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Journal Articles

National Hemophilia Foundation Champions a National Research Blueprint Defining a Community-Coordinated Research Ecosystem to Accelerate Progress in Inherited Bleeding Disorders

Michelle Witkop, Maria E. Santaella, Michael Recht, Keri Norris, Brett Spitale, Esmeralda Vasquez, Donna DiMichele, Kevin Mills

Blood (2022) 140 (Supplement 1): 5021–5022.

https://doi.org/10.1182/blood-2022-170842

Published: 2022

Journal Articles

Relationship between Perceived Social Support, Mental Health, Activity, and Chronic Pain in Persons with Inheritable Bleeding Disorders

Maria E Santaella, Cynthia Nichols, Samantha Carlson, Michelle Witkop

Blood (2022) 140 (Supplement 1): 13156–13158.

https://doi.org/10.1182/blood-2022-170856

Published: 2022

Journal Articles

National Hemophilia Foundation Convenes Diverse Community Voices to Define an Actionable National Research Blueprint for Inherited Bleeding Disorders

Michelle L Witkop, Michael Recht, Donna DiMichele, Kevin Mills, Leonard A. Valentino, Maria E Santaella

Blood (2021) 138 (Supplement 1): 4952.

https://doi.org/10.1182/blood-2021-149518

Published: 2021

Journal Articles

Bleeding Disorder Data Registry Reveals Racial/Ethnic Disparities That Could Significantly Impact Patient Journey

Maria E Santaella, Michelle L Witkop, Cynthia Nichols, Rosaura Vidal, Leonard A. Valentino

Blood (2021) 138 (Supplement 1): 5004.

https://doi.org/10.1182/blood-2021-148025

Published: 2021

Journal Articles

National Hemophilia Foundation Enlists Diverse Patient Voices to Inform a National Research Blueprint for Inherited Bleeding Disorders

Maria E Santaella, Michelle L Witkop, Kevin Mills, Michael Recht, Donna DiMichele, Leonard A. Valentino

Blood (2021) 138 (Supplement 1): 1904.

https://doi.org/10.1182/blood-2021-147857

Published: 2021

Journal Articles

Pain in the Bleeding Disorders Community: Patient and Caregiver Perspectives

Tyler W. Buckner, MD MSc, Nancy Durben, PT, MSPT, PCS, Christi Humphrey, LCSW, Eric Iglewski, LMSW, Jennifer Newman, MSPT, Maria E Santaella, RN-BC, MSN, CPHON, Michelle Witkop, DNP, FNP-BC

Blood (2016) 128 (22): 2591.

https://doi.org/10.1182/blood.V128.22.2591.2591

Published: 2016

NARROW

National Hemophilia Foundation Champions a National Research Blueprint Defining a Community-Coordinated Research Ecosystem to Accelerate Progress in Inherited Bleeding Disorders

Relationship between Perceived Social Support, Mental Health, Activity, and Chronic Pain in Persons with Inheritable Bleeding Disorders

National Hemophilia Foundation Convenes Diverse Community Voices to Define an Actionable National Research Blueprint for Inherited Bleeding Disorders

Bleeding Disorder Data Registry Reveals Racial/Ethnic Disparities That Could Significantly Impact Patient Journey

National Hemophilia Foundation Enlists Diverse Patient Voices to Inform a National Research Blueprint for Inherited Bleeding Disorders

Pain in the Bleeding Disorders Community: Patient and Caregiver Perspectives

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ASH Publications

American Society of Hematology

National Hemophilia Foundation Champions a National Research Blueprint Defining a Community-Coordinated Research Ecosystem to Accelerate Progress in Inherited Bleeding Disorders

Relationship between Perceived Social Support, Mental Health, Activity, and Chronic Pain in Persons with Inheritable Bleeding Disorders

National Hemophilia Foundation Convenes Diverse Community Voices to Define an Actionable National Research Blueprint for Inherited Bleeding Disorders

Bleeding Disorder Data Registry Reveals Racial/Ethnic Disparities That Could Significantly Impact Patient Journey

National Hemophilia Foundation Enlists Diverse Patient Voices to Inform a National Research Blueprint for Inherited Bleeding Disorders

Pain in the Bleeding Disorders Community: Patient and Caregiver Perspectives

Email alerts

ASH Publications

American Society of Hematology

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