Results 121 to 130 of about 61,963 (243)

The effect of in-arms-holding by mothers on sleep-wake states disorders of preterm neonates in neonatal intensive care unit: A pilot study

Nursing Practice Today, 2015
Background & Aim: Mother-infant separation is one of the main causes of sleep-wake states disorders in neonatal intensive care unit (NICU). The current study was conducted to investigate the effect of in-arms-holding by mothers on sleep-wake states ...
Elaheh Amini, Farideh Bastani, Nahid Rajai, Hamid Haghani   +3 more
doaj  

Seizure forecasting: The long and winding road to clinical translation

Epilepsia, EarlyView.
Abstract Seizure forecasting has progressed from theoretical aspiration to a rapidly advancing research domain, yet clinical translation remains limited. Over the past decades, advances in algorithm development, chronic electroencephalography (EEG), wearable sensors, and the characterization of seizure cycles have demonstrated that seizure risk is not ...
Philippa J. Karoly, Rachel E. Stirling, Mark J. Cook, Daniel M. Goldenholz, Maxime O. Baud, Vikram R. Rao, Solveig Vieluf, Benjamin H. Brinkmann   +7 more
wiley   +1 more source

Activation of LH orexin neurons and VTA dopamine neurons is involved in anesthesia/surgery-induced sleep-wake disorders and delirium-like behaviors in mice. [PDF]

Sci Rep
Han S, He K, Cao L, Li S, Huang L.
europepmc   +1 more source

Characterizing chapeau de gendarme in pediatric epilepsy through systematic video‐EEG evaluation

Epilepsia, EarlyView.
Abstract Objective Chapeau de gendarme (CdG) is a subtle but clinically relevant semiology that has been scarcely studied in children. Previous studies have primarily focused on its localizing value in small, surgical cohorts. This study aimed to systematically characterize frequency and clinical features of CdG across the pediatric age spectrum ...
Hanna Barbara Brinkmann, Lea Nakamura, Jan Schönberger, Julia Jacobs, Victoria San Antonio‐Arce, Kerstin Alexandra Klotz   +5 more
wiley   +1 more source

The Burden of Sleep/Wake Disorders: Excessive Daytime Sleepiness and Insomnia Project. [PDF]

Methods Protoc
Tüzün M, Kallweit U, Seidel S, Endrich O, Trelle S, Leone MA, Bruni O, Dodel R, Konti M, Lolich M, Pupillo E, Ramankulov D, Vignatelli L, Meyer-Massetti C, Schmidt M, Bassetti CLA.   +15 more
europepmc   +1 more source

Clinical significance of subclinical seizures in epilepsy presurgical evaluation: A systematic review and meta‐analysis

Epilepsia, EarlyView.
Abstract Objective Subclinical seizures (SCSs) remain an understudied aspect of presurgical evaluation in patients with drug‐resistant epilepsy (DRE), with uncertain prevalence, distribution among epilepsy types, and predictive value for surgical outcomes.
Pilar Bosque‐Varela, Panagiota‐Eleni Tsalouchidou, Petra Levicka, Lara Wadi, Elizabeth R. Blackwood, Eugen Trinka, Birgit Frauscher   +6 more
wiley   +1 more source

Integrating Assessment of Circadian Rhythmicity to Improve Treatment Outcomes for Circadian Rhythm Sleep-Wake Disorders: Updates on New Treatments. [PDF]

Curr Sleep Med Rep
Gloston GF, Ward KC, Rodriguez-Torres GC, Gamble KL, Thomas SJ.   +4 more
europepmc   +1 more source

Components of generalized onset seizures with focal evolution progressing to bilateral tonic–clonic seizures using quantitative electroencephalography in children: Focal or generalized?

Epilepsia, EarlyView.
Abstract Absence seizures evolving to bilateral tonic–clonic seizures may have focal or asymmetric clinical features. Using quantitative electroencephalography (EEG) may evaluate this phenomenon and the involved neuronal network. We conducted a retrospective chart review of pediatric patients with generalized epilepsy and normal brain magnetic ...
Juan Toro‐Perez, Erick Sell, Asif Doja, Ana Suller‐Marti, Katherine Muir, Sarah Healy, Srinivas Bulusu, Sharon Whiting, Roberto Caraballo   +8 more
wiley   +1 more source

Epilepsy syndromes classification

Epilepsia Open, EarlyView.
Abstract Epilepsy syndromes are distinct electroclinical entities which have been recently defined by the International League Against Epilepsy Nosology and Definitions Task Force. Each syndrome is associated with “a characteristic cluster of clinical and EEG features, often supported by specific etiologic findings”.
Elaine C. Wirrell, Nicola Specchio, Rima Nabbout, Phillip L. Pearl, Kate Riney   +4 more
wiley   +1 more source

Genetic epilepsies with myoclonic seizures: Mechanisms and syndromes

Epilepsia Open, EarlyView.
Abstract Genetic epilepsy with myoclonic seizures encompasses a heterogeneous spectrum of conditions, ranging from benign and self‐limiting forms to severe, progressive disorders. While their causes are diverse, a significant proportion stems from genetic abnormalities.
Antonietta Coppola, Marica Rubino, Antonella Riva, Pasquale Striano   +3 more
wiley   +1 more source