Results 181 to 190 of about 1,028,023 (313)

Anomia prehabilitation in temporal lobe epilepsy surgery: A pilot study

open access: yesEpilepsia, EarlyView.
Abstract Objective An emerging approach in surgery is to propose prehabilitation programs to strengthen the patient's functional abilities before surgical interventions, thus helping them cope better with its consequences. In drug‐resistant language‐dominant temporal lobe epilepsy (LdTLE), surgical treatment carries a risk of increasing cognitive ...
Véronique Sabadell   +12 more
wiley   +1 more source

Familial SYNGAP1 variants define the boundaries of a complex neurodevelopmental disorder with epilepsy

open access: yesEpilepsia, EarlyView.
Abstract Objective SYNGAP1‐related disorders are common neurodevelopmental conditions characterized by autism spectrum disorder, developmental delay, intellectual disability, and a range of generalized seizure types. Disease‐causing variants in SYNGAP1 typically occur de novo. This study aims to characterize inherited cases of SYNGAP1‐related disorders.
Alicia G. Harrison   +10 more
wiley   +1 more source

Overlap between genetic variants associated with schizophrenia spectrum disorders and intelligence quotient: a systematic review. [PDF]

open access: yesJ Psychiatry Neurosci, 2022
Murillo-García N   +6 more
europepmc   +1 more source

Can headache impair intellectual abilities in children? An observational study

open access: yesNeuropsychiatric Disease and Treatment, 2012
Maria Esposito,1 Antonio Pascotto,1 Beatrice Gallai,3 Lucia Parisi,2 Michele Roccella,2 Rosa Marotta,4 Serena Marianna Lavano,4 Antonella Gritti,5 Giovanni Mazzotta,6 Marco Carotenuto11Center for Childhood Headache, Clinic of Child and Adolescent ...
Esposito M   +9 more
doaj  

The Correlation between Children's Intelligence Quotient and Their Behavior in Dental Setting: A Cross-Sectional Study. [PDF]

open access: yesBiomed Res Int, 2022
Khosrozadeh M   +5 more
europepmc   +1 more source

Broadening the phenotype associated with pathogenic variants in the FGF12 gene: From developmental and epileptic encephalopathy to drug‐responsive epilepsy with favorable cognitive outcome

open access: yesEpilepsia, EarlyView.
Abstract The fibroblast growth factor 12 (FGF12) gene encodes a protein interacting with voltage‐gated sodium channels. Two variants, p.(Arg52His) and p.(Gly50Ser), have repeatedly been associated with developmental and epileptic encephalopathy‐47 (DEE47; Mendelian Inheritance in Man #617166) with poor outcome.
Clément Pierret   +17 more
wiley   +1 more source

Editorial

open access: yesCiência da Informação, 2018
Why do organizations need to increase their strategic intelligence quotient (IQ)?
Kimiz Dalkir
doaj  

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