| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| Matthew B Dopler, Keyshawn E Cox, Tyler L Petersen, Muhammad I Abeer, Juneessa M Pressley, Sanaz Arezoumandan, Michael A Gitch. Basic Science and Pathogenesis. Alzheimer's & dementia : the journal of the Alzheimer's Association. vol 20 Suppl 1. 2025-01-03. PMID:39750721. |
amyotrophic lateral sclerosis (als) is a progressive neurodegenerative disease that is characterized by upper and lower motor neuron death that leads to paralysis with the average survival being 3-5 years after diagnosis. |
2025-01-03 |
2025-01-05 |
Not clear |
| Carolina Sbarigia, Sophie Rome, Luciana Dini, Stefano Taccon. New perspectives of the role of skeletal muscle derived extracellular vesicles in the pathogenesis of amyotrophic lateral sclerosis: the 'dying back' hypothesis. Journal of extracellular biology. vol 3. issue 11. 2024-11-14. PMID:39534483. |
amyotrophic lateral sclerosis (als), is a progressive neurodegenerative disease that affects nerve cells in the brain and the spinal cord, and is characterized by muscle weakness, paralysis and ultimately, respiratory failure. |
2024-11-14 |
2024-11-17 |
Not clear |
| María Montiel-Troya, Himan Mohamed-Mohamed, Teresa Pardo-Moreno, Ana González-Díaz, Azahara Ruger-Navarrete, Mario de la Mata Fernández, María Isabel Tovar-Gálvez, Juan José Ramos-Rodríguez, Victoria García-Morale. Advancements in Pharmacological Interventions and Novel Therapeutic Approaches for Amyotrophic Lateral Sclerosis. Biomedicines. vol 12. issue 10. 2024-10-26. PMID:39457513. |
(1) amyotrophic lateral sclerosis (als) is a neurodegenerative disease in which the patient suffers from an affection of both upper and lower motor neurons at the spinal and brainstem level, causing a progressive paralysis that leads to the patient's demise. |
2024-10-26 |
2024-10-29 |
Not clear |
| Miguel Angrick, Shiyu Luo, Qinwan Rabbani, Shreya Joshi, Daniel N Candrea, Griffin W Milsap, Chad R Gordon, Kathryn Rosenblatt, Lora Clawson, Nicholas Maragakis, Francesco V Tenore, Matthew S Fifer, Nick F Ramsey, Nathan E Cron. Real-time detection of spoken speech from unlabeled ECoG signals: A pilot study with an ALS participant. medRxiv : the preprint server for health sciences. 2024-10-14. PMID:39371161. |
brain-computer interfaces (bcis) hold significant promise for restoring communication in individuals with partial or complete loss of the ability to speak due to paralysis from amyotrophic lateral sclerosis (als), brainstem stroke, and other neurological disorders. |
2024-10-14 |
2024-10-16 |
human |
| Ali Shojaie, Ahmad Al Khleifat, Sarah Garrahy, Haniah Habash-Bailey, Rachel Thomson, Sarah Opie-Martin, Sara Javidnia, P Nigel Leigh, Ammar Al-Chalab. Investigating the impact of socioeconomic status on amyotrophic lateral sclerosis. Amyotrophic lateral sclerosis & frontotemporal degeneration. 2024-09-01. PMID:39218010. |
amyotrophic lateral sclerosis (als) is a neurodegenerative disease characterized by the gradual death of motor neurons in the brain and spinal cord, leading to fatal paralysis. |
2024-09-01 |
2024-09-04 |
human |
| Junyang Liu, Weijia Zhao, Jie Guo, Kaiwen Kang, Hua Li, Xiaohang Yang, Jie Li, Qiang Wang, Haifa Qia. Electroacupuncture Alleviates Motor Dysfunction by Regulating Neuromuscular Junction Disruption and Neuronal Degeneration in SOD1 Brain research bulletin. 2024-07-31. PMID:39084570. |
