| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| Panlin Liao, Yanchun Yuan, Zhen Liu, Xiaorong Hou, Wanzhen Li, Jin Wen, Kexuan Zhang, Bin Jiao, Lu Shen, Hong Jiang, Jifeng Guo, Beisha Tang, Zhuohua Zhang, Zhonghua Hu, Junling Wan. Association of variants in the KIF1A gene with amyotrophic lateral sclerosis. Translational neurodegeneration. vol 11. issue 1. 2022-10-26. PMID:36284339. |
amyotrophic lateral sclerosis (als) is a devastating progressive neurodegenerative disease that affects neurons in the central nervous system and the spinal cord. |
2022-10-26 |
2023-08-14 |
Not clear |
| Alberto Albanese, Albert Christian Ludolph, Christopher J McDermott, Philippe Corcia, Philip Van Damme, Leonard H Van den Berg, Orla Hardiman, Gilberto Rinaldi, Nicola Vanacore, Brian Dicki. Tauroursodeoxycholic acid in patients with amyotrophic lateral sclerosis: The TUDCA-ALS trial protocol. Frontiers in neurology. vol 13. 2022-10-14. PMID:36237618. |
amyotrophic lateral sclerosis (als) is a chronic neurodegenerative rare disease that affects motor neurons in the brain, brainstem, and spinal cord, resulting in progressive weakness and atrophy of voluntary skeletal muscles. |
2022-10-14 |
2023-08-14 |
Not clear |
| Byung Jo Choi, Kang Ho Park, Min Hee Park, Eric J Huang, Seung Hyun Kim, Jae-Sung Bae, Hee Kyung Ji. Acid sphingomyelinase inhibition improves motor behavioral deficits and neuronal loss in an amyotrophic lateral sclerosis mouse model. BMB reports. 2022-10-13. PMID:36229415. |
amyotrophic lateral sclerosis (als) is an incurable neurodegenerative disease characterized by the degeneration of motor neurons in the spinal cord. |
2022-10-13 |
2023-08-14 |
mouse |
| Elif Kubat Oktem, Busra Aydin, Metin Yazar, Kazim Yalcin Arg. Integrative Analysis of Motor Neuron and Microglial Transcriptomes from SOD1 Journal of molecular neuroscience : MN. 2022-09-30. PMID:36178612. |
integrative analysis of motor neuron and microglial transcriptomes from sod1 amyotrophic lateral sclerosis (als) is a fatal disease of motor neurons that mainly affects the motor cortex, brainstem, and spinal cord. |
2022-09-30 |
2023-08-14 |
Not clear |
| Non-Nuoc Tran, Byung-Hoon Le. Functional implication of ubiquitinating and deubiquitinating mechanisms in TDP-43 proteinopathies. Frontiers in cell and developmental biology. vol 10. 2022-09-26. PMID:36158183. |
amyotrophic lateral sclerosis (als) is a fatal neurodegenerative disease in which motor neurons in spinal cord and motor cortex are progressively lost. |
2022-09-26 |
2023-08-14 |
Not clear |
| b' Bel\\xc3\\xa9n Proa\\xc3\\xb1o, Julia Casani-Cubel, Mar\\xc3\\xada Benlloch, Ana Rodriguez-Mateos, Esther Navarro-Illana, Jose Mar\\xc3\\xada Lajara-Romance, Jose Enrique de la Rubia Ort\\xc3\\xa. Is Dutasteride a Therapeutic Alternative for Amyotrophic Lateral Sclerosis? Biomedicines. vol 10. issue 9. 2022-09-23. PMID:36140184.' |
amyotrophic lateral sclerosis (als) is a neurodegenerative disease that is characterized by the loss of upper and lower motor neurons (mns) in the cerebral cortex, brainstem and spinal cord, with consequent weakness, atrophy and the progressive paralysis of all muscles. |
2022-09-23 |
2023-08-14 |
Not clear |
| Robert L Barry, Angel Torrado-Carvajal, John E Kirsch, Grae E Arabasz, Daniel S Albrecht, Zeynab Alshelh, Olivia Pijanowski, Austin J Lewis, Mackenzie Keegan, Beverly Reynolds, Paulina C Knight, Erin J Morrissey, Marco L Loggia, Nazem Atassi, Jacob M Hooker, Suma Bab. Selective atrophy of the cervical enlargement in whole spinal cord MRI of amyotrophic lateral sclerosis. NeuroImage. Clinical. vol 36. 2022-09-22. PMID:36137496. |
selective atrophy of the cervical enlargement in whole spinal cord mri of amyotrophic lateral sclerosis. |
2022-09-22 |
