Anti-N-methyl-D-aspartate receptor encephalitis is a clinical condition characterized by acute behavioral and mood changes, abnormal movements, autonomic instability, seizures, and encephalopathy.We describe a 7-year-old boy diagnosed with autoimmune encephalitis due to NMDAR antibody in associatio...

A woman from Lincoln who was sectioned after being wrongly diagnosed as mentally ill is raising awareness of what happened to her.

Encephalitis with antibodies against N-methyl-D-aspartate receptor (NMDA-R) is classified as an autoimmune disorder with psychotic symptoms, which are frequently dominant. However, it remains unclear how frequently NMDA-R antibodies lead to a condition ...

Anti-NMDA antibody encephalitis should not be ignored by gynecologists whose role in management is central.

Objective:To compare clinical, diagnostic, management, and outcome factors in children with anti–N-methyl-d-aspartate receptor (NMDAR) encephalitis and a history of herpes simplex encephalitis (HSE...

Clinical Neurophysiology Available online 31 March 2021 Letter to the Editor Oculomotor artefacts mimic extreme deltabrush EEG features of autoimmune anti NMDA receptor encephalitis Author links open overlay panel Show more Share Cite View full text © 2021 International Federation of Clinical Neurophysiology. Published by Elsevier B.V. All rights reserved.

This study evaluates residual fatigue and cognitive defects in patients after leucine-rich glioma-inactivated 1 antibody encephalitis.

This study examines the association of myelin oligodendrocyte glycoprotein immunoglobulin G–associated disorder with pediatric optic neuritis to guide prognosis...

SHARE February 2021; 11 (1) CASE Horizontal Saccadic Palsy as a Prominent Symptom of Anti-NMDAR Encephalitis Koen Delmotte, Thomas Claeys, Koen Poesen, Bénédicte Dubois, Maarten Schrooten, Josep Dalmau, Robin Lemmens First published October 16, 2019, DOI: https://doi.org/10.1212/CPJ.0000000000000750 FULL PDF CITATION PERMISSIONS MAKE COMMENT SEE COMMENTS Downloads53 This article requires a subscription to view the full text. If you have a subscription you may use the login form below to view the article. Access to this article can also be purchased. Consider the diagnosis of autoimmune encephalitis in patients with progressive disorders of voluntary eye movements in the context of encephalopathy. Footnotes Funding information and disclosures are provided at the end of the article. Full disclosure form information provided by the authors is available with the full text of this article at Neurology.org/cp. Received June 24, 2019. Accepted September 9, 2019. © 2019 American Academy of Neurology View Full Text AAN Members We have changed the login procedure to improve access between AAN.com and the Neurology journals. If you are experiencing issues, please log out of AAN.com and clear history and cookies. (For instructions by browser, please click the instruction pages below). After clearing, choose preferred Journal and select login for AAN Members. You will be redirected to a login page where you can log in with your AAN ID number and password. When you are returned to the Journal, your name should appear at the top right of the page. Google Safari Microsoft Edge Firefox CLICK HERE TO LOGIN AAN Non-Member Subscribers CLICK HERE TO LOGIN Purchase access For assistance, please contact: AAN Members (800) 879-1960 or (612) 928-6000 (International) Non-AAN Member subscribers (800) 638-3030 or (301) 223-2300 option 3, select 1 (international) Sign Up Information on how to subscribe to Neurology and Neurology: Clinical Practice can be found here  Purchase Individual access to articles is available through the Add to Cart option on the article page.  Access for 1 day (from the computer you are currently using) is US$ 39.00.  Pay-per-view content is for the use of the payee only, and content may not be further distributed by print or electronic means.  The payee may view, download, and/or print the article for his/her personal, scholarly, research, and educational use.  Distributing copies (electronic or otherwise) of the article is not allowed. YOU MAY ALSO BE INTERESTED IN Back to top Advertisement RELATED ARTICLES No related articles found. TOPICS DISCUSSED Autoimmune diseases ALERT ME

<span><b>Background:</b> In our previous single-center study of autoimmune encephalitis (AE) related autoantibody test results we found positivity in 60 patients out of 1,034 with suspected AE from 2012 through 2018 as part of a Hungarian nationwide program.

Please do not touch a service dog. My Auggie may be cuter than oxygen monitors and feeding tubes, but she is every bit as important.

Anti-N-methyl-D-aspartate receptor (NMDAR) encephalitis is an autoimmune synaptic encephalitis likely mediated by neuronal surface antibody. Clinically, it is characterized by a variety of neurological and psychiatric symptoms, predominantly affecting young women.

Anti-IgLON5 disease is a progressive neurological disorder associated with autoantibodies against a neuronal cell adhesion molecule, IgLON5. In human postmortem brain tissue, the neurodegeneration and accumulation of hyperphosphorylated tau (p-tau) are found.

COVID-19 patients are at increased risk for developing new or recurrent psychosis.(1) Viral infections—including SARS-CoV-2 (2-4)—can cause psychosis in the context of autoimmune encephalitis.(5) However, some individuals with para-infectious psychosis do not meet criteria for autoimmune...

Autoimmune encephalitis, inflammatory diseases of the brain, present with a wide range of neurological and psychiatric symptoms, most of them common in autism...

Anti-NMDAR encephalitis in infants and toddlers clinically presents with movement disorders, developmental regression, and abnormal behaviors. Interestingly, this group had a higher proportion of patients after viral encephalitis, which is regarded as the only risk factor for poor outcomes.

Anti-N-methyl-D-aspartate receptor (NMDAR) encephalitis patients demonstrate characteristic multistage progression and movement disorders, which are analogous to hystero-epilepsy in Jean-Martin Charcot's Tuesday Lessons.

Kerry Wallen began to display strange behaviour: confusion, repeating herself, showing signs of memory loss. Here's what doctors discovered.

The common co-occurrence of autoimmune systemic diseases in patients with neurological disorders and antibodies against glutamic acid decarboxylase 65 (GAD65) suggests a shared genetic predisposition to these disorders.

Autoimmune encephalitis (AIE) constitutes an important treatable cause of movement disorders.We aimed to highlight the spectrum of movement disorder and other salient features of AIE patients diagnosed at our tertiary care centre and describe their clinical symptoms, diagnostic approach, treatment,...

In addition to anti-NMDAR antibodies, anti-GABA_BR antibodies and antibodies against unknown neuronal surface antigens can trigger autoimmune encephalitis following JE. Patients who developed autoimmune encephalitis had a poorer prognosis at the one-year follow-up.