Page 94 - Characterization of genetic neurodevelopmental disorders at adult age, with a focus on 22q11.2 deletion syndrome - Emma Boersma
P. 94
Chapter 2
sTable 3. continued
Search
date and
study
number
First author Year of
publication Journal Reason for exclusion
55 Haack 2012 Am J Hum Genet Other: No patient data
(apart from genetic
data) is available.
56 Habermeyer 2009 j neuropsych clin n No clear genetic
diagnosis
57 Hama 2017 j neurol sci No clear genetic
diagnosis
58 Hermann 2017 Tremor Other Hyperkinet
parkinsonism unclear
Mov
59 Hernandez
2017 eur j neurol parkinsonism unclear
Navarro
60 Hestnes 1997 j neurol neurosur psy parkinsonism unclear
61 Hjalgrim 2011 epilepsia parkinsonism unclear
62 Humphreys 2016 can j neurol sci parkinsonism unclear
63 Humphreys 2010 can j neurol sci no new data
64 Illsinger 2011 eur j paediatr neuro parkinsonism unclear
65 Jacobsen 1998 j med genet parkinsonism unclear
66 Kaleka 2019 Cureus parkinsonism unclear
67 Kalsner 2013 ann neurol No clear genetic
diagnosis
68 Kara 2013 Movement disord parkinsonism unclear
69 Kim 2018 Int J Neurosci No clear genetic
diagnosis
70 Klysz 2014 neurol neurochir pol parkinsonism unclear
71 Konrad 1973 J of Pediatr parkinsonism unclear
72 Kruer 2009 dev med child neurol No clear genetic
diagnosis
73 Kuiper 2014 movement disord parkinsonism unclear
74 Kuipers 2019 parkinsonism relat d No/unclear
Neurodevelopmental
disorder
75 Larnaout 2008 j inherit metab dis parkinsonism unclear
76 Laxova 1985 am j med genet No clear genetic
diagnosis
77 Lee 2012 movement disord No/unclear
Neurodevelopmental
disorder
78 Leuzzi 2010 Clin Genet parkinsonism unclear
79 Lindsay 1996 Am J Hum Genet No clear genetic
diagnosis
80 Lohmann 2019 eur j hum genet Other: unclear which
participants with
genetic variants had
parkinsonism
81 Lorea 2015 j inherit metab dis parkinsonism unclear
92
