Provide informed written consentXx_NEWLINE_xXVoluntary agreement to provide written informed consent and the willingness and ability to comply with all aspects of the protocolXx_NEWLINE_xXWillingness and ability to provide written informed consent and to comply with the study protocol as judged by the investigatorXx_NEWLINE_xXProvide written informed consentXx_NEWLINE_xXAbility to understand and the willingness to provide written informed consent to participateXx_NEWLINE_xXInability to provide informed consentXx_NEWLINE_xXProvide informed written consentXx_NEWLINE_xXPatients or their legally authorized representative must provide written informed consentXx_NEWLINE_xXAbility to provide written informed consent which must be obtained prior to any screening procedures and according to local guidelinesXx_NEWLINE_xXProvide written informed consentXx_NEWLINE_xXVoluntary agreement to provide written informed consent and the willingness and ability to comply with all aspects of the protocolXx_NEWLINE_xXProvide written informed consent (Subject or legal representative)Xx_NEWLINE_xXWillingness and ability to provide written informed consent prior to any study?related procedures and to comply with all study requirements.Xx_NEWLINE_xXSubjects must provide written informed consent to participateXx_NEWLINE_xXWillingness and ability to provide written informed consent prior to any study-related procedures and to comply with all study requirementsXx_NEWLINE_xXProvide signed, written informed consent.Xx_NEWLINE_xXAbility to provide written informed consentXx_NEWLINE_xXSubject or legal representative has ability to read, understand and provide written informed consent for study related proceduresXx_NEWLINE_xXMust provide written informed consent.Xx_NEWLINE_xXProvide written informed consentXx_NEWLINE_xXProvide written informed consentXx_NEWLINE_xXWillingness to provide informed written consentXx_NEWLINE_xXPatients who can provide informed consentXx_NEWLINE_xXPatients must provide written consentXx_NEWLINE_xXWillingness and ability to provide written informed consent prior to any study-related procedures and to comply with all study requirementsXx_NEWLINE_xXPatients unable to provide informed consentXx_NEWLINE_xXParticipant must voluntarily agree to provide written informed consentXx_NEWLINE_xXAbility to provide and understand written informed consent prior to any study proceduresXx_NEWLINE_xXProvide written informed consentXx_NEWLINE_xXProvide informed written consentXx_NEWLINE_xXProvide written informed consent obtained prior to the initiation of study proceduresXx_NEWLINE_xXProvide informed consentXx_NEWLINE_xXProvide informed written consentXx_NEWLINE_xXPatient refuses or is unable to provide written informed consentXx_NEWLINE_xXWillingness and ability to provide written informed consent and to comply with the study protocol as judged by the investigatorXx_NEWLINE_xXProvide informed written consentXx_NEWLINE_xXProvide informed written consentXx_NEWLINE_xXAbility to provide written informed consentXx_NEWLINE_xXAbility to provide written informed consentXx_NEWLINE_xXPatients must provide written informed consent prior to any study proceduresXx_NEWLINE_xXProvide informed written consentXx_NEWLINE_xXProvide informed written consentXx_NEWLINE_xXProvide informed written consentXx_NEWLINE_xXAbility to provide written informed consent obtained prior to participation in the study and any related procedures being performedXx_NEWLINE_xXAbility to provide written informed consent.Xx_NEWLINE_xXAbility to provide written informed consent obtained prior to participation in the study and any related procedures being performedXx_NEWLINE_xXPatients must provide written informed consent.Xx_NEWLINE_xXProvide signed written informed consentXx_NEWLINE_xXAbility to understand and willing to provide informed consentXx_NEWLINE_xXAbility to provide written informed consent for the protocolXx_NEWLINE_xXAbility to understand and willingness to provide informed consentXx_NEWLINE_xXAbility to understand and willingness to provide informed consent.Xx_NEWLINE_xXPsychiatric illness/social situation that would limit ability to provide informed consentXx_NEWLINE_xXProvide written informed consent for the follow up protocol.Xx_NEWLINE_xXRefusal to provide written informed consentXx_NEWLINE_xXPatients must provide informed consentXx_NEWLINE_xXProvide written informed consentXx_NEWLINE_xXProvide written informed consentXx_NEWLINE_xXWillingness and ability