National Hemophilia Foundation Enlists Diverse Patient Voices to Inform a National Research Blueprint for Inherited Bleeding Disorders
Santaella M, Witkop M, Mills K, Recht M, DiMichele D, Valentino L. National Hemophilia Foundation Enlists Diverse Patient Voices to Inform a National Research Blueprint for Inherited Bleeding Disorders. Blood 2021, 138: 1904. DOI: 10.1182/blood-2021-147857.Peer-Reviewed Original ResearchNational Hemophilia FoundationResearch prioritiesListening sessionsSubject matter expertsOregon Health & Science UniversityParticipant groupsMulti-disciplinary working groupWorking GroupHealth professionalsPatient vignettesUnderserved populationsInherited bleeding disorderPatient voiceEnlists individualsPatient communityUnmet needsAmerican ThrombosisResearch SummitCommunity supportCommunity surveyCommunity needsCommunity segmentsDiverse populationsScience UniversityConsultation
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