Exosomal TAR DNA-binding protein-43 and neurofilaments in plasma of amyotrophic lateral sclerosis patients: A longitudinal follow-up study
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[1] Sojib Bin Zaman,et al. Global, regional, and national burden of neurological disorders, 1990-2016: a systematic analysis for the Global Burden of Disease Study 2016. , 2017, The Lancet. Neurology.
[2] P. Calabresi,et al. Neurofilament light chain as a biomarker in neurological disorders , 2019, Journal of Neurology, Neurosurgery, and Psychiatry.
[3] T. H. Nguyen,et al. Global, regional, and national burden of motor neuron diseases 1990–2016: a systematic analysis for the Global Burden of Disease Study 2016 , 2018, The Lancet Neurology.
[4] J. Kassubek,et al. Neurofilament light chain in serum for the diagnosis of amyotrophic lateral sclerosis , 2018, Journal of Neurology, Neurosurgery, and Psychiatry.
[5] V. Bonetto,et al. Role of Extracellular Vesicles in Amyotrophic Lateral Sclerosis , 2018, Front. Neurosci..
[6] O. Pansarasa,et al. Pathological Proteins Are Transported by Extracellular Vesicles of Sporadic Amyotrophic Lateral Sclerosis Patients , 2018, Front. Neurosci..
[7] Suzie Chen,et al. Exosomes released by metabotropic glutamate receptor 1 (GRM1) expressing melanoma cells increase cell migration and invasiveness , 2017, Oncotarget.
[8] P. van Damme,et al. Comparison of elevated phosphorylated neurofilament heavy chains in serum and cerebrospinal fluid of patients with amyotrophic lateral sclerosis , 2017, Journal of Neurology, Neurosurgery, and Psychiatry.
[9] Y. Itoyama,et al. Safety and efficacy of edaravone in well defined patients with amyotrophic lateral sclerosis: a randomised, double-blind, placebo-controlled trial , 2017, The Lancet Neurology.
[10] Baorong Zhang,et al. Exosomes in Parkinson’s Disease , 2017, Neuroscience Bulletin.
[11] Zhiqiang Gao,et al. Progress in Exosome Isolation Techniques , 2017, Theranostics.
[12] Robert G. Miller,et al. Gamma aminobutyric acid (GABA) modulators for amyotrophic lateral sclerosis/motor neuron disease. , 2017, The Cochrane database of systematic reviews.
[13] G. Sobue,et al. Exosome secretion is a key pathway for clearance of pathological TDP-43. , 2016, Brain : a journal of neurology.
[14] A. Chiò,et al. Projected increase in amyotrophic lateral sclerosis from 2015 to 2040 , 2016, Nature Communications.
[15] N. Pearce,et al. Neurofilament light chain , 2015, Neurology.
[16] C. Théry,et al. Biogenesis, secretion, and intercellular interactions of exosomes and other extracellular vesicles. , 2014, Annual review of cell and developmental biology.
[17] A. Ludolph,et al. Limited role of free TDP-43 as a diagnostic tool in neurodegenerative diseases , 2014, Amyotrophic lateral sclerosis & frontotemporal degeneration.
[18] M. Swash,et al. Delayed diagnosis in ALS: The problem continues , 2014, Journal of the Neurological Sciences.
[19] Gavin Giovannoni,et al. Plasma neurofilament heavy chain levels and disease progression in amyotrophic lateral sclerosis: insights from a longitudinal study , 2014, Journal of Neurology, Neurosurgery & Psychiatry.
[20] A Al-Chalabi,et al. Lithium in patients with amyotrophic lateral sclerosis (LiCALS): a phase 3 multicentre, randomised, double-blind, placebo-controlled trial , 2013, The Lancet Neurology.
[21] Gerry Shaw,et al. Phosphorylated neurofilament heavy subunit (pNF-H) in peripheral blood and CSF as a potential prognostic biomarker in amyotrophic lateral sclerosis , 2012, Journal of Neurology, Neurosurgery & Psychiatry.
[22] K. Tsai,et al. Autophagy activators rescue and alleviate pathogenesis of a mouse model with proteinopathies of the TAR DNA-binding protein 43 , 2012, Proceedings of the National Academy of Sciences.
[23] Veeranna,et al. Neurofilaments at a glance , 2012, Journal of Cell Science.
[24] O. Hardiman,et al. Amyotrophic lateral sclerosis , 2011, The Lancet.
[25] H. Mitsumoto,et al. Efficacy of minocycline in patients with amyotrophic lateral sclerosis: a phase III randomised trial , 2007, The Lancet Neurology.
[26] H. Akiyama,et al. TDP-43 is a component of ubiquitin-positive tau-negative inclusions in frontotemporal lobar degeneration and amyotrophic lateral sclerosis. , 2006, Biochemical and biophysical research communications.
[27] Bruce L. Miller,et al. Ubiquitinated TDP-43 in Frontotemporal Lobar Degeneration and Amyotrophic Lateral Sclerosis , 2006, Science.
[28] P. Verkade,et al. Alzheimer's disease beta-amyloid peptides are released in association with exosomes. , 2006, Proceedings of the National Academy of Sciences of the United States of America.
[29] V. Meininger. Clinical Trials in ALS: What Did We Learn from Recent Trials in Humans? , 2006, Neurodegenerative Diseases.
[30] D. Schoenfeld,et al. A randomized, placebo-controlled trial of topiramate in amyotrophic lateral sclerosis , 2003, Neurology.
[31] M. Swash,et al. El Escorial revisited: Revised criteria for the diagnosis of amyotrophic lateral sclerosis , 2000, Amyotrophic lateral sclerosis and other motor neuron disorders : official publication of the World Federation of Neurology, Research Group on Motor Neuron Diseases.
[32] V. Meininger,et al. A controlled trial of riluzole in amyotrophic lateral sclerosis. ALS/Riluzole Study Group. , 1994, The New England journal of medicine.