Search Results - "Appel, Stanley"
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Immune dysregulation in amyotrophic lateral sclerosis: mechanisms and emerging therapies
Published in Lancet neurology (01-02-2019)“…Neuroinflammation is a common pathological feature of many neurodegenerative diseases, including amyotrophic lateral sclerosis (ALS), and is characterised by…”
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Immune-mediated Mechanisms in the Pathoprogression of Amyotrophic Lateral Sclerosis
Published in Journal of neuroimmune pharmacology (01-09-2013)“…Amyotrophic lateral sclerosis (ALS) is a devastating neurodegenerative disease with selective loss of upper and lower motor neurons. At sites of motor neuron…”
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Neuroinflammatory mechanisms in amyotrophic lateral sclerosis pathogenesis
Published in Current opinion in neurology (01-10-2018)“…Neuroinflammation is increasingly recognized as an important mediator of disease progression in patients with amyotrophic lateral sclerosis (ALS), and is…”
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Amyotrophic lateral sclerosis is a systemic disease: peripheral contributions to inflammation-mediated neurodegeneration
Published in Current opinion in neurology (01-10-2021)“…Neuroinflammation is an important mediator of the pathogenesis of disease in amyotrophic lateral sclerosis (ALS). Genetic mutations such as C9orf72 have begun…”
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Protective and Toxic Neuroinflammation in Amyotrophic Lateral Sclerosis
Published in Neurotherapeutics (01-04-2015)“…Amyotrophic lateral sclerosis (ALS) is a clinically heterogeneous disorder characterized by loss of motor neurons, resulting in paralysis and death. Multiple…”
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Transformation from a neuroprotective to a neurotoxic microglial phenotype in a mouse model of ALS
Published in Experimental neurology (01-09-2012)“…Neuroinflammation is a prominent pathological feature in the spinal cords of patients with amyotrophic lateral sclerosis (ALS), as well as in transgenic mouse…”
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TDP-43 activates microglia through NF-κB and NLRP3 inflammasome
Published in Experimental neurology (01-11-2015)“…Transactive response DNA-binding protein-43 (TDP-43) is a multifunctional nucleic acid binding protein present in ubiquitinated inclusions in tissues of…”
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An antisense oligonucleotide against SOD1 delivered intrathecally for patients with SOD1 familial amyotrophic lateral sclerosis: a phase 1, randomised, first-in-man study
Published in Lancet neurology (01-05-2013)“…Summary Background Mutations in SOD1 cause 13% of familial amyotrophic lateral sclerosis. In the SOD1 Gly93Ala rat model of amyotrophic lateral sclerosis, the…”
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CD4+ T cells mediate cytotoxicity in neurodegenerative diseases
Published in The Journal of clinical investigation (01-01-2009)“…Neuroinflammation, characterized by activated microglia and infiltrating T cells, is a prominent pathological feature in neurodegenerative diseases. However,…”
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Serum C-Reactive Protein as a Prognostic Biomarker in Amyotrophic Lateral Sclerosis
Published in JAMA neurology (01-06-2017)“…Various factors have been proposed as possible candidates associated with the prognosis of amyotrophic lateral sclerosis (ALS); however, there is still no…”
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Increased activation ability of monocytes from ALS patients
Published in Experimental neurology (01-06-2020)“…Neuroinflammation is increasingly recognized as an important mediator of disease progression in patients with amyotrophic lateral sclerosis (ALS). Recent…”
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Blood–spinal cord barrier breakdown and pericyte reductions in amyotrophic lateral sclerosis
Published in Acta neuropathologica (01-01-2013)“…The blood–brain barrier and blood–spinal cord barrier (BSCB) limit the entry of plasma components and erythrocytes into the central nervous system (CNS)…”
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Genome-wide Analyses Identify KIF5A as a Novel ALS Gene
Published in Neuron (Cambridge, Mass.) (21-03-2018)“…To identify novel genes associated with ALS, we undertook two lines of investigation. We carried out a genome-wide association study comparing 20,806 ALS cases…”
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CD4+ T cells support glial neuroprotection, slow disease progression, and modify glial morphology in an animal model of inherited ALS
Published in Proceedings of the National Academy of Sciences - PNAS (07-10-2008)“…Neuroinflammation, marked by gliosis and infiltrating T cells, is a prominent pathological feature in diverse models of dominantly inherited neurodegenerative…”
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Characterization of Gene Expression Phenotype in Amyotrophic Lateral Sclerosis Monocytes
Published in JAMA neurology (01-06-2017)“…Amyotrophic lateral sclerosis (ALS) is a common adult-onset neurodegenerative disease characterized by selective loss of upper and lower motor neurons…”
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T cell-microglial dialogue in Parkinson's disease and amyotrophic lateral sclerosis: are we listening?
Published in Trends in immunology (01-01-2010)“…Neuroinflammation is a pathological hallmark in Parkinson's disease (PD) and amyotrophic lateral sclerosis (ALS), and is characterized by activated microglia…”
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Endogenous regulatory T lymphocytes ameliorate amyotrophic lateral sclerosis in mice and correlate with disease progression in patients with amyotrophic lateral sclerosis
Published in Brain (London, England : 1878) (01-05-2011)“…Amyotrophic lateral sclerosis is a relentless and devastating adult-onset neurodegenerative disease with no known cure. In mice with amyotrophic lateral…”
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Inflammation in Parkinson's disease: Cause or consequence?
Published in Movement disorders (01-08-2012)Get full text
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Regulatory T‐lymphocytes mediate amyotrophic lateral sclerosis progression and survival
Published in EMBO molecular medicine (01-01-2013)“…In amyotrophic lateral sclerosis (ALS) mice, regulatory T‐lymphocytes (Tregs) are neuroprotective, slowing disease progression. To address whether Tregs and…”
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TREM2 variant p.R47H as a risk factor for sporadic amyotrophic lateral sclerosis
Published in JAMA neurology (01-04-2014)“…Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disease in which microglia play a significant and active role. Recently, a rare missense…”
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