Page 84 - Characterization of genetic neurodevelopmental disorders at adult age, with a focus on 22q11.2 deletion syndrome - Emma Boersma
P. 84
Chapter 2
sTable 1. continued
Study specifications
Search
date study
number
First author Publication
year
Journal Publication
type
Countries of
study
146 Swaans147 2000 Ann hum genet Article The
Netherlands,
France
146
146
147 Burke148 2018 Clin genet Article U.S.A.
148 Galosi149 2019 Movement disord Abstract Italy
149 Horn150 2016 Clin case rep Article Norway
150 Serra Soler151 2017 Endocrinol diabetes
Letter Spain
nutr
151 Gupta152 2015 Parkinsonism Relat D Letter U.S.A.
151
June 15, 2021
152 Meytin153 2020 Movement disord Abstract U.S.A.
153 Buongarzone154 2020 Movement disord Abstract Italy
153
153
154 Maric155 2020 Eur j med genet Abstract Spain
155 Umehara156 2020 Neurol clin neuroschi Article Japan
156 Samanta157 2020 J pedriatr neurosci Article U.S.A.
157 Yunisova47 2020 Neurodegener dis Article Turkey
158 Munoz-
2020 Movement disord Abstract Spain
delgado158
159 Zadori159 2020 Front neurol Article Hungary
160 Jesus160 2021 Neurol genet Article Spain
Sleiman161 161 2009 Neurosci lett Article U.K.
162 Grimes162 2006 Movement dis Article Canada
163 Kanatani163 2021 Brain dev-jpn Article Japan
163
164 Malaquias164 2021 Parkinsonism Relat D Article Portugal
165 Witt165 2020 Movement disord Abstract Sweden
166 Kim166 2020 Ann neurol Article U.S.A.
166
82
