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Burden of Illness for Osteoporotic Fractures Compared With Other Serious Diseases Among Postmenopausal Women in the United States

Mayo Clinic proceedings, 2015, Vol.90 (1), p.53-62

2015

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Low hemoglobin increases risk for cerebrovascular disease, kidney disease, pulmonary vasculopathy, and mortality in sickle cell disease: A systematic literature review and meta-analysis

PloS one, 2020-04, Vol.15 (4), p.e0229959-e0229959

2020

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Systematic review of the impact of erythropoiesis-stimulating agents on fatigue in dialysis patients

Nephrology, dialysis, transplantation, 2012-06, Vol.27 (6), p.2418-2425

2012

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Hemoglobin and End-Organ Damage in Individuals with Sickle Cell Disease

Current therapeutic research, 2023-01, Vol.98, p.100696-100696, Article 100696

2023

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Denosumab for Elderly Men with Osteoporosis: A Cost-Effectiveness Analysis from the US Payer Perspective

Journal of Osteoporosis, 2015-01, Vol.2015, p.627631-9

2015

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Impact of voxelotor (GBT440) on unconjugated bilirubin and jaundice in sickle cell disease

Hematology reports, 2018-05, Vol.10 (2), p.7643-7643

2018

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Estimated Life Expectancy and Income of Patients With Sickle Cell Disease Compared With Those Without Sickle Cell Disease

JAMA network open, 2019-11, Vol.2 (11), p.e1915374-e1915374

2019

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Patient-Reported Outcomes in Chronic Heart Failure

JACC. Heart failure, 2016-10, Vol.4 (10), p.791-804

2016

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GBT021601, a Next Generation HbS Polymerization Inhibitor: Results of Safety, Tolerability, Pharmacokinetics and Pharmacodynamics in Adults Living with Sickle Cell Disease and Healthy Volunteers

Blood, 2021-11, Vol.138 (Supplement 1), p.3099-3099

2021

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9: A Simplified Case-Mix Adjuster Model for the Proposed End Stage Renal Disease (ESRD) Prospective Payment System (PPS)

American journal of kidney diseases, 2010, Vol.55 (4), p.B34-B34

Agodoa, Irene

2010

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10: Alternative Higher Predictive Model for the End Stage Renal Disease (ESRD) Prospective Payment System (PPS)

American journal of kidney diseases, 2010, Vol.55 (4), p.B34-B34

Agodoa, Irene

2010

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Estimating the Lifetime Medical Cost Burden of an Allogeneic Hematopoietic Cell Transplantation Patient and the Value of Addressing the Unmet Need

Blood, 2022-11, Vol.140 (Supplement 1), p.10833-10834

2022

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Cognition and education benefits of increased hemoglobin and blood oxygenation in children with sickle cell disease

PloS one, 2023-08, Vol.18 (8), p.e0289642-e0289642

2023

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Real-World Experience of Voxelotor for the Management of Complications in Sickle Cell Disease

Blood, 2021-11, Vol.138 (Supplement 1), p.2052-2052

2021

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Opioid utilization patterns in United States individuals with sickle cell disease

American journal of hematology, 2018-10, Vol.93 (10), p.E345-E347

2018

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Real-world effectiveness of voxelotor for treating sickle cell disease in the US: a large claims data analysis

Expert review of hematology, 2022-02, Vol.15 (2), p.167-173

2022

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Higher Hemoglobin Levels Achieved with Voxelotor Are Associated with Lower Vaso-occlusive Crisis Incidence: 72-Week Analysis from the HOPE Study

Blood, 2020-11, Vol.136 (Supplement 1), p.31-32

2020

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Voxelotor in adolescents and adults with sickle cell disease (HOPE): long-term follow-up results of an international, randomised, double-blind, placebo-controlled, phase 3 trial

The Lancet. Haematology, 2021-05, Vol.8 (5), p.e323-e333

2021

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The Role of Hemoglobin and Hemolysis on Transcranial Doppler Velocities in Children with Sickle Cell Disease: Data from a Natural History Cohort

Blood, 2021-11, Vol.138 (Supplement 1), p.3092-3092

2021

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Low Hemoglobin Increases Risk for Stroke, Kidney Disease, Elevated Estimated Pulmonary Artery Systolic Pressure, and Premature Death in Sickle Cell Disease: A Systematic Literature Review and Meta-Analysis

Blood, 2018-11, Vol.132 (Supplement 1), p.12-12

2018

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Patient-Reported Experiences in Voxelotor-Treated Children and Adults with Sickle Cell Disease: A Semistructured Interview Study