electroacupuncture alleviates motor dysfunction by regulating neuromuscular junction disruption and neuronal degeneration in sod1 amyotrophic lateral sclerosis (als) is a fatal neurological disease characterized by the progressive destruction of the neuromuscular junction (nmj) and the degeneration of motor neurons, eventually leading to atrophy and paralysis of voluntary muscles responsible for motion and breathing. |
2024-07-31 |
2024-08-03 |
Not clear |
| Ermanna Turano, Federica Virla, Ilaria Scambi, Sylwia Dabrowska, Oluwamolakun Bankole, Raffaella Mariott. Adipose mesenchymal stem cells-derived extracellular vesicles exert their preferential action in damaged central sites of SOD1 mice rather than peripherally. European journal of histochemistry : EJH. vol 68. issue 3. 2024-07-04. PMID:38963135. |
amyotrophic lateral sclerosis (als) is a neurodegenerative disorder involving motor neuron (mn) loss in the motor cortex, brainstem and spinal cord leading to progressive paralysis and death. |
2024-07-04 |
2024-07-10 |
mouse |
| Sylwia Dabrowska, Ermanna Turano, Ilaria Scambi, Federica Virla, Alice Nodari, Francesco Pezzini, Mirco Galiè, Bruno Bonetti, Raffaella Mariott. A Cellular Model of Amyotrophic Lateral Sclerosis to Study the Therapeutic Effects of Extracellular Vesicles from Adipose Mesenchymal Stem Cells on Microglial Activation. International journal of molecular sciences. vol 25. issue 11. 2024-06-19. PMID:38891895. |
amyotrophic lateral sclerosis (als) is a fatal neurodegenerative disease characterized by the progressive degeneration of upper and lower motor neurons (mns) in the brain and spinal cord, leading to progressive paralysis and death. |
2024-06-19 |
2024-06-21 |
human |
| Rumi Ueha, Cathrine Miura, Naoyuki Matsumoto, Taku Sato, Takao Goto, Kenji Kond. Vocal Fold Motion Impairment in Neurodegenerative Diseases. Journal of clinical medicine. vol 13. issue 9. 2024-05-11. PMID:38731036. |
vfmi in ndds is caused by the following: laryngeal muscle weakness due to muscular atrophy, caused by brainstem and motor neuron degeneration in amyotrophic lateral sclerosis; hyperactivity of laryngeal adductors in parkinson's disease; and varying degrees of laryngeal adductor hypertonia and abductor paralysis in multiple system atrophy. |
2024-05-11 |
2024-05-27 |
Not clear |
| Hongmei Zhu, Urvashi Dalvi, William Cazenave, Daniel Cattaert, Pascal Brancherea. Excitatory action of low frequency depolarizing GABA/glycine synaptic inputs is prevalent in prenatal spinal SOD1 The Journal of physiology. 2024-02-12. PMID:38345477. |
excitatory action of low frequency depolarizing gaba/glycine synaptic inputs is prevalent in prenatal spinal sod1 amyotrophic lateral sclerosis (als) is a fatal adult-onset neurodegenerative disease characterized by progressive motor neuron degeneration and muscle paralysis. |
2024-02-12 |
2024-02-15 |
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 |
| Xin Xiao, Min Li, Zhi Ye, Xiaoyan He, Jun Wei, Yunhong Zh. Amyotrophic lateral sclerosis & frontotemporal degeneration. 2023-11-05. PMID:37926865. |
amyotrophic lateral sclerosis (als) is a fatal neurodegenerative disease associated with upper and lower motor neuron degeneration and necrosis, characterized by progressive muscle weakness, atrophy, and paralysis. |
2023-11-05 |
2023-11-08 |
Not clear |
| Wonphorn Kandhavivorn, Hannes Glaß, Thomas Herrmannsdörfer, Tobias M Böckers, Marc Uhlarz, Jonas Gronemann, Richard H W Funk, Jens Pietzsch, Arun Pal, Andreas Herman. Restoring Axonal Organelle Motility and Regeneration in Cultured FUS-ALS Motoneurons through Magnetic Field Stimulation Suggests an Alternative Therapeutic Approach. Cells. vol 12. issue 11. 2023-06-11. PMID:37296623. |
