Disease: Amyotrophic lateral sclerosis type 6
- A human proteogenomic-cellular framework identifies KIF5A as a modulator of astrocyte process integrity with relevance to ALS
- Age-Related Modifications of Electroencephalogram Coherence in Mice Models of Alzheimer's Disease and Amyotrophic Lateral Sclerosis
- Differential Expression of MicroRNAs and Predicted Drug Target in Amyotrophic Lateral Sclerosis
- Focal limb weakness (monoparesis): when family history holds the key to diagnosis
- Genetic Downregulation of the Metabotropic Glutamate Receptor Type 5 Dampens the Reactive and Neurotoxic Phenotype of Adult ALS Astrocytes
- Genome-wide structural variant analysis identifies risk loci for non-Alzheimer's dementias
- IFNγ protects motor neurons from oxidative stress via enhanced global protein synthesis in FUS-associated amyotrophic lateral sclerosis
- Mesenchymal stem cell therapy in amyotrophic lateral sclerosis (ALS) patients: A comprehensive review of disease information and future perspectives
- Molecular dynamics and protein frustration analysis of human fused in Sarcoma protein variants in Amyotrophic Lateral Sclerosis type 6: An In Silico approach
- Mutations in FUS, an RNA processing protein, cause familial amyotrophic lateral sclerosis type 6
- omicSynth: an Open Multi-omic Community Resource for Identifying Druggable Targets across Neurodegenerative Diseases
- Optineurin deficiency impairs autophagy to cause interferon beta overproduction and increased survival of mice following viral infection
- Protein kinetics of superoxide dismutase-1 in familial and sporadic amyotrophic lateral sclerosis
- Rapid Conversion to a Completely Virtual Multidisciplinary ALS Clinic in Response to the COVID-19 Pandemic: Implications for Future Care Delivery
- Risk factors associated with amyotrophic lateral sclerosis based on the observational study: a systematic review and meta-analysis
- Short tandem repeat expansions in sporadic amyotrophic lateral sclerosis and frontotemporal dementia
- STING-Triggered CNS Inflammation in Human Neurodegenerative Diseases
- Werdnig-Hoffmann Disease