Page 72 - Characterization of genetic neurodevelopmental disorders at adult age, with a focus on 22q11.2 deletion syndrome - Emma Boersma

Chapter 2
sTable 1. List of included reports describing data on an individual level
Study specifications
Search
date study
number
First author Publication
year
Journal Publication
type
Countries of
study
May 31, 2020
1 Lipton2 2009 Neurology Letter U.S.A.
2 Roeben3 2019 Journal of Neurology Letter Germany
3 Baudoin4 2010 Movement disord Abstract France
4 Booij5 2010 Am J Med Genet
Part A
Article The
Netherlands
5 Boot6 2015 Am J Med Genet
Part A
Article Canada, The
Netherlands
5
6 Gambardella7 2018 Parkinsons Dis Article Italy
7 Hu8 2019 Clin Parkinsonism
Article China
Relat Disord
8 Krahn9 1998 Mayo Clin Proc Article U.S.A.
9 Mills10 2016 Ann Neurol Abstract U.S.A.
10 Moreira11 2018 Movement disord Abstract Portugal
11 Oki12 2016 Intern Med Article Japan
12 Pollard13 2016 Parkinsonism Relat D Article U.S.A.
13 Rehman14 2015 Movement disord Article U.S.A.
14 Verhoeven15 2017 Eur Arch Psychiatry
Clin Neurosci
Article The
Netherlands
14
15 Zaleski16 2009 Am J Med Genet
Part A
Article U.S.A.,
Canada
15
16 2016 Movement disord Article Foo17 17 Clayton18 1986 J neurol neurosur psy Article U.K.
18 Fan19 2020 Movement disord Article Taiwan
19 Park20 2020 BMC Neurology Article Korea
20 Sechi21 2008 Prog Neuro-Psychoph Letter Italy
21 Vázquez-Justes22 2020 Clin neurol neurosur Article Spain
22 Yoshida23 2011 Acta Neurol Scand Article Japan
22
23
24 Woodward25 2017 Movement disord Abstract U.S.A.
25 Akçakaya26 2019 Neuromol Med Article Turkey
26 Hornemann27 2020 Neuropediatrics Article Germany
27 Kumada28 2015 movement disord Abstract Japan
Singapore
23 Harbord24 2001 J clin neurosci Article Australia
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