TDP-43 deposition in prospectively followed, cognitively normal elderly individuals: correlation with argyrophilic grains but not other concomitant pathologies.
about
Hippocampal sclerosis of aging, a prevalent and high-morbidity brain diseaseExpanded C9ORF72 hexanucleotide repeat in depressive pseudodementia.Prevalence of mixed pathologies in the aging brainIncidence and extent of TDP-43 accumulation in aging human brain.Arizona Study of Aging and Neurodegenerative Disorders and Brain and Body Donation Program.Higher Prevalence of TDP-43 Proteinopathy in Cognitively Normal Asians: A Clinicopathological Study on a Multiethnic Sample.Altered Proteins in the Aging BrainDetection of TDP-43 oligomers in frontotemporal lobar degeneration-TDP.Hippocampal Sclerosis but Not Normal Aging or Alzheimer Disease Is Associated With TDP-43 Pathology in the Basal Forebrain of Aged PersonsTBK1 Mutation Spectrum in an Extended European Patient Cohort with Frontotemporal Dementia and Amyotrophic Lateral Sclerosis.Challenges of multimorbidity of the aging brain: a critical update.TDP-43 pathology and memory impairment in elders without pathologic diagnoses of AD or FTLD.Prevalence of TDP-43 proteinopathy in cognitively normal older adults: systematic review and meta-analysis.Overlapping but distinct TDP-43 and tau pathologic patterns in aged hippocampi.Pathology of Neurodegenerative Diseases.TDP-43 stage, mixed pathologies, and clinical Alzheimer's-type dementia.Adenoviral expression of TDP-43 and FUS genes and shRNAs for protein degradation pathways in rodent motoneurons in vitro and in vivo.Argyrophilic grain disease: An underestimated tauopathy.The Amygdala as a Locus of Pathologic Misfolding in Neurodegenerative Diseases.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.Possible concurrence of TDP-43, tau and other proteins in amyotrophic lateral sclerosis/frontotemporal lobar degeneration.Perry Syndrome: A Distinctive Type of TDP-43 Proteinopathy.Amygdala TDP-43 Pathology in Frontotemporal Lobar Degeneration and Motor Neuron Disease.Non-Alzheimer neurodegenerative pathologies and their combinations are more frequent than commonly believed in the elderly brain: a community-based autopsy series.Distribution and characteristics of transactive response DNA binding protein 43 kDa pathology in progressive supranuclear palsy.TDP-43 pathology in Alzheimer's disease, dementia with Lewy bodies and ageing.No interaction between tau and TDP-43 pathologies in either frontotemporal lobar degeneration or motor neurone disease.Updated TDP-43 in Alzheimer's disease staging scheme.Multiregional Age-Associated Reduction of Brain Neuronal Reserve Without Association With Neurofibrillary Degeneration or β-Amyloidosis.
P2860
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P2860
TDP-43 deposition in prospectively followed, cognitively normal elderly individuals: correlation with argyrophilic grains but not other concomitant pathologies.
description
2013 nî lūn-bûn
@nan
2013年の論文
@ja
2013年論文
@yue
2013年論文
@zh-hant
2013年論文
@zh-hk
2013年論文
@zh-mo
2013年論文
@zh-tw
2013年论文
@wuu
2013年论文
@zh
2013年论文
@zh-cn
name
TDP-43 deposition in prospecti ...... other concomitant pathologies.
@en
type
label
TDP-43 deposition in prospecti ...... other concomitant pathologies.
@en
prefLabel
TDP-43 deposition in prospecti ...... other concomitant pathologies.
@en
P2860
P1476
TDP-43 deposition in prospecti ...... other concomitant pathologies.
@en
P2093
Brittany N Dugger
Stacy J Arnold
P2860
P2888
P356
10.1007/S00401-013-1110-0
P577
2013-04-20T00:00:00Z