Disease: Degenerative motor system disease
- 14-3-3θ, a novel player in TDP-43 pathophysiology: Implications for ALS/FTD
- A comprehensive review on frontotemporal dementia: its impact on language, speech and behavior
- A dynamic regulatory switch for phase separation of FUS protein: Zinc ions and zinc finger domain
- A Poem About ALS
- A Potential Role of Interleukin-5 in the Pathogenesis and Progression of Amyotrophic Lateral Sclerosis: A New Molecular Perspective
- Ablation of Mitochondrial RCC1-L Induces Nigral Dopaminergic Neurodegeneration and Parkinsonian-like Motor Symptoms
- Abundant transcriptomic alterations in the human cerebellum of patients with a C9orf72 repeat expansion
- Add-on treatment with Cerebrolysin improves clinical symptoms in patients with ALS: results from a prospective, single-center, placebo-controlled, randomized, double-blind, phase II study
- Aging accelerates locomotor decline in PINK1 knockout rats in association with decreased nigral, but not striatal, dopamine and tyrosine hydroxylase expression
- Aging hastens locomotor decline in PINK1 knockout rats in association with decreased nigral, but not striatal, dopamine and tyrosine hydroxylase expression
- An aberrant fused in sarcoma liquid droplet of amyotrophic lateral sclerosis pathological variant, R495X, accelerates liquid-solid phase transition
- Analysis of Heart Rate Variability in Individuals Affected by Amyotrophic Lateral Sclerosis
- Animal Models of FUS-Proteinopathy: A Systematic Review
- Anterior insula is more vulnerable than posterior insula to TDP-43 pathology in common dementias and ALS
- Biomarkers for Managing Neurodegenerative Diseases
- Boosting BDNF in muscle rescues impaired axonal transport in a mouse model of DI-CMTC peripheral neuropathy
- Butyrate as a potential therapeutic agent for neurodegenerative disorders
- C9ORF72 patient-derived endothelial cells drive blood-brain barrier disruption and contribute to neurotoxicity
- Causal Relationship between Sex Hormones and Risk of Developing Common Neurodegenerative Diseases: A Mendelian Randomization Study
- CHCHD10<sup>S59L/+</sup> mouse model: Behavioral and neuropathological features of frontotemporal dementia
- Choroid plexus enlargement in amyotrophic lateral sclerosis patients and its correlation with clinical disability and blood-CSF barrier permeability
- Clinical heterogeneity within the ALS-FTD spectrum in a family with a homozygous optineurin mutation
- Concentric needle jitter analysis of the genioglossus muscle in patients with motor neuron disease
- Corticospinal tract hyperintensity in patients with LGI1-antibody encephalitis and other central nervous system disorders with neuroglial antibodies
- Cost-effectiveness of acceptance and commitment therapy for people living with motor neuron disease, and their health-related quality of life
- Developing a novel immune infiltration-associated mitophagy prediction model for amyotrophic lateral sclerosis using bioinformatics strategies
- Diagnostic value of neurofilaments in differentiating motor neuron disease from multifocal motor neuropathy
- Diaphragm weakness in late-onset Pompe disease: A complex interplay between lower motor neuron and muscle fibre degeneration
- Discovery of a novel homozygous SOD1 truncating variant bolsters infantile SOD1 deficiency syndrome
- Distinct transcriptomic profile of satellite cells contributes to preservation of neuromuscular junctions in extraocular muscles of ALS mice
- Dysregulation of innate immune signaling in animal models of spinal muscular atrophy
- Early Aggregation Mechanism of SOD1<sub>28-38</sub> Based on Force Field Parameter of 5-Cyano-Tryptophan
- Early deficits in an in vitro striatal microcircuit model carrying the Parkinson's GBA-N370S mutation
- Edaravone Oral Suspension: A Neuroprotective Agent to Treat Amyotrophic Lateral Sclerosis
- Embryonic motor neuron programming factors reactivate immature gene expression and suppress ALS pathologies in postnatal motor neurons
- Endurance exercise has a negative impact on the onset of SOD1-G93A ALS in female mice and affects the entire skeletal muscle-motor neuron axis
- Evaluation of cyanotoxin L-BMAA effect on α-synuclein and TDP43 proteinopathy
- Evolution of diagnostic criteria and new insights into clinical testing in mixed connective tissue disease; anti-survival motor neuron complex antibody as a novel marker of severity of the disease
- Experience of the treatment of spinal muscular atrophy type 3 Kugelberg-Welander with Nusinersen
- Experiences of predictive genetic testing in inherited motor neuron disease: Findings from a qualitative interview study
- Exploring antioxidant strategies in the pathogenesis of ALS
- Fatigue in Spinal Muscular Atrophy: a fundamental open issue
- Generation and characterization of monoclonal antibodies against pathologically phosphorylated TDP-43
- Genetic therapies and respiratory outcomes in patients with neuromuscular disease
- Halogen doped graphene quantum dots modulate TDP-43 phase separation and aggregation in the nucleus
- Improved synthesis and application of an alkyne-functionalized isoprenoid analogue to study the prenylomes of motor neurons, astrocytes and their stem cell progenitors
- Improved therapeutic approach for spinal muscular atrophy via ubiquitination-resistant survival motor neuron variant
- Increased Vulnerability to Ferroptosis in FUS-ALS
- Investigating Repeat Expansions in <em>NIPA1</em>, <em>NOP56</em>, and <em>NOTCH2NLC</em> Genes: A Closer Look at Amyotrophic Lateral Sclerosis Patients from Southern Italy
- KCNJ2 inhibition mitigates mechanical injury in a human brain organoid model of traumatic brain injury
