Page 76 - 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
52 De Coo53 1999 Ann neurol Article The
Netherlands
53 Sedel54 2006 Neurology Article France
54 Takahashi55 2017 Case rep neurol Article Japan
55 Porta56 2012 Mol genet metab Article Italy
55
56 Straniero57 2017 Ann neurol Article Canada
56
56
57 Anikster58 2017 Am J Hum Genet Article Israel
58 Koroglu59 2013 Parkinsonism relat d Article Turkey
58
58
58
59
59
59
59
59
59 Ng60 2020 Movement disord Article Pakistan
60 Termsarasab 61 2015 Movement disord Abstract U.S.A.
61 Edvardson62 2012 Plos one Article Israel
61
62 Elsayed63 2016 Ann neurol Letter France
63 Tassin64 2000 Brain Article France
63
63
64 Kikuchi65 2004 Movement disord Article Japan
65 Wirth66 2020 Movement disord Article France
65
66 Zielonka67 2015 J inherit metab dis Article Kuwait
67 Bodhireddy68 1994 Neurology Letter U.S.A.
68 Brandel69 1994 Neurology Letter France
69 Agarwal70 2010 Movement disord Abstract U.S.A.
74
