Page 251 - Characterization of genetic neurodevelopmental disorders at adult age, with a focus on 22q11.2 deletion syndrome - Emma Boersma

About the author
Emma von Scheibler, Agnies van Eeghen, Thérèse van Amelsvoort, Erik
Boot et al. Prevalence of Parkinson’s disease in 22q11.2 deletion syndrome:
A multicenter study. Article in progress.
Publications in national non-peer-reviewed journals
Emma N.M.M. von Scheibler, MD; Thérèse A.M.J. van Amelsvoort, MD,
PhD; Claudia Vingerhoets, PhD; Agnies M. van Eeghen, MD, PhD; Erik
Boot, MD, PhD. Post-traumatische stress bij volwassenen met 22q11.2
deletiesyndroom. TAVG, nummer 4, 2022. (Dutch)
Emma von Scheibler, Agnies van Eeghen, Tos Berendschot, Denise van
Barneveld, Josine Widdershoven, Therese van Amelsvoort, Erik Boot.
Zintuigproblematiek bij 22q11.2 deletiesyndroom. TAVG, nummer 3, 2020.
(Dutch)
Scientific communications with accepted/published abstracts
Agnies van Eeghen, Erik Boot, Emma von Scheibler, Annelieke Müller,
Hadassa Kwetsie, Hester Jaspers Faijer – Westerink. Workshops (oral
presentations) at the “Focus op Onderzoek” symposium, Amersfoort, The
Netherlands, 2023.
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. Poster presentation at
EuroNDD, Amsterdam, The Netherlands, 2023.
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. Poster presentation at Society of
the Study of Behavioral Phenotypes conference, Oslo, Norway, 2022.
Emma N.M.M. von Scheibler, Josine C.C. Widdershoven, Denise C.P.B.M.
Breukels-van Barneveld, Nina Schröder, Thérèse A.M.J. van Amelsvoort,
Agnies M. van Eeghen, Erik Boot. Age-related hearing loss in adults with
A4
249