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Sex-based differences in the manifestations and complications of sickle cell disease: Report from the Sickle Cell Disease Implementation Consortium

PloS one, 2021-10, Vol.16 (10), p.e0258638-e0258638

2021

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Emergency Provider Analgesic Practices and Attitudes Toward Patients With Sickle Cell Disease

Annals of emergency medicine, 2013-10, Vol.62 (4), p.293-302.e10

2013

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Publication of data collection forms from NHLBI funded sickle cell disease implementation consortium (SCDIC) registry

Orphanet journal of rare diseases, 2020-07, Vol.15 (1), p.178-178, Article 178

2020

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Identifying barriers to evidence-based care for sickle cell disease: results from the Sickle Cell Disease Implementation Consortium cross-sectional survey of healthcare providers in the USA

BMJ open, 2021-11, Vol.11 (11), p.e050880-e050880

2021

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"The project did not come to us with a solution": Perspectives of research teams on implementing a study about electronic health record-embedded individualized pain plans for emergency department treatment of vaso-occlusive episodes in adults with sickle cell disease

BMC health services research, 2023-11, Vol.23 (1), p.1245-1245, Article 1245

2023

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Improving Emergency Department-Based Care of Sickle Cell Pain

Hematology, 2017-12, Vol.2017 (1), p.412-417

Glassberg, Jeffrey A

2017

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3-D OCT imaging of hyalocytes in partial posterior vitreous detachment and vaso-occlusive retinal disease

American journal of ophthalmology case reports, 2023-06, Vol.30, p.101836, Article 101836

2023

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A Survey-Based Needs Assessment of Barriers to Optimal Sickle Cell Disease Care in the Emergency Department

Annals of emergency medicine, 2020-09, Vol.76 (3), p.S64-S72

2020

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Wheezing and asthma are independent risk factors for increased sickle cell disease morbidity

British journal of haematology, 2012-11, Vol.159 (4), p.472-479

2012

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Cough and wheeze events are temporally associated with increased pain in individuals with sickle cell disease without asthma

British journal of haematology, 2015-09, Vol.170 (5), p.732-734

2015

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Risk Factors for Increased ED Utilization in a Multinational Cohort of Children With Sickle Cell Disease

Academic emergency medicine, 2012-06, Vol.19 (6), p.664-672

2012

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Wheezing in children with sickle cell disease

Current opinion in pediatrics, 2014-02, Vol.26 (1), p.9-18

2014

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SARS-CoV-2 Neutralizing Antibody LY-CoV555 in Outpatients with Covid-19

The New England journal of medicine, 2021-01, Vol.384 (3), p.229-237

2021

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A multilevel mHealth intervention boosts adherence to hydroxyurea in individuals with sickle cell disease

Blood advances, 2023-12, Vol.7 (23), p.7190-7201

2023

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A randomized clinical trial of the efficacy and safety of rivipansel for sickle cell vaso-occlusive crisis

Blood, 2023-01, Vol.141 (2), p.168-179

2023

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Plasma Free Hemoglobin Is Associated with LDH, AST, Total Bilirubin, and the Hemolytic Component in Patients with Sickle Cell Anemia

Blood, 2022-11, Vol.140 (Supplement 1), p.5438-5439

2022

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Intravenous Fluid Boluses Are Commonly Administered to Adults with Sickle Cell Disease and Vaso-Occlusive Pain

Blood, 2019-11, Vol.134 (Supplement_1), p.4839-4839

2019

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Pharmacokinetics, Efficacy, and Safety of a SARS-CoV-2 Antibody Treatment in Pediatric Participants: An Open-Label Addendum of a Placebo-Controlled, Randomized Phase 2/3 Trial

Infectious diseases and therapy, 2023-07, Vol.12 (7), p.1861-1873

2023

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Mortality in Adults with Sickle Cell Disease: Results from the Sickle Cell Disease Implementation Consortium (SCDIC) Registry

