All Relations between spinal cord and brainstem

Publication Sentence Publish Date Extraction Date Species
Venkataramanan Srinivasan, Victoria Homer, Darren Barton, Abigail Clutterbuck-James, Siân Jenkins, Claire Potter, Kristian Brock, Ann Logan, Donna Smith, Lars Bruce, Zsuzsanna Nagy, Simon P Bac. A low molecular weight dextran sulphate, ILB®, for the treatment of amyotrophic lateral sclerosis (ALS): An open-label, single-arm, single-centre, phase II trial. PloS one. vol 19. issue 7. 2024-07-11. PMID:38990927. it is a fatal disease with specific loss of motor neurons in the spinal cord, brain stem, and motor cortex leading to progressive paralysis and usually death within five years of diagnosis. 2024-07-11 2024-07-14 Not clear
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
Laura Toussaint, Witold Matysiak, Claire Alapetite, Javier Aristu, Agata Bannink-Gawryszuk, Stephanie Bolle, Alessandra Bolsi, Felipe Calvo, Fernando Cerron Campoo, Frances Charlwood, Charlotte Demoor-Goldschmidt, Jérôme Doyen, Katarzyna Drosik-Rutowicz, Pauline Dutheil, Anna Embring, Jacob Engellau, Anneleen Goedgebeur, Farid Goudjil, Semi Harrabi, Renata Kopec, Ingrid Kristensen, Peter Lægsdmand, Carola Lütgendorf-Caucig, Arturs Meijers, Alfredo Mirandola, Fernand Missohou, Marta Montero Feijoo, Ludvig P Muren, Barbora Ondrova, Ester Orlandi, Erik Pettersson, Alessia Pica, Sandija Plaude, Roberto Righetto, Barbara Rombi, Beate Timmermann, Karen Van Beek, Anthony Vela, Sabina Vennarini, Anne Vestergaard, Marie Vidal, Vladimir Vondracek, Damien C Weber, Gillian Whitfield, Jens Zimmerman, John H Maduro, Yasmin Lassen-Ramsha. Clinical practice in European centres treating paediatric posterior fossa tumours with pencil beam scanning proton therapy. Radiotherapy and oncology : journal of the European Society for Therapeutic Radiology and Oncology. 2024-06-28. PMID:38942120. as no guidelines for pencil beam scanning (pbs) proton therapy (pt) of paediatric posterior fossa (pf) tumours exist to date, this study investigated planning techniques across european pt centres, with special considerations for brainstem and spinal cord sparing. 2024-06-28 2024-07-01 Not clear
Ching-Yi Lin, Veronica Vanoverbeke, David Trent, Kathryn Willey, Yu-Shang Le. The Spatiotemporal Expression of SOCS3 in the Brainstem and Spinal Cord of Amyotrophic Lateral Sclerosis Mice. Brain sciences. vol 14. issue 6. 2024-06-27. PMID:38928564. the spatiotemporal expression of socs3 in the brainstem and spinal cord of amyotrophic lateral sclerosis mice. 2024-06-27 2024-06-29 mouse
Nabil Belfeki, Nouha Ghriss, Montasar Fourati, Delphine Leclercq, David Saadou. Neuro-Behçet's disease: A review. La Revue de medecine interne. 2024-06-27. PMID:38937151. nbd can be subdivided into parenchymal nbd through an immune mediated meningoencephalitis with a predilection to the brainstem, basal ganglia, thalamus, cranial nerves, and spinal cord involvement, and extraparenchymal nbd encompassing cerebral veinous thrombosis and intracranial arterial involvement. 2024-06-27 2024-06-30 Not clear
Marlene Tahedl, Ee Ling Tan, Jana Kleinerova, Siobhan Delaney, Jennifer C Hengeveld, Mark A Doherty, Russell L Mclaughlin, Pierre-Francois Pradat, Cédric Raoul, Fabrice Ango, Orla Hardiman, Kai Ming Chang, Jasmin Lope, Peter Bed. Progressive Cerebrocerebellar Uncoupling in Sporadic and Genetic Forms of Amyotrophic Lateral Sclerosis. Neurology. vol 103. issue 2. 2024-06-20. PMID:38900989. amyotrophic lateral sclerosis (als) is predominantly associated with motor cortex, corticospinal tract (cst), brainstem, and spinal cord degeneration, and cerebellar involvement is much less well characterized. 2024-06-20 2024-06-23 Not clear
