Disease: Degenerative motor system disease
- A common variant in the iron regulatory gene (Hfe) alters the metabolic and transcriptional landscape in brain regions vulnerable to neurodegeneration
- A Novel De Novo Missense Mutation in <em>KIF1A</em> Associated with Young-Onset Upper-Limb Amyotrophic Lateral Sclerosis
- A patient-derived amyotrophic lateral sclerosis blood-brain barrier model for focused ultrasound-mediated anti-TDP-43 antibody delivery
- A rapid and easy-to-use spinal muscular atrophy screening tool based on primers with high specificity and amplification efficiency for SMN1 combined with single-stranded tag hybridization assay
- Absence of motor impairments or pathological changes in TMEM230 knockout rats
- Advance directives in amyotrophic lateral sclerosis - a systematic review and meta-analysis
- All-in-one wearable drug efficacy assessment systems for bulbar muscle function using amyotrophic lateral sclerosis animal models
- Allele-Selective Thiomorpholino Antisense Oligonucleotides as a Therapeutic Approach for Fused-in-Sarcoma Amyotrophic Lateral Sclerosis
- Amyloid fibril structures link CHCHD10 and CHCHD2 to neurodegeneration
- Amyotrophic lateral sclerosis associated with a new pathogenic variant of the ERBB4 gene
- An Accurate and Rapidly Calibrating Speech Neuroprosthesis
- Analysis of diffusion changes in cerebral tissues of Parkinson's patients who underwent subthalamic nucleus deep brain stimulation: Correlation of improvements in motor and neuropsychiatric symptoms
- Axonopathy Underlying Amyotrophic Lateral Sclerosis: Unraveling Complex Pathways and Therapeutic Insights
- Brain MRI Volumetric Assessment of Patients With Multiple Sclerosis: The Volume of Basal Ganglia, Thalamus, and Posterior Fossa
- Brain-Computer Interfaces for Restoring Communication
- Brazilian version of the Hammersmith Functional Motor Scale Expanded: cross-cultural adaptation and validation
- Camptocormia in a young man with anti-GAD-seropositive stiff-person syndrome
- Central neurodegeneration in Kennedy's disease accompanies peripheral motor dysfunction
- Cerebellar nuclei cells produce distinct pathogenic spike signatures in mouse models of ataxia, dystonia, and tremor
- Chemokine CX3CL1 (Fractalkine) Signaling and Diabetic Encephalopathy
- Circulating MAIT cells in multiple sclerosis and amyotrophic lateral sclerosis
- Clinical characterization of common pathogenic variants of SOD1-ALS in Germany
- Clinically relevant mouse models of severe spinal muscular atrophy with respiratory distress type 1
- Coadministration of 6-Shogaol and Levodopa Alleviates Parkinson's Disease-Related Pathology in Mice
- Coffee and amyotrophic lateral sclerosis (ALS)
- Cognitive reserve as a modulator of cognitive decline and of behavioral symptoms in patients with amyotrophic lateral sclerosis
- Correction to: Diagnostic value of neurofilaments in differentiating motor neuron disease from multifocal motor neuropathy
- Cortical inexcitability in ALS: correlating a clinical phenotype
- Cramp-Fasciculation Syndrome Associated with Natural and Added Chemicals in Popular Food Items
- D-Glutamate production by stressed Escherichia coli gives a clue for the hypothetical induction mechanism of the ALS disease
- Data and Process Harmonisation of Multi-National, Multi-Site Research Data
- Deep cervical lymph nodes in Parkinson's disease and atypical Parkinson's disease: A potential ultrasound biomarker for differential diagnosis
- Digital Biomarker for Muscle Function Assessment using Surface Electromyography with Electrical Stimulation and A Non-Invasive Wearable Device
- Dilemma in patients with amyotrophic lateral sclerosis and expectations from brain-machine interfaces
- Diverse Phenotypic Presentation of the Welander Distal Myopathy Founder Mutation, With Myopathy and Amyotrophic Lateral Sclerosis in the Same Family
