| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| Stephen A Goutman, Masha G Savelieff, Stacey A Sakowski, Eva L Feldma. Stem cell treatments for amyotrophic lateral sclerosis: a critical overview of early phase trials. Expert opinion on investigational drugs. vol 28. issue 6. 2019-07-09. PMID:31189354. |
amyotrophic lateral sclerosis (als) is a neurodegenerative disease of cortical, brainstem, and spinal motor neurons; it causes progressive muscle weakness and atrophy, respiratory failure, and death. |
2019-07-09 |
2023-08-13 |
Not clear |
| Shahram Darabi, Ali Noori-Zadeh, Farzad Rajaei, Hojjat Allah Abbaszadeh, Salar Bakhtiyari, Navid Ahmady Roozbahan. SMER28 Attenuates Dopaminergic Toxicity Mediated by 6-Hydroxydopamine in the Rats via Modulating Oxidative Burdens and Autophagy-Related Parameters. Neurochemical research. vol 43. issue 12. 2019-05-23. PMID:30288644. |
parkinson's disease is the second most common neurodegenerative disease that occurs due to cellular autophagy deficiency and the accumulation of alpha-synuclein in the dopaminergic neurons of the substantia nigra pars compacta (snc) of the brainstem. |
2019-05-23 |
2023-08-13 |
rat |
| Francesca Magri, Fiammetta Vanoli, Stefania Cort. miRNA in spinal muscular atrophy pathogenesis and therapy. Journal of cellular and molecular medicine. vol 22. issue 2. 2019-04-22. PMID:29160009. |
spinal muscular atrophy (sma) is an autosomal recessive neurodegenerative disease characterized by the selective death of lower motor neurons in the brain stem and spinal cord. |
2019-04-22 |
2023-08-13 |
Not clear |
| A Weerasekera, D M Sima, T Dresselaers, S Van Huffel, P Van Damme, U Himmelreic. Non-invasive assessment of disease progression and neuroprotective effects of dietary coconut oil supplementation in the ALS SOD1 NeuroImage. Clinical. vol 20. 2019-02-05. PMID:30368196. |
non-invasive assessment of disease progression and neuroprotective effects of dietary coconut oil supplementation in the als sod1 amyotrophic lateral sclerosis (als) is an incurable neurodegenerative disease primarily characterized by progressive degeneration of motor neurons in the motor cortex, brainstem and spinal cord. |
2019-02-05 |
2023-08-13 |
Not clear |
| Isabela Lopes Trevizan, Talita Dias Silva, Helen Dawes, Thais Massetti, Tânia Brusque Crocetta, Francis Meire Favero, Acary Souza Bulle Oliveira, Luciano Vieira de Araújo, Ana Carolina Costa Santos, Luiz Carlos de Abreu, Shelly Coe, Carlos Bandeira de Mello Monteir. Efficacy of different interaction devices using non-immersive virtual tasks in individuals with Amyotrophic Lateral Sclerosis: a cross-sectional randomized trial. BMC neurology. vol 18. issue 1. 2019-01-22. PMID:30558556. |
amyotrophic lateral sclerosis (als) is a rapid progressive neurodegenerative disease, characterized by a selective loss of motor neurons, brain stem and spinal cord which leads to deterioration of motor abilities. |
2019-01-22 |
2023-08-13 |
Not clear |
| Silvia Ravera, Tiziana Bonifacino, Martina Bartolucci, Marco Milanese, Elena Gallia, Francesca Provenzano, Katia Cortese, Isabella Panfoli, Giambattista Bonann. Characterization of the Mitochondrial Aerobic Metabolism in the Pre- and Perisynaptic Districts of the SOD1 Molecular neurobiology. vol 55. issue 12. 2019-01-18. PMID:29656361. |
characterization of the mitochondrial aerobic metabolism in the pre- and perisynaptic districts of the sod1 amyotrophic lateral sclerosis (als) is an adult-onset fatal neurodegenerative disease characterized by muscle wasting, weakness, and spasticity due to a progressive degeneration of cortical, brainstem, and spinal motor neurons. |
