Focality, stochasticity and neuroanatomic propagation in ALS pathogenesis
about
Recent advances in amyotrophic lateral sclerosisNeuropathology of Amyotrophic Lateral Sclerosis and Its Variants.Environmental insults: critical triggers for amyotrophic lateral sclerosisTDP-43 pathology in the basal forebrain and hypothalamus of patients with amyotrophic lateral sclerosis.Special Issue on amyotrophic lateral sclerosis.A Multiscale Mapping Assessment of Lake Champlain Cyanobacterial Harmful Algal BloomsIn vitro prion-like behaviour of TDP-43 in ALS.Stem cells therapy for ALS.The established and emerging roles of astrocytes and microglia in amyotrophic lateral sclerosis and frontotemporal dementiaEndocytic membrane trafficking and neurodegenerative disease.Disease Mechanisms in ALS: Misfolded SOD1 Transferred Through Exosome-Dependent and Exosome-Independent Pathways.Assessing Cyanobacterial Harmful Algal Blooms as Risk Factors for Amyotrophic Lateral Sclerosis.Novel therapies in development that inhibit motor neuron hyperexcitability in amyotrophic lateral sclerosis.Pathogenesis of amyotrophic lateral sclerosis.Prion-like propagation as a pathogenic principle in frontotemporal dementia.Neurodegeneration and RNA-binding proteins.Boundary Cap Neural Crest Stem Cells Promote Survival of Mutant SOD1 Motor Neurons.Clinical Spectrum of Amyotrophic Lateral Sclerosis (ALS).Biological Spectrum of Amyotrophic Lateral Sclerosis Prions.Chemotherapy-Induced Tissue Injury: An Insight into the Role of Extracellular Vesicles-Mediated Oxidative Stress Responses.Targeted Genetic Screen in Amyotrophic Lateral Sclerosis Reveals Novel Genetic Variants with Synergistic Effect on Clinical Phenotype.Escape from homeostasis: spinal microcircuits and progression of amyotrophic lateral sclerosis.Patterns of symptom development in patients with motor neuron disease.TDP-43 Proteinopathy: Aggregation and Propagation in the Pathogenesis of Amyotrophic Lateral Sclerosis.Clinical Significance of TDP-43 Neuropathology in Amyotrophic Lateral Sclerosis.Perfusion alterations converge with patterns of pathological spread in transactive response DNA-binding protein 43 proteinopathies.Sequence features governing aggregation or degradation of prion-like proteins
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P2860
Focality, stochasticity and neuroanatomic propagation in ALS pathogenesis
description
2014 nî lūn-bûn
@nan
2014 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2014 թվականի դեկտեմբերին հրատարակված գիտական հոդված
@hy
2014年の論文
@ja
2014年論文
@yue
2014年論文
@zh-hant
2014年論文
@zh-hk
2014年論文
@zh-mo
2014年論文
@zh-tw
2014年论文
@wuu
name
Focality, stochasticity and neuroanatomic propagation in ALS pathogenesis
@ast
Focality, stochasticity and neuroanatomic propagation in ALS pathogenesis
@en
Focality, stochasticity and neuroanatomic propagation in ALS pathogenesis
@nl
type
label
Focality, stochasticity and neuroanatomic propagation in ALS pathogenesis
@ast
Focality, stochasticity and neuroanatomic propagation in ALS pathogenesis
@en
Focality, stochasticity and neuroanatomic propagation in ALS pathogenesis
@nl
prefLabel
Focality, stochasticity and neuroanatomic propagation in ALS pathogenesis
@ast
Focality, stochasticity and neuroanatomic propagation in ALS pathogenesis
@en
Focality, stochasticity and neuroanatomic propagation in ALS pathogenesis
@nl
P2860
P3181
P1476
Focality, stochasticity and neuroanatomic propagation in ALS pathogenesis
@en
P2093
John Ravits
P2860
P3181
P356
10.1016/J.EXPNEUROL.2014.07.021
P407
P478
P577
2014-12-01T00:00:00Z