Evidence of multisystem disorder in whole-brain map of pathological TDP-43 in amyotrophic lateral sclerosis.
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Widespread structural and functional connectivity changes in amyotrophic lateral sclerosis: insights from advanced neuroimaging researchALS Patient Stem Cells for Unveiling Disease Signatures of Motoneuron Susceptibility: Perspectives on the Deadly Mitochondria, ER Stress and Calcium TriadWhat does imaging reveal about the pathology of amyotrophic lateral sclerosis?Intrinsic disorder in proteins involved in amyotrophic lateral sclerosis.TDP-43 transgenic mice develop spastic paralysis and neuronal inclusions characteristic of ALS and frontotemporal lobar degenerationCross-sectional evaluation of clinical neuro-ophthalmic abnormalities in an amyotrophic lateral sclerosis population.Whole-brain analysis of amyotrophic lateral sclerosis by using echo-planar spectroscopic imaging.The involvement of the cerebellum in amyotrophic lateral sclerosis.Mimicking aspects of frontotemporal lobar degeneration and Lou Gehrig's disease in rats via TDP-43 overexpression.Transactive response DNA-binding protein 43 burden in familial Alzheimer disease and Down syndromeOlfactory epithelium amyloid-beta and paired helical filament-tau pathology in Alzheimer disease.The role of transactive response DNA-binding protein-43 in amyotrophic lateral sclerosis and frontotemporal dementia.Biomarkers in frontotemporal lobar degenerations--progress and challenges.TAR DNA-binding protein 43 in neurodegenerative disease.Variations in the progranulin gene affect global gene expression in frontotemporal lobar degenerationNarrative discourse deficits in amyotrophic lateral sclerosisTDP-43 is directed to stress granules by sorbitol, a novel physiological osmotic and oxidative stressor.Extensive FUS-immunoreactive pathology in juvenile amyotrophic lateral sclerosis with basophilic inclusions.ALS-Plus syndrome: non-pyramidal features in a large ALS cohort.The cortical signature of amyotrophic lateral sclerosis.Grey and white matter changes across the amyotrophic lateral sclerosis-frontotemporal dementia continuum.Molecular imaging of microglial activation in amyotrophic lateral sclerosis.Behavior matters--cognitive predictors of survival in amyotrophic lateral sclerosis.Pathological 43-kDa transactivation response DNA-binding protein in older adults with and without severe mental illness.Mapping cortical degeneration in ALS with magnetization transfer ratio and voxel-based morphometry.Mice with mutation in dynein heavy chain 1 do not share the same tau expression pattern with mice with SOD1-related motor neuron diseaseTDP-43 pathology in the basal forebrain and hypothalamus of patients with amyotrophic lateral sclerosis.Risk genotypes at TMEM106B are associated with cognitive impairment in amyotrophic lateral sclerosis.Abnormal serine phosphorylation of insulin receptor substrate 1 is associated with tau pathology in Alzheimer's disease and tauopathies.Brain progranulin expression in GRN-associated frontotemporal lobar degenerationMotor neuron disease clinically limited to the lower motor neuron is a diffuse TDP-43 proteinopathy.Amyotrophic lateral sclerosis and frontotemporal lobar degeneration: a spectrum of TDP-43 proteinopathies.Microstructural changes across different clinical milestones of disease in amyotrophic lateral sclerosis.TDP-43 pathology and neuronal loss in amyotrophic lateral sclerosis spinal cordA patient carrying a homozygous p.A382T TARDBP missense mutation shows a syndrome including ALS, extrapyramidal symptoms, and FTDRodent models of TDP-43 proteinopathy: investigating the mechanisms of TDP-43-mediated neurodegeneration1H MRS of basal ganglia and thalamus in amyotrophic lateral sclerosisOn the development of markers for pathological TDP-43 in amyotrophic lateral sclerosis with and without dementia.Talampanel reduces the level of motoneuronal calcium in transgenic mutant SOD1 mice only if applied presymptomaticallyClinical and neuropathologic heterogeneity of c9FTD/ALS associated with hexanucleotide repeat expansion in C9ORF72
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P2860
Evidence of multisystem disorder in whole-brain map of pathological TDP-43 in amyotrophic lateral sclerosis.
description
2008 nî lūn-bûn
@nan
2008年の論文
@ja
2008年学术文章
@wuu
2008年学术文章
@zh
2008年学术文章
@zh-cn
2008年学术文章
@zh-hans
2008年学术文章
@zh-my
2008年学术文章
@zh-sg
2008年學術文章
@yue
2008年學術文章
@zh-hant
name
Evidence of multisystem disord ...... amyotrophic lateral sclerosis.
@en
Evidence of multisystem disord ...... amyotrophic lateral sclerosis.
@nl
type
label
Evidence of multisystem disord ...... amyotrophic lateral sclerosis.
@en
Evidence of multisystem disord ...... amyotrophic lateral sclerosis.
@nl
prefLabel
Evidence of multisystem disord ...... amyotrophic lateral sclerosis.
@en
Evidence of multisystem disord ...... amyotrophic lateral sclerosis.
@nl
P2093
P1433
P1476
Evidence of multisystem disord ...... amyotrophic lateral sclerosis.
@en
P2093
Felix Geser
John Q Trojanowski
Lauren Elman
Leo McCluskey
Linda K Kwong
Nicholas J Brandmeir
Sharon X Xie
Virginia M-Y Lee
P304
P356
10.1001/ARCHNEUR.65.5.636
P577
2008-05-01T00:00:00Z