All Relations between Neurodegenerative Diseases and brainstem

Publication Sentence Publish Date Extraction Date Species
Robert B Kargb. Microbiome-Gut-Brain Axis Modulation: New Approaches in Treatment of Parkinson's Disease and Amyotrophic Lateral Sclerosis. ACS medicinal chemistry letters. vol 14. issue 7. 2023-07-19. PMID:37465304. mitochondrial dysfunction plays a critical role in the disease's progression, while amyotrophic lateral sclerosis (als), or lou gehrig's disease, is a fatal progressive neurodegenerative disease characterized by significant motor neuron loss in the primary motor cortex, brainstem, and spinal cord. 2023-07-19 2023-08-14 Not clear
Bárbara Teruel-Peña, José Luís Gómez-Urquiza, Nora Suleiman-Martos, Isabel Prieto, Francisco José García-Cózar, Manuel Ramírez-Sánchez, Carmen Fernández-Martos, Germán Domínguez-Vía. Systematic Review and Meta-Analyses of Aminopeptidases as Prognostic Biomarkers in Amyotrophic Lateral Sclerosis. International journal of molecular sciences. vol 24. issue 8. 2023-04-28. PMID:37108335. amyotrophic lateral sclerosis (als) is a fatal neurodegenerative disease characterized by the progressive loss of motor neurons in the spinal cord, brain stem, and cerebral cortex. 2023-04-28 2023-08-14 human
Sena Boncuk Ulaş, Yeşim Güzey Aras, Sezen Irmak Gözükara, Türkan Acar, Bilgehan Atılgan Aca. Correlates of Zonulin and Claudin-5, markers of intestinal and brain endothelial permeability, in Parkinson's Disease: A pilot study. Parkinsonism & related disorders. vol 110. 2023-03-24. PMID:36963340. idiopathic parkinson's disease is a chronic, progressive, neurodegenerative disease that affects the substantia nigra pars compacta and dopaminergic neurons in the brain stem. 2023-03-24 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
Mohammed Al-Biltagi, Adel Salah Bediwy, Nermin Kamal Saee. Cough as a neurological sign: What a clinician should know. World journal of critical care medicine. vol 11. issue 3. 2022-11-04. PMID:36331984. cough reflex sensitivity could be increased in many neurological disorders such as brainstem space-occupying lesions, medullary lesions secondary to chiari type i malformations, tics disorders such as tourette's syndrome, somatic cough, cerebellar neurodegenerative diseases, and chronic vagal neuropathy due to allergic and non-allergic conditions. 2022-11-04 2023-08-14 Not clear
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
Banaja P Dash, Axel Freischmidt, Jochen H Weishaupt, Andreas Herman. Downstream Effects of Mutations in International journal of molecular sciences. vol 23. issue 17. 2022-09-09. PMID: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 2023-08-14 human
Kimberly Luttik, Victor Olmos, Ashley Owens, Aryaan Khan, Joy Yun, Terri Driessen, Janghoo Li. Identifying Disease Signatures in the Spinocerebellar Ataxia Type 1 Mouse Cortex. Cells. vol 11. issue 17. 2022-09-09. PMID:36078042. the neurodegenerative disease spinocerebellar ataxia type 1 (sca1) is known to lead to the progressive degeneration of specific neuronal populations, including cerebellar purkinje cells (pcs), brainstem cranial nerve nuclei and inferior olive nuclei, and spinocerebellar tracts. 2022-09-09 2023-08-14 mouse
Qianqian Zhang, Huihui Zhao, Maotao Luo, Xi Cheng, Yanan Li, Qingyang Li, Zheng Wang, Qi Ni. The Classification and Prediction of Ferroptosis-Related Genes in ALS: A Pilot Study. Frontiers in genetics. vol 13. 2022-07-25. PMID:35873477. amyotrophic lateral sclerosis (als) is a neurodegenerative disease characterized by progressive muscle paralysis, which is followed by degeneration of motor neurons in the motor cortex of the brainstem and spinal cord. 2022-07-25 2023-08-14 Not clear
Gabriela Bortolança Chiarotto, Luciana Politti Cartarozzi, Matheus Perez, Ana Laura Midori Rossi Tomiyama, Mateus Vidigal de Castro, Adriana S S Duarte, Ângela Cristina Malheiros Luzo, Alexandre Leite Rodrigues de Oliveir. Delayed onset, immunomodulation, and lifespan improvement of SOD1 Brain research bulletin. 2022-06-19. PMID: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. 2022-06-19 2023-08-14 human
Kadavigere V Rajagopal, Antony S D'Souza, Aparna Verma, Hosapatna Mamatha, Lokadolalu C Prasann. Comparative morphometric evaluation of the brainstem in neurodegenerative diseases with healthy individuals using magnetic resonance imaging. Journal of Taibah University Medical Sciences. vol 17. issue 1. 2022-02-10. PMID:35140570. comparative morphometric evaluation of the brainstem in neurodegenerative diseases with healthy individuals using magnetic resonance imaging. 2022-02-10 2023-08-13 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. 2021-11-29. PMID: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 2023-08-13 Not clear
Susanne G Muelle. Mapping internal brainstem structures using MP2RAGE derived T1 weighted and T1 relaxation images at 3 and 7 T. Human brain mapping. vol 41. issue 8. 2021-11-08. PMID:31971322. mapping internal brainstem structures using mp2rage derived t1 weighted and t1 relaxation images at 3 and 7 t. the brainstem is a site of early pathology in several neurodegenerative diseases. 2021-11-08 2023-08-13 human
Harry W M Steinbusch, Mohammad Amin Dolatkhah, David A Hopkin. Anatomical and neurochemical organization of the serotonergic system in the mammalian brain and in particular the involvement of the dorsal raphe nucleus in relation to neurological diseases. Progress in brain research. vol 261. 2021-10-22. PMID:33785137. the brainstem is a neglected brain area in neurodegenerative diseases, including alzheimer's and parkinson's disease, frontotemporal lobar degeneration and autonomic dysfunction. 2021-10-22 2023-08-13 Not clear
Vladimir A Martínez-Rojas, Daniele Arosio, Maria Pennuto, Carlo Musi. Clenbuterol-sensitive delayed outward potassium currents in a cell model of spinal and bulbar muscular atrophy. Pflugers Archiv : European journal of physiology. vol 473. issue 8. 2021-10-18. PMID:34021780. sbma is characterized by selective dysfunction and degeneration of motor neurons in the brainstem and spinal cord through still unclear mechanisms in which ion channel modulation might play a central role as for other neurodegenerative diseases. 2021-10-18 2023-08-13 mouse
Melissa A Walker, Maria Miranda, Amanda Allred, Vamsi K Mooth. On the dynamic and even reversible nature of Leigh syndrome: Lessons from human imaging and mouse models. Current opinion in neurobiology. vol 72. 2021-10-16. PMID:34656053. leigh syndrome (ls) is a neurodegenerative disease characterized by bilaterally symmetric brainstem or basal ganglia lesions. 2021-10-16 2023-08-13 mouse
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. 2021-09-07. PMID: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 2023-08-13 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. 2021-07-28. PMID: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 2023-08-13 rat
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. 2021-06-24. PMID:32282307. als, a progressive neurodegenerative disease affects the motor cortex, brain stem and spinal cord, causing muscular weakness, spasticity, and hyperreflexia. 2021-06-24 2023-08-13 human
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. 2021-06-21. PMID: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 2023-08-13 human