TDP-43 proteinopathies: pathological identification of brain regions differentiating clinical phenotypes.
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Assessment of amyloid β in pathologically confirmed frontotemporal dementia syndromes.Heterogeneity of cerebral TDP-43 pathology in sporadic amyotrophic lateral sclerosis: Evidence for clinico-pathologic subtypesPrevalence of TDP-43 proteinopathy in cognitively normal older adults: systematic review and meta-analysis."New Old Pathologies": AD, PART, and Cerebral Age-Related TDP-43 With Sclerosis (CARTS).ALS/FTLD: experimental models and reality.Synapse Dysfunction of Layer V Pyramidal Neurons Precedes Neurodegeneration in a Mouse Model of TDP-43 Proteinopathies.Reduced TDP-43 Expression Improves Neuronal Activities in a Drosophila Model of Perry Syndrome.Distinct TDP-43 inclusion morphologies in frontotemporal lobar degeneration with and without amyotrophic lateral sclerosis.Multiple neuronal pathologies are common in young patients with pathologically proven Frontotemporal lobar degeneration.Anterior Cingulate Cortex TDP-43 Pathology in Sporadic Amyotrophic Lateral Sclerosis.Longitudinal structural changes in ALS: a three time-point imaging study of white and gray matter degeneration.Imaging the pathoanatomy of amyotrophic lateral sclerosis in vivo: targeting a propagation-based biological marker.Perry Syndrome: A Distinctive Type of TDP-43 Proteinopathy.A Single Neonatal Exposure to BMAA in a Rat Model Produces Neuropathology Consistent with Neurodegenerative Diseases.Distribution and characteristics of transactive response DNA binding protein 43 kDa pathology in progressive supranuclear palsy.Can Astrocytes Be a Target for Precision Medicine?Emergence of an imaging biomarker for amyotrophic lateral sclerosis: is the end point near?von Economo Neuron Density and Thalamus Volumes in Behavioral Deficits in Frontotemporal Dementia Cases with and without a C9ORF72 Repeat Expansion.Progress and Challenges in Frontotemporal Dementia Research: A 20-Year Review.Dissecting the pathobiology of altered MRI signal in amyotrophic lateral sclerosis: A post mortem whole brain sampling strategy for the integration of ultra-high-field MRI and quantitative neuropathology.
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P2860
TDP-43 proteinopathies: pathological identification of brain regions differentiating clinical phenotypes.
description
2015 nî lūn-bûn
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2015年の論文
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2015年学术文章
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2015年学术文章
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2015年学术文章
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2015年学术文章
@zh-my
2015年学术文章
@zh-sg
2015年學術文章
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2015年學術文章
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2015年學術文章
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name
TDP-43 proteinopathies: pathol ...... entiating clinical phenotypes.
@en
TDP-43 proteinopathies: pathol ...... entiating clinical phenotypes.
@nl
type
label
TDP-43 proteinopathies: pathol ...... entiating clinical phenotypes.
@en
TDP-43 proteinopathies: pathol ...... entiating clinical phenotypes.
@nl
prefLabel
TDP-43 proteinopathies: pathol ...... entiating clinical phenotypes.
@en
TDP-43 proteinopathies: pathol ...... entiating clinical phenotypes.
@nl
P2093
P2860
P50
P356
P1433
P1476
TDP-43 proteinopathies: pathol ...... rentiating clinical phenotypes
@en
P2093
Andrew McGeachie
Heather McCann
John R Hodges
Manaal Fatima
Matthew C Kiernan
Shelley L Forrest
P2860
P304
P356
10.1093/BRAIN/AWV220
P407
P577
2015-07-31T00:00:00Z