Results 41 to 50 of about 73,644 (221)

Anti-GAD-associated limbic encephalitis: an unusual clinical manifestation from northwest of Ireland

open access: yesThe Egyptian Journal of Neurology, Psychiatry and Neurosurgery, 2020
We report an unusual manifestation of anti-GAD-associated limbic encephalitis in a 59-year-old man following pacemaker insertion for cardiac pauses. Clinically, the association of anti-GAD antibody with limbic encephalitis is rare.
Salman Mansoor, Kevin Murphy
doaj   +1 more source

Limbic encephalitis: Not a picture to forget [PDF]

open access: yesNeurology, 2004
A 36-year-old woman presented to the emergency department with three generalized seizures following 5 days of pyrexia. Over the subsequent week she had clouded consciousness, further generalized convulsions, and visual …
Chinnery PF   +3 more
openaire   +3 more sources

Rare paraneoplastic syndrome of prostatic cancer: limbic encephalitis: a case report

open access: yesJournal of Medical Case Reports, 2021
Introduction Limbic encephalitis is an autoimmune neurologic disorder, often of paraneoplastic origin, that seldom complicates prostatic tumors. The nonspecificity of symptoms makes the diagnosis sometimes difficult to establish. Prognosis is essentially
Omar Karray   +9 more
doaj   +1 more source

Olfactory dysfunction after autoimmune encephalitis depending on the antibody type and limbic MRI pathologies

open access: yesFrontiers in Neurology, 2023
ObjectivePatients’ olfactory function after autoimmune encephalitis (AE) involving limbic structures may be impaired. This study aimed to characterize olfactory function in patients after autoimmune encephalitides.MethodsA case–control study was ...
Martin Hänsel   +6 more
doaj   +1 more source

Seronegative limbic encephalitis manifesting as subacute amnestic syndrome: a case report and review of the literature

open access: yesJournal of Medical Case Reports, 2021
Background Limbic encephalitis (LE), a variant of autoimmune encephalitis, is inflammation of the limbic system of the brain. The disorder presents with subacute impairment of short-term memory, psychiatric manifestations, confusion and seizures ...
Ismail Ibrahim Ismail   +2 more
doaj   +1 more source

Limbic Encephalitis With Dual Positivity

open access: yesCureus, 2023
Limbic encephalitis is a well-defined clinical disorder among paraneoplastic neurological syndromes. Although it is not always possible to identify specific autoantibodies in limbic encephalitis, the presence of anti-neuronal nuclear antibody type 1 (ANNA1 or anti-Hu), anti-Ma2, collapsin response mediator protein 5 (CRMP-5-IgG or anti-CV2), anti-GABAB 
Erdil Yucesoy, Esra   +4 more
openaire   +2 more sources

Utility of the APE2 Score as a Diagnostic Tool for Autoimmune Encephalitis

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective To retrospectively evaluate the diagnostic performance of the Antibody Prevalence in Epilepsy and Encephalopathy (APE2) score relative to clinician‐adjudicated autoimmune encephalitis (AE) and the Graus criteria in a tertiary neuroimmunology referral cohort, including antibody‐negative AE.
Bijoya Basu   +3 more
wiley   +1 more source

Seronegative paraneoplastic limbic encephalitis associated with thymoma

open access: yes, 2020
Paraneoplastic limbic encephalitis is an autoimmune syndrome characterized by the acute or subacute onset of encephalopathy, memory loss, confusion, temporal lobe seizures, and behavioral and mood changes.
Duque, Alejandra   +5 more
core   +1 more source

A case of anti-VGKC antibody encephalitis and prolonged encephalopathy despite spontaneous resolution of imaging abnormalities

open access: yesJournal of Community Hospital Internal Medicine Perspectives, 2020
Anti-voltage-gated potassium channel (anti-VGKC) antibody encephalitis is a common form of autoimmune encephalitis (AE). AE is usually associated with autoimmune diseases or paraneoplastic phenomena such as seen in small cell lung cancer.
Victoria Novoselova   +3 more
doaj   +1 more source

Early Clinical and Cerebrospinal Fluid Predictors of 1‐Year Recurrence in Autoimmune GFAP Astrocytopathy

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Autoimmune glial fibrillary acidic protein astrocytopathy (GFAP‐A) is an inflammatory central nervous system disorder with variable outcomes. Relapse occurs in a subset of patients, but early predictors remain unclear. We aimed to identify admission‐available features associated with 1‐year recurrence and develop an interpretable ...
Qingting Hong   +10 more
wiley   +1 more source

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