2023-08-14 |
human |
| Robert L Barry, Angel Torrado-Carvajal, John E Kirsch, Grae E Arabasz, Daniel S Albrecht, Zeynab Alshelh, Olivia Pijanowski, Austin J Lewis, Mackenzie Keegan, Beverly Reynolds, Paulina C Knight, Erin J Morrissey, Marco L Loggia, Nazem Atassi, Jacob M Hooker, Suma Bab. Selective atrophy of the cervical enlargement in whole spinal cord MRI of amyotrophic lateral sclerosis. NeuroImage. Clinical. vol 36. 2022-09-22. PMID:36137496. |
amyotrophic lateral sclerosis (als) is a deadly neurodegenerative disorder affecting motor neurons in the spinal cord and brain. |
2022-09-22 |
2023-08-14 |
human |
| Banaja P Dash, Axel Freischmidt, Jochen H Weishaupt, Andreas Herman. Downstream Effects of Mutations in International journal of molecular sciences. vol 23. issue 17. 2022-09-09. PMID:36077049. |
downstream effects of mutations in amyotrophic lateral sclerosis (als) is a progressive and fatal neurodegenerative disease marked by death of motor neurons (mns) present in the spinal cord, brain stem and motor cortex. |
2022-09-09 |
2023-08-14 |
human |
| Stephanie L Rayner, Alison Hogan, Jennilee M Davidson, Flora Cheng, Luan Luu, Marco Morsch, Ian Blair, Roger Chung, Albert Le. Cyclin F, Neurodegeneration, and the Pathogenesis of ALS/FTD. The Neuroscientist : a review journal bringing neurobiology, neurology and psychiatry. 2022-09-05. PMID:36062310. |
amyotrophic lateral sclerosis (als) is the most common form of motor neuron disease and is characterized by the degeneration of upper and lower motor neurons of the brain and spinal cord. |
2022-09-05 |
2023-08-14 |
Not clear |
| Christoph Schweingruber, Eva Hedlun. The Cell Autonomous and Non-Cell Autonomous Aspects of Neuronal Vulnerability and Resilience in Amyotrophic Lateral Sclerosis. Biology. vol 11. issue 8. 2022-08-26. PMID:36009818. |
amyotrophic lateral sclerosis (als) is defined by the loss of upper motor neurons (mns) that project from the cerebral cortex to the brain stem and spinal cord and of lower mns in the brain stem and spinal cord which innervate skeletal muscles, leading to spasticity, muscle atrophy, and paralysis. |
2022-08-26 |
2023-08-14 |
Not clear |
| Liu-Lin Xiong, Li Chen, Isaac Bul Deng, Xin-Fu Zhou, Ting-Hua Wan. P75 neurotrophin receptor as a therapeutic target for drug development to treat neurological diseases. The European journal of neuroscience. 2022-08-26. PMID:36017737. |
the interaction of neurotrophins with their receptors is involved in the pathogenesis and progression of various neurological diseases, including alzheimer's disease (ad), parkinson's disease (pd), amyotrophic lateral sclerosis (als), spinal cord injury, and acute and chronic cerebral damage, etc. |
2022-08-26 |
2023-08-14 |
Not clear |
| Gordon S Mitchell, Tracy L Bake. Respiratory neuroplasticity: Mechanisms and translational implications of phrenic motor plasticity. Handbook of clinical neurology. vol 188. 2022-08-14. PMID:35965036. |
advances in our understanding of these novel and important forms of plasticity have been rapid and have already inspired translation in multiple respects: (1) development of novel therapeutic strategies to preserve/restore breathing function in humans with severe neurological disorders, such as spinal cord injury and amyotrophic lateral sclerosis; and (2) the discovery that similar plasticity also occurs in nonrespiratory motor systems. |
2022-08-14 |
2023-08-14 |
Not clear |
| Pan Si, Chenkai Zh. Biological and neurological activities of astaxanthin (Review). Molecular medicine reports. vol 26. issue 4. 2022-08-10. PMID:35946443. |
