Marked Involvement of the Striatal Efferent System in TAR DNA-Binding Protein 43 kDa-Related Frontotemporal Lobar Degeneration and Amyotrophic Lateral Sclerosis
Published 2016 View Full Article
- Home
- Publications
- Publication Search
- Publication Details
Title
Marked Involvement of the Striatal Efferent System in TAR DNA-Binding Protein 43 kDa-Related Frontotemporal Lobar Degeneration and Amyotrophic Lateral Sclerosis
Authors
Keywords
-
Journal
JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY
Volume 75, Issue 8, Pages 801-811
Publisher
Oxford University Press (OUP)
Online
2016-06-27
DOI
10.1093/jnen/nlw053
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- Fair play: social norm compliance failures in behavioural variant frontotemporal dementia
- (2015) Claire O’Callaghan et al. BRAIN
- Fronto-Striatal Atrophy in Behavioral Variant Frontotemporal Dementia and Alzheimer’s Disease
- (2015) Maxime Bertoux et al. Frontiers in Neurology
- Self-awareness in neurodegenerative disease relies on neural structures mediating reward-driven attention
- (2014) Tal Shany-Ur et al. BRAIN
- Neurogenesis in the Striatum of the Adult Human Brain
- (2014) Aurélie Ernst et al. CELL
- Similar effects of substance P on learning and memory function between hippocampus and striatal marginal division
- (2014) Changchun Zeng et al. Neural Regeneration Research
- Differential motor neuron involvement in progressive muscular atrophy: a comparative study with amyotrophic lateral sclerosis
- (2014) Yuichi Riku et al. BMJ Open
- Stages of pTDP-43 pathology in amyotrophic lateral sclerosis
- (2013) Johannes Brettschneider et al. ANNALS OF NEUROLOGY
- Amyotrophic lateral sclerosis—a model of corticofugal axonal spread
- (2013) Heiko Braak et al. Nature Reviews Neurology
- Basal ganglia involvement in amyotrophic lateral sclerosis
- (2013) P. Bede et al. NEUROLOGY
- Lower Motor Neuron Involvement in TAR DNA-Binding Protein of 43 kDa–Related Frontotemporal Lobar Degeneration and Amyotrophic Lateral Sclerosis
- (2013) Yuichi Riku et al. JAMA Neurology
- Pattern of ubiquilin pathology in ALS and FTLD indicates presence of C9ORF72 hexanucleotide expansion
- (2012) Johannes Brettschneider et al. ACTA NEUROPATHOLOGICA
- Japanese amyotrophic lateral sclerosis patients with GGGGCC hexanucleotide repeat expansion in C9ORF72
- (2012) T. Konno et al. JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY
- Distribution of GABAergic Interneurons and Dopaminergic Cells in the Functional Territories of the Human Striatum
- (2012) Javier Bernácer et al. PLoS One
- Motor neuron disease clinically limited to the lower motor neuron is a diffuse TDP-43 proteinopathy
- (2011) Felix Geser et al. ACTA NEUROPATHOLOGICA
- Neuropathological background of phenotypical variability in frontotemporal dementia
- (2011) Keith A. Josephs et al. ACTA NEUROPATHOLOGICA
- A harmonized classification system for FTLD-TDP pathology
- (2011) Ian R. A. Mackenzie et al. ACTA NEUROPATHOLOGICA
- National Institute on Aging–Alzheimer’s Association guidelines for the neuropathologic assessment of Alzheimer’s disease: a practical approach
- (2011) Thomas J. Montine et al. ACTA NEUROPATHOLOGICA
- Sensitivity of revised diagnostic criteria for the behavioural variant of frontotemporal dementia
- (2011) Katya Rascovsky et al. BRAIN
- Classification of primary progressive aphasia and its variants
- (2011) M. L. Gorno-Tempini et al. NEUROLOGY
- The Neural Basis of Intuitive Best Next-Move Generation in Board Game Experts
- (2011) X. Wan et al. SCIENCE
- Basal Ganglia Disorders Associated with Imbalances in the Striatal Striosome and Matrix Compartments
- (2011) Jill R. Crittenden et al. Frontiers in Neuroanatomy
- Functional Significance of Striatal Responses during Episodic Decisions: Recovery or Goal Attainment?
- (2010) S. Han et al. JOURNAL OF NEUROSCIENCE
- Early onset of aging-like changes is restricted to cognitive abilities and skin structure in Cnr1−/− mice
- (2010) Andras Bilkei-Gorzo et al. NEUROBIOLOGY OF AGING
- TDP-43 transgenic mice develop spastic paralysis and neuronal inclusions characteristic of ALS and frontotemporal lobar degeneration
- (2010) Hans Wils et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Evaluation of subcortical pathology and clinical correlations in FTLD-U subtypes
- (2009) Keith A. Josephs et al. ACTA NEUROPATHOLOGICA
- Clinicopathological characterization of Pick’s disease versus frontotemporal lobar degeneration with ubiquitin/TDP-43-positive inclusions
- (2009) Osamu Yokota et al. ACTA NEUROPATHOLOGICA
- Clinical and Pathological Continuum of Multisystem TDP-43 Proteinopathies
- (2009) Felix Geser et al. ARCHIVES OF NEUROLOGY
- Sporadic amyotrophic lateral sclerosis: two pathological patterns shown by analysis of distribution of TDP-43-immunoreactive neuronal and glial cytoplasmic inclusions
- (2008) Yasushi Nishihira et al. ACTA NEUROPATHOLOGICA
- Sporadic amyotrophic lateral sclerosis of long duration is associated with relatively mild TDP-43 pathology
- (2008) Yasushi Nishihira et al. ACTA NEUROPATHOLOGICA
- Effects of substance P microinjections into the globus pallidus and central nucleus of amygdala on passive avoidance learning in rats
- (2008) Erika Kertes et al. BEHAVIOURAL BRAIN RESEARCH
Find Funding. Review Successful Grants.
Explore over 25,000 new funding opportunities and over 6,000,000 successful grants.
ExploreCreate your own webinar
Interested in hosting your own webinar? Check the schedule and propose your idea to the Peeref Content Team.
Create Now