All Relations between Neurodegenerative Diseases and brainstem

Publication Sentence Publish Date Extraction Date Species
Yanran Li, Bo Sun, Zhanjun Wang, Zhengqing He, Fei Yang, Hongfen Wang, Fang Cui, Zhaohui Chen, Li Ling, Chaodong Wang, Xusheng Huan. Mutation Screening of the Frontiers in neuroscience. vol 15. 2021-05-26. PMID:34025336. mutation screening of the amyotrophic lateral sclerosis (als) is a fatal progressive neurodegenerative disease involving the upper and lower motor neurons of the spinal cord, brainstem, and cerebral cortex. 2021-05-26 2023-08-13 Not clear
Julia Post, Vanessa Kogel, Anja Schaffrath, Philipp Lohmann, N Jon Shah, Karl-Josef Langen, Dieter Willbold, Antje Willuweit, Janine Kutzsch. A Novel Anti-Inflammatory d-Peptide Inhibits Disease Phenotype Progression in an ALS Mouse Model. Molecules (Basel, Switzerland). vol 26. issue 6. 2021-05-12. PMID:33805709. amyotrophic lateral sclerosis (als) is a progressive neurodegenerative disease characterised by selective neuronal death in the brain stem and spinal cord. 2021-05-12 2023-08-13 mouse
Christine Marques, Thibaut Burg, Jelena Scekic-Zahirovic, Mathieu Fischer, Caroline Rouau. Upper and Lower Motor Neuron Degenerations Are Somatotopically Related and Temporally Ordered in the Brain sciences. vol 11. issue 3. 2021-04-13. PMID:33805792. upper and lower motor neuron degenerations are somatotopically related and temporally ordered in the amyotrophic lateral sclerosis (als) is a devastating and fatal neurodegenerative disease arising from the combined degeneration of upper motor neurons (umn) in the motor cortex, and lower motor neurons (lmn) in the brainstem and spinal cord. 2021-04-13 2023-08-13 Not clear
Pilar Rojas, Ana I Ramírez, Manuel Cadena, José A Fernández-Albarral, Elena Salobrar-García, Inés López-Cuenca, Irene Santos-García, Eva de Lago, José L Urcelay-Segura, José M Ramírez, Rosa de Hoz, Juan J Salaza. Retinal Ganglion Cell Loss and Microglial Activation in a SOD1G93A Mouse Model of Amyotrophic Lateral Sclerosis. International journal of molecular sciences. vol 22. issue 4. 2021-04-12. PMID:33562231. the neurodegenerative disease amyotrophic lateral sclerosis (als) affects the spinal cord, brain stem, and cerebral cortex. 2021-04-12 2023-08-13 mouse
Winston T Chu, Trina Mitchell, Kelly D Foote, Stephen A Coombes, David E Vaillancour. Functional imaging of the brainstem during visually-guided motor control reveals visuomotor regions in the pons and midbrain. NeuroImage. vol 226. 2021-03-01. PMID:33301937. we also determined the effect of physiological noise and task repetitions on the visuomotor signal that will be useful in future studies of neurodegenerative diseases affecting the brainstem. 2021-03-01 2023-08-13 Not clear
Banaja P Dash, Marcel Naumann, Jared Sterneckert, Andreas Herman. Genome Wide Analysis Points towards Subtype-Specific Diseases in Different Genetic Forms of Amyotrophic Lateral Sclerosis. International journal of molecular sciences. vol 21. issue 18. 2021-02-24. PMID:32967368. amyotropic lateral sclerosis (als) is a lethally progressive and irreversible neurodegenerative disease marked by apparent death of motor neurons present in the spinal cord, brain stem and motor cortex. 2021-02-24 2023-08-13 human
Yeomin Yun, Yoon H. CRISPR/Cas9-Mediated Gene Correction to Understand ALS. International journal of molecular sciences. vol 21. issue 11. 2021-02-16. PMID:32471232. amyotrophic lateral sclerosis (als) is a neurodegenerative disease caused by the death of motor neurons in the spinal cord and brainstem. 2021-02-16 2023-08-13 Not clear
Rachel Waller, Matthew Wyles, Paul R Heath, Mbombe Kazoka, Helen Wollff, Pamela J Shaw, Janine Kirb. Small RNA Sequencing of Sporadic Amyotrophic Lateral Sclerosis Cerebrospinal Fluid Reveals Differentially Expressed miRNAs Related to Neural and Glial Activity. Frontiers in neuroscience. vol 11. 2021-01-09. PMID:29375285. amyotrophic lateral sclerosis (als) is a clinical subtype of motor neurone disease (mnd), a fatal neurodegenerative disease involving the loss of both the upper and lower motor neurones from the motor cortex, brainstem, and spinal cord. 2021-01-09 2023-08-13 Not clear
Wenping Tang, Aiqun Wang, S Ramkumar, Radeep Krishna Radhakrishnan Nai. Signal identification system for developing rehabilitative device using deep learning algorithms. Artificial intelligence in medicine. vol 102. 2020-12-22. PMID:31980094. some of the neurodegenerative diseases like amyotrophic lateral sclerosis, brainstem leison, stupor and muscular dystrophy affect the muscle movements in the body. 2020-12-22 2023-08-13 human
Mustapha Bouhrara, Luis E Cortina, Abinand C Rejimon, Nikkita Khattar, Christopher Bergeron, Janet Bergeron, Denise Melvin, Linda Zukley, Richard G Spence. Quantitative age-dependent differences in human brainstem myelination assessed using high-resolution magnetic resonance mapping. NeuroImage. vol 206. 2020-12-14. PMID:31669302. several studies indicate early brainstem alterations in a myriad of neurodegenerative diseases and dementias. 2020-12-14 2023-08-13 human
