Are willing and able to provide signed informed consent.
Willing and able to provide informed consent.
Must be able and willing to participate in all aspects of the study and provide informed consent prior to study participation.
Willing and able to provide informed consent
Able to provide informed consent and be willing to participate in study schedule and events.
Willing and able to provide informed consent
Willing and able to provide informed consent
Willing and able to provide consent
Willing and able to provide consent
Patient able and willing to provide informed consent.
Willing and able to provide informed consent
All patients must be willing and capable to provide informed consent to participate in the protocol
All patients must be willing and capable to provide informed consent to participate in the protocol
Able and willing to provide informed consent
All patients must be willing and capable to provide informed consent to participate in the protocol
Able and willing to provide consent for required bone marrow biopsies.
Willing and able to provide informed consent
DONOR: Willing and able to provide informed consent
All patients must be willing and capable to provide informed consent to participate in the protocol
Willing and able to provide informed consent
COHORT A: The subject must be willing and able to provide informed consent
COHORT B: The subject must be willing and able to provide informed consent
Able to provide informed consent and be willing to sign an informed consent form
Willing and able to provide informed consent
All patients must be willing and capable to provide informed consent to participate in the protocol
Patients must be willing and able to provide signed informed consent and comply with the study protocol.
Patient or guardian willing and able to provide informed consent.
Willing and able to provide informed consent
At least  years of age and willing and able to provide informed consent.
Willing and able to provide informed consent
Willing and able to provide informed consent;
Willing and able to provide informed consent
Age  years or older and willing and able to provide informed consent;
PROVIDER ELIGIBILITY: The participant is willing to provide informed consent in English
Able and willing to provide informed consent
Willing and able to provide informed consent
Willing and able to provide informed consent
Not willing and able to provide informed consent
Capable and willing to provide Informed consent
Willing and able to provide informed consent
Not willing and able to provide informed consent
Willing and able to provide signed, informed consent
Able and willing to provide consent (both)
PATIENT: Be able and willing to provide informed consent
Able and willing to provide informed consent
Willing and able to provide, signed informed consent
The subject must be willing and able to provide informed consent
Cognitively able and willing to provide consent
Subjects willing and able to provide consent to participating in the study
Able to understand and willing to provide informed consent for the RPFNAs and study participation
Patients who are willing and capable to provide informed consent
Capable and willing to provide informed consent
The patient is willing and able to provide informed consent.
Patients must be capable and willing to provide informed consent
Patients must be capable and willing to provide informed consent.
Patient able and willing to provide informed consent
HCC PATIENTS: Patient is willing to provide informed consent
The patient must be willing and able to provide informed consent
Willing and able to provide informed consent
Be willing and able to provide informed consent
NORMAL VOLUNTEERS: Be willing and able to provide informed consent
Participants must be willing to participate and provide signed informed consent
Willing and able to provide informed consent and fill out demographic, disease, and pain assessment questionnaires