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With informed consent acquired from patients, collection of fasted blood samples was carried out followed by separation of plasma, which was kept frozen at − 70 °C.
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A written informed consent was acquired from all patients who participated in our study.
Blood samples were taken and demographic and clinical data were recorded from all patients enrolled in the study after written informed consent was acquired from patients or their next of kin.
Written consent was acquired from each participant prior to the experimental session.
Written consent was acquired from each participant prior to the experimental sessions.
Written informed consent was acquired from every participant prior to participation.
Written informed consent was acquired from all subjects participating in this study, according to the declaration of Helsinki.
Written informed consent was acquired prior to surgery from every patient for further studies on primary glioma cultures.
Ethical approval for this study was given by the respective institutional ethical committees (IEC, DMCH and IEC, UDSC) and informed written consent was acquired from the participants.
This study was approved by the Ethics Committee of the Vall d'Hebron Hospital and informed and written consent was acquired from all patients or relatives and from controls.
The following protocols conformed to the tenets of the Declaration of Helsinki and were approved by the institutional review board of the Singapore Eye Research Institute, and the written informed consent was acquired from all participating patients.
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