to provide written informed consent prior to any study-related procedures and to comply with all study requirementsXx_NEWLINE_xXProvide written informed consentXx_NEWLINE_xXProvide written informed consentXx_NEWLINE_xXProvide informed written consentXx_NEWLINE_xXProvide written informed consentXx_NEWLINE_xXProvide informed written consentXx_NEWLINE_xXPatients (female or male) must provide informed written consent and must complete all screening assessments as outlined in the protocolXx_NEWLINE_xXVoluntary agreement to provide written informed consent and the willingness and ability to comply with all aspects of the protocolXx_NEWLINE_xXThe patient or legal guardian must provide written informed consentXx_NEWLINE_xXWilling to provide informed written consentXx_NEWLINE_xXProvide written informed consentXx_NEWLINE_xXAbility to provide written informed consent obtained prior to participation in the study and any related procedures being performedXx_NEWLINE_xXAbility to understand and provide informed consentXx_NEWLINE_xXProvide informed written consentXx_NEWLINE_xXProvide informed written consentXx_NEWLINE_xXAbility to provide informed consent and adhere to the required follow-upXx_NEWLINE_xXPatients or their legally authorized representative must provide written informed consentXx_NEWLINE_xXAbility to provide written informed consentXx_NEWLINE_xXAbility to understand and provide informed consentXx_NEWLINE_xXProvide written, informed consent to participate in the study and follow the study proceduresXx_NEWLINE_xXProvide written informed consentXx_NEWLINE_xXAbility to understand and the willingness to provide informed consentXx_NEWLINE_xXCompetent to provide informed consentXx_NEWLINE_xXProvide written informed consentXx_NEWLINE_xXAbility to provide informed consentXx_NEWLINE_xXProvide informed written consentXx_NEWLINE_xXAdults who are unable to provide informed consent will NOT be enrolled on this studyXx_NEWLINE_xXAbility to provide written informed consentXx_NEWLINE_xXProvide informed written consentXx_NEWLINE_xXProvide informed written consentXx_NEWLINE_xXProvide written informed consentXx_NEWLINE_xXPatient or patient’s legal representative must provide written informed consentXx_NEWLINE_xXPatients must provide written informed consentXx_NEWLINE_xXProvide written informed consentXx_NEWLINE_xXPatients must provide written informed consent.Xx_NEWLINE_xXAbility to provide written informed consentXx_NEWLINE_xXPatients or their legally authorized representative must provide written informed consentXx_NEWLINE_xXAbility to provide informed consentXx_NEWLINE_xXPatients or their legally authorized representative must provide written informed consentXx_NEWLINE_xXProvide signed written informed consentXx_NEWLINE_xXPatients or their legally authorized representative must have the ability to understand and provide signed informed written consentXx_NEWLINE_xXProvide written informed consent (or legal representative)Xx_NEWLINE_xXAbility to provide written informed consent obtained prior to participation in the study and any related procedures being performedXx_NEWLINE_xXAbility to provide informed consent.Xx_NEWLINE_xXPatients must provide written informed consent prior to any screening proceduresXx_NEWLINE_xXAbility to understand and provide informed consentXx_NEWLINE_xXAbility to understand and provide informed consentXx_NEWLINE_xXINCLUSION CRITERIA FOR TNBC: Ability to understand and provide informed consentXx_NEWLINE_xXThe patient must provide informed consent.Xx_NEWLINE_xXProvide informed written consentXx_NEWLINE_xXProvide informed written consentXx_NEWLINE_xXProvide written, informed consent to participate in the study and follow the study proceduresXx_NEWLINE_xXPatients must provide informed written consentXx_NEWLINE_xXAbility to provide written informed consentXx_NEWLINE_xXWillingness and ability to provide written informed consent and to comply with the study protocol as judged by the investigatorXx_NEWLINE_xXPatients or their legally authorized representative must provide written informed consentXx_NEWLINE_xXPatients unable to provide informed consent.Xx_NEWLINE_xXUnable to provide written informed consentXx_NEWLINE_xXPatients or their legally authorized representative must provide written informed consentXx_NEWLINE_xXAbility to provide written informed consent.Xx_NEWLINE_xXPatients must provide written informed consentXx_NEWLINE_xXPatients or their legally authorized representative must provide written