2019-01-18 |
2023-08-13 |
Not clear |
| Aimee N Winter, Erika K Ross, Heather M Wilkins, Trisha R Stankiewicz, Tyler Wallace, Keith Miller, Daniel A Linsema. An anthocyanin-enriched extract from strawberries delays disease onset and extends survival in the hSOD1 Nutritional neuroscience. vol 21. issue 6. 2018-12-24. PMID:28276271. |
an anthocyanin-enriched extract from strawberries delays disease onset and extends survival in the hsod1 amyotrophic lateral sclerosis (als) is a neurodegenerative disease resulting from the death of motor neurons in the brain, brain stem, and spinal cord. |
2018-12-24 |
2023-08-13 |
Not clear |
| D Heidelberg, S Ronsin, F Bonneville, S Hannoun, C Tilikete, F Cotto. Main inherited neurodegenerative cerebellar ataxias, how to recognize them using magnetic resonance imaging? Journal of neuroradiology = Journal de neuroradiologie. vol 45. issue 5. 2018-11-26. PMID:29920348. |
ataxia is a neurodegenerative disease resulting from brainstem, cerebellar, and/or spinocerebellar tracts impairments. |
2018-11-26 |
2023-08-13 |
Not clear |
| Fulvio Zaccagna, Giulia Lucignani, Eytan Raz, Claudio Colonnes. Imaging techniques in ALS. Archives italiennes de biologie. vol 155. issue 4. 2018-08-28. PMID:29405031. |
amyotrophic lateral sclerosis (als) is a progressive neurodegenerative disease characterized by degeneration of both upper and lower motor neuron located in the spinal cord and brainstem. |
2018-08-28 |
2023-08-13 |
Not clear |
| Marios G Krokidis, Panagiotis Vlamo. Transcriptomics in amyotrophic lateral sclerosis. Frontiers in bioscience (Elite edition). vol 10. 2018-06-19. PMID:28930607. |
amyotrophic lateral sclerosis (als) is an adult-onset, incurable neurodegenerative disease characterized by the selective death of upper and lowers motor neurons in the spinal cord, brainstem and motor cortex, which ultimately leads to paralysis and death within 2-3 years of onset. |
2018-06-19 |
2023-08-13 |
human |
| Lihua Hou, Bin Jiao, Tingting Xiao, Lu Zhou, Zhifan Zhou, Juan Du, Xinxiang Yan, Junling Wang, Beisha Tang, Lu She. Screening of SOD1, FUS and TARDBP genes in patients with amyotrophic lateral sclerosis in central-southern China. Scientific reports. vol 6. 2018-05-18. PMID:27604643. |
amyotrophic lateral sclerosis (als) is a fatal neurodegenerative disease affecting motor neurons of the brain, brainstem and spinal cord. |
2018-05-18 |
2023-08-13 |
Not clear |
| Christine M Walsh, Leslie Ruoff, Kathleen Walker, Alaisa Emery, Jonathan Varbel, Elissaios Karageorgiou, Phi N Luong, Irida Mance, Hilary W Heuer, Adam L Boxer, Lea T Grinberg, Joel H Kramer, Bruce L Miller, Thomas C Neyla. Sleepless Night and Day, the Plight of Progressive Supranuclear Palsy. Sleep. vol 40. issue 11. 2018-03-26. PMID:29029214. |
to elucidate the unique sleep and waking characteristics in progressive supranuclear palsy (psp), a neurodegenerative disease associated with motor deficits and dementia that largely affects the brainstem and thalamic regions. |
2018-03-26 |
2023-08-13 |
Not clear |
| Can Sun, Yuanyuan Liu, Yaling Liu, Mei Zhao, Jingxu Zhai, Pengli Hao, Ying Wang, Yingxiao J. Characterization of aromatase expression in the spinal cord of an animal model of familial ALS. Brain research bulletin. vol 132. 2018-02-09. PMID:28583855. |
amyotrophic lateral sclerosis (als) is a neurodegenerative disease involving motor neurons in the motor cortex, brainstem and spinal cord. |
2018-02-09 |
2023-08-13 |
mouse |
