All Relations between Neurodegenerative Diseases and brainstem

Reference Sentence Publish Date Extraction Date Species
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 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 2022-09-14 Not clear
Gabriela Bortolan\\xc3\\xa7a Chiarotto, Luciana Politti Cartarozzi, Matheus Perez, Ana Laura Midori Rossi Tomiyama, Mateus Vidigal de Castro, Adriana S S Duarte, \\xc3\\x82ngela Cristina Malheiros Luzo, Alexandre Leite Rodrigues de Oliveir. Delayed onset, immunomodulation, and lifespan improvement of SOD1 Brain research bulletin vol 186 issue 2022 35718222 delayed onset, immunomodulation, and lifespan improvement of sod1 amyotrophic lateral sclerosis (als) is a neurodegenerative disease characterized by the selective and progressive loss of motor neurons from the spinal cord, brain stem, and motor cortex. 2022-06-24 2022-06-27 Not clear
Polina S Goncharova, Tatiana K Davydova, Tatiana E Popova, Maxim A Novitsky, Marina M Petrova, Oksana A Gavrilyuk, Mustafa Al-Zamil, Natalia G Zhukova, Regina F Nasyrova, Natalia A Shnayde. Nutrient Effects on Motor Neurons and the Risk of Amyotrophic Lateral Sclerosis. Nutrients vol 13 issue 11 2021 34836059 amyotrophic lateral sclerosis (als) is an incurable chronic progressive neurodegenerative disease with the progressive degeneration of motor neurons in the motor cortex and lower motor neurons in the spinal cord and the brain stem. 2021-11-29 2022-01-13 Not clear
A V Alessenko, U A Gutner, V O Nebogatikov, M A Shupik, A A Ustyugo. [The role of sphingolipids in pathogenesis of amyotrophic lateral sclerosis]. Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova vol 121 issue 8 2021 34481449 amyotrophic lateral sclerosis (als) is an incurable neurodegenerative disease characterized by selective degeneration of motor neurons of the spinal cord and motor cortex and brain stem. 2021-09-07 2022-01-14 Not clear
Sanjay Das, A Nalini, T R Laxmi, T R Raj. ALS-CSF-induced structural changes in spinal motor neurons of rat pups cause deficits in motor behaviour. Experimental brain research vol 239 issue 1 2021 33170340 amyotrophic lateral sclerosis (als) is a late-onset, neurodegenerative disease associated with the loss of motor neurons in the spinal cord, brain stem and primary motor cortex. 2021-07-28 2022-01-13 Not clear
Faizana Fayaz, Faheem H Pottoo, Sadat Shafi, Mushtaq A Wani, Sharad Wakode, Anjali Sharm. Denouement of Chemicals on Amyotrophic Lateral Sclerosis: Is Green Chemistry the Answer. Medicinal chemistry (Shariqah (United Arab Emirates)) vol 16 issue 8 2021 32282307 als, a progressive neurodegenerative disease affects the motor cortex, brain stem and spinal cord, causing muscular weakness, spasticity, and hyperreflexia. 2021-06-24 2022-01-13 Not clear
Jun Ma, Baofeng Feng, Desheng Kong, Jingjing He, Ruiyun Guo, Asiamah Ernest Amponsah, Wei Zhang, Shuhan Zhang, Fei Lv, Yongzhou Song, Aijing Liu, Huixian Cu. Production and validation of human induced pluripotent stem cell line from sporadic amyotrophic lateral sclerosis (SALS). Stem cell research vol 44 issue 2021 32203916 amyotrophic lateral sclerosis (als) is a neurodegenerative disease with the loss of upper motor neurons in the cortex and lower motor neurons in the brain stem and spinal cord regressively. 2021-06-21 2022-01-13 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 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 2022-01-13 Not clear
Pilar Rojas, Ana I Ram\\xc3\\xadrez, Manuel Cadena, Jos\\xc3\\xa9 A Fern\\xc3\\xa1ndez-Albarral, Elena Salobrar-Garc\\xc3\\xada, In\\xc3\\xa9s L\\xc3\\xb3pez-Cuenca, Irene Santos-Garc\\xc3\\xada, Eva de Lago, Jos\\xc3\\xa9 L Urcelay-Segura, Jos\\xc3\\xa9 M Ram\\xc3\\xadrez, 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 33562231 the neurodegenerative disease amyotrophic lateral sclerosis (als) affects the spinal cord, brain stem, and cerebral cortex. 2021-04-12 2022-01-13 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 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 2022-01-13 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 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 2022-01-13 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 issue 2020 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 2022-01-13 Not clear
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 issue 2020 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 2022-01-13 Not clear
Sandra Carrera-Juli\\xc3\\xa1, Mari Luz Moreno, Carlos Barrios, Jose Enrique de la Rubia Ort\\xc3\\xad, Eraci Drehme. Antioxidant Alternatives in the Treatment of Amyotrophic Lateral Sclerosis: A Comprehensive Review. Frontiers in physiology vol 11 issue 2020 32116773 amyotrophic lateral sclerosis (als) is a neurodegenerative disease that produces a selective loss of the motor neurons of the spinal cord, brain stem and motor cortex. 2020-09-28 2022-01-13 Not clear
Gitika Batra, Manav Jain, Rahul Soloman Singh, Amit Raj Sharma, Ashutosh Singh, Ajay Prakash, Bikash Medh. Novel therapeutic targets for amyotrophic lateral sclerosis. Indian journal of pharmacology vol 51 issue 6 2020 32029967 amyotrophic lateral sclerosis (als) is an untreatable and fatal neurodegenerative disease that is identified by the loss of motor neurons in the spinal cord, brain stem, and motor cortex which theatrically reduces life expectancy. 2020-06-03 2022-01-13 Not clear
Jia Liu, Fei Wan. Role of Neuroinflammation in Amyotrophic Lateral Sclerosis: Cellular Mechanisms and Therapeutic Implications. Frontiers in immunology vol 8 issue 2019 28871262 amyotrophic lateral sclerosis (als) is a progressive neurodegenerative disease that affects upper motor neurons (mns) comprising the corticospinal tract and lower mns arising from the brain stem nuclei and ventral roots of the spinal cord, leading to fatal paralysis. 2019-11-20 2022-01-13 Not clear
Andres Trostchansk. Overview of Lipid Biomarkers in Amyotrophic Lateral Sclerosis (ALS). Advances in experimental medicine and biology vol 1161 issue 2019 31562633 amyotrophic lateral sclerosis (als) is a multifactorial neurodegenerative disease involving motor neuron (mn) degeneration in the spinal cord, brain stem and primary motor cortex. 2019-10-02 2022-01-13 Not clear
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 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 2022-01-13 Not clear
Isabela Lopes Trevizan, Talita Dias Silva, Helen Dawes, Thais Massetti, T\\xc3\\xa2nia Brusque Crocetta, Francis Meire Favero, Acary Souza Bulle Oliveira, Luciano Vieira de Ara\\xc3\\xbajo, 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 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 2022-01-13 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 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 2022-01-13 Not clear
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