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HLA-haploidentical bone marrow transplantation with posttransplant cyclophosphamide expands the donor pool for patients with sickle cell disease

Blood, 2012-11, Vol.120 (22), p.4285-4291

2012

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Management of sickle cell disease: summary of the 2014 evidence-based report by expert panel members

JAMA : the journal of the American Medical Association, 2014-09, Vol.312 (10), p.1033

2014

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An evaluation of cardiopulmonary endurance and muscular strength in adults living with sickle cell disease

British journal of haematology, 2022-11, Vol.199 (4), p.597-602

2022

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2019 sickle cell disease guidelines by the American Society of Hematology: methodology, challenges, and innovations

Blood advances, 2019-12, Vol.3 (23), p.3945-3950

2019

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Current Evidence and Rationale to Guide Perioperative Management, Including Transfusion Decisions, in Patients With Sickle Cell Disease

Anesthesia and analgesia, 2023-06, Vol.136 (6), p.1107-1114

2023

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A case‐control analysis of hyperhemolysis syndrome in adults and laboratory correlates of complement involvement

Transfusion (Philadelphia, Pa.), 2019-10, Vol.59 (10), p.3129-3139

2019

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Silent cerebral infarction during immune TTP remission: prevalence, predictors, and impact on cognition

Blood, 2023-07, Vol.142 (4), p.325-335

2023

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Short-term air pollution levels and sickle cell disease hospital encounters in South Carolina: A case-crossover analysis

Environmental research, 2024-07, Vol.252 (Pt 1), p.118766-118766, Article 118766

2024

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Mortality and Access to Kidney Transplantation in Patients with Sickle Cell Disease-Associated Kidney Failure

Clinical journal of the American Society of Nephrology, 2021-03, Vol.16 (3), p.407-414

2021

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Implementation of national blood conservation recommendations at an adult sickle cell center

Transfusion (Philadelphia, Pa.), 2022-09, Vol.62 (9), p.1763-1771

2022

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Nonmydriatic Ultra-Widefield Fundus Photography in a Hematology Clinic Shows Utility for Screening of Sickle Cell Retinopathy

American journal of ophthalmology, 2022-04, Vol.236, p.241-248

2022

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Converting adults with sickle cell disease from full agonist opioids to buprenorphine: A reliable method with safety and early evidence of reduced acute care utilization

American journal of hematology, 2022-11, Vol.97 (11), p.1435-1442

2022

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Mental health, pain and likelihood of opioid misuse among adults with sickle cell disease

British journal of haematology, 2024-03, Vol.204 (3), p.1029-1038

2024

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Daily Opioid Use Fluctuates as a Function of Pain, Catastrophizing, and Affect in Patients With Sickle Cell Disease: An Electronic Daily Diary Analysis

The journal of pain, 2018-01, Vol.19 (1), p.46-56

2018

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Depressive and Insomnia Symptoms Sequentially Mediate the Association Between Racism-Based Discrimination in Healthcare Settings and Clinical Pain Among Adults With Sickle Cell Disease

The journal of pain, 2023-04, Vol.24 (4), p.643-654

2023

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A Preliminary Investigation of the Underlying Mechanism Associating Daily Sleep Continuity Disturbance and Prescription Opioid Use Among Individuals With Sickle Cell Disease

Annals of behavioral medicine, 2021-06, Vol.55 (6), p.580-591

2021

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Impact of disease- and race-based discrimination in health care on pain outcomes among adults living with sickle cell disease in the United States: The mediating roles of internalized stigma and depressive symptoms

Stigma and health (Washington, D.C.), 2024-09

2024

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Vasculopathy, inflammation, and blood flow in leg ulcers of patients with sickle cell anemia

American journal of hematology, 2014-01, Vol.89 (1), p.1-6

2014

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Examination of the Patient and Hospitalization Characteristics of 30-Day SCD Readmissions

Southern medical journal (Birmingham, Ala.), 2016-09, Vol.109 (9), p.583-587

2016

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Terminology for Retinal Findings in Sickle Cell Disease Research: A Scoping Review

Ophthalmology retina, 2024-01, Vol.8 (1), p.81-87

2024

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Genetic contributions to pain modulation in sickle cell: A focus on single nucleotide polymorphisms

Gene reports, 2024-09, Vol.36, p.101983, Article 101983

2024

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Evidence gaps in the management of sickle cell disease: A summary of needed research

American journal of hematology, 2015-04, Vol.90 (4), p.273-275

2015

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Idiopathic Acquired Hemophilia A with Undetectable Factor VIII Inhibitor

Case reports in hematology, 2014-01, Vol.2014 (2014), p.1-4

2014

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COVID-19 in Hospitalized Patients with Sickle Cell Disease

Blood, 2021-11, Vol.138 (Supplement 1), p.3090-3090

2021

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HLA-haploidentical bone marrow transplantation with posttransplant cyclophosphamide expands the donor pool for patients with sickle cell disease

Management of sickle cell disease: summary of the 2014 evidence-based report by expert panel members

An evaluation of cardiopulmonary endurance and muscular strength in adults living with sickle cell disease

2019 sickle cell disease guidelines by the American Society of Hematology: methodology, challenges, and innovations

Current Evidence and Rationale to Guide Perioperative Management, Including Transfusion Decisions, in Patients With Sickle Cell Disease

A case‐control analysis of hyperhemolysis syndrome in adults and laboratory correlates of complement involvement

Silent cerebral infarction during immune TTP remission: prevalence, predictors, and impact on cognition

Short-term air pollution levels and sickle cell disease hospital encounters in South Carolina: A case-crossover analysis

Mortality and Access to Kidney Transplantation in Patients with Sickle Cell Disease-Associated Kidney Failure

Implementation of national blood conservation recommendations at an adult sickle cell center

Nonmydriatic Ultra-Widefield Fundus Photography in a Hematology Clinic Shows Utility for Screening of Sickle Cell Retinopathy

Converting adults with sickle cell disease from full agonist opioids to buprenorphine: A reliable method with safety and early evidence of reduced acute care utilization

Mental health, pain and likelihood of opioid misuse among adults with sickle cell disease

Daily Opioid Use Fluctuates as a Function of Pain, Catastrophizing, and Affect in Patients With Sickle Cell Disease: An Electronic Daily Diary Analysis

Depressive and Insomnia Symptoms Sequentially Mediate the Association Between Racism-Based Discrimination in Healthcare Settings and Clinical Pain Among Adults With Sickle Cell Disease

A Preliminary Investigation of the Underlying Mechanism Associating Daily Sleep Continuity Disturbance and Prescription Opioid Use Among Individuals With Sickle Cell Disease

Impact of disease- and race-based discrimination in health care on pain outcomes among adults living with sickle cell disease in the United States: The mediating roles of internalized stigma and depressive symptoms

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

Vasculopathy, inflammation, and blood flow in leg ulcers of patients with sickle cell anemia

Examination of the Patient and Hospitalization Characteristics of 30-Day SCD Readmissions

Terminology for Retinal Findings in Sickle Cell Disease Research: A Scoping Review

Genetic contributions to pain modulation in sickle cell: A focus on single nucleotide polymorphisms

Evidence gaps in the management of sickle cell disease: A summary of needed research

Idiopathic Acquired Hemophilia A with Undetectable Factor VIII Inhibitor

COVID-19 in Hospitalized Patients with Sickle Cell Disease

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