He-Hai Jiang, Ruoxuan Xu, Xiupeng Nie, Zhenghui Su, Xiaoshan Xu, Ruiqi Pang, Yi Zhou, Fujun Lu. Neurexins control the strength and precise timing of glycinergic inhibition in the auditory brainstem. eLife. vol 13. 2024-05-30. PMID:38814174. however, it remains unknown whether and how neurexins are involved in shaping functional properties of the glycinergic synapses, which mediate prominent inhibition in the brainstem and spinal cord. 2024-05-30 2024-06-02 mouse
Shima Hassanpour, Hannan Algitami, Maya Umraw, Jessica Merletti, Brieana Keast, Patrick W Stroma. Investigating Descending Pain Regulation in Fibromyalgia and the Link to Altered Autonomic Regulation by Means of Functional MRI Data. Brain sciences. vol 14. issue 5. 2024-05-25. PMID:38790429. prior fmri studies have shown evidence of functional differences in fibromyalgia (fm) within brain regions associated with pain's motivational aspects, as well as differences in neural activity related to pain regulation, arousal, and autonomic homeostatic regulation within the brainstem and spinal cord regions. 2024-05-25 2024-05-27 Not clear
Shima Hassanpour, Hannan Algitami, Maya Umraw, Jessica Merletti, Brieana Keast, Patrick W Stroma. Investigating Descending Pain Regulation in Fibromyalgia and the Link to Altered Autonomic Regulation by Means of Functional MRI Data. Brain sciences. vol 14. issue 5. 2024-05-25. PMID:38790429. we, therefore, hypothesized that nociceptive processing is altered in fm compared to healthy controls (hcs) in the brainstem and spinal cord areas linked to autonomic function and descending pain regulation, including the parabrachial nuclei (pbn) and nucleus tractus solitarius (nts). 2024-05-25 2024-05-27 Not clear
Ilaria Martinelli, Jessica Mandrioli, Andrea Ghezzi, Elisabetta Zucchi, Giulia Gianferrari, Cecilia Simonini, Francesco Cavallieri, Franco Valzani. Multifaceted superoxide dismutase 1 expression in amyotrophic lateral sclerosis patients: a rare occurrence? Neural regeneration research. vol 20. issue 1. 2024-05-20. PMID:38767482. amyotrophic lateral sclerosis (als) is a neuromuscular condition resulting from the progressive degeneration of motor neurons in the cortex, brainstem, and spinal cord. 2024-05-20 2024-05-27 human
Sharon Natasha Cox, Claudio Lo Giudice, Anna Lavecchia, Maria Luana Poeta, Matteo Chiara, Ernesto Picardi, Graziano Pesol. Mitochondrial and Nuclear DNA Variants in Amyotrophic Lateral Sclerosis: Enrichment in the Mitochondrial Control Region and Sirtuin Pathway Genes in Spinal Cord Tissue. Biomolecules. vol 14. issue 4. 2024-04-27. PMID:38672428. amyotrophic lateral sclerosis (als) is a progressive disease with prevalent mitochondrial dysfunctions affecting both upper and lower motor neurons in the motor cortex, brainstem, and spinal cord. 2024-04-27 2024-04-29 human
David Gonzalez, Xiomara Cuenca, Miguel L Allend. Knockdown of Frontiers in cellular neuroscience. vol 18. 2024-04-22. PMID:38644973. knockdown of amyotrophic lateral sclerosis (als) corresponds to a neurodegenerative disorder marked by the progressive degeneration of both upper and lower motor neurons located in the brain, brainstem, and spinal cord. 2024-04-22 2024-04-24 mouse
Ricardo De Miguel, Devon Wallis Hague, Jennifer L Johnson, Amber M Zilinger, Anna Kukekova, Stephane Lezm. Congenital spongiform leukodystrophy in 2 female littermate German shepherd puppies. Journal of veterinary internal medicine. 2024-03-28. PMID:38544400. the white matter (wm) of the central nervous system (cns) showed bilateral diffuse severe spongiosis in the cerebellum, brainstem, spinal cord, and the neuropil of the oculomotor and red nuclei. 2024-03-28 2024-03-30 Not clear
