國立虎尾科技大學 |

Handbook of the Cerebellum and Cerebellar Disorders

Record Type:	Language materials, printed : Monograph/item
Title/Author:	Handbook of the Cerebellum and Cerebellar Disorders/ edited by Mario Manto, Donna Gruol, Jeremy Schmahmann, Noriyuki Koibuchi, Roy Sillitoe.
other author:	Manto, Mario.
Description:	online resource. :
Contained By:	Springer Nature Living Reference
Subject:	Neurosciences. -
Online resource:	https://doi.org/10.1007/978-3-319-97911-3
ISBN:	9783319979113

Handbook of the Cerebellum and Cerebellar Disorders
Handbook of the Cerebellum and Cerebellar Disorders[electronic resource] /edited by Mario Manto, Donna Gruol, Jeremy Schmahmann, Noriyuki Koibuchi, Roy Sillitoe. - online resource.

Chapter 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.

Our 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 authors are 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.

ISBN: 9783319979113

Standard No.: 10.1007/978-3-319-97911-3doiSubjects--Topical Terms:

593561
Neurosciences.

LC Class. No.: RC321-580

Dewey Class. No.: 612.8

Handbook of the Cerebellum and Cerebellar Disorders
LDR:04635nam a22003615i 4500 001 1027477
003 DE-He213
005 20200705003908.0
007 cr nn 008mamaa
008 210318s2020 gw | s |||| 0|eng d
020 $a 9783319979113 $9 978-3-319-97911-3
024 7 $a 10.1007/978-3-319-97911-3 $2 doi
035 $a 978-3-319-97911-3
050 4 $a RC321-580
072 7 $a PSAN $2 bicssc
072 7 $a MED057000 $2 bisacsh
072 7 $a PSAN $2 thema
082 0 4 $a 612.8 $2 23
245 1 0 $a Handbook of the Cerebellum and Cerebellar Disorders $h [electronic resource] / $c edited by Mario Manto, Donna Gruol, Jeremy Schmahmann, Noriyuki Koibuchi, Roy Sillitoe.
264 1 $a Cham : $b Springer International Publishing : $b Imprint: Springer, $c 2020.
300 $b online resource.
336 $a text $b txt $2 rdacontent
337 $a computer $b c $2 rdamedia
338 $a online resource $b cr $2 rdacarrier
347 $a text file $b PDF $2 rda
505 0 $a Chapter 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 $a Our 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 authors are 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 0 $a Neurosciences. $3 593561
650 0 $a Neurochemistry. $3 581832
650 0 $a Neurobiology. $3 573189
650 0 $a Neurology . $3 1253459
650 0 $a Neurosurgery. $3 673771
650 0 $a Human physiology. $3 636012
650 2 4 $a Neurology. $3 593894
650 2 4 $a Human Physiology. $3 668349
700 1 $a Manto, Mario. $4 edt $4 http://id.loc.gov/vocabulary/relators/edt $3 1071175
700 1 $a Gruol, Donna. $e editor. $4 edt $4 http://id.loc.gov/vocabulary/relators/edt $3 1323898
700 1 $a Schmahmann, Jeremy. $e editor. $4 edt $4 http://id.loc.gov/vocabulary/relators/edt $3 1323899
700 1 $a Koibuchi, Noriyuki. $4 edt $4 http://id.loc.gov/vocabulary/relators/edt $3 1071681
700 1 $a Sillitoe, Roy. $e editor. $4 edt $4 http://id.loc.gov/vocabulary/relators/edt $3 1323900
710 2 $a SpringerLink (Online service) $3 593884
773 0 $t Springer Nature Living Reference
856 4 0 $u https://doi.org/10.1007/978-3-319-97911-3
912 $a ZDB-2-SBL
912 $a ZDB-2-SXRB
912 $a ZDB-2-SLR
950 $a Biomedical and Life Sciences (SpringerNature-11642)
950 $a Reference Module Biomedical and Life Sciences (SpringerNature-43744)