- Dopaminergic progenitors generated by small molecule approach survived, integrated, and promoted functional recovery in (6-OHDA) mouse model of Parkinson's disease
- Dysregulation of cerebrospinal fluid metabolism profiles in spinal muscular atrophy patients: a case control study
- Electroacupuncture alleviates motor dysfunction by regulating neuromuscular junction disruption and neuronal degeneration in SOD1(G93A) mice
- Electrodiagnostic support in an atypical form of amyotrophic lateral sclerosis (Vulpian-Bernhardt syndrome)
- Emphasis on the importance of comprehensive clinical and genetic analysis - spinal muscular atrophy combined with phenylketonuria: A case report
- Excitatory to inhibitory synaptic ratios are unchanged at presymptomatic stages in multiple models of ALS
- Generation of Human-Induced Pluripotent Stem Cells from Peripheral Blood Mononuclear Cells of C9ORF72-Associated Amyotrophic Lateral Sclerosis Patients
- Genetic Associations With an Amyotrophic Lateral Sclerosis Reversal Phenotype
- Harnessing Mirror Neurons: A New Frontier in Parkinson's Disease Rehabilitation-A Scoping Review of the Literature
- Heterozygous knockout of Synaptotagmin13 phenocopies ALS features and TP53 activation in human motor neurons
- HucMSC extracellular vesicles increasing SATB 1 to activate the Wnt/beta-catenin pathway in 6-OHDA-induced Parkinson's disease model
- Impact of Disease-modifying Therapies on Respiratory Function in People with Neuromuscular Disorders
- Increased copy-number variant load of associated risk genes in sporadic cases of amyotrophic lateral sclerosis
- Induction of astrocyte reactivity promotes neurodegeneration in human pluripotent stem cell models
- Inflammasome-Inhibiting Nanoligomers Are Neuroprotective against Space-Induced Pathology in Healthy and Diseased Three-Dimensional Human Motor and Prefrontal Cortex Brain Organoids
- Integrated Approaches and Practical Recommendations in Patient Care Identified with 5q Spinal Muscular Atrophy through Newborn Screening
- Integrated elemental analysis supports targeting copper perturbations as a therapeutic strategy in multiple sclerosis
- Intranasal delivery of small extracellular vesicles reduces the progress of amyotrophic lateral sclerosis and the overactivation of complement-coagulation cascade and NF-ĸB signaling in SOD1<sup>G93A</sup> mice
- Isogenic patient-derived organoids reveal early neurodevelopmental defects in spinal muscular atrophy initiation
- Judicialization of Zolgensma in the Ministry of Health: costs and clinical profile of patients
- Learning From the Exception and Not the Rule: Genetic Associations With an Amyotrophic Lateral Sclerosis Reversal Phenotype
- Limbic Network and Papez Circuit Involvement in ALS: Imaging and Clinical Profiles in GGGGCC Hexanucleotide Carriers in <em>C9orf72</em> and <em>C9orf72</em>-Negative Patients
- Local protein synthesis at neuromuscular synapses is required for motor functions
- Longevity of a Brain-Computer Interface for Amyotrophic Lateral Sclerosis
- Loss of MEF2C function by enhancer mutation leads to neuronal mitochondria dysfunction and motor deficits in mice
- Mass spectrometry imaging of SOD1 protein-metal complexes in SOD1G93A transgenic mice implicates demetalation with pathology
- Meldonium, as a potential neuroprotective agent, promotes neuronal survival by protecting mitochondria in cerebral ischemia-reperfusion injury
- Mogroside V and mogrol: unveiling the neuroprotective and metabolic regulatory roles of Siraitia grosvenorii in Parkinson's disease
- Molsidomine provides neuroprotection against vincristine-induced peripheral neurotoxicity through soluble guanylyl cyclase activation
- Monoclonal antibodies to Respiratory Syncytial Virus (RSV) in patients with Spinal Muscular Atrophy Type 1
- Palliative care needs and utilisation of specialist services for people diagnosed with motor neuron disease: a national population-based study
- Palmatine Ameliorates Motor Deficits and Dopaminergic Neuron Loss by Regulating NLRP3 Inflammasome through Mitophagy in Parkinson's Disease Model Mice