BioMed research international, 2023, Vol.2023, p.7533111-12

2023

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Transcranial Doppler Velocities Conversion Rate Based on Increasing Hemoglobin Concentration: Analysies from the SCCRIP Cohort Study

Blood, 2019-11, Vol.134 (Supplement_1), p.1002-1002

2019

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Incidence of Vaso-Occlusive Crisis Does Not Increase with Achieving Higher Hemoglobin Levels on Voxelotor Treatment or after Discontinuation: Analyses of the HOPE Study

Blood, 2019-11, Vol.134 (Supplement_1), p.2313-2313

2019

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The Impact of Hemoglobin Level on Risk of End-Organ Damage among Patients with Sickle Cell Disease - A Large-Scale, Longitudinal Analysis

Blood, 2020-11, Vol.136 (Supplement 1), p.27-28

2020

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Efficacy and Safety of Voxelotor in Adolescents and Adults with Sickle Cell Disease: HOPE Trial 72-Week Analysis

Blood, 2020-11, Vol.136 (Supplement 1), p.19-19

2020

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Burden of Illness for Osteoporotic Fractures Compared With Other Serious Diseases Among Postmenopausal Women in the United States

Low hemoglobin increases risk for cerebrovascular disease, kidney disease, pulmonary vasculopathy, and mortality in sickle cell disease: A systematic literature review and meta-analysis

Systematic review of the impact of erythropoiesis-stimulating agents on fatigue in dialysis patients

Hemoglobin and End-Organ Damage in Individuals with Sickle Cell Disease

Denosumab for Elderly Men with Osteoporosis: A Cost-Effectiveness Analysis from the US Payer Perspective

Impact of voxelotor (GBT440) on unconjugated bilirubin and jaundice in sickle cell disease

Estimated Life Expectancy and Income of Patients With Sickle Cell Disease Compared With Those Without Sickle Cell Disease

Patient-Reported Outcomes in Chronic Heart Failure

GBT021601, a Next Generation HbS Polymerization Inhibitor: Results of Safety, Tolerability, Pharmacokinetics and Pharmacodynamics in Adults Living with Sickle Cell Disease and Healthy Volunteers

9: A Simplified Case-Mix Adjuster Model for the Proposed End Stage Renal Disease (ESRD) Prospective Payment System (PPS)

10: Alternative Higher Predictive Model for the End Stage Renal Disease (ESRD) Prospective Payment System (PPS)

Estimating the Lifetime Medical Cost Burden of an Allogeneic Hematopoietic Cell Transplantation Patient and the Value of Addressing the Unmet Need

Cognition and education benefits of increased hemoglobin and blood oxygenation in children with sickle cell disease

Real-World Experience of Voxelotor for the Management of Complications in Sickle Cell Disease

Opioid utilization patterns in United States individuals with sickle cell disease

Real-world effectiveness of voxelotor for treating sickle cell disease in the US: a large claims data analysis

Higher Hemoglobin Levels Achieved with Voxelotor Are Associated with Lower Vaso-occlusive Crisis Incidence: 72-Week Analysis from the HOPE Study

Voxelotor in adolescents and adults with sickle cell disease (HOPE): long-term follow-up results of an international, randomised, double-blind, placebo-controlled, phase 3 trial

The Role of Hemoglobin and Hemolysis on Transcranial Doppler Velocities in Children with Sickle Cell Disease: Data from a Natural History Cohort

Low Hemoglobin Increases Risk for Stroke, Kidney Disease, Elevated Estimated Pulmonary Artery Systolic Pressure, and Premature Death in Sickle Cell Disease: A Systematic Literature Review and Meta-Analysis

Patient-Reported Experiences in Voxelotor-Treated Children and Adults with Sickle Cell Disease: A Semistructured Interview Study

Transcranial Doppler Velocities Conversion Rate Based on Increasing Hemoglobin Concentration: Analysies from the SCCRIP Cohort Study

Incidence of Vaso-Occlusive Crisis Does Not Increase with Achieving Higher Hemoglobin Levels on Voxelotor Treatment or after Discontinuation: Analyses of the HOPE Study

The Impact of Hemoglobin Level on Risk of End-Organ Damage among Patients with Sickle Cell Disease - A Large-Scale, Longitudinal Analysis

Efficacy and Safety of Voxelotor in Adolescents and Adults with Sickle Cell Disease: HOPE Trial 72-Week Analysis

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