Ellen Plasschaert
Leuven, VLG 3000, Belgium
Last Updated: 09/26/2026
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Found 14 publications
Examination of the genetic factors underlying the cognitive variability associated with neurofibromatosis type 1.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: September 04, 2019
Emotional and behavioral problems in children and adolescents with neurofibromatosis type 1.
Journal: American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics
Published: June 24, 2017
Disease Burden and Symptom Structure of Autism in Neurofibromatosis Type 1: A Study of the International NF1-ASD Consortium Team (INFACT).
Journal: JAMA psychiatry
Published: October 21, 2016
Visuoperceptual processing in children with neurofibromatosis type 1: True deficit or artefact?
Journal: American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics
Published: September 02, 2016
Choroidal abnormalities in café-au-lait syndromes: a new differential diagnostic tool?
Journal: Clinical genetics
Published: July 08, 2016
Executive functioning deficits in children with neurofibromatosis type 1: The influence of intellectual and social functioning.
Journal: American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics
Published: April 21, 2015
Behavioral and cognitive outcomes for clinical trials in children with neurofibromatosis type 1.
Journal: Neurology
Published: April 16, 2015
Autism spectrum disorder profile in neurofibromatosis type I.
Journal: Journal of autism and developmental disorders
Published: December 06, 2014
Deficient motor timing in children with neurofibromatosis type 1.
Journal: Research in developmental disabilities
Published: April 14, 2014
Prevalence of Autism Spectrum Disorder symptoms in children with neurofibromatosis type 1.
Journal: American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics
Published: March 24, 2014
Characterizing the microstructural basis of "unidentified bright objects" in neurofibromatosis type 1: A combined in vivo multicomponent T2 relaxation and multi-shell diffusion MRI analysis.
Journal: NeuroImage. Clinical
Published: January 30, 2014
Last Updated: 09/26/2026