Language:
English
繁體中文
Help
Login
Back
Switch To:
Labeled
|
MARC Mode
|
ISBD
Frontotemporal Dementias = Emerging...
~
Boeve, Bradley.
Frontotemporal Dementias = Emerging Milestones of the 21st Century /
Record Type:
Language materials, printed : Monograph/item
Title/Author:
Frontotemporal Dementias / edited by Bernardino Ghetti, Emanuele Buratti, Bradley Boeve, Rosa Rademakers.
Reminder of title:
Emerging Milestones of the 21st Century /
other author:
Ghetti, Bernardino.
Description:
X, 320 p. 46 illus.online resource. :
Contained By:
Springer Nature eBook
Subject:
Neurosciences. -
Online resource:
https://doi.org/10.1007/978-3-030-51140-1
ISBN:
9783030511401
Frontotemporal Dementias = Emerging Milestones of the 21st Century /
Frontotemporal Dementias
Emerging Milestones of the 21st Century /[electronic resource] :edited by Bernardino Ghetti, Emanuele Buratti, Bradley Boeve, Rosa Rademakers. - 1st ed. 2021. - X, 320 p. 46 illus.online resource. - Advances in Experimental Medicine and Biology,12812214-8019 ;. - Advances in Experimental Medicine and Biology,889.
1. Behavioural variant FTD: recent advances in the diagnosis and understanding of the disorder -- 2. The neuropsychiatry of frontotemporal dementia -- 3. Nosology and Neuropathology of Language in Primary Progressive Aphasia -- 4. Measuring Behavior and Cognition in FTLD -- 5. Clinical update on C9orf72: FTD, ALS and beyond -- 6. Clinical aspects of familial FTLD associated with MAPT and GRN mutations -- 7. Neuroimaging in Frontotemporal Lobar Degeneration -- 8. The FTD Prevention Initiative - linking together genetic FTD cohort studies -- 9. Fluid Biomarkers of Frontotemporal Lobar Degeneration -- 10. Cross-cultural perspectives on frontotemporal degeneration -- 11. Clinical characteristics and Neuropathology of PSP, CBD and Related 4R-Tauopathies -- 12. Tau protein and frontotemporal dementias -- 13. FTLD-TDP pathological subtypes: clinical and mechanistic significance -- 14. Lysosomal dysfunction as a pathogenic mechanism in FTD: Evidence from PGRN and TMEM106B genetics and biology -- 15. Future trends in understanding the pathological role of TDP-43 and FUS proteins -- 16. Description of a new data resource for FTD including multiomic data on human post mortem brain (MAPT, GRN, C9orf72), matching mouse models and iPS models -- 17. Mendelian and sporadic FTD: avenues from genetics to disease pathways through in-silico prediction and modeling -- 18. FTLD treatment: Current Practice and Future Possibilities.
Under the name of Frontotemporal Dementias (FTD) numerous hereditary and sporadic disorders are listed. FTD may take away speech and language, social skills and ethical judgement, wishes and will, empathy and emotions; it may also impair motor functions. FTD may affect men and women in midlife or during old age leading to the demolition of the uniqueness of the human mind. In the last decade of the 20th century and in the first two decades of the 21st century, progress in the understanding of clinical, neuropathological, biochemical, and genetic aspects of FTD has accelerated. The novel awareness about FTD has directed young generations of researchers toward the study of this complex group of disorders. This Volume has been formulated with the participation of some of the leading scientists who have contributed to the development of knowledge in the clinical and basic science arenas. It captures the current central elements that are relevant to an up-to-date understanding of causes and pathogenesis of multiple forms of FTD. The volume is an opus that represents a distillation of the work of many scientists and addresses the current directions in the study of one of the most complex groups of diseases. In view of its structure, the book could also be used as a textbook, that offers both a broad and deep analysis of major areas in FTD. This book, planned by the International Society for Frontotemporal Dementias, is distinctive as it opens a window to a wide landscape about the biology of FTD. Thus, the book represents a moment of reflection on the present state of our knowledge of FTD and a collective vision toward scientific progress. The authors of each chapter share their knowledge and vision aimed at reducing the suffering which is caused by FTD.
ISBN: 9783030511401
Standard No.: 10.1007/978-3-030-51140-1doiSubjects--Topical Terms:
593561
Neurosciences.
LC Class. No.: RC321-580
Dewey Class. No.: 612.8
Frontotemporal Dementias = Emerging Milestones of the 21st Century /
LDR
:04710nam a22004095i 4500
001
1051851
003
DE-He213
005
20210930180543.0
007
cr nn 008mamaa
008
220103s2021 sz | s |||| 0|eng d
020
$a
9783030511401
$9
978-3-030-51140-1
024
7
$a
10.1007/978-3-030-51140-1
$2
doi
035
$a
978-3-030-51140-1
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
Frontotemporal Dementias
$h
[electronic resource] :
$b
Emerging Milestones of the 21st Century /
$c
edited by Bernardino Ghetti, Emanuele Buratti, Bradley Boeve, Rosa Rademakers.
