Page 80 - Characterization of genetic neurodevelopmental disorders at adult age, with a focus on 22q11.2 deletion syndrome - Emma Boersma

Chapter 2
sTable 1. continued
Study specifications
Search
date study
number
First author Publication
year
Journal Publication
type
Countries of
study
101 Araki102 2020 Epilepsy res Article Japan
102 Namihira103 2004 Psychiat Clin Neuros Letter Japan
103 Garraux104 2012 Arch neurol Article Belgium
104 Daelman105 2014 Rev Neurol Article France
105 Evans106 2004 Movement disord Article U.K.
106 Velema107 2015 JIMD Reports Article The
Netherlands
107 Leuzzi108 1995 J Inher Metab Dis Article Italy
108 Konrad109 1973 J of Pediatr Article U.S.A.
109 Sakaue110 2016 NPJ Parkinson’s dis Article Japan
110 Virmani111 2014 Movement disord Article U.S.A.
110
111 Morales-
Briceno112
2019 Parkinsonism relat d Article Australia
111
111
112 Rotstein113 2012 Movement disord Abstract Israel
113 Sotiriou114 2010 Muscle nerve Article U.S.A.
114 Echaniz-
2019 J inherit metab dis Article France
Laguna115
87 Martikainen88 2016 JAMA neurol Article U.K.
87
87
87
87
115 Bandettini di
Poggio116
2013 BMC med genet Article Italy
116 De Pue117 2016 Eur j neurol Abstract Belgium
117 Khodadadi118 2017 Movement disord Article Iran
117
118 Jaberi119 2016 Movement disord Article Iran
118
119 Kuipers120 2018 Movement disord Article Netherlands
119
119
120 Ortez121 2013 Gene Article Spain
121 Ciammola122 2017 Parkinsonism relat d Article
121
78