María José Castellanos-Montiel, Mathilde Chaineau, Thomas M Durca. The Neglected Genes of ALS: Cytoskeletal Dynamics Impact Synaptic Degeneration in ALS. Frontiers in cellular neuroscience. vol 14. 2020-12-08. PMID:33281562. amyotrophic lateral sclerosis (als) is a neurodegenerative disease that selectively affects motor neurons (mns) of the cortex, brainstem, and spinal cord. 2020-12-08 2023-08-13 Not clear
A V Alessenko, U A Gutner, V O Nebogatikov, M A Shupik, A A Ustyugo. [The role of lipids in the pathogenesis of lateral amyotrophic sclerosis]. Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova. vol 120. issue 10. 2020-11-30. PMID:33244966. amyotrophic lateral sclerosis (als) is an incurable neurodegenerative disease characterized by selective degeneration of motor neurons of the motor cortex, brain stem and brain stem. 2020-11-30 2023-08-13 Not clear
Manoj Kumar Jaiswa. Therapeutic opportunities and challenges of induced pluripotent stem cells-derived motor neurons for treatment of amyotrophic lateral sclerosis and motor neuron disease. Neural regeneration research. vol 12. issue 5. 2020-10-01. PMID:28616022. amyotrophic lateral sclerosis (als) and motor neuron diseases (mnds) are progressive neurodegenerative diseases that affect nerve cells in the brain affecting upper and lower motor neurons (umns/lmns), brain stem and spinal cord. 2020-10-01 2023-08-13 human
Rebecca F D'Cruz, Patrick B Murphy, Georgios Kaltsaka. Sleep disordered breathing in motor neurone disease. Journal of thoracic disease. vol 10. issue Suppl 1. 2020-10-01. PMID:29445532. motor neurone disease (mnd) is a neurodegenerative disease defined by axonal loss and gliosis of upper and lower motor neurones in the motor cortex, lower brainstem nuclei and ventral horn of the spinal cord. 2020-10-01 2023-08-13 Not clear
Irina Alecu, Steffany A L Bennet. Dysregulated Lipid Metabolism and Its Role in α-Synucleinopathy in Parkinson's Disease. Frontiers in neuroscience. vol 13. 2020-10-01. PMID:31031582. parkinson's disease (pd) is the second most common neurodegenerative disease, the main pathological hallmark of which is the accumulation of α-synuclein (α-syn) and the formation of filamentous aggregates called lewy bodies in the brainstem, limbic system, and cortical areas. 2020-10-01 2023-08-13 Not clear
Audrey M G Ragagnin, Sina Shadfar, Marta Vidal, Md Shafi Jamali, Julie D Atki. Motor Neuron Susceptibility in ALS/FTD. Frontiers in neuroscience. vol 13. 2020-10-01. PMID:31316328. amyotrophic lateral sclerosis (als) is a neurodegenerative disease characterized by the death of both upper and lower motor neurons (mns) in the brain, brainstem and spinal cord. 2020-10-01 2023-08-13 human
Luke McAlary, J Andrew Aquilina, Justin J Yerbur. Susceptibility of Mutant SOD1 to Form a Destabilized Monomer Predicts Cellular Aggregation and Toxicity but Not Frontiers in neuroscience. vol 10. 2020-09-30. PMID:27867347. susceptibility of mutant sod1 to form a destabilized monomer predicts cellular aggregation and toxicity but not amyotrophic lateral sclerosis (als) is a fatal neurodegenerative disease characterized by the rapid and progressive degeneration of upper and lower motor neurons in the spinal cord, brain stem and motor cortex. 2020-09-30 2023-08-13 Not clear
Roberta Bonafede, Raffaella Mariott. ALS Pathogenesis and Therapeutic Approaches: The Role of Mesenchymal Stem Cells and Extracellular Vesicles. Frontiers in cellular neuroscience. vol 11. 2020-09-30. PMID:28377696. amyotrophic lateral sclerosis (als) is a fatal neurodegenerative disease characterized by progressive muscle paralysis determined by the degeneration of motoneurons in the motor cortex brainstem and spinal cord. 2020-09-30 2023-08-13 Not clear
Rossana Sirabella, Valeria Valsecchi, Serenella Anzilotti, Ornella Cuomo, Antonio Vinciguerra, Pasquale Cepparulo, Paola Brancaccio, Natascia Guida, Nicolas Blondeau, Lorella M T Canzoniero, Cristina Franco, Salvatore Amoroso, Lucio Annunziato, Giuseppe Pignatar. Ionic Homeostasis Maintenance in ALS: Focus on New Therapeutic Targets. Frontiers in neuroscience. vol 12. 2020-09-30. PMID:30131665. amyotrophic lateral sclerosis (als) is one of the most threatening neurodegenerative disease since it causes muscular paralysis for the loss of motor neurons in the spinal cord, brainstem and motor cortex. 2020-09-30 2023-08-13 Not clear
Jeremy Jeffrey, Hannah D'Cunha, Masatoshi Suzuk. Blood Level of Glial Fibrillary Acidic Protein (GFAP) Does not Correlate With Disease Progression in a Rat Model of Familial ALS (SOD1 Frontiers in neurology. vol 9. 2020-09-30. PMID:30487774. blood level of glial fibrillary acidic protein (gfap) does not correlate with disease progression in a rat model of familial als (sod1 amyotrophic lateral sclerosis (als) is a neurodegenerative disease characterized by specific loss of motor neurons in the spinal cord and brain stem. 2020-09-30 2023-08-13 rat