Results 61 to 70 of about 3,617 (131)
Efficacy of Tocilizumab in Limbic Encephalitis with Anti-CASPR2 Antibodies
We report the case of a 64-year-old man who presented with subacute memory, balance impairment, behavioral and mood changes, and epileptic seizures. Magnetic resonance imaging (MRI) showed bilateral hippocampal abnormalities.
Maurizio Benucci +9 more
doaj +1 more source
Epilepsy: Epidemiology, Molecular Pathogenesis, and Clinical Management
Epilepsy is a heterogeneous and chronically evolving brain network disorder. This review integrates epidemiological burden, psychiatric comorbidities, and cyclic seizure patterns with multiscale pathogenic mechanisms, including ion‐channel dysfunction, synaptic transmission defects, neuroinflammation, metabolic and mitochondrial dysfunction, and ...
Jian Liu +8 more
wiley +1 more source
ObjectivesThis case report aims to highlight the atypical presentation and management of a patient diagnosed with CASPR2-associated autoimmune encephalitis and NF155 antibody-positive autoimmune nodopathies (AN), initially presenting with limb weakness ...
Wen-Ya Wang +23 more
doaj +1 more source
MOG-AD and CASPR2 Encephalitis (Overlap Syndrome) in an Adolescent Girl: A Case Report
Background: Although myelin oligodendrocytes glycoprotein antibody-associated disease (MOG-AD) and anti-contactin-associated protein-like 2 (CASPR2) antibody-mediated encephalitis are distinct neurological disorders, combined existence has rarely been ...
Dona Teresa Thomas +4 more
doaj +1 more source
In myelinated fibers, the voltage-gated sodium channels Nav1 are concentrated at the nodal gap to ensure the saltatory propagation of action potentials.
Giulia Bonetto +5 more
doaj +1 more source
IntroductionMultiple system atrophy (MSA) is a sporadic, adult-onset neurodegenerative disorder characterized by rapid progression. Early diagnosis remains particularly challenging, especially when CASPR2 antibodies are detected during the early stages ...
Jun Zhang, Yueming Wang, Le Chen, Jun Li
doaj +1 more source
Neuronal Antibodies in Children with or without Narcolepsy following H1N1-AS03 Vaccination.
Type 1 narcolepsy is caused by deficiency of hypothalamic orexin/hypocretin. An autoimmune basis is suspected, but no specific antibodies, either causative or as biomarkers, have been identified. However, the AS03 adjuvanted split virion H1N1 (H1N1-AS03)
Simon Thebault +9 more
doaj +1 more source
Case report: Recurring potassium channel complex autoimmunity-related neuropathic pain
Voltage-gated potassium channel (VGKC) complex autoimmunity associated with nerve hyperexcitability is an uncommon clinical spectrum. It is mostly characterized by limbic encephalitis, continuous neuromyotonia, and dysautonomia. Pain, however, has rarely
Yun-Qing Zhu +7 more
doaj +1 more source
Isaacs Syndrome (IS) is an autoimmune disease characterized by fasciculations, dysautonomia, and hyperactivity of muscle fibers due to hyperexcitability of the peripheral nerve system.
Rasa Zafari, Mona Ahmadi
doaj +1 more source
Antibody-Dependent Cellular Phagocytosis and Cytotoxicity in Patients With LGI1 and CASPR2 Encephalitis. [PDF]
Businaro P +24 more
europepmc +1 more source

