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001			76727
003			ES-MaUEC
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007			cr nn 008mamaa
008			120913s2013 ne | s |||| 0|eng d
020			_a9789400713338
024	7		_a10.1007/978-94-007-1333-8 _2doi
040			_aES-MaUEC
050		4	_aQP379 _b.H36 2013 EB
082	0	4	_a612.8
700	1		_aManto, Mario _eeditor literario. _984532 _0Local _0http://id.loc.gov/authorities/names/nb2002003465 _1http://viaf.org/viaf/29755942
245	0	0	_aHandbook of the Cerebellum and Cerebellar Disorders _cedited by Mario Manto, Jeremy D. Schmahmann, Ferdinando Rossi, Donna L. Gruol, Noriyuki Koibuchi.
264		1	_aDordrecht, Netherlands _bSpringer International Publishing _c2013
300			_a1 recurso en línea (XXXIV, 2424 páginas) _b450 ilustraciones, 400 ilustraciones en color eReference.
336			_aTexto (visual) _btxt _2rdacontent
337			_aelectrónico _bc _2rdamedia
338			_arecurso electrónico _bcr _2rdacarrier
505	0		_aChapter 1. Embryology -- Chapter 2. Anatomy -- Chapter 3. Neuroimaging of the cerebellum -- Chapter 4. Neurotransmitters and neuromodulators -- Chapter 5. Fructose metabolism and the cerebellum -- Chapter 6. Physiology of the cerebellum -- Chapter 7. Cerebellum and pain processing -- Chapter 8. Computational models of cerebellar function -- Chapter 9. Animal models of cerebellar ataxias -- Chapter 10. Symptoms of cerebellar disorders in human -- Chapter 11. Clinical deficits -- Chapter 12. Cerebellum and cognitive processes -- Chapter 13. Cerebellum and emotion regulation -- Chapter 14. Developmental disorders -- Chapter 15. Autism spectrum disorders and ataxia -- Chapter 16. Cerebellum and schizophrenia -- Chapter 17. Progressive myoclonic epilepsies -- Chapter 18. Cerebellar stroke -- Chapter 19. Immune diseases -- Chapter 20. Endocrine disorders -- Chapter 21. Infectious diseases -- Chapter 22. Tumors and paraneoplastic disorders -- Chapter 23. Trauma of the posterior fossa -- Chapter 24. Cerebellotoxic agents -- Chapter 25. Multiple system atrophy (MSA) -- Chapter 26. Essential tremor -- Chapter 27. Autosomal Recessive Cerebellar Ataxias (ARCAs) -- Chapter 28. Mitochondrial disorders -- Chapter 29. X-linked ataxias -- Chapter 30. Dominant ataxias -- Chapter 31. Overview of the differential diagnosis of cerebellar disorders -- Chapter 32. Overview of the general management of cerebellar disorders.
520			_aOur knowledge of cerebellar functions and cerebellar disorders, called ataxias, is increasing considerably. Studies of the cerebellum are now a central focus in neuroscience. During the last four decades, many laboratories worldwide have dedicated their research activities to understanding the roles of the cerebellum in motor control, cognitive processes and biology of mental processes, behavioral symptoms, and emotion. It is now accepted that the cerebellum acts as a cognitive operator in learning, perception, and attention. Moreover, major improvements in our assessment of in vivo cerebellar architecture using imaging techniques have occurred. A typical example is the accurate description of cerebellar anatomy during fetal development with MRI, a progress which has direct impacts on patient care. These advances have been associated with discoveries of new clinical disorders, in particular in the field of genetic ataxias. More than 20 new genes have been identified these last 10 years. Only for dominant ataxias, more than 30 diseases have now been unravelled. The number of ataxic disorders will increase with aging, the cerebellum being the structure of the brain with the most important loss of neurons with age. More than 300 different cerebellar disorders are encountered during daily practice, but we are missing a single source of information explaining their pathogenesis. Despite the immense amount of knowledge acquired about the cerebellar circuitry these last years, a large book covering the neuroscience of the cerebellum is missing. The goal of this endeavour is to bring up to date information relevant for basic science and also for clinical activities. To reach this goal, the most renowned authorsÂ{u1CA5} gathered in a unique and in-depth book with a format of a handbook. We emphasize the connections between molecular findings, imaging features, behavioural/neuropsychological aspects, and clinical implications.
650		7	_aFisiología humana _2embne _9140024
700	1		_aGruol, Donna L. _eeditor literario _0Local _1http://viaf.org/viaf/1742148122891195200003 _986019
700	1		_aKoibuchi, Noriyuki _eeditor literario _0Local _0http://id.loc.gov/authorities/names/nb2012023935 _1http://viaf.org/viaf/272506043 _986020
700	1		_aRossi, Ferdinando _eeditor literario _929953 _0comprobar BNE19990525103 _1http://viaf.org/viaf/92492500
700	1		_aSchmahmann, Jeremy D _eeditor literario _986018 _0Local _1http://viaf.org/viaf/64312986
856	4	0	_uhttps://go.openathens.net/redirector/universidadeuropea.es?url=https://link.springer.com/book/10.1007/978-94-007-1333-8 _zAcceso a este recurso digital (usuarios Universidad Europea de Madrid)
907			_a.b12823454 _b10-10-17 _c01-10-14
942			_2lcc _cLE
945			_aRC321-580 EB _g1 _ieBOOK _j0 _lmae _o- _pEUR0.00 _q- _r- _sb _t15 _u0 _v0 _w0 _x0 _y.i11552669 _z06-04-17
988	0	0	_aEBOOK, EBSPRINGER, GOBI_sep2018
988			_aEbook_one2one
998			_aSI _a_alco _a_vill _b10/2018 _cm _dz _ef _feng _gne _h0
999			_c76727 _d76727 _x1