All Relations between Paralysis and Amyotrophic Lateral Sclerosis

Publication Sentence Publish Date Extraction Date Species
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
Silvia Scaricamazza, Illari Salvatori, Susanna Amadio, Valentina Nesci, Alessio Torcinaro, Giacomo Giacovazzo, Aniello Primiano, Michela Gloriani, Niccolò Candelise, Luisa Pieroni, Jean-Philippe Loeffler, Frederique Renè, Cyril Quessada, Tesfaye W Tefera, Hao Wang, Frederik J Steyn, Shyuan T Ngo, Gabriella Dobrowolny, Elisa Lepore, Andrea Urbani, Antonio Musarò, Cinzia Volonté, Elisabetta Ferraro, Roberto Coccurello, Cristiana Valle, Alberto Ferr. Repurposing of Trimetazidine for Amyotrophic Lateral Sclerosis: a study in SOD1 British journal of pharmacology. 2021-11-16. PMID:34783031. repurposing of trimetazidine for amyotrophic lateral sclerosis: a study in sod1 amyotrophic lateral sclerosis (als), a neurodegenerative disease characterized by the degeneration of upper and lower motor neurons, progressive wasting and paralysis of voluntary muscles is currently incurable despite intense research and numerous unsuccessful clinical trials. 2021-11-16 2023-08-13 Not clear
A Bakiya, K Kamalanand, V Rajinikant. Automated diagnosis of amyotrophic lateral sclerosis using electromyograms and firefly algorithm based neural networks with fractional position update. Physical and engineering sciences in medicine. 2021-08-16. PMID:34398392. amyotrophic lateral sclerosis (als) is a disorder of the neuromuscular system that causes the impairment of nerve cells from brain to spinal cord and to the voluntary muscles in every part of the human physiological system, which totally leads to paralysis. 2021-08-16 2023-08-13 human
Wenting Liu, Sharmila Venugopal, Sana Majid, In Sook Ahn, Graciel Diamante, Jason Hong, Xia Yang, Scott H Chandle. Single-cell RNA-seq analysis of the brainstem of mutant SOD1 mice reveals perturbed cell types and pathways of amyotrophic lateral sclerosis. Neurobiology of disease. vol 141. 2021-07-14. PMID:32360664. amyotrophic lateral sclerosis (als) is a neurodegenerative disease in which motor neurons throughout the brain and spinal cord progressively degenerate resulting in muscle atrophy, paralysis and death. 2021-07-14 2023-08-13 mouse
Veronica Granatiero, Nicole M Sayles, Angela M Savino, Csaba Konrad, Michael G Kharas, Hibiki Kawamata, Giovanni Manfred. Modulation of the IGF1R-MTOR pathway attenuates motor neuron toxicity of human ALS SOD1 Autophagy. 2021-03-27. PMID:33749521. modulation of the igf1r-mtor pathway attenuates motor neuron toxicity of human als sod1 als (amyotrophic lateral sclerosis), the most common motor neuron disease, causes muscle denervation and rapidly fatal paralysis. 2021-03-27 2023-08-13 human
Benjamin E Clarke, Rickie Patan. The microglial component of amyotrophic lateral sclerosis. Brain : a journal of neurology. vol 143. issue 12. 2021-03-01. PMID:33427296. microglia have been implicated in playing a role in amyotrophic lateral sclerosis (als), a neurodegenerative disease characterized by extensive motor neuron loss leading to paralysis and premature death. 2021-03-01 2023-08-13 Not clear
Toshifumi Asano, Daniel Boon Loong Teh, Hiromu Yaw. Application of Optogenetics for Muscle Cells and Stem Cells. Advances in experimental medicine and biology. vol 1293. 2021-02-15. PMID:33398826. there are potential therapeutic applications of optogenetics in cardiac pacemaking, muscle regeneration/maintenance, locomotion recovery for the treatment of muscle paralysis due to motor neuron diseases such as amyotrophic lateral sclerosis (als). 2021-02-15 2023-08-13 Not clear