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  1. 1081
    por Kollmer, Jennifer, Bendszus, Martin
    Publicado 2021
    “…Innovative studies in hereditary, metabolic or inflammatory polyneuropathies, and motor neuron diseases have contributed to a better understanding of the underlying pathomechanism. …”
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    Magnetic Resonance Neurography: Improved Diagnosis of Peripheral Neuropathies
  2. 1082
    “…However, provision of intrasalivary gland botox remains inconsistent and sialorrhoea is often poorly controlled in motor neuron disease (MND). Sialorrhoea in association with bulbar dysfunction can cause intolerance of non-invasive ventilation (NIV) and respiratory infection, so its treatment is critical within a home ventilation service (HVS). …”
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    Developing an intrasalivary gland botox service for patients receiving long-term non-invasive ventilation at home: a single-centre experience
  3. 1083
    “…We will evaluate observational studies (eg, cohort and case–control) conducted using routinely collected health data for investigating the associations between cancer and neurodegenerative diseases (such as Alzheimer’s disease, amyotrophic lateral sclerosis/motor neuron disease, Huntington’s disease, multiple sclerosis and Parkinson’s disease). …”
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    Design and methodological characteristics of studies using observational routinely collected health data for investigating the link between cancer and neurodegenerative diseases: protocol for a meta-research study
  4. 1084
    “…ELIGIBILITY CRITERIA FOR SELECTING STUDIES: All epidemiological studies reporting data on the possible association between a clinical diagnosis of amyotrophic lateral sclerosis (ALS)/motor neuron disease (MND), dementia or mild cognitive impairment (MCI), Parkinson’s disease (PD), chronic traumatic encephalopathy (CTE) at any stage and with any clinical pattern and the former participation in any types of sport at a varsity and professional level were included. …”
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    A systematic review on the risk of neurodegenerative diseases and neurocognitive disorders in professional and varsity athletes
  5. 1085
    “…Eighty FTLD patients (including cases with behavioral variant of frontotemporal dementia, primary progressive aphasia, progressive supranuclear palsy syndrome, motor neuron disease) and 65 healthy controls underwent rs-functional MRI. …”
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    Resting state functional brain networks associated with emotion processing in frontotemporal lobar degeneration
  6. 1086
    “…Amyotrophic lateral sclerosis (ALS) is a fatal, neurodegenerative motor neuron disease. Although an early diagnosis is crucial to provide adequate care and improve survival, patients with ALS experience a significant diagnostic delay. …”
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    Symptoms timeline and outcomes in amyotrophic lateral sclerosis using artificial intelligence
  7. 1087
    “…Mutations in RNA binding proteins (RBPs) have been linked to the motor neuron disease amyotrophic lateral sclerosis (ALS). …”
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    Digital color-coded molecular barcoding reveals dysregulation of common FUS and FMRP targets in soma and neurites of ALS mutant motoneurons
  8. 1088
    “…Vitamin D3 has an important role in reversing the COVID-19 infection in patients who have previously suffered from a neurological disease, such as Alzheimer’s disease, Parkinson disease, motor neuron disease, multiple sclerosis, Creutzfeldt–Jakob disease, stroke, cardiovascular problems, headache, sleep-associated disorder, and others. …”
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    A review article on neuroprotective, immunomodulatory, and anti-inflammatory role of vitamin-D3 in elderly COVID-19 patients
  9. 1089
    “…The most frequent differential diagnosis was motor neuron disease particularly of bulbar onset which showed remarkably overlapping clinical and electrophysiological features with MuSK MG at presentation. …”
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    Clinical pitfalls and serological diagnostics of MuSK myasthenia gravis
  10. 1090
    “…METHODS: 270 ALS patients referring to the Motor Neuron Disease Clinic of the University of Padova and Modena (Italy) accepted to compile the Italian version of the ROADS and results were correlated with the ALSFRSr and ALSAQ-40 scores, FVC values, and creatinine or albumin blood levels. …”
