Results 291 to 300 of about 2,272,583 (371)

Leucine-rich glioma-inactivated protein 1 antibody-positive limbic encephalitis in a patient with an early-stage asymptomatic breast cancer. [PDF]

BMJ Case Rep
Niño Uribe MF, Van Cutsem G, Kerschen P.   +2 more
europepmc   +1 more source

Evaluation of the etiology of epilepsy and/or developmental delay in children via next-generation sequencing: a single-center experience. [PDF]

Front Pediatr
Kava H, Akgun-Dogan O, Yesilyurt A, Alanay Y, Isik U.   +4 more
europepmc   +1 more source

Developmental and Epileptic Encephalopathy: Pathogenesis of Intellectual Disability Beyond Channelopathies. [PDF]

Biomolecules
Medyanik AD, Anisimova PE, Kustova AO, Tarabykin VS, Kondakova EV.   +4 more
europepmc   +1 more source

Expert-Agreed Practical Recommendations on the Use of Fenfluramine in Developmental and Epileptic Encephalopathies Based on Clinical Experience and Literature Review. [PDF]

Neurol Ther
Villanueva V, Soto-Insuga V, Smeyers P, Aledo-Serrano Á, Sánchez-Carpintero R, García-Peñas J, Gil-Nagel A.   +6 more
europepmc   +1 more source

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Pain behavior without pain sensation: an epileptic syndrome of "symbolism for pain"?

Pain, 2019
'Asymbolia for pain' (AP) has shown the potentiality of diseased insular networks to dissociate sensory from affective-behavioral dimensions of pain, resulting in the lack of appropriate motor and affective responses despite preserved sensory aspect of ...
K. Hagiwara, L. Garcia-Larrea, L. Tremblay, A. Montavont, H. Catenoix, S. Rheims, M. Guenot, J. Isnard   +7 more
semanticscholar   +1 more source

Epileptic

Late Self-Portraits, 2022
Terminology of the International League against epilepsy (1989) a syndrome is 'a cluster of signs and symptoms customarily occurring together'. An epileptic syndrome is usually based on all the information available from the patient's and his/her family ...
A. Ebner
semanticscholar   +1 more source

Both gain‐of‐function and loss‐of‐function de novo CACNA1A mutations cause severe developmental epileptic encephalopathies in the spectrum of Lennox‐Gastaut syndrome

Epilepsia, 2019
Developmental epileptic encephalopathies (DEEs) are genetically heterogeneous severe childhood‐onset epilepsies with developmental delay or cognitive deficits.
Xiao Jiang, P. K. Raju, N. D’Avanzo, M. Lachance, Julie Pépin, F. Dubeau, W. Mitchell, L. Bello-Espinosa, T. Pierson, B. Minassian, J. Lacaille, E. Rossignol   +11 more
semanticscholar   +1 more source