Page 74 - 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
28 Machado29 2017 Neurology Abstract unknown
29 Ohi30 2017 J of Neur Sci Abstract Japan
30 Fonderico31 2017 Front Neurol Article Italy
31 Ichinose32 2014 Neurol Clin Pract Article Japan
32 Verhoeven33 2014 Parkinsonism Related
Article The
D
Netherlands
32
33 Zhang34 2019 Neurology Abstract U.S.A.
34 Zitser35 2018 Movement disorders Article Israel
35 Endo36 2017 Neurol Clin Neurosci Article Japan
36 Dotti37 2000 Movement disord Article Italy
37 Fujiyama38 1991 Jpn J Med Article Japan
38 Grandas39 2002 Movement disord Letter Spain
39 Kuwabara40 1996 j neurol sci Article Japan
40 Li41 2020 Movement disord Letter China
41 Mignarri42 2012 Parkinsonism Relat D Letter Italy
42 Pilo de la
2008 J Neurol Article Spain
Fuente43
43 Schotsmans44 2012 Acta Neurol Belg Article Belgian
44 Su45 2010 Movement disord Article Taiwan
44
45 Wakamatsu46 1999 J Neurol Neurosurg
Article Japan
Ps
45
45
47
48
46 Yunisova47 2020 Neurodegener Dis Article Turkey
47 Zadori48 2017 Neurol Sci Article Hungary
48 Rubio Agusti49 2012 Movement disorders Abstract U.K.
49 Manti50 2019 Parkinsonism relat d Article Italy
50 Fernandez51 2000 Movement disord Other U.S.A.
51 Rana52 2018 J am geriatr soc Abstract U.S.A.
72
