Page 92 - Characterization of genetic neurodevelopmental disorders at adult age, with a focus on 22q11.2 deletion syndrome - Emma Boersma

Chapter 2
sTable 3. Studies excluded from data-extraction
Search
date and
study
number
First author Year of
publication Journal Reason for exclusion
May 31,
2020
1 Aggarwal 2010 Movement disord parkinsonism unclear
2 Air 2011 J neurosurg pediat No clear genetic
diagnosis
3 Al-Thihli 2010 j inherit metab dis parkinsonism unclear
4 Aljaafari 2017 Neurology parkinsonism unclear
5 Alvarez 2018 European J of Epilepsy parkinsonism unclear
6 Baide-Mairena 2018 Movement disord No clear genetic
diagnosis
7 Banka S. et al 2011 am j hum genet parkinsonism unclear
8 Banuelos 2017 F1000res parkinsonism unclear
9 Barnes 2011 ann neurol parkinsonism unclear
10 Barnes 2011 ann neurol parkinsonism unclear
11 Behnecke 2018 med genet parkinsonism unclear
12 Belezhanska 2017 Arch Balkan Med Union parkinsonism unclear
13 Bijarnia-Mahay 2018 j inherit metab dis parkinsonism unclear
14 Blau 2015 mol genet metab no new data
15 Bodzioch 2011 Movement disord parkinsonism unclear
16 Bouchereau 2018 mol genet metab no new data
17 Brahem 2017 Movement disord Other: not clear
which patient had
parkinsonism (with or
without GND)
18 Brahm 2007 Clinical Schizophrenia and
No clear genetic
Related Psychoses
diagnosis
19 Brajkovic 2010 Eur J Nucl Med Mol I No clear genetic
diagnosis
20 Brajkovic 2012 Hell J nucl med No clear genetic
diagnosis
21 Brautigam 1999 cin chem parkinsonism unclear
22 Buckley 2017 NeuroReport parkinsonism unclear
23 Burt 1980 Eur Neurol Other: unclear of
the patient with
Down syndrome had
parkinsonism, also for
other GNDs outcome
measures are on group
level
24 Butcher 2016 Biol Psychiat no new data
25 Butcher 2014 Mov Disord no new data
26 Butcher 2015 Mov Disord no new data
27 Butcher 2017 PLOS ONE no new data
28 Byrne 2015 neuromuscular disord parkinsonism unclear
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