| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| Jian Lu, An-Xu He, Zhuo-Ying Jin, Meng Zhang, Zhong-Xin Li, Fan Zhou, Lin Ma, Hong-Ming Jin, Jia-Ying Wang, Xu She. Desloratadine alleviates ALS-like pathology in hSOD1 Acta pharmacologica Sinica. 2024-01-29. PMID:38286832. |
desloratadine alleviates als-like pathology in hsod1 amyotrophic lateral sclerosis (als) is a fatal neurodegenerative disease with progressive loss of motor neurons in the spinal cord, cerebral cortex and brain stem. |
2024-01-29 |
2024-02-01 |
Not clear |
| Mario Díaz, Noemí Fabelo, M Virginia Martín, Guido Santos, Isidre Ferre. Evidence for alterations in lipid profiles and biophysical properties of lipid rafts from spinal cord in sporadic amyotrophic lateral sclerosis. Journal of molecular medicine (Berlin, Germany). 2024-01-29. PMID:38285093. |
evidence for alterations in lipid profiles and biophysical properties of lipid rafts from spinal cord in sporadic amyotrophic lateral sclerosis. |
2024-01-29 |
2024-01-31 |
human |
| Mario Díaz, Noemí Fabelo, M Virginia Martín, Guido Santos, Isidre Ferre. Evidence for alterations in lipid profiles and biophysical properties of lipid rafts from spinal cord in sporadic amyotrophic lateral sclerosis. Journal of molecular medicine (Berlin, Germany). 2024-01-29. PMID:38285093. |
amyotrophic lateral sclerosis (als) is an age-dependent neurodegenerative disease affecting motor neurons in the spinal cord and brainstem whose etiopathogenesis remains unclear. |
2024-01-29 |
2024-01-31 |
human |
| Mario Díaz, Noemí Fabelo, M Virginia Martín, Guido Santos, Isidre Ferre. Evidence for alterations in lipid profiles and biophysical properties of lipid rafts from spinal cord in sporadic amyotrophic lateral sclerosis. Journal of molecular medicine (Berlin, Germany). 2024-01-29. PMID:38285093. |
key messages: the lipid matrix of multimolecular membrane complexes named lipid rafts are altered in human spinal cord in sporadic amyotrophic lateral sclerosis (als). |
2024-01-29 |
2024-01-31 |
human |
| Younghwi Kwon, Minsung Kang, Yu-Mi Jeon, Shinrye Lee, Ho-Won Lee, Jin-Sung Park, Hyung-Jun Ki. Identification and characterization of novel ERBB4 variant associated with sporadic amyotrophic lateral sclerosis (ALS). Journal of the neurological sciences. 2024-01-26. PMID:38278691. |
amyotrophic lateral sclerosis (als) is the most common type of motor neuron disease characterized by progressive motor neuron degeneration in brain and spinal cord. |
2024-01-26 |
2024-01-29 |
Not clear |
| Samuel Lundt, Nannan Zhang, Luis Polo-Parada, Xinglong Wang, Shinghua Din. Dietary NMN supplementation enhances motor and NMJ function in ALS. Experimental neurology. 2024-01-24. PMID:38266764. |
amyotrophic lateral sclerosis (als) is an adult-onset neurodegenerative disease that causes the degeneration of motor neurons in the motor cortex and spinal cord. |
2024-01-24 |
2024-01-27 |
Not clear |
| Graziantonio Lauria, Rosita Curcio, Paola Tucc. A Machine Learning Approach for Highlighting microRNAs as Biomarkers Linked to Amyotrophic Lateral Sclerosis Diagnosis and Progression. Biomolecules. vol 14. issue 1. 2024-01-23. PMID:38254647. |
amyotrophic lateral sclerosis (als) is a fatal neurodegenerative disease characterized by the progressive loss of motor neurons in the brain and spinal cord. |
2024-01-23 |
2024-01-25 |
Not clear |
| Daniel J Robertson, Paul M Jeziorczak, Charles J Aprahamia. Diaphragmatic pacing for respiratory failure in children. Seminars in pediatric surgery. vol 33. issue 1. 2024-01-21. PMID:38245992. |
most of the literature on pacing involves adults with common indications being spinal cord injury and amyotrophic lateral sclerosis (als). |
2024-01-21 |
2024-01-24 |
Not clear |
| Shir Zaccai, Anna Nemirovsky, Livnat Lerner, Leenor Alfahel, Ekaterina Eremenko, Adrian Israelson, Alon Monsoneg. CD4 T-cell aging exacerbates neuroinflammation in a late-onset mouse model of amyotrophic lateral sclerosis. Journal of neuroinflammation. vol 21. issue 1. 2024-01-11. PMID:38212835. |
amyotrophic lateral sclerosis (als) is an adult-onset progressive neurodegenerative disorder characterized by the loss of upper and lower motor neurons in the brain and spinal cord. |
2024-01-11 |
2024-01-14 |
mouse |
| Shumin Zhao, Ranran Chen, Ying Gao, Yanchao Lu, Xue Bai, Jingjing Zhan. Fundamental roles of the Optineurin gene in the molecular pathology of Amyotrophic Lateral Sclerosis. Frontiers in neuroscience. vol 17. 2024-01-05. PMID:38178841. |
amyotrophic lateral sclerosis (als) is a neurodegenerative disease characterized by the progressive loss of motor neurons (mns) in the brain and spinal cord. |
2024-01-05 |
2024-01-07 |
Not clear |
| Rachel Waller, Joanna J Bury, Charlie Appleby-Mallinder, Matthew Wyles, George Loxley, Aditi Babel, Saleh Shekari, Mbombe Kazoka, Helen Wollff, Ammar Al-Chalabi, Paul R Heath, Pamela J Shaw, Janine Kirb. Establishing mRNA and microRNA interactions driving disease heterogeneity in amyotrophic lateral sclerosis patient survival. Brain communications. vol 6. issue 1. 2024-01-01. PMID:38162899. |