Blood, 2022-11, Vol.140 (Supplement 1), p.2586-2588

2022

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Hepcidin Predicts Decrease in Erythroid Expansion in Sickle Cell Disease Patients Treated with Inhaled Steroids

Blood, 2018-11, Vol.132 (Supplement 1), p.2339-2339

2018

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Sickle Cell Disease and Venous Thromboembolism: Hospital Mortality, Length of Stay and Cost

Blood, 2018-11, Vol.132 (Supplement 1), p.2378-2378

2018

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Cerebrovascular Accidents Among African American Adults with Sickle Cell Disease: A Nationwide Outcomes and Trend Analysis over Two Decades

Blood, 2017-12, Vol.130, p.4644-4644

2017

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Predictors of Maternal Morbidity Among Participants Enrolled in the Sickle Cell Disease Implementation Consortium Registry

Blood, 2020-11, Vol.136 (Supplement 1), p.3-3

2020

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Sex Based Differences in Sickle Cell Disease

Blood, 2020-11, Vol.136 (Supplement 1), p.37-37

2020

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Sex-based differences in the manifestations and complications of sickle cell disease: Report from the Sickle Cell Disease Implementation Consortium

Emergency Provider Analgesic Practices and Attitudes Toward Patients With Sickle Cell Disease

Publication of data collection forms from NHLBI funded sickle cell disease implementation consortium (SCDIC) registry

Identifying barriers to evidence-based care for sickle cell disease: results from the Sickle Cell Disease Implementation Consortium cross-sectional survey of healthcare providers in the USA

"The project did not come to us with a solution": Perspectives of research teams on implementing a study about electronic health record-embedded individualized pain plans for emergency department treatment of vaso-occlusive episodes in adults with sickle cell disease

Improving Emergency Department-Based Care of Sickle Cell Pain

3-D OCT imaging of hyalocytes in partial posterior vitreous detachment and vaso-occlusive retinal disease

A Survey-Based Needs Assessment of Barriers to Optimal Sickle Cell Disease Care in the Emergency Department

Wheezing and asthma are independent risk factors for increased sickle cell disease morbidity

Cough and wheeze events are temporally associated with increased pain in individuals with sickle cell disease without asthma

Risk Factors for Increased ED Utilization in a Multinational Cohort of Children With Sickle Cell Disease

Wheezing in children with sickle cell disease

SARS-CoV-2 Neutralizing Antibody LY-CoV555 in Outpatients with Covid-19

A multilevel mHealth intervention boosts adherence to hydroxyurea in individuals with sickle cell disease

A randomized clinical trial of the efficacy and safety of rivipansel for sickle cell vaso-occlusive crisis

Plasma Free Hemoglobin Is Associated with LDH, AST, Total Bilirubin, and the Hemolytic Component in Patients with Sickle Cell Anemia

Intravenous Fluid Boluses Are Commonly Administered to Adults with Sickle Cell Disease and Vaso-Occlusive Pain

Pharmacokinetics, Efficacy, and Safety of a SARS-CoV-2 Antibody Treatment in Pediatric Participants: An Open-Label Addendum of a Placebo-Controlled, Randomized Phase 2/3 Trial

Mortality in Adults with Sickle Cell Disease: Results from the Sickle Cell Disease Implementation Consortium (SCDIC) Registry

Hepcidin Predicts Decrease in Erythroid Expansion in Sickle Cell Disease Patients Treated with Inhaled Steroids

Sickle Cell Disease and Venous Thromboembolism: Hospital Mortality, Length of Stay and Cost

Cerebrovascular Accidents Among African American Adults with Sickle Cell Disease: A Nationwide Outcomes and Trend Analysis over Two Decades

Predictors of Maternal Morbidity Among Participants Enrolled in the Sickle Cell Disease Implementation Consortium Registry

Sex Based Differences in Sickle Cell Disease

Identifying Clinical and Research Priorities in Sickle Cell Lung Disease. An Official American Thoracic Society Workshop Report

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