| Sonam Parakh, Julie D Atki. Protein folding alterations in amyotrophic lateral sclerosis. Brain research. vol 1648. issue Pt B. 2018-01-17. PMID:27064076. |
amyotrophic lateral sclerosis (als) is a neurodegenerative disease that targets motor neurons in the brain, brainstem and spinal cord. |
2018-01-17 |
2023-08-13 |
Not clear |
| Jerri L Jaffa, Marlene Dufault, Mary Lavi. An Interprofessional Approach to Amyotrophic Lateral Sclerosis Care. The Journal of neuroscience nursing : journal of the American Association of Neuroscience Nurses. vol 49. issue 5. 2017-10-31. PMID:28817498. |
amyotrophic lateral sclerosis (als) is a progressive fatal neurodegenerative disease that is characterized by the death of motor neurons in the spinal cord, brain stem, and motor cortex that are responsible for voluntary movement. |
2017-10-31 |
2023-08-13 |
Not clear |
| Zhang-Yu Zou, Ming-Sheng Liu, Xiao-Guang Li, Li-Ying Cu. H46R SOD1 mutation is consistently associated with a relatively benign form of amyotrophic lateral sclerosis with slow progression. Amyotrophic lateral sclerosis & frontotemporal degeneration. vol 17. issue 7-8. 2017-10-23. PMID:27348463. |
amyotrophic lateral sclerosis (als) is a fatal neurodegenerative disease caused by progressive loss of motor neurons in the motor cortex, brainstem, and spinal cord. |
2017-10-23 |
2023-08-13 |
Not clear |
| Yulia Solomonov, Nurit Hadad, Rachel Lev. Reduction of cytosolic phospholipase A2α upregulation delays the onset of symptoms in SOD1G93A mouse model of amyotrophic lateral sclerosis. Journal of neuroinflammation. vol 13. issue 1. 2017-10-10. PMID:27250836. |
amyotrophic lateral sclerosis (als) is a fatal multifactorial neurodegenerative disease characterized by selective death of motor neurons in the cortex, brainstem, and spinal cord. |
2017-10-10 |
2023-08-13 |
mouse |
| Stefania Marcuzzo, Silvia Bonanno, Matteo Figini, Alessandro Scotti, Ileana Zucca, Ludovico Minati, Nilo Riva, Teuta Domi, Andrea Fossaghi, Angelo Quattrini, Barbara Galbardi, Sara D'Alessandro, Maria Grazia Bruzzone, José Manuel García-Verdugo, Victoria Moreno-Manzano, Renato Mantegazza, Pia Bernascon. A longitudinal DTI and histological study of the spinal cord reveals early pathological alterations in G93A-SOD1 mouse model of amyotrophic lateral sclerosis. Experimental neurology. vol 293. 2017-08-17. PMID:28351750. |
amyotrophic lateral sclerosis (als) is a neurodegenerative disease characterized by selective motor neuron degeneration in the motor cortex, brainstem and spinal cord. |
2017-08-17 |
2023-08-13 |
mouse |
| Mingchun Yang, Hongkuan Yang, Hongpeng Guan, Jean-Pierre Bellier, Shiguang Zhao, Ikuo Tooyam. Mapping of mitochondrial ferritin in the brainstem of Macaca fascicularis. Neuroscience. vol 328. 2017-07-18. PMID:27133573. |
the distribution of ftmt which we found in the brainstem implies possible involvement of ftmt in several physiological mechanisms, especially in the catecholaminergic neurons, and the possibility of significant involvement in neurodegenerative disease. |
2017-07-18 |
2023-08-13 |
mouse |
| Liyan Hou, Cong Zhang, Ke Wang, Xiaofang Liu, Hongwei Wang, Yuning Che, Fuqiang Sun, Xueying Zhou, Xiulan Zhao, Qingshan Wan. Paraquat and maneb co-exposure induces noradrenergic locus coeruleus neurodegeneration through NADPH oxidase-mediated microglial activation. Toxicology. vol 380. 2017-05-12. PMID:28202386. |
the loss of noradrenergic locus coeruleus (lc/ne) neurons in brainstem is a common feature shared by multiple neurodegenerative diseases, including pd. |
2017-05-12 |
2023-08-13 |
mouse |