Subject has given written informed consent
Patient must have given written informed consent
Written informed consent
Able to give a written informed consent.
Written informed consent
Written informed consent
Written informed consent has been obtained
Has read and understands the informed consent form and has given written informed consent prior to any study procedures
Written informed consent prior to any procedure.
Provides written informed consent on the approved informed consent form
Able to give written informed consent.
Subjects given written informed consent
Written informed consent must be obtained from the patient.
Written informed consent.
Written informed consent.
Written informed consent
PRE-SCREENING: Written informed consent for prescreening
FULL STUDY INCLUSION CRITERIA: Written informed consent for full study
Written informed consent
Written informed consent for transplant
Written informed consent is given
Patient has given written informed consent.
Written informed consent
DONOR: Written informed consent
Age ? 18 years with the capacity to give written informed consent
Subjects must give written informed consent to participate in this trial
Written informed consent obtained
Written informed consent is given
Subjects given written informed consent
Subjects given written informed consent
Written informed consent for the trial
Written informed consent prior to admission to this study
Patients must give written informed consent prior to registration on the study
Written informed consent
Written informed consent
Subjects who are ?18 years of age on the date of written informed consent.
Able to give written informed consent to participate in the study
Has read and understands the informed consent form and has given written informed consent prior to any study procedures.
Written informed consent
Patient’s written informed consent
Able to give informed written consent
Written informed consent
Written informed consent
Written Informed Consent
Able to give a written informed consent.
Written informed consent for the transplant phase
Written informed consent
Patient must give written informed consent
Written informed consent is given
Obtained written informed consent
Written informed consent must be obtained before any assessment is performed.
Written informed consent to participate in this study
Patient must give written informed consent
Written informed consent prior to any procedure
Subjects must give written informed consent to participate in this trial
Written informed consent must be obtained
Written informed consent
Written informed consent
Written informed consent.
Written informed consent must be obtained from all patients before entry into the study
Written informed consent
Written informed consent has been obtained
Written informed consent
Written informed consent
Written informed consent prior to registration on study
Has given written Informed Consent
Patients must give written informed consent
Written informed consent
Written informed consent and assent as is age appropriate
Written informed consent
Written Informed Consent
Written informed consent
Written informed consent or assent
Has given written informed consent.
Written informed consent
Subjects must give written informed consent to participate in this trial
Able to give informed written consent
Written informed consent;
patient had given written informed consent.
Written informed consent obtained before undergoing any study-related activities
Has the subject given written informed consent?
Written informed consent has been obtained
Patients who give a written informed consent
Written informed consent.
Capable of given written informed consent, which includes compliance with the requirements and restrictions listed in the consent form.
Patients must give written informed consent
Subjects must have given written informed consent to agree to participate
Subjects must have given written informed consent
Written informed consent and any locally required authorization
Subjects given written informed consent.
Written, informed consent
Written informed consent.
Documented written informed consent of the participant
Able to give written informed consent
HSCT CGs: Able to give written informed consent
Written, informed consent
Written informed consent
Must give written study consent
Any patient with cholestasis due to suspected MHO who provides written informed consent.
Properly obtained written informed consent
Gives written informed consent
Gives written informed consent
All patients to give written informed consent to participate
Written informed consent
Adequately informed of the nature and risks of the study with written informed consent
Give written informed consent
Properly obtained written informed consent
Able to perform written, informed consent
Written consent
Written informed consent
Given written informed consent (patient and donor)
Written informed consent obtained from the subject.
Written informed consent obtained from the subject
Patient provides written informed consent
Written informed consent
Give written informed consent
Patient provides written informed consent
Patient provides written informed consent
Patients must give written informed consent
Able to give written informed consent to participate in the study
Provides written informed consent
Provides written informed consent document
Patients who have granted written informed consent for the study
Written informed consent will be obtained from patients
Provides written informed consent
Written informed consent
Provides written informed consent
Written informed consent
Written informed consent
Provides written informed consent
Provides written informed consent
Written informed consent
All patients must give written informed consent
Written informed consent.
Provides written informed consent