Judith R. Baker, D.P.H.
Affiliations: | 2013 | Health Services | University of California, Los Angeles, Los Angeles, CA |
Area:
Public Health, Public and Social Welfare, Health Care ManagementGoogle:
"Judith Baker"Cross-listing: SocTree
Parents
Sign in to add mentor| Jack Needleman | grad student | 2013 | UCLA | |
| (Design for an Evaluation of Hemophilia Treatment Center 340B Drug Pricing Programs.) | ||||
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Publications
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| Curtis R, Manco-Johnson M, Konkle BA, et al. (2022) Comorbidities, Health-Related Quality of Life, Health-care Utilization in Older Persons with Hemophilia-Hematology Utilization Group Study Part VII (HUGS VII). Journal of Blood Medicine. 13: 229-241 |
| Valentino LA, Baker JR, Butler R, et al. (2021) Integrated Hemophilia Patient Care via a National Network of Care Centers in the United States: A Model for Rare Coagulation Disorders. Journal of Blood Medicine. 12: 897-911 |
| Kanter J, Smith WR, Desai PC, et al. (2020) Building access to care in adult sickle cell disease: defining models of care, essential components, and economic aspects. Blood Advances. 4: 3804-3813 |
| Curtis R, Ding Y, Aliyev ER, et al. (2019) Pro53 Clotting Factor Utilization And Bleeding Rates Among Persons With Hemophilia A From A Longitudinal Study Value in Health. 22 |
| Claster S, Roland M, Tucker J, et al. (2018) Poor Access to Care Is a Risk Factor for Iron Overload in Adults with Sickle Cell Disease in Southern California Blood. 132: 3527-3527 |
| Chen CX, Baker JR, Nichol MB. (2017) 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. Value in Health : the Journal of the International Society For Pharmacoeconomics and Outcomes Research. 20: 1074-1082 |
| Mazepa MA, Monahan PE, Baker JR, et al. (2016) Men with severe hemophilia in the United States: birth cohort analysis of a large national database. Blood |
| Curtis R, Baker J, Riske B, et al. (2015) Young adults with hemophilia in the U.S.: demographics, comorbidities, and health status. American Journal of Hematology. 90: S11-6 |
| Niu X, Baker JR, Riske B, et al. (2015) Clustering Health Status Among Adults With Hemophilia Using Sf-12 Health Survey. Value in Health : the Journal of the International Society For Pharmacoeconomics and Outcomes Research. 18: A673-4 |
| Zhou ZY, Koerper MA, Johnson KA, et al. (2015) Burden of illness: direct and indirect costs among persons with hemophilia A in the United States. Journal of Medical Economics. 18: 457-65 |