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Treatment and prognostic factors for long-term outcome in patients with anti-NMDA receptor encephalitis: an observational cohort study
A clinical approach to diagnosis of autoimmune encephalitis
Recommended diagnostic criteria for paraneoplastic neurological syndromes
An international panel of neurologists interested in PNS recommended new criteria for those in whom no clinical consensus was reached in the past and defined “classical” syndrome and onconeural antibody as “well characterised”.
Investigation of LGI1 as the antigen in limbic encephalitis previously attributed to potassium channels: a case series
Anti-Hu-associated paraneoplastic encephalomyelitis: analysis of 200 patients.
The predictors of mortality and PEM evolution found in the study may be important in the design of future therapeutic protocols, and emphasize the importance of early diagnosis and treatment of the underlying tumour.
AMPA receptor antibodies in limbic encephalitis alter synaptic receptor location
To report the clinical and immunological features of a novel autoantigen related to limbic encephalitis (LE) and the effect of patients' antibodies on neuronal cultures.
Anti‐Hu-Associated Paraneoplastic Encephalomyelitis/Sensory Neuronopathy A Clinical Study of 71 Patients
Patients with rapidly developing sensory neuropathy or symptoms of encephalomyelitis should be studied for the presence of the anti-Hu antibody; if the antibody is found, the possibility of small-cell lung cancer should be investigated.
Antibodies to the GABAB receptor in limbic encephalitis with seizures: case series and characterisation of the antigen
Antibody titres at diagnosis and during follow-up of anti-NMDA receptor encephalitis: a retrospective study
The category of autoimmune encephalitides constitutes disorders with relatively distinct characteristics such as psychosis, seizures, abnormal movements, coma, and dysautonomia that can be successfully treated.