informed consentXx_NEWLINE_xXInability to provide informed consentXx_NEWLINE_xXProvide informed written consentXx_NEWLINE_xXWillingness to provide informed consent to undergo pre- and post-dose biopsyXx_NEWLINE_xXPatient or legal guardian must provide written informed consentXx_NEWLINE_xXAbility to provide written informed consent obtained prior to participation in the study and any related procedures being performedXx_NEWLINE_xXAbility to provide written informed consentXx_NEWLINE_xXPatient must have the ability to understand the requirements of the study and provide informed consent.Xx_NEWLINE_xXPatients must provide informed written consentXx_NEWLINE_xXAbility to provide written informed consentXx_NEWLINE_xXPatients or their legally authorized representative must provide written informed consentXx_NEWLINE_xXPatients or their legally authorized representative must provide written informed consentXx_NEWLINE_xXPatients must provide written informed consentXx_NEWLINE_xXAbility to provide informed consent for participationXx_NEWLINE_xXProvide informed written consentXx_NEWLINE_xXPatients must provide written informed consentXx_NEWLINE_xXAll patients must be willing and capable to provide informed consent to participate in the protocolXx_NEWLINE_xXProvide written informed consent for the trialXx_NEWLINE_xXPatients or their legally authorized representative must provide written informed consentXx_NEWLINE_xXProvide informed consent and agree to all assessments and study proceduresXx_NEWLINE_xXAbility to provide written informed consent obtained prior to participation in the study and any related procedures being performedXx_NEWLINE_xXProvide informed written consentXx_NEWLINE_xXMust provide written informed consentXx_NEWLINE_xXAbility to understand and the willingness to provide written informed consentXx_NEWLINE_xXProvide signed written informed consentXx_NEWLINE_xXAbility to provide written, informed consentXx_NEWLINE_xXParticipant must provide informed consentXx_NEWLINE_xXPatients must provide written informed consentXx_NEWLINE_xXProvide informed written consentXx_NEWLINE_xXPatients or their legal representatives must have the ability to read, understand and provide written informed consent for the initiation of any study related procedures.Xx_NEWLINE_xXFor Phase I and II: Patients must provide written informed consent.Xx_NEWLINE_xXAbility to provide written informed consent obtained prior to participation in the study and any related procedures being performedXx_NEWLINE_xXProvide signed written informed consentXx_NEWLINE_xXAbility to understand and provide informed consentXx_NEWLINE_xXPatient must have ability to understand and willingness to provide written informed consent prior to participation in the study and any related procedures being performedXx_NEWLINE_xXAbility to provide informed consentXx_NEWLINE_xXSubjects who provide written informed consent to participate in the studyXx_NEWLINE_xXCOHORTS 1 AND 2: HEALTHY VOLUNTEERS: Ability of subject to understand and provide written informed consentXx_NEWLINE_xXWillingness to provide written informed consent for the study.Xx_NEWLINE_xXProvide written informed consent prior to any study related procedure.Xx_NEWLINE_xXProvide informed written consentXx_NEWLINE_xXProvide written informed consent to participate on the studyXx_NEWLINE_xXAbility to provide written informed consentXx_NEWLINE_xXAll patients must be willing and capable to provide informed consent to participate in the protocolXx_NEWLINE_xXPatients must provide written consentXx_NEWLINE_xXInability to provide informed consent.Xx_NEWLINE_xXAbility of patient to provide informed consentXx_NEWLINE_xXProvide written informed consentXx_NEWLINE_xXProvide written informed consentXx_NEWLINE_xXProvide written informed consentXx_NEWLINE_xXParticipant unwilling to provide written informed consentXx_NEWLINE_xXUnable to provide informed consent or, in the opinion of the Principal Investigator, comply with the protocol.Xx_NEWLINE_xXAbility to provide informed consent.Xx_NEWLINE_xXAbility to understand the requirements of the study, provide written informed consent.Xx_NEWLINE_xXAbility to provide written informed consentXx_NEWLINE_xXPatients must provide written informed consent.Xx_NEWLINE_xXProvide written informed consentXx_NEWLINE_xXAbility to provide written informed consentXx_NEWLINE_xXAbility to provide written informed consent and to understand and comply with the requirements of the studyXx_NEWLINE_xXCan