Publications
Linking Frailty Instruments to the International Classification of Functioning, Disability, and Health Vrije Universiteit Brussel Ghent University
To date, the major dilemma concerning frailty is the lack of a standardized language regarding its operationalization. Considering the demographic challenge that the world is facing, standardization of frailty identification is indeed the first step in tackling the burdensome consequences of frailty. To demonstrate this diversity in frailty assessment, the available frailty instruments have been linked to the International Classification of ...
The impact of intellectual disability and sport expertise on cognitive and executive functions KU Leuven
Deciphering the pathology of PP2A-related intellectual disability KU Leuven
An intersectional approach towards parental employment in families with a child with a disability University of Antwerp KU Leuven
Cross-sectional and longitudinal associations of environmental factors with frailty and disability in older people University of Antwerp
The role of psychological factors in the perpetuation of pain intensity and disability in people with chronic shoulder pain: a systematic review University of Antwerp
Problem Behaviours and Major Depressive Disorder in Intellectual Disability and Autism: A Contribution of PET and MRI Ghent University
The relationship of multimorbidity with disability and frailty in the oldest patients: A cross-sectional analysis of three measures of multimorbidity in the BELFRAIL cohort KU Leuven Ghent University
Sporadic male patients with intellectual disability Vrije Universiteit Brussel KU Leuven
Genome-wide array comparative genome hybridization has become the first in line diagnostic tool in the clinical work-up of patients presenting with intellectual disability. As a result, chromosome X-copy number variations are frequently being detected in routine diagnostics. We retrospectively reviewed genome wide array-CGH data in order to determine the frequency and nature of chromosome X-copy number variations (X-CNV) in a cohort of 2222 ...