Results 101 to 110 of about 53,157 (259)
Chronic Inflammatory Demyelinating Polyneuropathy (CIDP): A Comprehensive Review of Types, Pathophysiology, and Treatment Approaches
Brain and Behavior, Volume 16, Issue 5, May 2026.Chronic inflammatory demyelinating polyneuropathy is an autoimmune disorder causing demyelination, leading to distal weakness, sensory loss, and autonomic dysfunction. Immune activation triggers macrophage‐mediated myelin damage and conduction failure.Ayesha Khan, Arsal Khan, Kuldeep Dalpat Rai, Anzel Saeed, Harsh Kumar, Aneesh Kumar Sangtiani, Tehreem Fatima, Muhammad Tanveer Alam, Faiza Rajput, Sakshi Chawla, Hussain Haider Shah, Humaira Kalam +11 morewiley +1 more sourceGuillain–Barré Syndrome After Malaria: A Case Report of a 7‐Year‐Old Child With Asymmetric Onset of Acute Motor Axonal Neuropathy
Clinical Case Reports, Volume 14, Issue 5, May 2026.ABSTRACT
This case highlights that acute motor axonal neuropathy can present with asymmetric, relapsing weakness in children. In malaria‐endemic and resource‐limited settings, clinicians should consider atypical Guillain–Barré variants early, as timely recognition and treatment can significantly improve outcomes despite diagnostic and systemic ...Muath Ibrahim Mohammed Abusaada, Mustafa Mohamed Ibrahim Ali, Muotaman Mohammed Abdalla Adam, Mohammed Hishameldeen Omer Ali, Mohamed Abdallah Mohamed Baraka, Amjad Ali Mohamedelhassan Bakheit, Khabab Abbasher Hussien Mohamed Ahmed, Isameldin Yousif Khidir Mohmed +7 morewiley +1 more sourceShort‐Term Oral Spermidine Supplementation Modifies Aspects of Neurodegenerative Disease in Flies and Mice With MPS III
Journal of Inherited Metabolic Disease, Volume 49, Issue 3, May 2026.ABSTRACT
Mucopolysaccharidosis type III (MPS III) is a group of autosomal recessive neurodegenerative lysosomal storage disorders that causes progressive cognitive and physical impairment, predominantly in child/early adulthood. The median age of death is 17 years as there is no safe, effective treatment approved.Helen Beard, Sonia Dayan, Karissa Barthelson, Laura Hewson, Louise V. O'Keefe, Kim M. Hemsley +5 morewiley +1 more sourceIncreased Circulating T Cell Reactivity to GM1 Ganglioside in Patients with Guillain-Barre Syndrome [PDF]
, 2005 This study was performed to determine whether increased ganglioside-specific T cell reactivity can be detected in the peripheral blood of patients with Guillain-Barre syndrome (GBS) and chronic inflammatory demyelinating polyradiculoneuropathy (CIDP).Alaedini, Alice-Ann Sullivan, Ariga, Asbury, Borsellino, Chiba, Cooper, Cooper, Dyck, Fujioka, Galli, Gong, Heidenreich, Hitoshi, Ho, Hughes, Illes, Judith M. Greer, Kaida, Kaida, Kerryn Green, Kieseier, Kleyweg, Koga, Kracun, Kusunoki, Kusunoki, Kuwabara, McCombe, Michael P. Pender, Odaka, Ogawa-Goto, Pamela A. McCombe, Pan, Pender, Pender, Peter A. Csurhes, Pollard, Prendergast, Press, Raschetti, Rees, Schwerer, Shamshiev, Shamshiev, Susuki, Tagawa, van den Berg, van Doorn, Vincent, Visser, Wicklein, Willison, Winer, Yan, Yu, Yuki, Yuki, Yuki, Yuki +59 morecore +1 more sourceDynamics of Nerve Conduction Studies in Patients With Guillain–Barré Syndrome
Muscle &Nerve, Volume 73, Issue 5, Page 832-842, May 2026.ABSTRACT Introduction/Aims
The value of electrodiagnostic subtyping of Guillain–Barré syndrome (GBS) is still debated. This study aimed to determine the diagnostic yield, timing, and changes of the electrodiagnostic subtyping in patients with GBS in serial nerve conduction studies (NCS).Samuel Arends, Laura de Koning, Judith Drenthen, Mahova Zhu, Peter Y. K. van den Bergh, Robert M. Hadden, Nortina Shahrizaila, Ricardo C. Reisin, Satoshi Kuwabara, Senda Ajroud‐Driss, Giovanni Antonini, Claudia Balducci, Fabio A. Barroso, Thomas H. Brannagan, Jan Buermann, Carlos Casasnovas, Guido Cavaletti, Chi‐Chao Chao, Ulrich Dillmann, Mazen M. Dimachkie, Giuliana