- Knockdown of <em>tgfb1a</em> partially improves ALS phenotype in a transient zebrafish model
- LINC complex alterations are a key feature of sporadic and familial ALS/FTD
- Long-Term Alterations in Motor Skills, Neurogenesis and Astrocyte Numbers following Transient Cerebral Ischemia in Mice
- Lycium barbarum glycopeptide ameliorates motor and visual deficits in autoimmune inflammatory diseases
- Massive ER protein disposal by reticulophagy receptors and selective disposal by TOLLIP
- Meta-analysis of differential gene expression in lower motor neurons isolated by laser capture microdissection from post-mortem ALS spinal cords
- Metabolomics of cerebrospinal fluid reveals candidate diagnostic biomarkers to distinguish between spinal muscular atrophy type II and type III
- Mitochondrial and Nuclear DNA Variants in Amyotrophic Lateral Sclerosis: Enrichment in the Mitochondrial Control Region and Sirtuin Pathway Genes in Spinal Cord Tissue
- Molecular mechanisms and therapeutic strategies for neuromuscular diseases
- Neurodegeneration and glial morphological changes are both prevented by TRPM2 inhibition during the progression of a Parkinson's disease mouse model
- Neurodegeneration Biomarkers in Adult Spinal Muscular Atrophy (SMA) Patients Treated with Nusinersen
- Neurofilaments in Sporadic and Familial Amyotrophic Lateral Sclerosis: A Systematic Review and Meta-Analysis
- Neuroinflammation in Neurodegenerative Disorders: Current Knowledge and Therapeutic Implications
- Neuropathology of the Neurodegenerative Diseases
- Neurophysiological and imaging biomarkers of lower motor neuron dysfunction in motor neuron diseases/amyotrophic lateral sclerosis: IFCN handbook chapter
- Online speech synthesis using a chronically implanted brain-computer interface in an individual with ALS
- Optimizing breathlessness management in amyotrophic lateral sclerosis: insights from a comprehensive systematic review
- Pan-neuronal expression of human mutant SOD1 in Drosophila impairs survival and motor performance, induces early neuroinflammation and chromosome aberrations
- Patients' experiences with methylcobalamin injections in amyotrophic lateral sclerosis
- Peripheral Immune Profiles Predict ALS Progression in an Age- and Sex-Dependent Manner
- Plasminogen degrades alpha-synuclein, Tau and TDP-43 and decreases dopaminergic neurodegeneration in mouse models of Parkinson's disease
- Profound hypoxemia and hypotension during posterior spinal fusion in a spinal muscular atrophy child with severe scoliosis: a case report
- Promising approaches to the pathogenetic therapy of amyotrophic lateral sclerosis
- Publisher Correction: Chlamydia psittaci Pneumonia in a patient with motor neuron disease: a case report
- Quantitative analysis of noninvasive deep temporal interference stimulation: A simulation and experimental study
- Rare association between spinocerebellar ataxia and amyotrophic lateral sclerosis: a case series
- Real-time ultrasound-guided sacral plexus block combined with mild sedation for hemorrhoidectomy and hemorrhoidal artery ligation in a patient with amyotrophic lateral sclerosis: a case report
- Recent research on home rehabilitation and nursing for spinal muscular atrophy
- Regulated cell death and its role in Alzheimer's disease and amyotrophic lateral sclerosis
- Reversal of <em>C9orf72</em> mutation-induced transcriptional dysregulation and pathology in cultured human neurons by allele-specific excision
- Role of NLRP3 in Parkinson's disease: Specific activation especially in dopaminergic neurons
- RVG29 Peptide-Modified Exosomes Loaded with Mir-133b Mediate the RhoA-ROCK Pathway to Improve Motor and Neurological Symptoms in Parkinson's Disease
- Small peptide CSF fingerprint of amyotrophic lateral sclerosis
- SOD1 gene therapy delays ALS disease progression
- Spatial enrichment and genomic analyses reveal the link of NOMO1 with amyotrophic lateral sclerosis
- Spinal Muscular Atrophy with early presentation, perspectives for its treatment in Chile
- Stasimon/Tmem41b is required for cell proliferation and adult mouse survival
- Stathmin 2 is a potential treatment target for TDP-43 proteinopathy in amyotrophic lateral sclerosis
- Stepwise combined cell transplantation using mesenchymal stem cells and induced pluripotent stem cell-derived motor neuron progenitor cells in spinal cord injury
- Targeting Mitochondrial Complex I Deficiency in MPP(+)/MPTP-induced Parkinson's Disease Cell Culture and Mouse Models by Transducing Yeast NDI1 Gene
- Testosterone Reduces Myelin Abnormalities in the Wobbler Mouse Model of Amyotrophic Lateral Sclerosis
- Thalamic Alterations in Motor Neuron Diseases: A Systematic Review of MRI Findings
- The burden of neurological conditions in north Africa and the Middle East, 1990-2019: a systematic analysis of the Global Burden of Disease Study 2019
- The usage and advantages of several common amyotrophic lateral sclerosis animal models
- Transsynaptic degeneration of ventral horn motor neurons exists but plays a minor role in lower motor system dysfunction in acute ischemic rats
- Type selective ablation of postnatal slow and fast fatigue-resistant motor neurons in mice induces late onset kinetic and postural tremor following fiber-type transition and myopathy
- Unraveling Axonal Transcriptional Landscapes: Insights from iPSC-Derived Cortical Neurons and Implications for Motor Neuron Degeneration
- Upper motor neuron signs in primary lateral sclerosis and hereditary spastic paraplegia
- Use of Muscle Ultrasonography in Morphofunctional Assessment of Amyotrophic Lateral Sclerosis (ALS)
- Variant-specific effects of GBA1 mutations on dopaminergic neuron proteostasis