provide informed consentXx_NEWLINE_xXProvide written informed consentXx_NEWLINE_xXProvide written informed consentXx_NEWLINE_xXAbility to understand and willingness to provide informed consent.Xx_NEWLINE_xXProvide informed written consentXx_NEWLINE_xXAbility to provide written informed consentXx_NEWLINE_xXProvide informed written consentXx_NEWLINE_xXInability to understand or provide informed consentXx_NEWLINE_xXProvide informed written consentXx_NEWLINE_xXARM A: Ability to provide informed written consentXx_NEWLINE_xXARM B: Ability to provide informed written consentXx_NEWLINE_xXAbility to provide informed consentXx_NEWLINE_xXAbility to provide informed consentXx_NEWLINE_xXPatients must provide informed written consentXx_NEWLINE_xXProvide written informed consentXx_NEWLINE_xXAbility to provide written informed consentXx_NEWLINE_xXAbility to provide informed consentXx_NEWLINE_xXInability to provide informed consentXx_NEWLINE_xXAbility and willingness to provide informed consent to participate in this studyXx_NEWLINE_xXProvide informed written consentXx_NEWLINE_xXAbility to provide informed consentXx_NEWLINE_xXAbility to provide informed consentXx_NEWLINE_xXWillingness to provide informed consentXx_NEWLINE_xXProvide written informed consentXx_NEWLINE_xXProvide written informed consentXx_NEWLINE_xXPatients must provide written informed consent prior to any screening proceduresXx_NEWLINE_xXAbility to provide written informed consent obtained prior to participation in the study and any related procedures being performedXx_NEWLINE_xXAbility to provide written informed consent obtained prior to participation in the study and any related procedures being performedXx_NEWLINE_xXAbility to provide informed consentXx_NEWLINE_xXPatients must provide verbal and written informed consent to participate in the studyXx_NEWLINE_xXAbility to provide written informed consentXx_NEWLINE_xXPatients must provide written informed consent.Xx_NEWLINE_xXProvide written, informed consent to participate in the study and follow the study proceduresXx_NEWLINE_xXAll patients must be willing and capable to provide informed consent to participate in the protocolXx_NEWLINE_xXWillingness to provide written informed consent for the study.Xx_NEWLINE_xXWillingness and ability to provide written informed consent and to comply with the study protocol as judged by the investigatorXx_NEWLINE_xXVoluntary agreement to provide written informed consent and the willingness and ability to comply with all aspects of the protocol.Xx_NEWLINE_xXWilling to provide written informed consentXx_NEWLINE_xXProvide informed written consentXx_NEWLINE_xXAbility to provide informed written consentXx_NEWLINE_xXPatients must provide written informed consent prior to any screening proceduresXx_NEWLINE_xXParticipant must voluntarily agree to provide written informed consent.Xx_NEWLINE_xXPatients must provide written informed consentXx_NEWLINE_xXPatients must provide written informed consentXx_NEWLINE_xXAbility to understand and the willingness to provide written informed consentXx_NEWLINE_xXAbility to understand and the willingness to provide informed consentXx_NEWLINE_xXProvide written informed consentXx_NEWLINE_xXAbility to understand and provide written informed consentXx_NEWLINE_xXProvide written informed consentXx_NEWLINE_xXSubject or Authorized Representative is unable to provide informed consent.Xx_NEWLINE_xXAbility to provide informed consentXx_NEWLINE_xXAbility to provide written informed consent obtained prior to participation in the study and any related procedures being performedXx_NEWLINE_xXAbility to provide written informed consent prior to participation in the study and any related procedures being performedXx_NEWLINE_xXAbility to provide informed consentXx_NEWLINE_xXAbility and willingness to provide written informed consent, and to comply with the requirements of the protocolXx_NEWLINE_xXProvide written, informed consent to participate in the study and follow the study proceduresXx_NEWLINE_xXAbility to provide and understand written informed consent prior to any study proceduresXx_NEWLINE_xXPatients or their legally authorized representative must provide written informed consentXx_NEWLINE_xXProvide informed written consentXx_NEWLINE_xXProvide informed written consentXx_NEWLINE_xXPatients or their legally authorized representative must provide written informed consentXx_NEWLINE_xXAbility to provide informed consentXx_NEWLINE_xXAbility and willingness