250
$a
1st ed. 2021.
264
1
$a
Cham :
$b
Springer International Publishing :
$b
Imprint: Springer,
$c
2021.
300
$a
X, 320 p. 46 illus.
$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
490
1
$a
Advances in Experimental Medicine and Biology,
$x
2214-8019 ;
$v
1281
505
0
$a
1. Behavioural variant FTD: recent advances in the diagnosis and understanding of the disorder -- 2. The neuropsychiatry of frontotemporal dementia -- 3. Nosology and Neuropathology of Language in Primary Progressive Aphasia -- 4. Measuring Behavior and Cognition in FTLD -- 5. Clinical update on C9orf72: FTD, ALS and beyond -- 6. Clinical aspects of familial FTLD associated with MAPT and GRN mutations -- 7. Neuroimaging in Frontotemporal Lobar Degeneration -- 8. The FTD Prevention Initiative - linking together genetic FTD cohort studies -- 9. Fluid Biomarkers of Frontotemporal Lobar Degeneration -- 10. Cross-cultural perspectives on frontotemporal degeneration -- 11. Clinical characteristics and Neuropathology of PSP, CBD and Related 4R-Tauopathies -- 12. Tau protein and frontotemporal dementias -- 13. FTLD-TDP pathological subtypes: clinical and mechanistic significance -- 14. Lysosomal dysfunction as a pathogenic mechanism in FTD: Evidence from PGRN and TMEM106B genetics and biology -- 15. Future trends in understanding the pathological role of TDP-43 and FUS proteins -- 16. Description of a new data resource for FTD including multiomic data on human post mortem brain (MAPT, GRN, C9orf72), matching mouse models and iPS models -- 17. Mendelian and sporadic FTD: avenues from genetics to disease pathways through in-silico prediction and modeling -- 18. FTLD treatment: Current Practice and Future Possibilities.
520
$a
Under the name of Frontotemporal Dementias (FTD) numerous hereditary and sporadic disorders are listed. FTD may take away speech and language, social skills and ethical judgement, wishes and will, empathy and emotions; it may also impair motor functions. FTD may affect men and women in midlife or during old age leading to the demolition of the uniqueness of the human mind. In the last decade of the 20th century and in the first two decades of the 21st century, progress in the understanding of clinical, neuropathological, biochemical, and genetic aspects of FTD has accelerated. The novel awareness about FTD has directed young generations of researchers toward the study of this complex group of disorders. This Volume has been formulated with the participation of some of the leading scientists who have contributed to the development of knowledge in the clinical and basic science arenas. It captures the current central elements that are relevant to an up-to-date understanding of causes and pathogenesis of multiple forms of FTD. The volume is an opus that represents a distillation of the work of many scientists and addresses the current directions in the study of one of the most complex groups of diseases. In view of its structure, the book could also be used as a textbook, that offers both a broad and deep analysis of major areas in FTD. This book, planned by the International Society for Frontotemporal Dementias, is distinctive as it opens a window to a wide landscape about the biology of FTD. Thus, the book represents a moment of reflection on the present state of our knowledge of FTD and a collective vision toward scientific progress. The authors of each chapter share their knowledge and vision aimed at reducing the suffering which is caused by FTD.
650
0
$a
Neurosciences.
$3
593561
650
0
$a
Neurology .
$3
1253459
650
0
$a
Human genetics.
$3
596505
650
2 4
$a
Neurology.
$3
593894
650
2 4
$a
Human Genetics.
$3
593893
700
1
$a
Ghetti, Bernardino.
$e
editor.
$4
edt
$4
http://id.loc.gov/vocabulary/relators/edt
$3
1356456
700
1
$a
Buratti, Emanuele.
$e
editor.
$4
edt
$4
http://id.loc.gov/vocabulary/relators/edt
$3
1356457
700
1
$a
Boeve, Bradley.
$e
editor.
$4
edt
$4
http://id.loc.gov/vocabulary/relators/edt
$3
1356458
700
1
$a
Rademakers, Rosa.
$e
editor.
$4
edt
$4
http://id.loc.gov/vocabulary/relators/edt
$3
1356459
710
2
$a
SpringerLink (Online service)
$3
593884
773
0
$t
Springer Nature eBook
776
0 8
$i
Printed edition:
$z
9783030511395
776
0 8
$i
Printed edition:
$z
9783030511418
776
0 8
$i
Printed edition:
$z
9783030511425
830
0
$a
Advances in Experimental Medicine and Biology,
$x
0065-2598 ;
$v
889
$3
1253792
856
4 0
$u
https://doi.org/10.1007/978-3-030-51140-1
912
$a
ZDB-2-SBL
912
$a
ZDB-2-SXB
950
$a
Biomedical and Life Sciences (SpringerNature-11642)
950
$a
Biomedical and Life Sciences (R0) (SpringerNature-43708)
based on 0 review(s)
Multimedia
Reviews
Add a review
and share your thoughts with other readers
Export
pickup library
Processing
...
Change password
Login