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    Italian version of the Rasch-Built Overall Amyotrophic Lateral Sclerosis Disability Scale (ROADS): validation and longitudinal performance
  11. 1091
    “…Mutations in the human Superoxide dismutase 1 (hSOD1) gene are well‐established cause of the motor neuron disease ALS. Patients and transgenic (Tg) ALS model mice carrying mutant variants develop hSOD1 aggregates in the CNS. …”
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    Mutant SOD1 aggregates formed in vitro and in cultured cells are polymorphic and differ from those arising in the CNS
  12. 1092
    “…The EphA4 signaling pathway plays an important role in regulating motor neuron ferroptosis in motor neuron disease. To investigate whether EphA4 signaling is involved in ferroptosis in spinal cord ischemia/reperfusion injury, in this study we established a rat model of spinal cord ischemia/reperfusion injury by clamping the left carotid artery and the left subclavian artery. …”
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    Eph receptor A4 regulates motor neuron ferroptosis in spinal cord ischemia/reperfusion injury in rats
  13. 1093
    “…Her condition was misdiagnosed as “motor neuron disease” at the time. Three years after onset, her condition was revisited because of nephrotic syndrome, and she was diagnosed with nephrotic syndrome and peripheral nerve injury caused by systemic lupus erythematosus. …”
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    Progressive muscle weakness and amyotrophy during pregnancy as the first manifestation of systemic lupus erythematosus: A case report and review of literature
  14. 1094
    “…People (>14 years old) with NMD and vital capacity <80% predicted were eligible, stratified by disease subgroup (amyotrophic lateral sclerosis/motor neuron disease or other NMDs), and randomized to 3 months of twice-daily LVR or breathing exercises. …”
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    A Randomized Controlled Clinical Trial of Lung Volume Recruitment in Adults with Neuromuscular Disease
  15. 1095
    “…Indications for chronic home NIV were categorised into: neuromuscular diseases (NMD) [including motor neuron disease (MND)]; obstructive sleep apnoea/obesity hypoventilation (OSA/OHS); pulmonary disease; and others. …”
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    O029 Clinical features and outcomes of patients referred to a Respiratory Failure service
  16. 1096
    “…To determine if gait disturbances due to MPTP and 3NP, drugs affecting the basal ganglia, were comparable to gait disturbances associated with motor neuron diseases, we also studied gait dynamics in a mouse model of amyotrophic lateral sclerosis (ALS). …”
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    Gait dynamics in mouse models of Parkinson's disease and Huntington's disease
  17. 1097
    “…CONCLUSION: Our results indicate that HIV-1-based lentiviral vectors pseudotyped with the Rabies PV glycoprotein might provide important vehicles for CNS targeting by peripheral injection in the treatment of motor neuron diseases (MND), pain, and neuropathy.…”
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    Comparative analysis of HIV-1-based lentiviral vectors bearing lyssavirus glycoproteins for neuronal gene transfer
  18. 1098
    “…BACKGROUND: Cerebral palsy (CP) is an upper motor neuron disease that results in a progressive movement disorder. …”
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    Novel transcriptional profile in wrist muscles from cerebral palsy patients
  19. 1099
    “…BACKGROUND: The slow Wallerian Degeneration (Wld(S)) gene specifically protects axonal and synaptic compartments of neurons from a wide variety of degeneration-inducing stimuli, including; traumatic injury, Parkinson's disease, demyelinating neuropathies, some forms of motor neuron disease and global cerebral ischemia. The Wld(S )gene encodes a novel Ube4b-Nmnat1 chimeric protein (Wld(S )protein) that is responsible for conferring the neuroprotective phenotype. …”
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    Expression of the neuroprotective slow Wallerian degeneration (Wld(S)) gene in non-neuronal tissues
  20. 1100
    por Hideyama, Takuto, Kwak, Shin
    Publicado 2011
    “…Amyotrophic lateral sclerosis (ALS) is the most common adult-onset motor neuron disease. More than 90% of ALS cases are sporadic, and the majority of sporadic ALS patients do not carry mutations in genes causative of familial ALS; therefore, investigation specifically targeting sporadic ALS is needed to discover the pathogenesis. …”
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    When Does ALS Start? ADAR2–GluA2 Hypothesis for the Etiology of Sporadic ALS
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