J. Baker

发表

Comorbidities, Health-Related Quality of Life, Health-care Utilization in Older Persons with Hemophilia—Hematology Utilization Group Study Part VII (HUGS VII)

M. Nichol, Joanne Wu, B. Konkle, 2022, Journal of blood medicine.

Building access to care in adult sickle cell disease: defining models of care, essential components, and economic aspects.

John D. Roberts, A. King, J. Little, 2020, Blood advances.

Burden of illness: direct and indirect costs among persons with hemophilia A in the United States

Kathleen A. Johnson, M. Nichol, B. Riske, 2015, Journal of medical economics.

Men with severe hemophilia in the United States: birth cohort analysis of a large national database.

B. Riske, P. Monahan, J. Soucie, 2016, Blood.

Capacity Building for Rare Bleeding Disorders in the Remote Commonwealth of the Northern Mariana Islands.

James N. Huang, Tiffany F Lin, J. Baker, 2016, American journal of public health.

Sickle cell disease among Latinx in California

Susan T. Paulukonis, J. Baker, Susan Paulukonis, 2022, PloS one.

Integrated Hemophilia Patient Care via a National Network of Care Centers in the United States: A Model for Rare Coagulation Disorders

L. Valentino, M. Recht, R. Butler, 2021, Journal of blood medicine.

Insurance, home therapy, and prophylaxis in U.S. youth with severe hemophilia.

B. Riske, S. Cutter, R. Presley, 2011, American journal of preventive medicine.

Economic Burden of Illness among Persons with Hemophilia B from HUGS Vb: Examining the Association of Severity and Treatment Regimens with Costs and Annual Bleed Rates.

M. Nichol, J. Baker, Christina X Chen, 2017, Value in health : the journal of the International Society for Pharmacoeconomics and Outcomes Research.

Physical functioning in boys with hemophilia in the U.S.

B. Riske, P. Monahan, J. Soucie, 2011, American journal of preventive medicine.

Young adults with hemophilia in the U.S.: demographics, comorbidities, and health status

M. Nichol, B. Riske, R. Curtis, 2015, American journal of hematology.

US Hemophilia Treatment Center population trends 1990–2010: patient diagnoses, demographics, health services utilization

B. Riske, A. Forsberg, R. Shearer, 2013, Haemophilia : the official journal of the World Federation of Hemophilia.

Self-reported barriers to hemophilia care in people with factor VIII deficiency.

Kathleen A. Johnson, B. Riske, A. Forsberg, 2011, American journal of preventive medicine.

A model for a regional system of care to promote the health and well-being of people with rare chronic genetic disorders.

B. Riske, A. Forsberg, S. Crudder, 2005, American journal of public health.

Physical activity and health outcomes in persons with haemophilia B

M. Nichol, B. Riske, J. Poon, 2014, Haemophilia : the official journal of the World Federation of Hemophilia.

Physical activity and health outcomes in persons with haemophilia

M. Nichol, B. Riske, J. Poon, 2014 .

Haemophilia Utilization Group Study – Part Va (HUGS Va): design, methods and baseline data

B. Riske, A. Forsberg, A. Shapiro, 2011, Haemophilia : the official journal of the World Federation of Hemophilia.

Design for an Evaluation of Hemophilia Treatment Center 340B Drug Pricing Programs

J. Baker, 2013 .

Surveillance of female patients with inherited bleeding disorders in United States Haemophilia Treatment Centres

B. Konkle, J. Gill, P. Kouides, 2011, Haemophilia : the official journal of the World Federation of Hemophilia.

Building the foundation for a community-generated national research blueprint for inherited bleeding disorders: research priorities in health services; diversity, equity, and inclusion; and implementation science

A. Dinno, T. Buckner, V. Byams, 2023, Expert review of hematology.

Patient satisfaction with US Hemophilia Treatment Center Care, Teams and Services: The First National Survey

B. Riske, R. Shearer, J. Baker, 2020, Haemophilia : the official journal of the World Federation of Hemophilia.

Trends in prescribing practices for management of haemophilia: 1999–2021

M. Nichol, Joanne Wu, M. Koerper, 2023, Haemophilia.

Trends in Prescribing Practices for Management of Hemophilia

M. Nichol, Joanne Wu, M. Koerper, 2021, Blood.

Depression and anxiety in persons with Von Willebrand disease

M. Nichol, Joanne Wu, B. Konkle, 2021, Haemophilia : the official journal of the World Federation of Hemophilia.

Burden of illness: direct and indirect costs among persons with hemophilia A in the United States

Kathleen A. Johnson, M. Nichol, B. Riske, 2015, Journal of medical economics.

High school completion rates among men with hemophilia.

B. Riske, A. Forsberg, J. Soucie, 2010, American journal of preventive medicine.

Physical functioning in boys with hemophilia in the U.S.

B. Riske, J. Baker, J. M. Soucie, 2011, American journal of preventive medicine.

Depression and anxiety in persons with Von Willebrand disease

M. Nichol, Joanne Wu, B. Konkle, 2022, Haemophilia : the official journal of the World Federation of Hemophilia.

Healthcare Utilization and Health Related Quality of Life in Persons with Von Willebrand Disease

M. Nichol, Joanne Wu, B. Konkle, 2020 .

Insurance, home therapy, and prophylaxis in U.S. youth with severe hemophilia.

B. Riske, S. Cutter, R. Presley, 2011, American journal of preventive medicine.