Galassi, Gerardo Gutiérrez‐Gutiérrez, Thomas Harbo, Sung‐Tsang Hsieh, Badrul Islam, Hans Katzberg, Lynette Kiers, Giorgia Mataluni, Julio Pardo, Yann Peréon, Yusuf A. Rajabally, Mark Stettner, Camiel Verhamme, Michal Vytopil, Waheed Waqar, David R. Cornblath, Bart C. Jacobs, IGOS Consortium, James M. Addington, Senda Ajroud‐Driss, Hiroshi Amino, Giovanni Antonini, Sharam Attarian, Umesh A. Badrising, Claudia Balducci, Fabio A. Barroso, Kathleen Bateman, Isabelita Bella, Luana Benedetti, Tulio Bertorini, Ratna Bhavaraju‐Sanka, Davide Binda, Thomas Brannagan, Chiara Briani, Jan Buermann, Mark Busby, Steven Butterworth, Carlos Casasnovas, Guido Cavaletti, Govind Chavada, Chi‐Chao Chao, Shan Chen, Kristl Claeys, Eugenia Conti, Jeremy S. Cosgrove, Marinos Dalakas, Philip van Damme, Efthimios Dardiotis, Amy Davidson, Ulrich Dillmann, Mazen Dimachkie, Alex Doets, Pieter van Doorn, Andoni Echaniz‐Laguna, Filip Eftimov, Karin G. Faber, Raffaella Fazio, Thomas E. Feasby, Janev Fehmi, Chris Fokke, Toshiki Fujioka, Ernesto Fulgenzi, Giuliana Galassi, Marcel P.J. Garssen, Cees J. Gijsbers, James M. Gilchrist, Job Gilhuis, Jonathan M. Goldstein, Kenneth C. Gorson, Namita Goyal, Volkan Granit, Gerardo Gutiérrez‐Gutiérrez, Ludwig Gutmann, Thomas Harbo, Hans‐Peter Hartung, James K.L. Holt, Sung‐Tsang Hsieh, Min Htut, Richard A.C. Hughes, Badrul Islam, Zhahirul Islam, Ivonne Jericó‐Pascual, Kenichi Kaida, Summer Karafiath, Hans Katzberg, Mohammad Ali Khoshnoodi, Lynette Kiers, Ruud P. Kleiweg, Norito Kokubun, Noah A. Kolb, Rinske van Koningsveld, Anneke J. van der Kooi, Hans Kramers, Krista Kuitwaard, Justin Y. Kwan, Shafeeq S. Ladha, Lisbeth Landschoff Lassen, Victoria H. Lawson, Helmar Lehmann, Luciana Leon Cejas, Linda Luijten, Michael P.T. Lunn, Fiore Manganelli, Hadi Manji, Girolama A. Marfia, Celedonio Márquez Infante, Lorena Martín‐Aguilar, Eugenia Martinez‐Hernandez, Giorgia Mataluni, Marcelo Mattiazzi, Christopher McDermott, Gregg Meekins, Quazi Deen Mohammad, Soledad Monges, Germán Moris de la Tassa, Caterina Nascimbene, Eduardo Nobile‐Orazio, Richard J. Nowak, Michael Osei‐Bonsu, Julio Pardo, Farah Pelouto, Yann Péreon, Michael T. Pulley, Luis Querol Gutiérrez, Yusuf Rajabally, Stephen W. Reddel, Taco van der Ree, Simon Rinaldi, Paolo Ripellino, Rhys C. Roberts, Iñigo Rojas‐Marcos, Stacy A. Rudnicki, George M. Sachs, Johnny P.A. Samijn, Lucio Santoro, Angelo Schenone, Maria José Sedano Tous, Yukari Sekiguchi, Kazim A. Sheikh, Nicholas Joseph Silvestri, Soeren H. Sundrup, Claudia Sommer, Beth Stein, Mark Stettner, Amro Maher Stino, Robin C.M. Thomma, Paul Twydell, Giovanni Uncini, Jay D. Varrato, Camiel Verhamme, Frederique H. Vermeij, Jan Verschuuren, Leo H. Visser, Michal Vytopil, Christa Walgaard, Min Wang, Yuzhong Wang, Waheed Waqar, Hugh J. Willison, Paul W. Wirtz, Marieke van Woerkom, Sascha A. Zivkovic +181 morewiley +1 more sourceCharacterization of a hamster melanoma-associated ganglioside antigen as 7-O-acetylated disialoganglioside GD3
Journal of Lipid Research, 1993 We previously reported a hamster animal model of melanoma in which the tumor tissue expresses gangliosides GM3, GD3, and O-acetyl GD3. This ganglioside pattern is similar to that in human melanomas (Ren, S., A. Slominski, and R. K. Yu.S Ren, T Ariga, JN Scarsdale, Y Zhang, A Slominski, PO Livingston, G Ritter, Y Kushi, RK Yu +8 moredoaj +1 more sourceStructural analysis of brain ganglioside acetylation patterns in mice with altered ganglioside biosynthesis [PDF]
, 2013 Gangliosides are sialylated membrane glycosphingolipids especially abundant in mammalian brain tissue. Sialic acid O-acetylation is one of the most common structural modifications of gangliosides which considerably influences their chemical properties ...Fabris, Dragana, Heffer, Marija, Kalanj Bognar, Svjetlana, Mlinac, Kristina, Rožman, Marko, Vukelić, Željka +5 morecore +1 more source