Caregiving Quality Across Development and Secure Base Knowledge among Adolescents with a History of Institutional Care. [PDF]
Hare MM +6 more
europepmc +1 more source
Tracking Motor Progression and Device‐Aided Therapy Eligibility in Parkinson's Disease
ABSTRACT Objective To characterise the progression of motor symptoms and identify eligibility for device‐aided therapies in Parkinson's disease, using both the 5‐2‐1 criteria and a refined clinical definition, while examining differences across genetic subgroups.
David Ledingham +7 more
wiley +1 more source
High-resolution chronologies of anthropogenic soil substrates based on portable luminescence reader data. [PDF]
Brill D +6 more
europepmc +1 more source
Change in Cognition Following Ischaemic Stroke
ABSTRACT Objective Cognitive decline can occur following ischaemic stroke. How cognition changes over time and associations with cognitive change are poorly understood. This study aimed to explore these issues over 2 years following ischaemic stroke.
Wenci Yan +8 more
wiley +1 more source
Airflow trajectories in childhood asthma: what data-driven research can teach us. [PDF]
Vollmond AV, Håkansson KEJ, Rastogi D.
europepmc +1 more source
Visual Recovery Reflects Cortical MeCP2 Sensitivity in Rett Syndrome
ABSTRACT Objective Rett syndrome (RTT) is a devastating neurodevelopmental disorder with developmental regression affecting motor, sensory, and cognitive functions. Sensory disruptions contribute to the complex behavioral and cognitive difficulties and represent an important target for therapeutic interventions.
Alex Joseph Simon +12 more
wiley +1 more source
A thermochronological transect across the Trento platform: constraints for the evolution of the European Eastern Southern Alps. [PDF]
Klotz T +4 more
europepmc +1 more source
ON ORNAMENTAL DETAILS OF THE ZEN-STYLE ARCHITECTURE OF THE EARLY MIDDLE AGES (3)
Kinya Sekiguchi
openalex +2 more sources
The Diverse Neuromuscular Spectrum of VPS13A Disease
ABSTRACT Objective VPS13A disease (chorea‐acanthocytosis) is a rare neurodegenerative disorder caused by biallelic variants in VPS13A, typically presenting with hyperkinetic movement disorders, while neuromuscular signs are often mild. The aim of the project was to investigate the frequency and severity of neuromuscular impairment in VPS13A disease ...
Anne Buchberger +16 more
wiley +1 more source
Structural connectome gradients and their relationship to IQ in childhood. [PDF]
Hong Y +9 more
europepmc +1 more source

