Results 81 to 90 of about 11,808 (215)
Neuropsychopharmacology Reports, Volume 46, Issue 2, June 2026.Combined IVIg and 500 mg/day IVMP achieve superior efficacy over monotherapies in anti‐LGI1 encephalitis, with optimal safety. Higher‐dose IVMP (1000 mg) accelerates response but increases adverse events, particularly in diabetic patients. Cognitive deficits persist post‐treatment, necessitating long‐term management.
Yao Tan +6 more
wiley +1 more source
A review of psychiatric co-morbidity described in genetic and immune mediated movement disorders [PDF]
, 2017 Psychiatric symptoms are an increasingly recognised feature of movement disorders. Recent identification of causative genes and autoantibodies has allowed detailed analysis of aetiologically homogenous subgroups, thereby enabling determination of the ...
Dale, R.C. +6 more
core +3 more sources
Catatonia em Encefalite Anti-Receptor N-Metil-D-Aspartato (NMDA) Confundida com Esquizofrenia [PDF]
, 2020 Anti-N-Mmethyl-D-aspartate receptor encephalitis is an autoimmune disease of the central nervous system with prominent neurologic and psychiatric features.
Brito, A +4 more
core +1 more source
Encephalatrophy and anti-N-methyl-D-aspartate receptor encephalitis [PDF]
, 2020 Abstract Objective: This study aims to find whether there are differences of clinical and laboratory features between anti-NMDAR encephalitis patients with and without brain atrophy. We also compare brain atrophy scale in anti-NMDAR positive patients with and without teratomas.
Yinyao Lin +9 more
openaire +1 more source
CNS Neuroscience &Therapeutics, Volume 32, Issue 5, May 2026.MOG antibody‐associated cortical encephalitis (MOG‐CCE) presents a distinct clinical phenotype characterized by seizure‐dominant onset, unilateral cortical lesions, and favorable immunotherapy response, highlighting the diagnostic and prognostic value of antibody profiling in autoimmune cortical encephalitis.
Qing Yin +7 more
wiley +1 more source
Clinical and Immunologic Investigations in Patients With Stiff-Person Spectrum Disorder [PDF]
, 2016 Importance: Symptoms of stiff-person syndrome (SPS), stiff-limb syndrome (SLS), or progressive encephalomyelitis with rigidity, myoclonus, or other symptoms (SPS-plus) can occur with several autoantibodies, but the relative frequency of each antibody ...
Ariño, H +13 more
core +2 more sources
Is Favorable Outcome Possible After Prolonged Refractory Status Epilepticus? [PDF]
, 2016 When status epilepticus (SE) remains refractory to appropriate therapy, it is associated with high mortality and with substantial morbidity in survivors.
Alvarez, V., Drislane, F.W.
core +1 more source
Genetic Diagnosis and Discovery Enabled by Large Language Models
Advanced Science, Volume 13, Issue 22, 17 April 2026.We demonstrate that large language models (LLMs) can facilitate genetic diagnosis and discovery. LLMs were used to solve four types of genetic problems of sequentially increased complexity. An LLM‐based pipeline could analyze genetic variants in the genomic sequences of human hearing loss or rare genetic disease patients and assist in identifying ...
Tao Tu +25 more
wiley +1 more source
Anti-N-Methyl-D-Aspartate Receptor Encephalitis: Response to Early Treatment
Pediatric Neurology Briefs, 2010 A 5-year-old girl with anti-N-methyl-D-aspartate (NMDA) receptor encephalitis and near-complete recovery following early diagnosis and treatment with immune globulin and steroids is reported from Indiana University, University of Pennsylvania, and Mayo ...
J Gordon Millichap
doaj +1 more source
Infectious profiles in pediatric anti-N-methyl-d-aspartate receptor encephalitis
Journal of Neuroimmunology, 2023 Anti-N-methyl-d-aspartate receptor autoimmune encephalitis (NMDAR AE) is an antibody-mediated neurological disorder that may be caused by post-herpes simplex virus-1 meningoencephalitis (HSV ME) and ovarian teratomas, although most pediatric cases are idiopathic.
Alexander J, Sandweiss +10 more
openaire +2 more sources