Results 11 to 20 of about 11,674 (220)

Conversion disorder in children and adolescents : Clinical features of pseudoneurological symptoms

open access: yesEuropean Psychiatry, 2021
Introduction Pseudoneurological symptoms are frequent among children consulting in neuropediatrics. Psychogenic origin is often unrecognized, which may cause a major disruption and an increase of medical care expenses.
R. Gadhoum   +6 more
doaj   +1 more source

Neuropathology of Congenital Heart Disease in an Inpatient Autopsy Cohort 2000–2017

open access: yesJournal of the American Heart Association: Cardiovascular and Cerebrovascular Disease, 2020
Background As a result of medical and surgical advancements in the management of congenital heart disease (CHD), survival rates have improved substantially, which has allowed the focus of CHD management to shift toward neurodevelopmental outcomes ...
Leigh A. Rettenmaier   +4 more
doaj   +1 more source

Trends in Neuropediatric Physical Therapy [PDF]

open access: yesFrontiers in Public Health, 2013
Among the various diseases that cause neuromotor deficits in children, the chronic non-progressive encephalopathy [cerebral palsy (CP)] is one of the most frequent. Children affected by PC may present: sensory disorders, cognitive disorders, abnormal patterns of posture, and postural tone change (1).
Eduardo Borba Neves, Eduardo Borba Neves
openaire   +3 more sources

Scalp HFO rates decrease after successful epilepsy surgery and are not impacted by the skull defect resulting from craniotomy

open access: yesScientific Reports, 2022
Epilepsy surgery can achieve seizure freedom in selected pediatric candidates, but reliable postsurgical predictors of seizure freedom are missing. High frequency oscillations (HFO) in scalp EEG are a new and promising biomarker of treatment response ...
Dorottya Cserpan   +6 more
doaj   +1 more source

Lennox-Gastaut Syndrome: A State of the Art Review. [PDF]

open access: yes, 2017
Lennox-Gastaut syndrome (LGS) is a severe age-dependent epileptic encephalopathy usually with onset between 1 and 8 years of age. Functional neuroimaging studies recently introduced the concept of Lennox-Gastaut as "secondary network epilepsy" resulting ...
Mastrangelo, Mario
core   +1 more source

Short-Term Neurodevelopmental Outcome in Term Neonates Treated with Phenobarbital versus Levetiracetam: A Single-Center Experience [PDF]

open access: yes, 2019
BACKGROUND: Phenobarbital (PB) has been traditionally used as the first-line treatment for neonatal seizures. More recently, levetiracetam (LEV) has been increasingly used as a promising newer antiepileptic medication for treatment of seizures in ...
Barbagallo, M.   +7 more
core   +3 more sources

Scalp high‐frequency oscillations differentiate neonates with seizures from healthy neonates

open access: yesEpilepsia Open, 2023
Objective We aimed to investigate (1) whether an automated detector can capture scalp high‐frequency oscillations (HFO) in neonates and (2) whether scalp HFO rates can differentiate neonates with seizures from healthy neonates.
Dorottya Cserpan   +7 more
doaj   +1 more source

Dynamic imaging of coherent sources reveals different network connectivity underlying the generation and perpetuation of epileptic seizures [PDF]

open access: yes, 2013
The concept of focal epilepsies includes a seizure origin in brain regions with hyper synchronous activity (epileptogenic zone and seizure onset zone) and a complex epileptic network of different brain areas involved in the generation, propagation, and ...
Anwar, Abdul Rauf   +6 more
core   +6 more sources

Diffusion tensor imaging discriminates focal cortical dysplasia from normal brain parenchyma and differentiates between focal cortical dysplasia types

open access: yesInsights into Imaging, 2023
Key points 1. DTI derived indices may be a useful tool for FCD characterisation. 2. FA and MD discriminated between FCD and contralateral brain parenchyma (CBP). 3. Status epilepticus increased the FA difference values between FCD and CBP. 4.
Antonio Giulio Gennari   +5 more
doaj   +1 more source

Pinpointing brainstem mechanisms responsible for autonomic dysfunction in Rett syndrome:therapeutic perspectives for 5-HT1A agonists [PDF]

open access: yes, 2014
Rett syndrome is a neurological disorder caused by loss of function of methyl-CpG-binding protein 2 (MeCP2). Reduced function of this ubiquitous transcriptional regulator has a devastating effect on the central nervous system.
Abdala, Ana Paula   +2 more
core   +3 more sources

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