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A comprehensive review of amyotrophic lateral sclerosis

A comprehensive review of amyotrophic lateral sclerosis

http://www.wikidata.org/entity/Q26775401

about

Amyotrophic lateral sclerosis mimic syndromes Major Histocompatibility Complex I Expression by Motor Neurons and Its Implication in Amyotrophic Lateral Sclerosis Anti-Inflammatory Applications of Melittin, a Major Component of Bee Venom: Detailed Mechanism of Action and Adverse Effects Correlations between slow-rate repetitive nerve stimulation and characteristics associated with amyotrophic lateral sclerosis in Chinese patients Endoplasmic reticulum stress and inflammation in the central nervous system Pathological correlations between traumatic brain injury and chronic neurodegenerative diseases.Immune response in peripheral axons delays disease progression in SOD1(G93A) mice.Increased Expressions of Plasma Galectin-3 in Patients with Amyotrophic Lateral Sclerosis.ALS Pathogenesis and Therapeutic Approaches: The Role of Mesenchymal Stem Cells and Extracellular Vesicles Induced Pluripotent Stem Cell Neuronal Models for the Study of Autophagy Pathways in Human Neurodegenerative Disease.Caregiver burden in amyotrophic lateral sclerosis: A systematic review.Drugs in clinical development for the treatment of amyotrophic lateral sclerosis.Expression and Distribution of Arylsulfatase B are Closely Associated with Neuron Death in SOD1 G93A Transgenic Mice.AMPK in Neurodegenerative Diseases.TBK1: a new player in ALS linking autophagy and neuroinflammation.Can cannabinoids be a potential therapeutic tool in amyotrophic lateral sclerosis?Interaction of Mitochondria with the Endoplasmic Reticulum and Plasma Membrane in Calcium Homeostasis, Lipid Trafficking and Mitochondrial Structure Role of Neuroinflammation in Amyotrophic Lateral Sclerosis: Cellular Mechanisms and Therapeutic Implications.Inflammatory and non-inflammatory monocytes as novel prognostic biomarkers of survival in SOD1G93A mouse model of Amyotrophic Lateral Sclerosis.Autophagy Dysregulation in ALS: When Protein Aggregates Get Out of Hand.Frontotemporal Dementia in Amyotrophic Lateral Sclerosis: From Rarity to Reality?Novel miR-b2122 regulates several ALS-related RNA-binding proteins.Therapeutic implication of autophagy in neurodegenerative diseases.Implications of white matter damage in amyotrophic lateral sclerosis (Review).Edaravone and its clinical development for amyotrophic lateral sclerosis.The Utility of the Laboratory Work Up at the Time of Diagnosis of Amyotrophic Lateral Sclerosis.Integrated molecular landscape of amyotrophic lateral sclerosis provides insights into disease etiology.Ageing as a risk factor for ALS/FTD.Hypothalamic Alterations in Neurodegenerative Diseases and Their Relation to Abnormal Energy Metabolism.A Regulatory Circuitry Between Gria2, miR-409, and miR-495 Is Affected by ALS FUS Mutation in ESC-Derived Motor Neurons.A Possible Role for Platelet-Activating Factor Receptor in Amyotrophic Lateral Sclerosis Treatment.Epigenetic Mechanisms of Gene Regulation in Amyotrophic Lateral Sclerosis.The African turquoise killifish: A research organism to study vertebrate aging and diapause.Animal Toxins as Therapeutic Tools to Treat Neurodegenerative Diseases.Rab GTPases and Membrane Trafficking in Neurodegeneration.The Rules and Functions of Nucleocytoplasmic Shuttling Proteins.Antisense oligonucleotides in neurological disorders.DISCUSSING ANT1 ROLE IN AMYOTROPHIC LATERAL SCLEROSIS PATHOGENESIS.Strain Map of the Tongue in Normal and ALS Speech Patterns from Tagged and Diffusion MRI.Active nuclear import and passive nuclear export are the primary determinants of TDP-43 localization.

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A comprehensive review of amyotrophic lateral sclerosis

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Avoiding false positive diagnoses of motor neuron disease: lessons from the Scottish Motor Neuron Disease Register

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Antioxidant treatment for amyotrophic lateral sclerosis or motor neuron disease

Mutation of SOD1 in ALS: a gain of a loss of function

Effects of ALS-related SOD1 mutants on dynein- and KIF5-mediated retrograde and anterograde axonal transport

DNA/RNA helicase gene mutations in a form of juvenile amyotrophic lateral sclerosis (ALS4)

Prevalence of depression by race/ethnicity: findings from the National Health and Nutrition Examination Survey III

RNA toxicity from the ALS/FTD C9ORF72 expansion is mitigated by antisense intervention

Olesoxime, a cholesterol-like neuroprotectant for the potential treatment of amyotrophic lateral sclerosis

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