Kouis, Panayiotis
,
Goutaki, Myrofora
Halbeisen, Florian S.
Gioti, Ifigeneia
Middleton, Nicos
Amirav, Israel
Barbato, Angelo
Behan, Laura
Boon, Mieke
Emiralioglu, Nagehan
Haarman, Eric G.
Karadag, Bulent
Koerner-Rettberg, Cordula
Lazor, Romain
Loebinger, Michael R.
Maitre, Bernard
Mazurek, Henryk
Morgan, Lucy
Nielsen, Kim Gjerum
Omran, Heymut
Özçelik, Ugur
Price, Mareike
Pogorzelski, Andrzej
Snijders, Deborah
Thouvenin, Guillaume
Werner, Claudius
Zivkovic, Zorica
Kuehni, Claudia E.
Yiallouros, Panayiotis K.
,
,
,
,
,
Funding for this research was provided by:
FP7 Health (305404)
Swiss National Science Foundation (SNF 320030_173044)
Ministry of Science Republic of Serbia (III 41004)
Article History
Received: 25 March 2019
Accepted: 10 September 2019
First Online: 18 September 2019
Ethics approval and consent to participate
: Local Primary Investigators (PIs) received ethics approval and informed consent for collecting patient data for local research use or national registries. In countries where informed consent is required even for anonymised observational data, PIs are responsible for obtaining ethics approval and informed consent in their country for the contribution of their anonymised data to the iPCD Cohort for research purposes. The iPCD cohort database is maintained at University of Bern (Approval Number: 060/15, Kantonale Ethikkommission für die Forschung Bern).
: Not applicable.
: DS and MB report grants from Italian Health Ministry and Horizon 2020 respectively, outside the submitted work. All other authors wish to declare that they have no competing interests.