Page 78 - 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
70 Marui71 1999 Neuropathology Article Japan
71 Palat72 2018 Case Rep Neurol Med Article U.S.A.
72 Singer73 1990 Eur j neurol Article U.S.A.
73 Storm74 1990 Res dev disabil Article Germany
74 Sturman75 1989 Lancet Letter U.K.
75 Camargos76 2008 Lancet neurol Article Brazil
75
75
75
76 Keogh77 2014 Neurogenetics Letter U.K.
77 Rezazadeh78 2019 Epilepsy behav Article Canada
78 Yildiz79 2017 Seizure Article Turkey
79 Hall80 2010 Movement disord Article U.S.A.
80 Rosario81 2018 Movement disord Abstract Portugal
81 Chen82 2015 Movement disord Abstract U.S.A.
82 Bach83 2008 Movement Disord Letter Germany
83 Lee84 2019 Acta Neurol Belgica Letter Korea
84 Yu85 2019 Movement disord Abstract China
Fabbri86 86 Owens87 2004 J neurol neurosur ps Letter U.S.A.
87 Martikainen88 2016 JAMA neurol Article U.K.
88 Baumgartner89 2013 J neurol sci Abstract Austria
89 Hemelsoet90 2018 Neurol genet Article Belgium
90 Martikainen91 2013 Mitochondrion Article Finland
91 Zyss92 2011 Movement disord Abstract France
92 Alkufri93 2013 Movement disord Article United
Kingdom
93 Hara94 2013 Brain dev-jpn Article Japan
94 Choi95 2018 Mov disord Article Korea
95 Pradotto96 2014 Clin neuropathol Abstract Italy
96 Wattanapanom97 2011 J am geriatr soc Abstract U.S.A.
97 D’Ambrosio98 1984 Acta neurol Napoli Article Israel
98 Hattori99 1998 Pathol res prac Article Japan
99 Chandra100 2018 Movement Disord Abstract U.S.A.
100 Pescosolido101 2019 Mol Neuropsychiatry Article U.S.A.
100
85 2018 Neurol sci Letter Portugal
76
