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  1. 1061
    “…Amyotrophic lateral sclerosis (ALS) is the most common motor neuron disease, and ALS incidence is increasing worldwide. …”
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    Impact of the Amyotrophic Lateral Sclerosis Disease on the Biomechanical Properties and Oxidative Stress Metabolism of the Lung Tissue Correlated With the Human Mutant SOD1(G93A) Protein Accumulation
  2. 1062
    “…Spinal muscular atrophy (SMA) is an autosomal recessive motor neuron disease that is caused by deletions or mutations in the Survival Motor Neuron 1 (SMN1) gene but retention of its nearly perfect orthologue SMN2. …”
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    Comprehensive In Silico Analysis of Retrotransposon Insertions within the Survival Motor Neuron Genes Involved in Spinal Muscular Atrophy
  3. 1063
    “…Amyotrophic lateral sclerosis (ALS) is a severe adult motor neuron disease that causes progressive neuromuscular atrophy, muscle wasting, weakness, and depressive-like symptoms. …”
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    Activation of IGF-1/GLP-1 Signalling via 4-Hydroxyisoleucine Prevents Motor Neuron Impairments in Experimental ALS-Rats Exposed to Methylmercury-Induced Neurotoxicity
  4. 1064
    “…It progresses variably for 2-3 years followed by stabilization without progression to Motor neuron disease.…”
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    Monomelic amyotrophy with clinico-radiological and electrophysiological evaluation: A study from Eastern India
  5. 1065
    “…METHODS: The study included 146 autopsy‐confirmed cases of FTLD‐TDP and 55 cases of FTLD‐TDP with motor neuron disease (FTLD‐MND). Sections from the basal forebrain were screened for tau pathology with phosphorylated‐tau immunohistochemistry. …”
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    Concurrent tau pathologies in frontotemporal lobar degeneration with TDP‐43 pathology
  6. 1066
    “…Genetic mutations that cause amyotrophic lateral sclerosis (ALS), a progressively lethal motor neuron disease, are commonly found in ubiquitously expressed genes. …”
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    Targeting TNFα produced by astrocytes expressing amyotrophic lateral sclerosis‐linked mutant fused in sarcoma prevents neurodegeneration and motor dysfunction in mice
  7. 1067
    “…OBJECTIVES: Transplantation of neural progenitor cells (NPCs) derived from human‐induced pluripotent stem cells (hiPSCs) is one of the promising treatment strategies for motor neuron diseases (MNDs). However, the inefficiency in committed differentiation of NPCs in vivo limits its application. …”
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    Inducible motor neuron differentiation of human induced pluripotent stem cells in vivo
  8. 1068
    “…INTRODUCTION: Objective biomarkers for the fatal neurodegenerative disease amyotrophic lateral sclerosis or motor neuron disease (ALS/MND) are critical for diagnosis, drug development, clinical trials, and insight into disease pathology. …”
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    Profiling non-coding RNA expression in cerebrospinal fluid of amyotrophic lateral sclerosis patients
  9. 1069
    “…BACKGROUND: Amyotrophic lateral sclerosis (ALS) is a motor neuron disease that results in a progressive increase in dysfunctions, limitations and restrictions over time, which can impact on quality of life (QoL). …”
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    Quality of life, disability, and clinical variables in amyotrophic lateral sclerosis
  10. 1070
    “…RESULTS: Fifty participants were studied: bvFTD = 20, semantic variant FTD (svFTD) = 11, non-fluent variant FTD (nfvFTD) = 9, FTD with motor neuron disease (MND) = 4, phFTD = 2, slow progressors = 3, FTD mimic = 1, mean age 67.2 (SD 8.4) years. …”
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    Plasma Neurofilament Light Chain and Clinical Diagnosis in Frontotemporal Dementia Syndromes
  11. 1071
    por Dweikat, Imad, Khalaf-Nazzal, Reham
    Publicado 2022
    “…Nervous system involvement was common, progressive, and presented with signs of upper motor neuron disease as well as variable degrees of cognitive impairment. …”
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    Clinical heterogeneity of hyperornithinemia-hyperammonemia-homocitrullinuria syndrome in thirteen palestinian patients and report of a novel variant in the SLC25A15 gene
  12. 1072
    “…In the early onset motor neuron disease spinal muscular atrophy (SMA), many motor axons are not ensheathed by Schwann cells nor grow sufficiently in radial diameter to become myelinated. …”
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    Boosting neuregulin 1 type-III expression hastens SMA motor axon maturation
  13. 1073
    “…OBJECTIVE: To determine the prevalence of autoimmune disease in symptomatic C9ORF72 (C9) mutation carriers and frontotemporal dementia with motor neuron disease (FTD/MND) cohorts. METHODS: In this case-control study, we reviewed the clinical histories of 66 patients with FTD/MND and 57 symptomatic C9 carriers (24 overlapping cases), a total of 99 charts, for history of autoimmune disease. …”
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    Increased prevalence of autoimmune disease within C9 and FTD/MND cohorts: Completing the picture
  14. 1074
    “…CONCLUSION: The results suggest that more extensive training with the proposed control system can be an effective and safe option that will allow the displacement of a wheelchair in a controlled environment for potential users suffering from some types of motor neuron diseases.…”
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    Brain-Computer Interface application: auditory serial interface to control a two-class motor-imagery-based wheelchair
  15. 1075
    “…MRI and CT myelography findings revealed spinal canal stenosis at the level of C5–6 and C6 root compression of the right side. Motor neuron disease was excluded because of findings from electromyography. …”
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    Surgical treatment for dropped head syndrome with cervical spondylotic amyotrophy: a case report
  16. 1076
    “…The parameters of kinematic analysis could be used to quantitatively evaluate dysphagia in motor neuron disease.…”
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    Application of Automatic Kinematic Analysis Program for the Evaluation of Dysphagia in ALS patients
  17. 1077
    “…The patients were attending the National ALS/Motor Neuron Disease Multidisciplinary Clinic at Beaumont Hospital, Dublin. …”
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    Prediction of caregiver burden in amyotrophic lateral sclerosis: a machine learning approach using random forests applied to a cohort study
  18. 1078
    “…Background  Amyotrophic lateral sclerosis (ALS) is a rare motor neuron disease with progressive degeneration of motor neurons. …”
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    Association of Plasma Biomarkers for Angiogenesis and Proteinopathy in Indian Amyotrophic Lateral Sclerosis Patients
  19. 1079
    “…In this exploratory study, we quantified the levels of both anti-TDP-43 NAb and TDP-43 protein as putative accessible markers for improving the ALS diagnostic process by using ELISA in N = 70 ALS patients (N = 4 carrying TARDBP mutations), N = 40 age-comparable healthy controls (CTRL), N = 20 motor neuron disease mimics (MN-m), N = 20 Alzheimer’s disease (AD) and N = 15 frontotemporal lobar degeneration (FTLD) patients. …”
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    Serum naturally occurring anti-TDP-43 auto-antibodies are increased in amyotrophic lateral sclerosis
  20. 1080
    “…Amyotrophic lateral sclerosis (ALS) is a form of motor neuron disease (MND) that is characterized by the progressive loss of motor neurons within the spinal cord, brainstem, and motor cortex. …”
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    In vivo Validation of Bimolecular Fluorescence Complementation (BiFC) to Investigate Aggregate Formation in Amyotrophic Lateral Sclerosis (ALS)
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