Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Dorinde Korteling"'
Autor:
Mirjam van der Ende-van Loon, Dorinde Korteling, Hilde Willekens, Monique Schilders, Wouter Curvers, Raf Bisschops, Erik Schoon, Caroline Terwee
Publikováno v:
Journal of Patient-Reported Outcomes, Vol 7, Iss 1, Pp 1-11 (2023)
Abstract Purpose To translate the eight PROMIS® GastrointestinaI Symptom Scales into Dutch–Flemish and to evaluate their psychometric properties. Methods This study consisted of two parts: (1) translation according to the Functional Assessment of
Externí odkaz:
https://doaj.org/article/fb151be69cae4aef9eb4d342d233e69e
Autor:
Dorinde Korteling, Marco P. Boks, Ania M. Fiksinski, Ilja N. van Hoek, Jacob A. S. Vorstman, Nanda M. Verhoeven-Duif, Judith J. M. Jans, Janneke R. Zinkstok
Publikováno v:
Translational Psychiatry, Vol 12, Iss 1, Pp 1-7 (2022)
Abstract The 22q11.2 deletion syndrome (22q11.2DS) is characterized by a well-defined microdeletion and is associated with increased risk of neurodevelopmental phenotypes including autism spectrum disorders (ASD) and intellectual impairment. The typi
Externí odkaz:
https://doaj.org/article/813bd39245924393afee3b6cedb922b1
Autor:
Dorinde Korteling, Marco P. Boks, Ania M. Fiksinski, Ilja N. van Hoek, Jacob A. S. Vorstman, Nanda M. Verhoeven-Duif, Judith J. M. Jans, Janneke R. Zinkstok
Publikováno v:
Translational Psychiatry, 12, 1
Translational Psychiatry, 12(1):97. Nature Publishing Group
Translational Psychiatry, 12
Translational Psychiatry, 12(1):97. Nature Publishing Group
Translational Psychiatry, 12
Contains fulltext : 252344.pdf (Publisher’s version ) (Open Access) The 22q11.2 deletion syndrome (22q11.2DS) is characterized by a well-defined microdeletion and is associated with increased risk of neurodevelopmental phenotypes including autism s
Autor:
Dorinde Korteling, Janneke Zinkstok, Judith J.M. Jans, Ania Fiksinski, Marco P. Boks, Nanda M. Verhoeven
Publikováno v:
European Neuropsychopharmacology. 51:e130