Page 82 - Characterization of genetic neurodevelopmental disorders at adult age, with a focus on 22q11.2 deletion syndrome - Emma Boersma
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Chapter 2
sTable 1. continued
Study specifications
Search
date study
number
First author Publication
year
Journal Publication
type
Countries of
study
121
122 Guldner123 2016 Parkinsonism relat d Letter Germany
123 Lesage124 2015 Neurol genet Article France
124 Wilson125 2014 Am j human genet Article Australia
124
125 Roze126 2007 Movement disord Other France
126 Chahil127 2018 Cureus Article U.S.A.
127 Venkateswaran128 2014 Dev med child neurol Article Canada
128 Pollini129 2020 Movement disord Letter Italy
129 Ollivier130 2015 Neuromuscular
Disord
Article France
130 Goizet131 2009 Hum mutat Other France
130
131 Anheim132 2009 J neurol Article France
131
132 Guidubaldi133 2011 Movement disord Article Italy
133 Kang134 2004 Parkinsonism relat d Article South Korea
134 Damasio135 2014 Movement disord Abstract Portugal
135 Mallaret136 2014 j neurol Letter France
136 Schicks137 2011 Movement disord Letter Germany
136
137 Groth138 2018 Tremor Other
Article U.S.A.
Hyperkinet Mov
2018 Movement disord Article U.S.A.
138 Ebrahimi-
Fakhari139
139 Nitschke140 2011 Schweitz arch neurol Abstract Switzerland
140 Westenberger141 2013 Movement disord Article Germany
141 De Rijk-van
2000 Neurology Article The
Andel142
Netherlands
141
141
141
142 Pons143 2010 Movement disord Other Greece
142
142
143 Grattan-Smith144 2002 Movement disord Article Australia
144 Haugarvoll145 2011 J parkinson dis Article Norway
145 Ludecke146 1996 Hum mol genet Article Norway
80
