Page 96 - Characterization of genetic neurodevelopmental disorders at adult age, with a focus on 22q11.2 deletion syndrome - Emma Boersma
P. 96
Chapter 2
First author sTable 3. continued
Search
date and
study
number
Year of
publication Journal Reason for exclusion
112 Schicks 2010 movement disord no new data
113 Sheehan 2017 bmj brit med j No clear genetic
diagnosis
114 shi 2016 movement disorders parkinsonism unclear
115 Singh 1986 brit j psychiat parkinsonism unclear
116 Soto 2017 J Inborn Errors Metab
parkinsonism unclear
Screen
117 Stagnaro 2018 eur j paediatr neuro parkinsonism unclear
118 Stelten 2018 Neurology parkinsonism unclear
119 Straniero 2019 eur j hum genet no new data
120 Surtees 1998 movement disord no new data
121 Tan 2016 Lancet Neurol Not relevant
122 Tanaka 1989 Eur J Pediatr parkinsonism unclear
123 Temudo 2008 movement disord parkinsonism unclear
124 Troncoso 2015 j neurol sci No clear genetic
diagnosis
125 Tufekcioglu 2016 Neurocase parkinsonism unclear
126 Valadares 2011 arq neuro-psiquiat parkinsonism unclear
127 Vellingiri 2018 Parkinsonism Relat Disord Other: Aim, methods,
and results all unclear
128 Verhoeven 2015 Eur Arch Psychiatry Clin
no new data
Neurosci
129 Wang 2017 Stem cel res not relevant
130 Waschbisch 2010 j neurol sci parkinsonism unclear
131 Weinshenker 2008 nature not relevant
132 Wille 2018 neuropediatrics parkinsonism unclear
133 Wise 2012 dev med child neurol no new data
134 Yemni 2019 nature No/unclear
Neurodevelopmental
disorder
135 Yoon 2008 J Neurol Neurosurg Ps parkinsonism unclear
136 Zouari 2018 movement disord Other: unclear which
participants had a GND
with parkinsonism
137 Zweije-Hofman 1982 clin neurol neurosur parkinsonism unclear
June 15,
2021
138 Agabna 2021 dev med child neurol parkinsonism unclear
139 De Jesus 2020 movement disord parkinsonism unclear
140 Di lazarro 2020 parkinsonism relat d Parkinsonism unclear
141 Eis 2020 front neurol No/unclear
Neurodevelopmental
disorder
142 Jan 2021 nature Parkinsonism unclear
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