amyotrophic lateral sclerosis (als) is a devastating motoneuron disease characterized by sustained loss of neuromuscular junctions, degenerating corticospinal motoneurons and rapidly progressing muscle paralysis. |
2023-06-11 |
2023-08-14 |
Not clear |
| Xiaojiao Xu, Qiu Yang, Zheyi Liu, Rong Zhang, Hang Yu, Manli Wang, Sheng Chen, Guowang Xu, Yaping Shao, Weidong L. Integrative analysis of metabolomics and proteomics unravels purine metabolism disorder in the SOD1 Neurobiology of disease. 2023-03-31. PMID:37001614. |
integrative analysis of metabolomics and proteomics unravels purine metabolism disorder in the sod1 amyotrophic lateral sclerosis (als) is a fatal neurodegenerative disease with progressive paralysis of limbs and bulb in patients, the cause of which remains unclear. |
2023-03-31 |
2023-08-14 |
Not clear |
| Francesca De Lorenzo, Patrick Lüningschrör, Jinhan Nam, Liam Beckett, Federica Pilotto, Emilia Galli, Päivi Lindholm, Cora Rüdt von Collenberg, Simon Tii Mungwa, Sibylle Jablonka, Julia Kauder, Nadine Thau-Habermann, Susanne Petri, Dan Lindholm, Smita Saxena, Michael Sendtner, Mart Saarma, Merja H Voutilaine. CDNF rescues motor neurons in models of amyotrophic lateral sclerosis by targeting endoplasmic reticulum stress. Brain : a journal of neurology. 2023-03-17. PMID:36928391. |
amyotrophic lateral sclerosis is a progressive neurodegenerative disease that affects motor neurons (mns) in the spinal cord, brainstem, and motor cortex, leading to paralysis and eventually to death within 3 to 5 years of symptom onset. |
2023-03-17 |
2023-08-14 |
mouse |
| Elisa Duranti, Chiara Vill. Molecular Investigations of Protein Aggregation in the Pathogenesis of Amyotrophic Lateral Sclerosis. International journal of molecular sciences. vol 24. issue 1. 2023-01-08. PMID:36614144. |
amyotrophic lateral sclerosis (als) is a devastating progressive neurodegenerative disorder characterized by selective loss of lower and upper motor neurons (mns) in the brain and spinal cord, resulting in paralysis and eventually death due to respiratory insufficiency. |
2023-01-08 |
2023-08-14 |
Not clear |
| Anastasia Sarikidi, Ekaterini Kefalakes, Christine S Falk, Ruth Esser, Arnold Ganser, Nadine Thau-Habermann, Susanne Petr. Altered Immunomodulatory Responses in the CX3CL1/CX3CR1 Axis Mediated by hMSCs in an Early In Vitro SOD1 Biomedicines. vol 10. issue 11. 2022-11-26. PMID:36428484. |
altered immunomodulatory responses in the cx3cl1/cx3cr1 axis mediated by hmscs in an early in vitro sod1 amyotrophic lateral sclerosis (als) is a fatal motor neuron (mn) disease characterized by progressive mn loss and muscular atrophy resulting in rapidly progressive paralysis and respiratory failure. |
2022-11-26 |
2023-08-14 |
human |
| 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 |
| 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 |
| Andrea David Re Cecconi, Mara Barone, Simona Gaspari, Massimo Tortarolo, Caterina Bendotti, Luca Porcu, Giulia Terribile, Rosanna Piccirill. The p97-Nploc4 ATPase complex plays a role in muscle atrophy during cancer and amyotrophic lateral sclerosis. Journal of cachexia, sarcopenia and muscle. 2022-05-25. PMID:35611892. |
we investigated whether and how it might also be involved in muscle wasting in cancer, where loss of appetite occurs, or amyotrophic lateral sclerosis (als), where motoneuron death causes muscle denervation and fatal paralysis. |
2022-05-25 |
2023-08-13 |
Not clear |