Motor-Sensory Learning in Children with Disabilities: Does Piano Practice Help? [PDF]
Strübbe S, Roy S, Sidorenko I, Lampe R.
europepmc +1 more source
Objective Endovascular thrombectomy (EVT) is increasingly used for pediatric large vessel occlusion (LVO) stroke, however, its role in isolated M2 occlusions remains underexplored. This study compared clinical outcomes in children with isolated M2 occlusion treated with EVT versus best medical therapy (BMT). Methods This multicenter cohort study pooled
Peter B. Sporns +24 more
wiley +1 more source
Effect of multidisciplinary interventions using the Enabling Inclusion® program on gross motor function and functional independence in children with disabilities in rural South India. [PDF]
Bhrasadiya N +8 more
europepmc +1 more source
Brain Atrophy Associated With Risk Variant rs10191329 Extends Beyond Multiple Sclerosis
The risk allele rs10191329*A is associated with disease severity and brain atrophy in people with multiple sclerosis (MS). We investigated the association of rs10191329 with age‐related brain atrophy in a population‐based cohort using 10,308 magnetic resonance imaging (MRI) scans of 4,815 participants aged ≥ 45 years without MS in cross‐sectional and ...
Cato E. A. Corsten +10 more
wiley +1 more source
The Socio-Ecological Factors of Physical Activity Participation in Preschool-Aged Children with Disabilities. [PDF]
Sung MC, Mahmoudkhani M, Ku B.
europepmc +1 more source
Diverse Genetic Etiologies of Unilateral Polymicrogyria
Objective Polymicrogyria (PMG) is one of the most common human malformations of cortical development and is often classified by its radiographic pattern of distribution. Unilateral polymicrogyria (uPMG) is a subtype of PMG affecting a portion or all of one cerebral hemisphere.
Abbe Lai +21 more
wiley +1 more source
Association of physical activity and screen time with vitamin D status among children with disabilities. [PDF]
Wang W +5 more
europepmc +1 more source
Fibroblast Transcriptomics in Molecular Diagnostics of a Comprehensive Dystonia Cohort
Objective Genomic sequencing leaves >50% of dystonia‐affected individuals without a diagnosis. Where DNA‐oriented approaches remain insufficient, integrating multiomics is essential to advance genome interpretation. Herein, we incorporated RNA sequencing (RNA‐seq) data from 167 patients with dystonia across a range of ages and presentations. Methods We
Alice Saparov +42 more
wiley +1 more source
Telenursing on primary family caregivers and children with disabilities: a scoping review. [PDF]
Nishigaki K +6 more
europepmc +1 more source
A Cross-Sectional Examination of Movement Behaviours and Guideline Adherence Rates Among Preschool-Aged Children With Disabilities. [PDF]
James ME +4 more
europepmc +1 more source