- Phagocytosis of aggrecan-positive perineuronal nets surrounding motor neurons by reactive microglia expressing MMP-9 in TDP-43(Q331K) ALS model mice
- Phenotype distinctions in mice deficient in the neuron-specific alpha3 subunit of Na,K-ATPase: Atp1a3(tm1Ling/+)and Atp1a3 (+/D801Y)
- Physiological Features of the Neural Stem Cells Obtained from an Animal Model of Spinal Muscular Atrophy and Their Response to Antioxidant Curcumin
- Plasma, brain and spinal cord concentrations of caffeine are reduced in the SOD1<sup>G93A</sup> mouse model of amyotrophic lateral sclerosis following oral administration
- Poly-GR repeats associated with ALS/FTD gene <em>C9ORF72</em> impair translation elongation and induce a ribotoxic stress response in neurons
- Postural instability and lower extremity dysfunction in upper motor neuron-dominant amyotrophic lateral sclerosis
- Prognostic communication in amyotrophic lateral sclerosis: findings from a Nationwide Italian survey
- Pyrrole adducts mediated mitochondrial dysfunction activates SARM1-dependent axon degeneration in 2,5-hexanedione-induced neuropathy
- Quantitative Analysis of Glutathione and Carnosine Adducts with 4-Hydroxy-2-nonenal in Muscle in a hSOD1<sup>G93A</sup> ALS Rat Model
- Rare Variants of the <em>SMN1</em> Gene Detected during Neonatal Screening
- Recognising dying in motor neurone disease: A scoping review
- Repetitive magnetic stimulation prevents dorsal root ganglion neuron death and enhances nerve regeneration in a sciatic nerve injury rat model
- Schwann cell JUN expression worsens motor performance in an amyotrophic lateral sclerosis mouse model
- Scientific plurality and amyotrophic lateral sclerosis (ALS): A philosophical and historical perspective on Charcot's texts
- SIGMAR1 targets AMPK/ULK1 pathway to inhibit SH-SY5Y cell apoptosis by regulating endoplasmic reticulum stress and autophagy
- SoDCoD: a comprehensive database of Cu/Zn superoxide dismutase conformational diversity caused by ALS-linked gene mutations and other perturbations
- Study of Language Function in Bengali-Speaking Population with Motor Neuron Disease
- Surface electromyography of the vastus lateralis and gluteus medius muscles in post-operative T3-L3 hemilaminectomy dogs: a prospective controlled observational study
- Targeting the NRF2 pathway for disease modification in neurodegenerative diseases: mechanisms and therapeutic implications
- The ALS-associated KIF5A P986L variant is not pathogenic for Drosophila motoneurons
- The burden of upper motor neuron involvement is correlated with the bilateral limb involvement interval in patients with amyotrophic lateral sclerosis: a retrospective observational study
- The effect of growth hormone on motor findings and dendrite morphology in an experimental Parkinson's disease model
- The Impact of Nusinersen and Risdiplam on Motor Function for Spinal Muscular Atrophy Type 2 and 3: A Meta-Analysis
- The molecular mechanisms that underlie IGHMBP2-related diseases
- Therapeutics Targeting Skeletal Muscle in Amyotrophic Lateral Sclerosis
- Timeline of hypoglossal motor neuron death and intrinsic tongue muscle denervation in high-copy number SOD1(G93A) mice
- Tirbanibulin (KX2-391) analog KX2-361 inhibits botulinum neurotoxin serotype A mediated SNAP-25 cleavage in pre- and post-intoxication models in cells
- User expectations and experiences of an assistive robotic arm in amyotrophic lateral sclerosis: a multicenter observational study
- Utility of the Repetitive Nerve Stimulation Test and Needle EMG in the Trapezius Muscle for the Early Diagnosis of ALS
- Veterans with familial ALS and bulbar and respiratory presentations at onset had shorter survival
- Visualization and Quantification of Organelle Axonal Transport in Cultured Neurons
- Watch for inclusion body myositis
- Why should we care about astrocytes in a motor neuron disease?