Sleep problems are commonly reported in Rett syndrome (RTT); however the electroen-cephalographic (EEG) biomarkers underlying sleep dysfunction are poorly understood. The aim of this study was to analyze the temporal evolution of quantitative EEG (qEEG) bio-markers in overnight EEGs recorded from girls (2–9 yrs. old) diagnosed with RTT using a non-traditional automated protocol. In this study, EEG spectral analysis identified high delta power cycles representing slow wave sleep (SWS) in 8–9h overnight sleep EEGs from the frontal, central and occipital leads (AP axis), comparing age-matched girls with and without RTT. Automated algorithms quantitated the area under the curve (AUC) within identified SWS cycles for each spectral frequency wave...
Sleep disorders are frequently seen in patients with Parkinson disease (PD), including rapid eye mov...
Study objectives: Increased phase synchronization in electroencephalography (EEG) bands might reflec...
Rett syndrome is a rare but severe neurological disorder associated with a mutation in the methyl Cp...
Sleep problems are commonly reported in Rett syndrome (RTT); however the electroencephalographic (EE...
Rett syndrome (RTT), a severe neurodevelopmental disorder caused by MECP2 gene abnormalities, is cha...
OBJECTIVE/BACKGROUND: Methyl-CpG-binding protein 2 (MeCP2) is of utmost importance in neuronal funct...
Rett Syndrome (RTT, OMIM 312750), a unique rare neurodevelopmental disorder, mostly affects females ...
j Abstract Vulnerability markers for affective dis-orders have focused on stress hormone regulation ...
Rett Syndrome (RTT, OMIM 312750), a unique rare neurodevelopmental disorder, mostly affects females ...
Rett Syndrome (RTT, OMIM 312750), a unique rare neurodevelopmental disorder, mostly affects females ...
Rett syndrome is characterized by loss of motor and social functions, development of stereotypic han...
Rapid eye movement (REM) sleep behavior disorder (RBD) is characterized by disrupting motor enactmen...
Polysomnography (PSG) is an objective assessment used to diagnose sleep disorders and includes recor...
Insomnia disorder (ID) has become the second-most common mental disorder. Despite burgeoning evidenc...
STUDY OBJECTIVES: We aimed to analyze quantitatively rapid eye movement (REM) sleep electroencephalo...
Sleep disorders are frequently seen in patients with Parkinson disease (PD), including rapid eye mov...
Study objectives: Increased phase synchronization in electroencephalography (EEG) bands might reflec...
Rett syndrome is a rare but severe neurological disorder associated with a mutation in the methyl Cp...
Sleep problems are commonly reported in Rett syndrome (RTT); however the electroencephalographic (EE...
Rett syndrome (RTT), a severe neurodevelopmental disorder caused by MECP2 gene abnormalities, is cha...
OBJECTIVE/BACKGROUND: Methyl-CpG-binding protein 2 (MeCP2) is of utmost importance in neuronal funct...
Rett Syndrome (RTT, OMIM 312750), a unique rare neurodevelopmental disorder, mostly affects females ...
j Abstract Vulnerability markers for affective dis-orders have focused on stress hormone regulation ...
Rett Syndrome (RTT, OMIM 312750), a unique rare neurodevelopmental disorder, mostly affects females ...
Rett Syndrome (RTT, OMIM 312750), a unique rare neurodevelopmental disorder, mostly affects females ...
Rett syndrome is characterized by loss of motor and social functions, development of stereotypic han...
Rapid eye movement (REM) sleep behavior disorder (RBD) is characterized by disrupting motor enactmen...
Polysomnography (PSG) is an objective assessment used to diagnose sleep disorders and includes recor...
Insomnia disorder (ID) has become the second-most common mental disorder. Despite burgeoning evidenc...
STUDY OBJECTIVES: We aimed to analyze quantitatively rapid eye movement (REM) sleep electroencephalo...
Sleep disorders are frequently seen in patients with Parkinson disease (PD), including rapid eye mov...
Study objectives: Increased phase synchronization in electroencephalography (EEG) bands might reflec...
Rett syndrome is a rare but severe neurological disorder associated with a mutation in the methyl Cp...