Results 171 to 180 of about 272,493 (246)
Abstract The 15q11.2 microdeletion is a chromosomal condition associated with a broad epileptic phenotype. It is differentiated from Angelman syndrome, which is typically a larger maternal deletion in an overlapping area. We describe a patient with a 15q11.2 microdeletion that has clinical and EEG biomarker features similar to those seen in Angelman ...
Hok Leong Chin +2 more
wiley +1 more source
Knowledge and Perceptions of Human Papillomavirus Infection and Vaccination Among Adolescents in French Rural Family Homes: A Mixed-Methods Study. [PDF]
Le Stang N +5 more
europepmc +1 more source
Pediatric new‐onset seizure‐like events: Yield of diagnostic work‐up
Abstract Objective To assess the diagnostic yield of ancillary investigations in children presenting with new‐onset seizure‐like events (SLEs) at a tertiary first seizure clinic (FSC). Methods We conducted a retrospective cohort study including 1213 children evaluated for new‐onset SLEs at a tertiary FSC.
Geertruida Slinger +8 more
wiley +1 more source
Rising incidence of central precocious puberty in Thailand: a nationwide population-based study before, during, and after the COVID-19 pandemic (2018-2024). [PDF]
Wiromrat P +5 more
europepmc +1 more source
Climate‐related exposures and seizures in children: A systematic review
Abstract Objective Climate‐related exposures, including air pollution, temperature extremes, humidity, and atmospheric conditions, are increasingly recognized as potential seizure triggers. As climate change intensifies, understanding the environmental contributors to pediatric seizure risk has important implications for anticipatory guidance and ...
Caroline Sarpy +5 more
wiley +1 more source
Incomplete male puberty: a new nosographic entity. [PDF]
La Vignera S, Condorelli RA.
europepmc +1 more source
Inherited metabolic epilepsies–established diseases, new approaches
Abstract Inherited metabolic epilepsies (IMEs) represent the inherited metabolic disorders (IMDs) in which epilepsy is a prevailing component, often determining other neurodevelopmental outcomes associated with the disorder. The different metabolic pathways affected by individual IMEs are the basis of their rarity and heterogeneity.
Itay Tokatly Latzer, Phillip L. Pearl
wiley +1 more source
COVID-19 Preventive Practices, Parent-Child Conflict, and Depressive Symptoms Among Chinese Adolescents. [PDF]
Zhou T, Xu L, Bian X, Wei L, Liu J.
europepmc +1 more source