to provide informed consentXx_NEWLINE_xXPatients or their legally authorized representative must provide written informed consentXx_NEWLINE_xXAbility to understand and the willingness to provide written informed assent or consentXx_NEWLINE_xXProvide written informed consentXx_NEWLINE_xXWillingness and ability to provide written informed consent prior to any study-related procedures and to comply with all study requirements.Xx_NEWLINE_xXProvide informed written consentXx_NEWLINE_xXAll patients must be willing and capable to provide informed consent to participate in the protocolXx_NEWLINE_xXAbility to provide written informed consent and comply with study requirementsXx_NEWLINE_xXAbility to provide informed consentXx_NEWLINE_xXProvide informed written consentXx_NEWLINE_xXProvide informed written consentXx_NEWLINE_xXProvide informed written consentXx_NEWLINE_xXProvide informed written consentXx_NEWLINE_xXAbility to provide informed written consentXx_NEWLINE_xXAdults who are unable to provide informed consent will NOT be enrolled on this studyXx_NEWLINE_xXPatients must provide informed consentXx_NEWLINE_xXPatients must provide verbal and written informed consent to participate in the studyXx_NEWLINE_xXPatients must provide written informed consent prior to any registration on studyXx_NEWLINE_xXAbility to provide written informed consentXx_NEWLINE_xXAbility and willingness to provide written informed consentXx_NEWLINE_xXUnable to provide informed consentXx_NEWLINE_xXAbility to provide informed consentXx_NEWLINE_xXProvide written, informed consent to participate in the study and follow the study proceduresXx_NEWLINE_xXProvide informed written consentXx_NEWLINE_xXProvide written informed consentXx_NEWLINE_xXProvide informed written consentXx_NEWLINE_xXProvide written informed consent (Screen 1 and Screen 2)Xx_NEWLINE_xXProvide informed written consentXx_NEWLINE_xXAbility and willingness to provide written informed consentXx_NEWLINE_xXProvide informed written consentXx_NEWLINE_xXPatients must provide informed written consentXx_NEWLINE_xXAbility to provide informed written consentXx_NEWLINE_xXAbility to provide written informed consent obtained prior to participation in the study and any related procedures being performedXx_NEWLINE_xXInability to provide informed consentXx_NEWLINE_xXAbility to provide written informed consent obtained prior to participation in the study and any related procedures being performedXx_NEWLINE_xXAbility to understand and the willingness to provide informed consentXx_NEWLINE_xXCognitively impaired patients who cannot provide informed consentXx_NEWLINE_xXProvide informed written consentXx_NEWLINE_xXPatients who provide written informed consent for participation in this trialXx_NEWLINE_xXInability to provide informed consent.Xx_NEWLINE_xXAbility to provide written informed consent obtained prior to participation in the study and any related procedures being performedXx_NEWLINE_xXProvide informed written consentXx_NEWLINE_xXProvide written informed consentXx_NEWLINE_xXAbility to provide written informed consent obtained prior to participation in the study and any related procedures being performedXx_NEWLINE_xXVoluntary agreement to provide written informed consent and the willingness and ability to comply with all aspects of the protocolXx_NEWLINE_xXProvide informed consentXx_NEWLINE_xXAbility to provide written informed consent obtained prior to participation in the study and any related procedures being performedXx_NEWLINE_xXInability to provide informed consentXx_NEWLINE_xXAll patients must be willing and capable to provide informed consent to participate in the protocolXx_NEWLINE_xXAbility to provide written informed consentXx_NEWLINE_xXInability to provide informed consentXx_NEWLINE_xXAbility to provide informed consentXx_NEWLINE_xXProvide written informed consentXx_NEWLINE_xXAbility to provide informed consent.Xx_NEWLINE_xXAbility to provide informed consentXx_NEWLINE_xXUnderstands the potential risks and benefits of study participation and is willing to provide written informed consent.Xx_NEWLINE_xXAbility to understand and provide informed consentXx_NEWLINE_xXWillingness and ability to provide written informed consent prior to any study-related procedures and comply with all study requirements.Xx_NEWLINE_xXPatients must provide written informed consentXx_NEWLINE_xXProvide signed written informed consentXx_NEWLINE_xXInability to provide informed consentXx_NEWLINE_xXProvide