Page 95 - Characterization of genetic neurodevelopmental disorders at adult age, with a focus on 22q11.2 deletion syndrome - Emma Boersma

Parkinsonism in GNDs
sTable 3. continued
Search
date and
study
number
First author Year of
publication Journal Reason for exclusion
82 Masingue 2017 eur j neurol parkinsonism unclear
83 Matsuura 2019 Movement disord Other: no GND
(specifically mentioned)
with parkinsonism.
There may be patients in
the group “other”.
84 Melberg 1996 muscle nerve No clear genetic
diagnosis
85 Mellick 2004 movement disord No clear genetic
diagnosis
86 Morales 2017 Movement disord No new data
87 Morton 1997 dev med child neurol parkinsonism unclear
88 Neri 2012 neuromuscular disord No clear genetic
diagnosis
89 Nissenkorn 2012 J Child Neurol parkinsonism unclear
90 Olszewska 2018 movement disord no new data
91 Ortez 2015 mol genet metab parkinsonism unclear
92 Palumbo 2016 Mol Syndromol parkinsonism unclear
93 Panteghini 2016 Movement disord parkinsonism unclear
94 Papendreou 2017 dev med child neurol Other: unclear
which participant/
genetic disorder had
parkinsonism
95 Park 2014 Movement disord parkinsonism unclear
96 Peer Zada 2015 movement disord No new data
97 Pilotto 2017 Eur J Neurol parkinsonism unclear
98 Pilotto 2017 J Inborn Errors Metab
parkinsonism unclear
Screen
99 Pilotto 2019 Eur J Neurol parkinsonism unclear
100 Porta 2010 mol genet metab no new data
101 Porta 2009 Neurology parkinsonism unclear
102 Raghavan 1993 can j neurol sci parkinsonism unclear
103 Ramerman 2018 rev des disabil No clear genetic
diagnosis
104 Riahi 2016 Eur J Neurol No clear genetic
diagnosis
105 Rodan 2018 mol genet metab parkinsonism unclear
106 Rosini 2014 J Neurol parkinsonism unclear
107 Rubio-Agusti 2011 movement disord parkinsonism unclear
108 Russo 2019 Movement disord parkinsonism unclear
109 Sarpong 2009 clin genet parkinsonism unclear
110 Scheifes 2016 j clin pharmacol No clear genetic
diagnosis
111 Schicks 2011 movement disord parkinsonism unclear
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