Affiliation: Katholieke Universiteit Leuven
- Early motor development in young children with 22q.11 deletion syndrome and a conotruncal heart defectAnn Swillen
Department of Human Genetics, University Hospital Gasthuisberg, University of Leuven, Herestraat 49, 3000 Leuven, Belgium
Dev Med Child Neurol 47:797-802. 2005..These data reveal a significant motor delay in many young children with del22q.11, which is not caused by the presence of a congenital heart defect or by behavioural features...
- Basic number processing and difficulties in single-digit arithmetic: evidence from Velo-Cardio-Facial SyndromeBert De Smedt
Centre for Disability, Special Needs Education, and Child Care, University of Leuven, Belgium
Cortex 45:177-88. 2009..s model (2003). Most importantly, the correlational analyses showed that basic number processing skills directly accounted for single-digit arithmetic performance and strategy use in the children of the present study...
- Ocular findings in children with a microdeletion in chromosome 22q11.2Ingele Casteels
Department of Ophthalmology, University Hospitals Leuven St Rafael, Leuven, Belgium
Eur J Pediatr 167:751-5. 2008..2. Ophthalmological examination at a young age and refractive correction in those children is warranted. On the other hand, ocular findings can give a clue to the diagnosis of del 22q11.2...
- Interstitial 6q deletion: clinical and array CGH characterisation of a new patientCedric Le Caignec
Centre for Human Genetics, University Hospital Gasthuisberg, Herestraat 49, 3000 Leuven, Belgium
Eur J Med Genet 48:339-45. 2005....
- Velocardiofacial syndrome presenting as distal arthrogryposisKoen Devriendt
Centre for Human Genetics, University Hospital Leuven, Herestraat 49, 3000 Leuven, Belgium
Eur J Pediatr 163:329-30. 2004
- Numerical magnitude processing impairments in genetic syndromes: a cross-syndrome comparison of Turner and 22q11.2 deletion syndromesCarmen Brankaer
Parenting and Special Education Research Unit, Faculty of Psychology and Educational Sciences, University of Leuven, Belgium
Dev Sci . 2016....
- Atypical neuropsychological profile in a boy with 22q11.2 Deletion SyndromePeter Stiers
Department of Pediatrics, K U Leuven, Medical School, Herestraat 49, B 3000 Leuven, Belgium
Child Neuropsychol 11:87-108. 2005..At least in this boy the microdeletion seems to have interfered with the development and functioning of particular neural subsystems, while the structure and functioning of other subsystems was left intact...
- Pulmonary atresia/ventricular septal defect associated with facial port-wine stain and retinal vascular abnormality: a new constellation or deletion in chromosome 22q11.2?Koen Devriendt
Am J Med Genet A 132:340-1. 2005
- Motor development in school-aged children with 22q11 deletion (velocardiofacial/DiGeorge syndrome)Katrijn Van Aken
Faculty of Kinesiology and Rehabilitation Sciences, Katholieke Universiteit Leuven, Leuven, Belgium
Dev Med Child Neurol 49:210-3. 2007..To conclude, primary school children with a del22q11 syndrome showed a significant deficit in motor performance compared with a control group. A significant effect of IQ on motor performance in del22q11 was found...
- Middle and inner ear malformations in velocardiofacial syndromeKoenraad Devriendt
Am J Med Genet A 131:225-6. 2004
- Involvement of hyperprolinemia in cognitive and psychiatric features of the 22q11 deletion syndromeGregory Raux
Department of Genetics and Inserm U614, IFRMP, Faculty of Medicine, Rouen, France
Hum Mol Genet 16:83-91. 2007....
- No evidence for a parental inversion polymorphism predisposing to rearrangements at 22q11.2 in the DiGeorge/Velocardiofacial syndromeGabriel Stefan Gebhardt
Eur J Hum Genet 11:109-11. 2003
- VEGF: a modifier of the del22q11 (DiGeorge) syndrome?Ingeborg Stalmans
The Center for Transgene Technology and Gene Therapy, Flanders Interuniversity Institute for Biotechnology, Katholieke Universiteit Leuven, Leuven, Belgium
Nat Med 9:173-82. 2003..These genetic data in mouse, fish and human indicate that VEGF is a modifier of cardiovascular birth defects in the del22q11 syndrome...