Cargando…

Increased overall cortical connectivity with syndrome specific local decreases suggested by atypical sleep-EEG synchronization in Williams syndrome

Williams syndrome (7q11.23 microdeletion) is characterized by specific alterations in neurocognitive architecture and functioning, as well as disordered sleep. Here we analyze the region, sleep state and frequency-specific EEG synchronization of whole night sleep recordings of 21 Williams syndrome a...

Descripción completa

Detalles Bibliográficos
Autores principales:	Gombos, Ferenc, Bódizs, Róbert, Kovács, Ilona
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Nature Publishing Group UK 2017
Materias:	Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5522417/ https://www.ncbi.nlm.nih.gov/pubmed/28733679 http://dx.doi.org/10.1038/s41598-017-06280-2

Ejemplares similares

Sigma frequency dependent motor learning in Williams syndrome
por: Berencsi, Andrea, et al.
Publicado: (2017)

Perceptual Learning in Williams Syndrome: Looking Beyond Averages
por: Gervan, Patricia, et al.
Publicado: (2012)

Overnight dynamics in scale-free and oscillatory spectral parameters of NREM sleep EEG
por: G. Horváth, Csenge, et al.
Publicado: (2022)

Sleep spindling and fluid intelligence across adolescent development: sex matters
por: Bódizs, Róbert, et al.
Publicado: (2014)

The interrelated effect of sleep and learning in dogs (Canis familiaris); an EEG and behavioural study
por: Kis, Anna, et al.
Publicado: (2017)

Topographical relocation of adolescent sleep spindles reveals a new maturational pattern in the human brain
por: Gombos, Ferenc, et al.
Publicado: (2022)

Scale-free and oscillatory spectral measures of sleep stages in humans
por: Schneider, Bence, et al.
Publicado: (2022)

Face processing in Williams syndrome is already atypical in infancy
por: D’Souza, Dean, et al.
Publicado: (2015)

The sleep EEG spectrum is a sexually dimorphic marker of general intelligence
por: Ujma, Péter P., et al.
Publicado: (2017)

Atypical deletion of Williams–Beuren syndrome reveals the mechanism of neurodevelopmental disorders
por: Zhou, Jianrong, et al.
Publicado: (2022)

A set of composite, non-redundant EEG measures of NREM sleep based on the power law scaling of the Fourier spectrum
por: Bódizs, Róbert, et al.
Publicado: (2021)

Dynamic sustained attention markers differentiate atypical development: The case of Williams syndrome and Down's syndrome
por: Shalev, Nir, et al.
Publicado: (2019)

An EEG investigation of alpha and beta activity during resting states in adults with Williams syndrome
por: Greer, Joanna M. H., et al.
Publicado: (2021)

A Different Brain: Anomalies of Functional and Structural Connections in Williams Syndrome
por: Gagliardi, Chiara, et al.
Publicado: (2018)

Typical visual search performance and atypical gaze behaviors in response to faces in Williams syndrome
por: Hirai, Masahiro, et al.
Publicado: (2016)

Serotonergic innervation of the amygdala is increased in autism spectrum disorder and decreased in Williams syndrome
por: Lew, C. H., et al.
Publicado: (2020)

Basal Dendritic Morphology of Cortical Pyramidal Neurons in Williams Syndrome: Prefrontal Cortex and Beyond
por: Hrvoj-Mihic, Branka, et al.
Publicado: (2017)

Williams Syndrome with a “Twist”
por: Maritsi, Despoina, et al.
Publicado: (2010)

Dentofacial characteristics in William's syndrome
por: Poornima, P., et al.
Publicado: (2012)

Cleft palate in Williams syndrome
por: Domenico, Scopelliti, et al.
Publicado: (2013)

Regional Brain Differences in Cortical Thickness, Surface Area and Subcortical Volume in Individuals with Williams Syndrome
por: Meda, Shashwath A., et al.
Publicado: (2012)

Connectivity of EEG synchronization networks increases for Parkinson’s disease patients with freezing of gait
por: Asher, Eitan E., et al.
Publicado: (2021)

Myelodysplastic syndrome with synchronous gastric cancer: when the symptoms suggest something else
por: de Melo Campos, Paula, et al.
Publicado: (2014)

Autistic Disorder in Patients with Williams-Beuren Syndrome: A Reconsideration of the Williams-Beuren Syndrome Phenotype
por: Tordjman, Sylvie, et al.
Publicado: (2012)

New Field Suggested by Dr. Williams’s Paper
por: Mills, G. A.
Publicado: (1897)

Atypical cortical connectivity and visuospatial cognitive impairments are related in children with chromosome 22q11.2 deletion syndrome
por: Simon, Tony J, et al.
Publicado: (2008)

Differences in pre-sleep activity and sleep location are associated with variability in daytime/nighttime sleep electrophysiology in the domestic dog
por: Bunford, Nóra, et al.
Publicado: (2018)

Williams syndrome presenting with findings consistent with Alagille syndrome
por: Sakhuja, Pankaj, et al.
Publicado: (2015)

Music training is associated with cortical synchronization reflected in EEG coherence during verbal memory encoding
por: Cheung, Mei-chun, et al.
Publicado: (2017)

Correction: Regional Brain Differences in Cortical Thickness, Surface Area and Subcortical Volume in Individuals with Williams Syndrome
por: Meda, Shashwath A., et al.
Publicado: (2012)

Abnormalities in early visual processes are linked to hypersociability and atypical evaluation of facial trustworthiness: An ERP study with Williams syndrome
por: Shore, Danielle M., et al.
Publicado: (2017)

Epileptic Phenotype and Cannabidiol Efficacy in a Williams–Beuren Syndrome Patient With Atypical Deletion: A Case Report
por: Nicotera, Antonio G., et al.
Publicado: (2021)

Supravalvular aortic stenosis in William's syndrome
por: Mohan, Bishav, et al.
Publicado: (2011)

Neural Correlates of Amusia in Williams Syndrome
por: Lense, Miriam D., et al.
Publicado: (2014)

Oral findings in Williams-Beuren syndrome
por: Ferreira, Shirlene-Barbosa-Pimentel, et al.
Publicado: (2018)

Williams Syndrome With Rare Ureteric Abnormality
por: Khan, Jaffar, et al.
Publicado: (2021)

Social orienting is reduced in williams syndrome
por: Kleberg, J., et al.
Publicado: (2021)

Late phonological development in Williams syndrome
por: Pérez, Vanesa, et al.
Publicado: (2022)

Emotion Priming in People with Williams Syndrome
por: Hsu, Ching-Fen, et al.
Publicado: (2023)

Prenatal phenotype of Williams–Beuren syndrome and of the reciprocal duplication syndrome
por: Marcato, Livia, et al.
Publicado: (2014)

Cannot write session to /tmp/vufind_sessions/sess_rv7vf4emlmo1k9itnilbe4m4vs