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Michelle L Witkop

Showing results (1-10 of 12) with videos related to

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Expert Review of Hematology|March 15, 2023
Soliciting international perspectives on an American national research agenda for inherited bleeding disordersMichelle L Witkop, Fiona Robinson, Donna DiMichele
International Journal of Laboratory Hematology|June 17, 2020
Patient advocacy and its importance to laboratory medicine practice: A response from patient advocacy groupsMichelle L Witkop, Maria Santaella, Caroline Kruse, et al.
Expert Review of Hematology|March 15, 2023
The National Hemophilia Foundation State of the Science Research Summit initiative: executive summaryLeonard A Valentino, Michelle L Witkop, Maria E Santaella, et al.
Expert Review of Hematology|March 15, 2023
The National Hemophilia Foundation's State of the Science Research Summit: the foundation of a national research blueprint for inherited bleeding disordersLeonard A Valentino, Michelle L Witkop, Maria E Santaella, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|June 14, 2022
Building the blueprint: Formulating a community-generated national plan for future research in inherited bleeding disordersLeonard A Valentino, Michelle L Witkop, Maria E Santaella, et al.
Journal of Racial and Ethnic Health Disparities|February 21, 2016
Racial Differences in Chronic Pain and Quality of Life among Adolescents and Young Adults with Moderate or Severe HemophiliaJohn M McLaughlin, Angela Lambing, Michelle L Witkop, et al.
Health and Quality of Life Outcomes|April 9, 2017
Predictors of quality of life among adolescents and young adults with a bleeding disorderJohn M McLaughlin, James E Munn, Terry L Anderson, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|August 15, 2017
Patient, caregiver, and provider perceptions of pain and pain management in adolescents and young adults with bleeding disordersAngela Lambing, Cynthia D Nichols, James E Munn, et al.
Expert Review of Hematology|December 15, 2023
Cross-cultural assessment of the influence of the COVID-19 pandemic on the perceived mental health and medical experiences of persons with inherited bleeding disorders and their parents/guardiansSylvia von Mackensen, Maria E Santaella, Cynthia D Nichols, et al.
Patient Preference and Adherence|October 2, 2019
Interrelationship between depression, anxiety, pain, and treatment adherence in hemophilia: results from a US cross-sectional surveyMichelle L Witkop, Angela Lambing, Cynthia D Nichols, et al.
Pageof 2

Showing results (1-10 of 12) with videos related to

Sort By:
Pageof 2
Expert Review of Hematology|March 15, 2023
Soliciting international perspectives on an American national research agenda for inherited bleeding disordersMichelle L Witkop, Fiona Robinson, Donna DiMichele
International Journal of Laboratory Hematology|June 17, 2020
Patient advocacy and its importance to laboratory medicine practice: A response from patient advocacy groupsMichelle L Witkop, Maria Santaella, Caroline Kruse, et al.
Expert Review of Hematology|March 15, 2023
The National Hemophilia Foundation State of the Science Research Summit initiative: executive summaryLeonard A Valentino, Michelle L Witkop, Maria E Santaella, et al.
Expert Review of Hematology|March 15, 2023
The National Hemophilia Foundation's State of the Science Research Summit: the foundation of a national research blueprint for inherited bleeding disordersLeonard A Valentino, Michelle L Witkop, Maria E Santaella, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|June 14, 2022
Building the blueprint: Formulating a community-generated national plan for future research in inherited bleeding disordersLeonard A Valentino, Michelle L Witkop, Maria E Santaella, et al.
Journal of Racial and Ethnic Health Disparities|February 21, 2016
Racial Differences in Chronic Pain and Quality of Life among Adolescents and Young Adults with Moderate or Severe HemophiliaJohn M McLaughlin, Angela Lambing, Michelle L Witkop, et al.
Health and Quality of Life Outcomes|April 9, 2017
Predictors of quality of life among adolescents and young adults with a bleeding disorderJohn M McLaughlin, James E Munn, Terry L Anderson, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|August 15, 2017
Patient, caregiver, and provider perceptions of pain and pain management in adolescents and young adults with bleeding disordersAngela Lambing, Cynthia D Nichols, James E Munn, et al.
Expert Review of Hematology|December 15, 2023
Cross-cultural assessment of the influence of the COVID-19 pandemic on the perceived mental health and medical experiences of persons with inherited bleeding disorders and their parents/guardiansSylvia von Mackensen, Maria E Santaella, Cynthia D Nichols, et al.
Patient Preference and Adherence|October 2, 2019
Interrelationship between depression, anxiety, pain, and treatment adherence in hemophilia: results from a US cross-sectional surveyMichelle L Witkop, Angela Lambing, Cynthia D Nichols, et al.
Pageof 2