owing to its ability to cross the blood‑brain barrier, astaxanthin has received attention for its protective effects against neurological disorders, including alzheimer's disease, parkinson's disease, amyotrophic lateral sclerosis, cerebral ischemia/reperfusion, subarachnoid hemorrhage, traumatic brain injury, spinal cord injury, cognitive impairment and neuropathic pain. |
2022-08-10 |
2023-08-14 |
Not clear |
| Ivan Rulik, Md Samiul Haque Sunny, Javier Dario Sanjuan De Caro, Md Ishrak Islam Zarif, Brahim Brahmi, Sheikh Iqbal Ahamed, Katie Schultz, Inga Wang, Tony Leheng, Jason Peng Longxiang, Mohammad H Rahma. Control of a Wheelchair-Mounted 6DOF Assistive Robot With Chin and Finger Joysticks. Frontiers in robotics and AI. vol 9. 2022-08-08. PMID:35937617. |
people with limited upper limb function due to stroke, spinal cord injury, cerebral palsy, amyotrophic lateral sclerosis, and other conditions find the controls of assistive devices such as power wheelchairs difficult to use. |
2022-08-08 |
2023-08-14 |
Not clear |
| Yining Zhu, Yining Xu, Rongrong Xuan, Jialu Huang, Bíró István, Gusztáv Fekete, Yaodong G. Mixed Comparison of Different Exercise Interventions for Function, Respiratory, Fatigue, and Quality of Life in Adults With Amyotrophic Lateral Sclerosis: Systematic Review and Network Meta-Analysis. Frontiers in aging neuroscience. vol 14. 2022-07-28. PMID:35898325. |
amyotrophic lateral sclerosis (als) is a progressive neuromuscular disease whose primary hallmark is the progressive degeneration of motor neurons in the brainstem, spinal cord, and cerebral cortex that leads to weakness, spasticity, fatigue, skeletal muscle atrophy, paralysis, and even death. |
2022-07-28 |
2023-08-14 |
Not clear |
| Qianqian Zhang, Huihui Zhao, Maotao Luo, Xi Cheng, Yanan Li, Qingyang Li, Zheng Wang, Qi Ni. The Classification and Prediction of Ferroptosis-Related Genes in ALS: A Pilot Study. Frontiers in genetics. vol 13. 2022-07-25. PMID:35873477. |
amyotrophic lateral sclerosis (als) is a neurodegenerative disease characterized by progressive muscle paralysis, which is followed by degeneration of motor neurons in the motor cortex of the brainstem and spinal cord. |
2022-07-25 |
2023-08-14 |
Not clear |
| Evelien Van Schoor, Simona Ospitalieri, Sebastiaan Moonen, Sandra O Tomé, Alicja Ronisz, Orkun Ok, Jochen Weishaupt, Albert C Ludolph, Philip Van Damme, Ludo Van Den Bosch, Dietmar Rudolf Tha. Increased pyroptosis activation in white matter microglia is associated with neuronal loss in ALS motor cortex. Acta neuropathologica. 2022-07-22. PMID:35867112. |
amyotrophic lateral sclerosis (als) is characterized by the degeneration of motor neurons in the motor cortex, brainstem, and spinal cord. |
2022-07-22 |
2023-08-14 |
Not clear |
| Jessica M Collins, Rachel A K Atkinson, Lyzette M Matthews, Isabella C Murray, Sharn E Perry, Anna E Kin. Sarm1 knockout modifies biomarkers of neurodegeneration and spinal cord circuitry but not disease progression in the mSOD1 Neurobiology of disease. 2022-07-21. PMID:35863521. |
sarm1 knockout modifies biomarkers of neurodegeneration and spinal cord circuitry but not disease progression in the msod1 the mechanisms underlying the loss of motor neuron axon integrity in amyotrophic lateral sclerosis (als) are unclear. |
2022-07-21 |
2023-08-14 |
Not clear |
| Yiyan Sun, Xiaohuan Xia, Diksha Basnet, Jialin C Zheng, Jian Huang, Jianhui Li. Mechanisms of Ferroptosis and Emerging Links to the Pathology of Neurodegenerative Diseases. Frontiers in aging neuroscience. vol 14. 2022-07-15. PMID:35837484. |
neurodegenerative diseases are a diverse class of diseases attributed to chronic progressive neuronal degeneration and synaptic loss in the brain and/or spinal cord, including alzheimer's disease, parkinson's disease, huntington's disease, amyotrophic lateral sclerosis and multiple sclerosis. |
2022-07-15 |
2023-08-14 |
Not clear |