Results 71 to 80 of about 33,305 (301)

Added Prognostic Value of EEG Reactivity in Comatose Patients Following Cardiac Arrest

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objectives To evaluate the added prognostic value of EEG reactivity for favorable outcome compared with background analysis during and after targeted temperature management (TTM). Methods Prospective observational cohort study of comatose post–cardiac arrest patients admitted to a single academic center between 2017 and 2022, all undergoing ...
Sarah Caroyer, Marie Obrecht, Charlotte de Maeseneire, Charlotte Damien, Chantal Depondt, Lorenzo Ferlini, Estelle Rikir, Filippo Annoni, Fabio Silvio Taccone, Nicolas Mavroudakis, Benjamin Legros, Nicolas Gaspard   +11 more
wiley   +1 more source

Pharmacotherapy of idiopathic generalized epilepsies

, 2009
Idiopathic generalized epilepsies (IGE) represent about 20% of all epilepsies, are genetically determined and comprise several subgroups of syndromes.
Cerminara, C, Moavero, R, Curatolo, P, CURATOLO, PAOLO, MOAVERO, ROMINA, LO CASTRO, A, LO CASTRO, ADRIANA, Cerminara, C.   +7 more
core   +1 more source

Memory and Resting‐State Connectivity in Acute Transient Global Amnesia: A Case–Control fMRI Study

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Background and Objectives Transient global amnesia (TGA) is a striking model of isolated amnesia. While hippocampal lesions are well described, the network‐level mechanisms and the precise neuropsychological profile remain debated. Our objective was thus to characterize functional and neuropsychological correlates of acute TGA and their ...
Elias El Otmani, Emmanuel Barbeau, Béatrice Lemesle, Emilie Milongo‐Rigal, Sophie Fernandez, Sandrine Charpentier, Jean‐François Albucher, Nicolas Raposo, Fabrice Bonneville, Patrice Péran, Jérémie Pariente   +10 more
wiley   +1 more source

Ketogenic diet in pharmacoresistant epilepsies: a clinical nutritional assessment

Arquivos de Neuro-Psiquiatria
Background Epilepsies are among the most prevalent chronic neurological diseases, usually beginning in childhood. About 30% of children with epilepsies develop seizures that are difficult to control with medication.
Cecilia Nascimento de Mendonça, Adelia Maria de Miranda Henriques-Souza, Larissa de Andrade Viana, Paula Azoubel de Souza, Luis Bandeira Alves Neto, Maria Júlia Gonçalves de Mello   +5 more
doaj   +1 more source

The epilepsies 3 /

, 2009
This title in the acclaimed Blue Books of Neurology series highlights advances in epileptology and new ways of managing seizure disorders. Contributors from around the world, most new to this volume, lend a global perspective and provide the latest ...
Pedley, Timothy A., Shorvon, S. D.(Simon D.)   +1 more
core  

Movement Disorders in Aicardi–Goutières Syndrome and Response to Immunomodulation

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT This study characterizes movement disorders and treatment responses in seven children with Aicardi–Goutières syndrome (AGS). We retrospectively evaluated motor phenotypes, neuroimaging, and interferon signatures in patients treated with baricitinib or anifrolumab. Spasticity affected all patients, while dystonia was present in 4/7.
Enrique Gonzalez Saez‐Diez, Monica Ferrer Socorro, Kathryn Yang, Nicole Battaglia, Zainab Zaman, Mariko Bennett, Adeline Vanderver, Pui Y. Lee, Lauren A. Henderson, Milena M. Andzelm, Darius Ebrahimi‐Fakhari   +10 more
wiley   +1 more source

AFG2A-related encephalopathy, expanding the neurodevelopmental and epileptic spectrum

Orphanet Journal of Rare Diseases
Objectives To expand the clinical features, epilepsy phenotype, and genotype in individuals with AFG2A-related encephalopathy (AFG2A-RE), previously known SPATA5-related encephalopathy, and to explore potential associations between genotype and epilepsy ...
Laia Nou-Fontanet, Gaetano Cantalupo, Frederik Braun, Alia Ramírez Camacho, Verónica González Álvarez, Verónica Delgadillo Chilavert, Víctor Soto Insuga, Luisa Arrabal Fernández, Itziar Alonso-Colmenero, Alexis Arzimanoglou, Carmen Fons   +10 more
doaj   +1 more source

Gene Panel Testing in Epileptic Encephalopathies and Familial Epilepsies [PDF]

, 2016
In recent years, several genes have been causally associated with epilepsy. However, making a genetic diagnosis in a patient can still be difficult, since extensive phenotypic and genetic heterogeneity has been observed in many monogenic epilepsies. This
Miranda, Maria J, Frangu, Mimoza, Krag-Olsen, Bente, Farooq, Muhammad, Møller, Rikke S; id_orcid, Linnet, Karen M, Talvik, Inga, Pal, Deb K, Hjalgrim, Helle, Talvik, Tiina, Born, A P, Svendsen, L Lavard, Baig, Shahid M, Abdullah, U, Gellert, Pia, Al-Zehhawi, Lana I K, Olofsson, Kern, Svendsen, Lene Lavard, Vaher, Ulvi, Abdullah, Uzma, Born, Alfred P, Nielsen, Jens E K, Larsen, Line H G, Tommerup, Niels, Kjelgaard, Ditte B, Rubboli, G, Johannesen, Katrine M, Peñalva, Sofia J, Marjanovic, Dragan, Pal, Deb K; id_orcid, Rubboli, Guido, Brusgaard, Klaus, Hao, Qin; id_orcid, Møller, Rikke S, Jepsen, Birgit, Hao, Qin, Uldall, Peter, Dahl, Hans A, Nikanorova, Marina   +38 more
core   +1 more source

Persistent Bilateral [18F]THK5351 and Migrating Unilateral [18F]FDG Uptake in Anti‐LGI1 Encephalitis

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Anti–leucine‐rich glioma‐inactivated 1 encephalitis (LGI1‐E) can cause persistent cognitive deficits, but the mechanisms remain unclear. A 40‐year‐old woman with LGI1‐E presented with subacute cognitive deficits and showed mild left medial temporal lobe (MTL) swelling and fluid‐attenuated inversion recovery (FLAIR) hyperintensity on initial ...
Yusuke Akitomi, Kenichiro Taira, Masanori Kurihara, Kenji Ishibashi, Kenji Ishii, Fumio Suzuki, Aya Midori Tokumaru, Makoto Hara, Atsushi Iwata   +8 more
wiley   +1 more source

Editorial: Epilepsy syndromes: pathophysiology and managements

Frontiers in Neurology, 2023
Hua-Jun Feng, Hua-Jun Feng, Tao Sun, Tao Sun, Bo Xiao, Bo Xiao, Bo Xiao   +6 more
doaj   +1 more source