Results 261 to 270 of about 4,670,463 (363)

Long‐Term Efficacy of Immunotherapy in Autoimmune Autonomic Ganglionopathy—A 10‐Year Follow Up Study

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Autoimmune autonomic ganglionopathy (AAG) is a rare but potentially treatable cause of severe autonomic failure. Evidence guiding long‐term immunotherapy, treatment sequencing, and residual autonomic impairment is limited. We evaluated long‐term treatment response, residual autonomic dysfunction, and relapse patterns in patients with
Giacomo Chiaro, Shiwen Koay, Gordon T. Ingle, Patricia McNamara, Laura Watson, Fion Bremner, Valeria Iodice   +6 more
wiley   +1 more source

Syntaxin1A in synaptopathies: From molecular mechanisms to therapeutic implications in neurological disorders (Review). [PDF]

Biomed Rep
Huang Y, Xi J, Su B, Wang P, Xie C, Yuan Y, Yin X, Bao B.   +7 more
europepmc   +1 more source

MOGAD Is the Most Common Cause of Isolated Optic Neuritis in Children

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objectives The study aimed to characterize the clinical features, etiologies, and outcomes of isolated, first‐time pediatric ON in the post‐MOG‐IgG era. Methods This was a single‐center retrospective cohort study at Texas Children's Hospital of patients diagnosed with first‐time ON between 2018–2024, with follow‐up data collected through 2025.
Chaitanya Aduru, Akansha Chandrasekar, Kyla Blasingame, Jonathan Rosen, Jesse M. Levine, Karla Salazar, Madhuri Chilakapati, Rod Foroozan, Victoria Hardwick, Jonathan M. Yarimi, Nikita Shukla, Timothy E. Lotze, Kristen S. Fisher, Alexander J. Sandweiss   +13 more
wiley   +1 more source

Supplementary data for: Prepulse inhibition of the blink reflex in functional neurological disorder and fibromyalgia

Nováková, Lucia, Sojka, Petr, Voženílek, David, Sieger, Tomáš, Hasíková, Lenka, Šenolt, Ladislav, Závada, Jakub, Edwards, Mark J., Serranová, Tereza   +8 more
openalex   +1 more source

Correction: Protective effects of Hif2 inhibitor PT-2385 on a neurological disorder induced by deficiency of Irp2 [PDF]

Jiaqi Shen, Li Xu, Yuxuan Li, Weichen Dong, Jing Cai, Yutong Liu, Hongting Zhao, Tianze Xu, Esther Meyron Holtz, Yan‐Zhong Chang, Tong Qiao, Kuanyu Li   +11 more
openalex   +1 more source

Impact of Plasma p‐tau181 on Cognition, Motor Phenotypes, and Disease Course in ALS

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Phosphorylated tau181 (p‐tau181), an Alzheimer's disease biomarker, was recently evaluated in amyotrophic lateral sclerosis (ALS). We investigated plasma p‐tau181 in 202 ALS/ALS‐FTD patients and 94 healthy controls, assessing cognitive performance, motor function, and longitudinal dynamics.
Elisabeth Kasper, Annaliis Lehto, Nina Nordmann, Oliver Peters, Julian Hellmann, Josef Priller, Eike Jakob Spruth, Gabor C. Petzold, Ina Vogt, Patrick Weydt, Sarah Bernsen, Elisabeth Dinter, Björn Falkenburger, René Günther, Emrah Düzel, Wenzel Glanz, Matthis Synofzik, Lukas Beichert, Annika Spottke, Michael Wagner, Frederic Brosseron, Matthias C. Schmid, Anja Schneider, Stefan Teipel, Johannes Prudlo, Andreas Hermann   +25 more
wiley   +1 more source

A Scoping Review of Gut Dysbiosis and Malnutrition in Neurological Disorders: Implications, Indications, and Promising Therapeutic Approaches. [PDF]

J Clin Med
Aljaraedah T, Al-Thnaibat S, Nawasreh AA, Alraei W, Al-Trad E.   +4 more
europepmc   +1 more source

Autonomic regulation during sleep and wakefulness: a review with implications for defining the pathophysiology of neurological disorders

, 2018
Anne M. Fink, Ulf G. Bronas, Michael W. Calik   +2 more
openalex   +2 more sources

Comprehensive Characterization of 98 Chinese Cases of Genetic Creutzfeldt‐Jakob Disease With T188K Mutation

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective To characterize the demographic, clinical, and laboratory features of the Chinese patients of genetic Creutzfeldt‐Jakob disease with T188K variant (T188K‐gCJD), the most common subtype of genetic prion diseases (gPrDs) in China. Methods In this nationwide retrospective study, data from 98 genetically confirmed T188K‐gCJD patients ...
Chun‐Jie Li, Dong‐Lin Liang, Li‐Ping Gao, Wei‐Wei Zhang, Wei Zhou, A. Ruhan, Bing Xu, Run‐Dong Cao, Kang Xiao, Cao Chen, Qi Shi, Xiao‐Ping Dong   +11 more
wiley   +1 more source

Strategic consensus on the clinical translation of advanced therapies in paediatric rare neurological disorders. [PDF]

Neurotherapeutics
Lim NY, Meagher CE, Bye A, Lorentzos M, Dale RC, Mohammad S, Howell KB, Palmer EE, Woodcock IR, Macdonald-Laurs E, Preisz A, Badawi N, Cooper ST, Hille SC, Trahair TN, Cairns A, Smith N, Farrar MA, Kariyawasam DS.   +18 more
europepmc   +1 more source