Epilepsia Open, EarlyView., 2022 Abstract Epilepsy is a heterogeneous disorder characterized by spontaneous seizures and behavioral comorbidities. The underlying mechanisms of seizures and epilepsy across various syndromes lead to diverse clinical presentation and features. Similarly, animal models of epilepsy arise from numerous dissimilar inciting events.
Melissa Barker‐Haliski +3 more
wiley +1 more source
The neurobiological basis of ADHD [PDF]
, 2010 Attention-Deficit/Hyperactivity Disorder is not a single pathophysiological entity and appears to have a complex etiology. There are multiple genetic and environmental risk factors with small individual effect that act in concert to create a spectrum of ...
Curatolo, Paolo +2 more
core +3 more sources
A Pilot Study to Evaluate Neurodevelopmental Outcomes in a Pediatric Cohort With Genodermatoses
American Journal of Medical Genetics Part A, EarlyView.ABSTRACT Our study aimed to evaluate cognitive function in individuals with genetic skin disorders involving neuroectoderm (n = 8) compared to individuals with only ectoderm or mesoderm (n = 16) involvement. We hypothesized that neuroectodermal involvement would result in poorer neurocognitive performance.
Sneha A. Rangu +10 more
wiley +1 more source
TERAPI DO’A UNTUK MENINGKATKAN KONSENTRASI ANAK DENGAN GANGGUAN ATTENTION DEFICIT HYPERACTIVITY DISORDER (ADHD) DI RUMAH TERAPI AL-BIRRU [PDF]
, 2023 ABSTRAK Perkembangan anak usia 0-6 tahun merupakan masa emas anak yang sangat menentukan tumbuh kembang anak di kehidupan selanjutnya. Masalah dengan Attention Deficit Hyperactivity Disorder (ADHD) umumnya terjadi saat anak memasuki tahun-tahun ...
Mutia, Fuji Juhilna
core
American Journal of Medical Genetics Part A, EarlyView.ABSTRACT Nabais Sá‐De Vries syndrome (NSDVS) is an extremely rare autosomal dominant disorder caused by SPOP mutations. To date, only 10 cases have been described presenting with intellectual disability, neurological signs and symptoms, and a variable association of dysmorphic features.
Jessica Galli +10 more
wiley +1 more source
State-related electroencephalographic deviances in attention deficit hyperactivity disorder [PDF]
, 2014 Objective: This study aimed to provide more insight into the functional significance of electroencephalographic (EEG) deviances in attention-deficit/hyperactivity disorder (ADHD) by evaluating quantitative EEG during performance on a task with a low ...
Buyck, Inez, Wiersema, Roeljan
core +4 more sources
Attention-deficit/hyperactivity disorder: a closer look [PDF]
, 1999 Includes bibliographical ...
O'Neill, Michael J.
core +1 more source
The Study of the Effect of Magnetic Therapy on Improvement of Neuropsychological Functions in Children with Attention Deficit Disorder and Hyperactivity [PDF]
, 2016 This study aims to evaluate the effect of magnetic therapy on improvement of neuropsychological functions in those with attention deficit disorder with hyperactivity. The statistical population of present study includes 30 children with attention deficit-
Emami Poo, Susan +3 more
core +3 more sources
Attention Deficit Hyperactivity Disorder Intervention: Strategies & Counselling Tips for Primary School Teachers. [PDF]
, 2010 This paper addresses attention deficit hyperactivity disorder intervention strategies for primary school teachers. Wrong labelling of children with attention deficit hyperactivity disorder has given rise to this paper.
Abikwi, M.I
core +2 more sources
MTSS2‐Related Disorder: Refining the Phenotype in Four New Cases and Literature Review
American Journal of Medical Genetics Part A, EarlyView.ABSTRACT MTSS2 encodes a protein highly expressed in the central nervous system, with a crucial role in neurodevelopment. The de novo recurrent variant c.2011C>T (p.Arg671Trp) was first identified in 2022 as cause of Intellectual Developmental Disorder with ocular anomalies and distinctive facial features (OMIM#620086).
Angela De Dominicis +12 more
wiley +1 more source