Makoto Urushitani, Hitoshi Warita, Naoki Atsuta, Yuishin Izumi, Osamu Kano, Toshio Shimizu, Yuki Nakayama, Yugo Narita, Hiroyuki Nodera, Takuji Fujita, Koichi Mizoguchi, Mitsuya Morita, Masashi Aok. The clinical practice guideline for the management of amyotrophic lateral sclerosis in Japan-update 2023. Rinsho shinkeigaku = Clinical neurology. 2024-03-24. PMID:38522911. amyotrophic lateral sclerosis (als) is an adult-onset intractable motor neuron disease characterized by selective degeneration of cortical neurons in the frontotemporal lobe and motor neurons in the brainstem and spinal cord. 2024-03-24 2024-03-27 Not clear
H Willemijn van Bruggen, Camiel A Wijngaarde, Faylynn Asselman, Marloes Stam, Nico H J Creugers, Renske I Wadman, W Ludo van der Pol, Stanimira I Kalaykov. Natural History of Mandibular Function in Spinal Muscular Atrophy Types 2 and 3. Journal of neuromuscular diseases. 2024-03-22. PMID:38517801. hereditary proximal spinal muscular atrophy (sma) is characterized by abnormal alpha motor neuron function in brainstem and spinal cord. 2024-03-22 2024-03-25 Not clear
LiJun Zhou, RenShi X. Invertebrate genetic models of amyotrophic lateral sclerosis. Frontiers in molecular neuroscience. vol 17. 2024-03-19. PMID:38500677. amyotrophic lateral sclerosis (als) is a common adult-onset neurodegenerative disease characterized by the progressive death of motor neurons in the cerebral cortex, brain stem, and spinal cord. 2024-03-19 2024-03-21 human
Jelena Scekic-Zahirovic, Cristina Benetton, Aurore Brunet, XiaoQian Ye, Evgeny Logunov, Vincent Douchamps, Salim Megat, Virginie Andry, Vanessa Wing Yin Kan, Geoffrey Stuart-Lopez, Johan Gilet, Simon J Guillot, Sylvie Dirrig-Grosch, Charlotte Gorin, Margaux Trombini, Stéphane Dieterle, Jérôme Sinniger, Mathieu Fischer, Frédérique René, Zeynep Gunes, Pascal Kessler, Luc Dupuis, Pierre-François Pradat, Yannick Goumon, Romain Goutagny, Véronique Marchand-Pauvert, Sabine Liebscher, Caroline Rouau. Cortical hyperexcitability in mouse models and patients with amyotrophic lateral sclerosis is linked to noradrenaline deficiency. Science translational medicine. vol 16. issue 738. 2024-03-13. PMID:38478631. amyotrophic lateral sclerosis (als) is a devastating neurodegenerative disease, characterized by the death of upper (umn) and lower motor neurons (lmn) in the motor cortex, brainstem, and spinal cord. 2024-03-13 2024-03-16 mouse
Cyril Jones Jagaraj, Sina Shadfar, Sara Assar Kashani, Sayanthooran Saravanabavan, Fabiha Farzana, Julie D Atki. Molecular hallmarks of ageing in amyotrophic lateral sclerosis. Cellular and molecular life sciences : CMLS. vol 81. issue 1. 2024-03-02. PMID:38430277. amyotrophic lateral sclerosis (als) is a fatal, severely debilitating and rapidly progressing disorder affecting motor neurons in the brain, brainstem, and spinal cord. 2024-03-02 2024-03-04 Not clear
Linjun Cai, Xu Liu, Hongyu Zhou, Jinmei Li, Dong Zhou, Zhen Hon. Case report: Identification of Hepatitis B Virus in the cerebrospinal fluid of neuromyelitis optica spectrum disorders and successful treatment with ofatumumab and inebilizumab. Frontiers in immunology. vol 15. 2024-03-01. PMID:38426084. neuromyelitis optica spectrum disorder (nmosd) is a rare demyelinating disease of the central nervous system primarily affecting the optic nerves, spinal cord, and brainstem. 2024-03-01 2024-03-03 Not clear
Jean-Charles Viemar. Isoproterenol modulates expiratory activities in the brainstem spinal cord preparation in neonatal mice in vitro. Respiratory physiology & neurobiology. 2024-02-28. PMID:38417565. isoproterenol modulates expiratory activities in the brainstem spinal cord preparation in neonatal mice in vitro. 2024-02-28 2024-03-02 mouse