Page 252 - Characterization of genetic neurodevelopmental disorders at adult age, with a focus on 22q11.2 deletion syndrome - Emma Boersma

Appendix lV
microdeletion 22q11.2. Oral presentation at the Biennial international
22q11.2 deletion syndrome conference, Split, Croatia, 2022.
Emma N.M.M. von Scheibler, Emy S. van der Valk Bouman, Myrthe A. Nuijts,
Noël J.C. Bauer, Tos T.J.M. Berendschot, Pit Vermeltfoort, Levinus A. Bok,
Agnies M. van Eeghen, Michiel L. Houben, Thérèse A.M.J. van Amelsvoort,
Erik Boot, Michelle B. van Egmond-Ebbeling. Ocular findings in 22q11.2
deletion syndrome: A systematic literature review and results of a Dutch
multicenter study. Oral presentation at the Biennial international 22q11.2
deletion syndrome conference, Split, Croatia, 2022.
Emma N.M.M. von Scheibler, Thérèse A.M.J. van Amelsvoort, Claudia
Vingerhoets, Agnies M. van Eeghen, Erik Boot. Post-traumatic stress in
adults with 22q11.2 deletion syndrome. Oral presentation at the Biennial
international 22q11.2 deletion syndrome conference, Split, Croatia, 2022.
Emma N.M.M. von Scheibler, Abhishek Appaji, Tos T.J.M. Berendschot,
Noël J.C. Bauer, Naren P. Rao, Thérèse A.M.J. van Amelsvoort, Agnies M.
van Eeghen, Erik Boot. Retinal vessel geometry: A biomarker for major
neurocognitive decline in 22q11.2 deletion syndrome? Oral presentation
at the Biennial international 22q11.2 deletion syndrome conference, Split,
Croatia, 2022.
Emma N.M.M. von Scheibler, Agnies M. van Eeghen, Tom J. de Koning,
Mark L. Kuijf, Janneke R. Zinkstok, Annelieke R. Müller; Thérèse A.M.J. van
Amelsvoort, Erik Boot, MD PhD. Parkinsonism in genetic neurodevelopmental
disorders: A systematic review. Lecture at the Dutch Parkinson Scientists
Congress, Amsterdam UMC, Amsterdam, The Netherlands, 2021.
E.N.M.M. von Scheibler, M. Kuijf, T.J. de Koning, J.R. Zinkstok, A. Muller,
T.A.M.J. van Amelsvoort, A.M. van Eeghen, H.J.G. Boot. Parkinsonism in
individuals with rare genetic neurodevelopmental disorders: A systematic
review. Oral presentation at the International Parkinson and Movement
Disorder Society Congress, 2021.
250