informed written consentXx_NEWLINE_xXMust have the ability to understand and the willingness to provide a written informed consent to participate in the studyXx_NEWLINE_xXPatients must provide informed consentXx_NEWLINE_xXProvide informed written consentXx_NEWLINE_xXWillingness to provide written informed consent for the study.Xx_NEWLINE_xXProvide written informed consent.Xx_NEWLINE_xXAbility to provide written informed consent obtained prior to participation in the study and any related procedures being performedXx_NEWLINE_xXProvide informed written consentXx_NEWLINE_xXPatients unable to provide informed consentXx_NEWLINE_xXAbility to provide written informed consentXx_NEWLINE_xXPatients must provide written informed consent.Xx_NEWLINE_xXProvide written informed consent prior to any study procedures.Xx_NEWLINE_xXWillingness and ability to provide written informed consent and to comply with the protocol requirementsXx_NEWLINE_xXAbility to provide written informed consent, comply with protocol visits and procedures, take oral medication, and not have any active infection or chronic comorbidity that would interfere with therapyXx_NEWLINE_xXAbility to read, understand and provide written consent to participate in the studyXx_NEWLINE_xXProvide written informed consent prior to any screening proceduresXx_NEWLINE_xXPatients or their legally authorized representative must provide written informed consentXx_NEWLINE_xXAbility to understand and provide informed consentXx_NEWLINE_xXAbility to provide written informed consent. Evidence of a personally signed informed consent.Xx_NEWLINE_xXAbility to provide informed consentXx_NEWLINE_xXInability to provide informed consentXx_NEWLINE_xXProvide written informed consent prior to any screening proceduresXx_NEWLINE_xXProvide signed written informed consentXx_NEWLINE_xXProvide informed written consentXx_NEWLINE_xXProvide written informed consentXx_NEWLINE_xXProvide informed written consentXx_NEWLINE_xXAbility to provide informed consentXx_NEWLINE_xXAbility to provide informed written consentXx_NEWLINE_xXAbility to provide written informed consentXx_NEWLINE_xXAbility to understand and the willingness to provide informed consent to participateXx_NEWLINE_xXAbility to provide written informed consent obtained prior to participation in the study and any related procedures being performedXx_NEWLINE_xXProvide informed written consentXx_NEWLINE_xXAbility to provide informed consentXx_NEWLINE_xXProvide informed written consentXx_NEWLINE_xXVoluntary agreement to provide written informed consent and the willingness and ability to comply with all aspects of the protocol.Xx_NEWLINE_xXProvide written informed consentXx_NEWLINE_xXInability to provide informed consentXx_NEWLINE_xXProvide written informed consent and willing to comply with protocol requirements.Xx_NEWLINE_xXAbility to understand and provide written informed consent to participate in this study.Xx_NEWLINE_xXInability to provide adequate informed consentXx_NEWLINE_xXAbility to provide written informed consentXx_NEWLINE_xXProvide informed written consentXx_NEWLINE_xXPatients must provide written informed consentXx_NEWLINE_xXProvide informed written consentXx_NEWLINE_xXHave ability to provide full written consentXx_NEWLINE_xXPatients or their legally authorized representative must provide written informed consentXx_NEWLINE_xXAbility to provide informed written consentXx_NEWLINE_xXProvide informed written consentXx_NEWLINE_xXProvide written informed consentXx_NEWLINE_xXProvide informed written consentXx_NEWLINE_xXBoth must provide informed consentXx_NEWLINE_xXUnable to provide consentXx_NEWLINE_xXPatient/caregiver can provide informed consentXx_NEWLINE_xXInability to provide informed consentXx_NEWLINE_xXUnable to provide informed consentXx_NEWLINE_xXPatients must provide written informed consent prior to any screening proceduresXx_NEWLINE_xXVoluntary agreement to provide written informed consent and the willingness and ability to comply with all aspects of the protocolXx_NEWLINE_xXPatients unable to understand the research protocol and/or provide informed consentXx_NEWLINE_xXThe ability to provide informed consentXx_NEWLINE_xXProvide written informed consentXx_NEWLINE_xXInability to provide a fully informed consent.Xx_NEWLINE_xXUnwilling to provide informed consentXx_NEWLINE_xXPatients who are unable to provide informed consent in English will be excludedXx_NEWLINE_xXCannot provide meaningful informed consentXx_NEWLINE_xXPatients