amyotrophic lateral sclerosis is a fatal neurodegenerative disease, associated with the degeneration of both upper and lower motor neurons of the motor cortex, brainstem and spinal cord. |
2024-01-01 |
2024-01-05 |
Not clear |
| Qin Kang, Shishi Jiang, Jun Min, Fan Hu, Renshi X. Parvalbumin interneurons dysfunction is potentially associated with FαMNs decrease and NRG1-ErbB4 signaling inhibition in spinal cord in amyotrophic lateral sclerosis. Aging. vol 15. 2023-12-29. PMID:38157256. |
parvalbumin interneurons dysfunction is potentially associated with fαmns decrease and nrg1-erbb4 signaling inhibition in spinal cord in amyotrophic lateral sclerosis. |
2023-12-29 |
2024-01-05 |
Not clear |
| Saadat Ullah Khan, Muhammad Majid, Marius George Linguraru, Syed Muhammad Anwa. Upper Limb Movement Execution Classification using Electroencephalography for Brain Computer Interface. Annual International Conference of the IEEE Engineering in Medicine and Biology Society. IEEE Engineering in Medicine and Biology Society. Annual International Conference. vol 2023. 2023-12-12. PMID:38082727. |
decoding eeg-based upper limb movements can be of great help to people with spinal cord injury (sci) or other neuro-muscular diseases such as amyotrophic lateral sclerosis (als), primary lateral sclerosis, and periodic paralysis. |
2023-12-12 |
2023-12-17 |
human |
| Haiyang Ma, Jia Huo, Cheng Xin, Jing Yang, Qi Liu, Hui Dong, Rui Li, Yaling Li. RABGGTB plays a critical role in ALS pathogenesis. Brain research bulletin. 2023-12-02. PMID:38042502. |
amyotrophic lateral sclerosis (als) is a progressive neurodegenerative disease with unknown causes, which mainly affects motor neurons in the anterior horn of the spinal cord, brain stem, and cerebral cortex, also known as motor neuron disease. |
2023-12-02 |
2023-12-10 |
Not clear |
| Alexander Fröhlich, Abigail L Pfaff, Vivien J Bubb, John P Quinn, Sulev Kok. Transcriptomic profiling of cerebrospinal fluid identifies ALS pathway enrichment and RNA biomarkers in MND individuals. Experimental biology and medicine (Maywood, N.J.). 2023-11-25. PMID:38001563. |
amyotrophic lateral sclerosis (als) is a fatal neurodegenerative disorder and the most common form of motor neurone disease (mnd) which is characterized by the damage and death of motor neurons in the brain and spinal cord of affected individuals. |
2023-11-25 |
2023-11-28 |
Not clear |
| Elisa Duranti, Chiara Vill. Muscle Involvement in Amyotrophic Lateral Sclerosis: Understanding the Pathogenesis and Advancing Therapeutics. Biomolecules. vol 13. issue 11. 2023-11-25. PMID:38002264. |
amyotrophic lateral sclerosis (als) is a fatal condition characterized by the selective loss of motor neurons in the motor cortex, brainstem, and spinal cord. |
2023-11-25 |
2023-11-28 |
Not clear |
| Chung-Min Wu, Yeou-Jiunn Chen, Shih-Chung Chen, Sheng-Feng Zhen. Creating an AI-Enhanced Morse Code Translation System Based on Images for People with Severe Disabilities. Bioengineering (Basel, Switzerland). vol 10. issue 11. 2023-11-25. PMID:38002405. |
(1) background: patients with severe physical impairments (spinal cord injury, cerebral palsy, amyotrophic lateral sclerosis) often have limited mobility due to physical limitations, and may even be bedridden all day long, losing the ability to take care of themselves. |
2023-11-25 |
2023-11-28 |
Not clear |
| Shaherin Basith, Balachandran Manavalan, Gwang Le. Unveiling local and global conformational changes and allosteric communications in SOD1 systems using molecular dynamics simulation and network analyses. Computers in biology and medicine. vol 168. 2023-11-21. PMID:37988788. |
amyotrophic lateral sclerosis (als) is a serious neurodegenerative disorder affecting nerve cells in the brain and spinal cord that is caused by mutations in the superoxide dismutase 1 (sod1) enzyme. |
2023-11-21 |
2023-11-29 |
Not clear |
| Aniket Saini, Pooja A Chawl. Breaking barriers with tofersen: Enhancing therapeutic opportunities in amyotrophic lateral sclerosis. European journal of neurology. 2023-11-17. PMID:37975798. |
amyotrophic lateral sclerosis (als) is a progressive neurodegenerative disease that primarily affects adults, characterized by muscle weakness resulting from the specific death of motor neurons in the spinal cord and brain. |
2023-11-17 |
2023-11-20 |
Not clear |
| Dipnarine Maharaj, Kawaljit Kaur, Adrian Saltese, Jacqueline Gouve. Personalized Precision Immunotherapy for Amyotrophic Lateral Sclerosis (ALS). Critical reviews in immunology. vol 43. issue 2. 2023-11-08. PMID:37938192. |
neurological syndrome amyotrophic lateral sclerosis (als) affects motor neurons and is characterized by progressive motor neuron loss in the brain and spinal cord. |
2023-11-08 |
2023-11-20 |
Not clear |