Results 191 to 200 of about 43,466 (261)

Sleep deprivation increases levels of the synaptic density marker SV2A in the human brain. [PDF]

PLoS Biol
Elmenhorst D, Foerges AL, Gordji-Nejad A, Elmenhorst EM, Kroll T, Matusch A, Beer S, Neumaier B, Krapf P, Lerche C, Drzezga A, Bauer A.   +11 more
europepmc   +1 more source

Night-time heat: How real-world exposure and human diversity redefine vulnerability. [PDF]

Eco Environ Health
Debarnot U.
europepmc   +1 more source

Diagnosis and management guidelines for infantile epileptic spasms syndrome around the world: A scoping review and comparative study of international approaches

Epilepsia, EarlyView.
Abstract Objective Infantile epileptic spasms syndrome (IESS) is an epileptic encephalopathy requiring rapid diagnosis and treatment to optimize neurodevelopmental outcomes. Although multiple national and regional guidelines exist, recommendations vary.
Gozde Erdemir, Chethan K. Rao, Anne Francine Pino, Christina Briscoe, Debopam Samanta, Jo M. Wilmshurst, Sonal Bhatia, Jessica L. Carpenter, Christina Hoei‐Hansen, Puneet Jain, Tommy Stodberg, Robyn Whitney, Ryuki Matsuura, Karina Rosso Astorga, Keryma Acevedo Gallinato, Pratibha Singhi, Aristides Hadijinicolaou, Gia Melikishvili, Patricia Smeyers, Nicola Specchio, Stéphane Auvin, Pediatric Epilepsy Research Consortium Infantile Spasm Work Group and International Committee   +21 more
wiley   +1 more source

One Step Further: Integrating Evidence-Based Guidelines into Practice to Address Environmental Challenges at the Men's 2026 FIFA World Cup. [PDF]

Sports Med
Esh CJ, Carter S, Bougault V, Girard O, van Rensburg DCJ, Chrismas BCR, Meyer T, Taylor L.   +7 more
europepmc   +1 more source

Insights into ANKRD11‐related epilepsy from 163 people

Epilepsia, EarlyView.
Abstract Objective Ankyrin repeat domain 11 gene (ANKRD11) is the key disease gene for autosomal dominant KBG syndrome, and a subset of affected individuals develop epilepsy. However, comprehensive characterization of epilepsy‐related phenotypes and genotype–phenotype correlations in ANKRD11 variant carriers remains limited.
Song Su, Jian Ma, Qi Zhang, Wandong Hu, Ying Ren, Wenchao Zhang, Hongwei Zhang   +6 more
wiley   +1 more source

Frequency-specific microstate correlates of ciprofol-induced alterations of consciousness. [PDF]

Front Neurosci
Yan F, Li Y, Xiong N, Zhang Y, Zhu Y.
europepmc   +1 more source

REST, Exploring Sleep Patterns and Influencing Factors in Elite Female Football Athletes. [PDF]

Sci Data
Boeker M, Alexandersen A, Thambawita V, Midoglu C, Johansen D, Riegler MA, Halvorsen P.   +6 more
europepmc   +1 more source

Pathological hippocampal–cortical hypersynchronization disrupts memory in temporal lobe epilepsy: A multimodal intracranial electroencephalographic–functional magnetic resonance imaging study

Epilepsia, EarlyView.
Abstract Objective Memory impairment is a common comorbidity in temporal lobe epilepsy (TLE) and is thought to arise from hippocampal dysfunction and disrupted interactions within a distributed memory network involving medial temporal, frontal, and parietal cortical regions.
Ruxue Gong, Xiaolong Peng, Rebecca W. Roth, Haris Rashid, William Yun, Daniel L. Drane, Leonardo Bonilha, Lisa McTeague, Ezequiel Gleichgerrcht   +8 more
wiley   +1 more source

Efficacy and Safety of Intravenous Thrombolysis with Tenecteplase in Patients with Wake-Up Branch Atheromatous Disease. [PDF]

Transl Stroke Res
Zhu L, Zhang Y, Li J, Song L, Li H, Yang Y, Liu L, Zhang S, Gao X, Chen W, Rui G, Qin H, Tian M, Fu S.   +13 more
europepmc   +1 more source

Complete seizure freedom following minimally invasive laser callosotomy in a patient with lissencephaly type 1: Challenging the traditional paradigm

Epileptic Disorders, EarlyView.
Agilda Dema, Archie Baskaran, Joshua Chang, Douglas Nordli III, Peter Warnke   +4 more
wiley   +1 more source