unable to provide informed consentXx_NEWLINE_xXAbility to provide informed consentXx_NEWLINE_xXAbility to provide a written physician's clearanceXx_NEWLINE_xXAbility to provide informed consentXx_NEWLINE_xXAbility to provide informed consentXx_NEWLINE_xXCan provide informed consent (e.g., no cognitive impairment)Xx_NEWLINE_xXCAREGIVER: Can provide Informed consentXx_NEWLINE_xXMust provide written informed consentXx_NEWLINE_xXSubject is willing to provide written informed consentXx_NEWLINE_xXAbility to provide informed written consentXx_NEWLINE_xXUnable to provide informed consentXx_NEWLINE_xXAre unable to provide informed consentXx_NEWLINE_xXAbility and Willingness to provide informed consentXx_NEWLINE_xXUnwilling to provide informed consentXx_NEWLINE_xXProvide written informed consentXx_NEWLINE_xXCapable and willing to provide Informed consentXx_NEWLINE_xXPatients unable to provide informed consentXx_NEWLINE_xXProvide written informed consentXx_NEWLINE_xXProvide written informed consent prior to screeningXx_NEWLINE_xXWilling to provide informed written consentXx_NEWLINE_xXAbility to provide informed written consentXx_NEWLINE_xXInability to provide informed consentXx_NEWLINE_xXInability to provide informed consentXx_NEWLINE_xXAny participant who is not competent to provide informed consent for study participation per the investigatorXx_NEWLINE_xXAbility to provide informed consentXx_NEWLINE_xXAbility to provide informed written consentXx_NEWLINE_xXCan provide informed consentXx_NEWLINE_xXAbility to provide informed written consentXx_NEWLINE_xXInability to provide informed consentXx_NEWLINE_xXUnable to provide informed consentXx_NEWLINE_xXProvide informed written consentXx_NEWLINE_xXAbility to provide written informed consentXx_NEWLINE_xXProvide informed written consentXx_NEWLINE_xXUnwilling to provide informed consentXx_NEWLINE_xXUnwilling to provide informed consentXx_NEWLINE_xXUnwilling to provide informed consentXx_NEWLINE_xXAbility to understand and the willingness to provide written informed consentXx_NEWLINE_xXAll participants must have the ability to understand the willingness to provide informed consentXx_NEWLINE_xXProvide informed written consentXx_NEWLINE_xXInability to provide informed consentXx_NEWLINE_xXPatients must provide written informed consent prior to any screening proceduresXx_NEWLINE_xXPatients must provide written informed consent to participate in the studyXx_NEWLINE_xXProvide informed written consentXx_NEWLINE_xXUnable to provide informed consentXx_NEWLINE_xXProvide informed consentXx_NEWLINE_xXPatients who cannot provide a valid consentXx_NEWLINE_xXSubjects unable to provide consentXx_NEWLINE_xXPatients can provide informed consentXx_NEWLINE_xXUnable to provide informed consentXx_NEWLINE_xXCONTROL (HEALTHY) GROUP: Unable to provide informed consentXx_NEWLINE_xXParticipant is unable to provide informed consentXx_NEWLINE_xXAbility to provide informed written consentXx_NEWLINE_xXUnable to provide informed consentXx_NEWLINE_xXInability to provide informed consentXx_NEWLINE_xXUnable to provide informed consentXx_NEWLINE_xXProvide informed consent and agree to all assessments and study procedures.Xx_NEWLINE_xXPatients unable or unwilling to provide informed consent or sign a written informed consent document (ICD)Xx_NEWLINE_xXProvide informed consent and agree to all assessments and study proceduresXx_NEWLINE_xXAbility to read and provide written informed consentXx_NEWLINE_xXWillingness to provide written informed consentXx_NEWLINE_xXProvide informed consent and agree to all assessments and study proceduresXx_NEWLINE_xXProvide written informed consent.Xx_NEWLINE_xXAbility to understand and the willingness to provide informed consent.Xx_NEWLINE_xXUnable to provide informed consentXx_NEWLINE_xXUnable to provide informed consentXx_NEWLINE_xXInability to provide informed consentXx_NEWLINE_xXHave the ability to provide informed consent in EnglishXx_NEWLINE_xXFOLLOW UP ASSESSMENTS: Have the ability to provide informed consent in EnglishXx_NEWLINE_xXAbility to provide written informed consentXx_NEWLINE_xXInability to provide informed consentXx_NEWLINE_xXPatients who are willing and capable to provide informed consentXx_NEWLINE_xXthe ability to comply with the study protocol and provide informed consentXx_NEWLINE_xXCapable and willing to provide informed consentXx_NEWLINE_xXPatients unable to provide informed consentXx_NEWLINE_xXProvide written informed consent for the studyXx_NEWLINE_xXPatients