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Indirect Economic Burden of Sickle Cell Disease
Value in health, 2021-08, Vol.24 (8), p.1095-1101
2021
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Feasibility and Quality Validation of a Mobile Application for Enhancing Adherence to Opioids in Sickle Cell Disease
Healthcare (Basel), 2022-08, Vol.10 (8), p.1506
2022
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Improved Utilization Amongst Adult Sickle Cell Disease Patients: A Multi-Disciplinary Medical Home Approach
Blood, 2020-11, Vol.136 (Supplement 1), p.22-23
2020
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Screening for Adverse Childhood Experiences (ACEs) As a Way to Predict Overdose Risk in Adult Sickle Cell Patients
Blood, 2022-11, Vol.140 (Supplement 1), p.13039-13040
2022
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Inpatient Reliance Ratio Versus Emergency Department Reliance Ratio in a Sickle Cell Disease Medical Home
Blood, 2022-11, Vol.140 (Supplement 1), p.7881-7882
2022
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Sickle Cell Disease May Qualify As an Ambulatory Care Sensitive Condition
Blood, 2022-11, Vol.140 (Supplement 1), p.7862-7863
2022
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Intensive Case Management in an Adult Sickle Cell Medical Home: Annual Effects on Utilization Efficiency Using Community Health Workers
Blood, 2022-11, Vol.140 (Supplement 1), p.1625-1626
2022
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COVID Symptoms and COVID Anxiety in Sickle Cell Disease
Blood, 2020-11, Vol.136 (Supplement 1), p.16-17
2020
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Responsivity of Utilization Rates to the Intensity of Case Management over Time Among High-Utilizing Adults with Sickle Cell Disease
Blood, 2019-11, Vol.134 (Supplement_1), p.5803-5803
2019
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A randomised controlled provider‐blinded trial of community health workers in sickle cell anaemia: effects on haematologic variables and hydroxyurea adherence
British journal of haematology, 2022-01, Vol.196 (1), p.193-203
2022
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Tiered Oral Therapy Protocol for Sickle Cell Vaso-Occlusive Crisis
Blood, 2019-11, Vol.134 (Supplement_1), p.3446-3446
2019
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Development and Validation of a Functional Status-Based Pain Assessment Tool
Blood, 2019-11, Vol.134 (Supplement_1), p.416-416
2019
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The Effect of Patient Navigators on Laboratory Parameters of Hydroxyurea Adherence in Sickle Cell Anemia: The SHIP-HU Study
Blood, 2019-11, Vol.134 (Supplement_1), p.2309-2309
2019
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Using Lean Six Sigma to Develop a Patient Centered Medical Home for Adults with Sickle Cell Disease
Blood, 2019-11, Vol.134 (Supplement_1), p.3408-3408
2019
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The Effect of Patient Navigators on Health-Related Quality of Life in Sickle Cell Anemia: The SHIP-HU Study
Blood, 2019-11, Vol.134 (Supplement_1), p.2168-2168
2019
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Case Management Featuring Community Health Workers Reduces Inpatient Health Care Utilization in Adults with Sickle Cell Disease
Blood, 2019-11, Vol.134 (Supplement_1), p.2104-2104
2019
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Development of a Framework to Describe Roles and Responsibilities for Sickle Cell Community Health Workers
Blood, 2018-11, Vol.132 (Supplement 1), p.5831-5831
2018
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Enhancing Adherence to Prescribed Opioids Using a Mobile-Based App: A Feasibility Study in Non-Cancer Pain
Blood, 2017-12, Vol.130, p.3418-3418
2017
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The Association of Painful Crises with Patient Reported Outcomes in Sickle Cell Disease: The SHIP-HU Study
Blood, 2018-11, Vol.132 (Supplement 1), p.3509-3509
2018
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Access to Care, and Emergency Department Utilization for Adults and Adolescents with Sickle Cell Disease: Ascq-Me and the SHIP-HU Study
Blood, 2017-12, Vol.130, p.2257-2257
2017
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Reducing Hospital Use of Urban Sickle Cell Adults Using Multidisciplinary Adult Care and Instrumental Support
Blood, 2017-12, Vol.130, p.5661-5661
2017
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Comparison of Adult and Adolescent Quality of Ambulatory and Emergency Care in Sickle Cell Disease: Ascq-Me and the SHIP-HU Study
Blood, 2017-12, Vol.130, p.2258-2258
2017
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Solution-derived Ge–Sb–Se–Te phase-change chalcogenide films
Scientific reports, 2024-08, Vol.14 (1), p.18151-11, Article 18151
2024
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Efficacy of an iron‐fortified infant cereal to reduce the risk of iron deficiency anemia in young children in East Cameroon
Food science & nutrition, 2020-07, Vol.8 (7), p.3566-3577
2020
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CAID prediction portal: a comprehensive service for predicting intrinsic disorder and binding regions in proteins
Nucleic acids research, 2023-07, Vol.51 (W1), p.W62
2023
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