Neuropharmacology 39: 765–776 69. Jackson JH (1879) On affections of speech from disease of the brain. Brain 1879: 323–356 70. Jacobs KM, Donoghue JP (1991) Reshaping the cortical motor map by unmasking latent intracortical connections. Science 251: 944–947 71. Krainik A, Lehericy S, Duffau H, Capelle L, Chainay H, Cornu P, Cohen L, Boch AL, Mangin JF, Le Bihan D, Marsault C (2003) Postoperative speech disorder after medial frontal surgery: role of the supplementary motor area.

93 Extreme lateral approach . . . . . . . . . . . . . . . . . 93 Radiotherapy . . . . . . . . . . . . . . . . . . . . . . . 99 Conventional radiotherapy . . . . . . . . . . . . . . . . . 102 LINAC based stereotactic radiotherapies . . . . . . . . . . . . 102 Gamma-Knife radiosurgery . . . . . . . . . . . . . . . . . 103 Brachytherapy. . . . . . . . . . . . . . . . . . . . . . 104 Charged particle radiation therapies.

109 Abstract Chordomas are rare, slow growing tumors of the axial skeleton, which derive from the remnants of the fetal notochord. They can be encountered anywhere along the axial skeleton, most commonly in the sacral area, skull base and less commonly in the spine. Chordomas have a benign histopathology but exhibit malignant clinical behavior with invasive, destructive and metastatic potential. Genetic and molecular pathology studies on oncogenesis of chordomas are very limited and there is little known on mechanisms governing the disease.

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