unable or unwilling to provide informed consent or sign a written informed consent document (ICD)Xx_NEWLINE_xXAre unable to provide informed consentXx_NEWLINE_xXAbility to understand and willingness to provide informed consentXx_NEWLINE_xXAbility to understand and the willingness to provide informed consentXx_NEWLINE_xXPatients must be capable and willing to provide informed consentXx_NEWLINE_xXUnable to provide written consentXx_NEWLINE_xXAbility to provide written informed consent in accordance with institutional policiesXx_NEWLINE_xXSubject must provide written informed consent prior to any study-related procedures being performedXx_NEWLINE_xXPatients must be capable and willing to provide informed consent.Xx_NEWLINE_xXCannot provide written informed consentXx_NEWLINE_xXCannot provide written informed consentXx_NEWLINE_xXAbility to provide informed consentXx_NEWLINE_xXUnable to provide informed consentXx_NEWLINE_xXPatients or their legal representatives must have the ability to read, understand and provide written informed consent for the initiation of any study related proceduresXx_NEWLINE_xXPatients unable or unwilling to provide informed consent or sign a written informed consent document (ICD)Xx_NEWLINE_xXPatients or their legal representatives must have the ability to read, understand and provide written informed consent for the initiation of any study related proceduresXx_NEWLINE_xXProvide informed written consent if >= 18 years; if < 18 years, provide informed written assent and parent or legal guardian provide informed written consentXx_NEWLINE_xXProvide written informed consentXx_NEWLINE_xXRefusal to provide informed consentXx_NEWLINE_xXPatients must provide written informed consentXx_NEWLINE_xXPatients or their legal representatives must have the ability to read, understand and provide written informed consent for the initiation of any study related proceduresXx_NEWLINE_xXFemales unable to provide informed consentXx_NEWLINE_xXSubjects unable to provide own consent are not eligibleXx_NEWLINE_xXCannot provide written informed consentXx_NEWLINE_xXAbility to provide informed consentXx_NEWLINE_xXInability to provide informed consentXx_NEWLINE_xXHCC PATIENTS: Patient is willing to provide informed consentXx_NEWLINE_xXInability to provide written informed consentXx_NEWLINE_xXParticipant willing to provide a written informed consentXx_NEWLINE_xXPatient unable to provide informed consentXx_NEWLINE_xXThose who are pregnant, claustrophobic, or unable to provide informed consentXx_NEWLINE_xXAre unable to provide informed consentXx_NEWLINE_xXAbility to provide written informed consentXx_NEWLINE_xXSubjects unable to provide own consent are not eligibleXx_NEWLINE_xXUnable to provide informed consentXx_NEWLINE_xXAbility to provide informed consentXx_NEWLINE_xXInability to provide informed consentXx_NEWLINE_xXUnable to provide consentXx_NEWLINE_xXProvide informed written consentXx_NEWLINE_xXPatients must provide informed written consentXx_NEWLINE_xXPatients must provide written informed consentXx_NEWLINE_xXCannot provide written informed consentXx_NEWLINE_xXInability to provide informed consentXx_NEWLINE_xXUnable to provide informed consentXx_NEWLINE_xXhas the ability to read, understand and provide written informed consent for the initiation of any study related procedures (or legal representative)Xx_NEWLINE_xXPatients unable to provide informed consentXx_NEWLINE_xXAbility to provide written, informed consent.Xx_NEWLINE_xXAre unable to provide informed consentXx_NEWLINE_xXUnable to provide informed consentXx_NEWLINE_xXProvide written informed consent and willing to comply with protocol requirementXx_NEWLINE_xXSubject or his or her legal representative has the ability to read, understand and provide written informed consent for the initiation of any study related proceduresXx_NEWLINE_xXProvide informed written consentXx_NEWLINE_xXAbility to provide informed consentXx_NEWLINE_xXAbility to provide written informed consent obtained prior to participation in the studyXx_NEWLINE_xXAbility to provide consentXx_NEWLINE_xXPATIENTS: The ability to provide informed consentXx_NEWLINE_xXCan provide informed consentXx_NEWLINE_xXPatients unable to provide informed consentXx_NEWLINE_xXMen who are unable to provide their own informed consentXx_NEWLINE_xXAbility and willingness to provide written informed consentXx_NEWLINE_xXParticipants must voluntarily agree to provide written informed consent.Xx_NEWLINE_xX