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Structural Racism and Impact on Sickle Cell Disease: Sickle Cell Lives Matter

Hematology/oncology clinics of North America, 2022-12, Vol.36 (6), p.1063-1076

2022

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Crizanlizumab for the Prevention of Pain Crises in Sickle Cell Disease

The New England journal of medicine, 2017-02, Vol.376 (5), p.429-439

2017

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Intraindividual pain variability and phenotypes of pain in sickle cell disease: a secondary analysis from the Pain in Sickle Cell Epidemiology Study

Pain (Amsterdam), 2022-06, Vol.163 (6), p.1102-1113

2022

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A Phase 3 Trial of l-Glutamine in Sickle Cell Disease

The New England journal of medicine, 2018-07, Vol.379 (3), p.226-235

2018

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The Routledge International Handbook of New Digital Practices in Galleries, Libraries, Archives, Museums and Heritage Sites

1, 2019

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Sickle cell disease

Nature reviews. Disease primers, 2018-03, Vol.4 (1), p.18010-18010, Article 18010

2018

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Impact of community health workers on quality of life in adolescents and young adults with sickle cell disease: The SHIP‐HU study

British journal of haematology, 2024-02, Vol.204 (2), p.649-657

2024

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Interactive technology and human–animal encounters at the zoo

International journal of human-computer studies, 2017-02, Vol.98, p.150-168

2017

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Use of Community-Engaged Research Approaches in Clinical Interventions for Neurologic Disorders in the United States: A Scoping Review and Future Directions for Improving Health Equity Research

Neurology, 2023-08, Vol.101 (7 Suppl 1), p.S27

2023

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Randomized phase 2 study of GMI-1070 in SCD: reduction in time to resolution of vaso-occlusive events and decreased opioid use

Blood, 2015-04, Vol.125 (17), p.2656-2664

2015

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How Would You Treat This Patient With Acute and Chronic Pain From Sickle Cell Disease? : Grand Rounds Discussion From Beth Israel Deaconess Medical Center

Annals of internal medicine, 2022-04, Vol.175 (4), p.566

2022

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Satisfaction and access to care for adults and adolescents with sickle cell disease: ASCQ‐Me quality of care and the SHIP‐HU study

Pediatric blood & cancer, 2022-12, Vol.69 (12), p.e29948-n/a

2022

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Dysphagia in patients with sickle cell disease: An understudied problem

Journal of the National Medical Association, 2024-04, Vol.116 (2), p.126-130

2024

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Early Initiation of Sub−Anesthetic Ketamine Infusion in Adults with Vaso-Occlusive Crises Is Associated with Greater Reduction in Sickle Cell Pain Intensity: A Single Center’s Experience

Pain medicine (Malden, Mass.), 2022-12, Vol.23 (12), p.2042-2049

2022

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Sickle-cell pain: advances in epidemiology and etiology

Hematology, 2010, Vol.2010 (1), p.409-415

2010

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Community Health Workers as Support for Sickle Cell Care

American journal of preventive medicine, 2016-07, Vol.51 (1), p.S87-S98

2016

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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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Development and validation of the sickle cell stress scale‐adult

European journal of haematology, 2022-09, Vol.109 (3), p.215-225

2022

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Moving Toward a Multimodal Analgesic Regimen for Acute Sickle Cell Pain with Non-Opioid Analgesic Adjuncts: A Narrative Review

Journal of pain research, 2022-04, Vol.15, p.879-894

2022

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AAAPT Diagnostic Criteria for Acute Sickle Cell Disease Pain

The journal of pain, 2019-07, Vol.20 (7), p.746-759

2019

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Improvements in haemolysis and indicators of erythrocyte survival do not correlate with acute vaso‐occlusive crises in patients with sickle cell disease: a phase III randomized, placebo‐controlled, double‐blind study of the gardos channel blocker senicapoc (ICA‐17043)

British journal of haematology, 2011-04, Vol.153 (1), p.92-104

2011

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Daily assessment of pain in adults with sickle cell disease

Annals of internal medicine, 2008-01, Vol.148 (2), p.94

2008

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Quality of care in sickle cell disease: Cross-sectional study and development of a measure for adults reporting on ambulatory and emergency department care

Medicine (Baltimore), 2016-08, Vol.95 (35), p.e4528-e4528

2016

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Biopsychosocial Factors Associated With Pain and Pain-Related Outcomes in Adults and Children With Sickle Cell Disease: A Multivariable Analysis of the GRNDaD Multicenter Registry

The journal of pain, 2024-01, Vol.25 (1), p.153-164

2024

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A mobile app offering distractions and tips to cope with cigarette craving: a qualitative study

JMIR mHealth and uHealth, 2014-05, Vol.2 (2), p.e23-e23

2014

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Structural Racism and Impact on Sickle Cell Disease: Sickle Cell Lives Matter

Crizanlizumab for the Prevention of Pain Crises in Sickle Cell Disease

Intraindividual pain variability and phenotypes of pain in sickle cell disease: a secondary analysis from the Pain in Sickle Cell Epidemiology Study

A Phase 3 Trial of l-Glutamine in Sickle Cell Disease

The Routledge International Handbook of New Digital Practices in Galleries, Libraries, Archives, Museums and Heritage Sites

Sickle cell disease

Impact of community health workers on quality of life in adolescents and young adults with sickle cell disease: The SHIP‐HU study

Interactive technology and human–animal encounters at the zoo

Use of Community-Engaged Research Approaches in Clinical Interventions for Neurologic Disorders in the United States: A Scoping Review and Future Directions for Improving Health Equity Research

Randomized phase 2 study of GMI-1070 in SCD: reduction in time to resolution of vaso-occlusive events and decreased opioid use

How Would You Treat This Patient With Acute and Chronic Pain From Sickle Cell Disease? : Grand Rounds Discussion From Beth Israel Deaconess Medical Center

Satisfaction and access to care for adults and adolescents with sickle cell disease: ASCQ‐Me quality of care and the SHIP‐HU study

Dysphagia in patients with sickle cell disease: An understudied problem

Early Initiation of Sub−Anesthetic Ketamine Infusion in Adults with Vaso-Occlusive Crises Is Associated with Greater Reduction in Sickle Cell Pain Intensity: A Single Center’s Experience

Sickle-cell pain: advances in epidemiology and etiology

Community Health Workers as Support for Sickle Cell Care

A randomised controlled provider‐blinded trial of community health workers in sickle cell anaemia: effects on haematologic variables and hydroxyurea adherence

Development and validation of the sickle cell stress scale‐adult

Moving Toward a Multimodal Analgesic Regimen for Acute Sickle Cell Pain with Non-Opioid Analgesic Adjuncts: A Narrative Review

AAAPT Diagnostic Criteria for Acute Sickle Cell Disease Pain

Improvements in haemolysis and indicators of erythrocyte survival do not correlate with acute vaso‐occlusive crises in patients with sickle cell disease: a phase III randomized, placebo‐controlled, double‐blind study of the gardos channel blocker senicapoc (ICA‐17043)

Daily assessment of pain in adults with sickle cell disease

Quality of care in sickle cell disease: Cross-sectional study and development of a measure for adults reporting on ambulatory and emergency department care

Biopsychosocial Factors Associated With Pain and Pain-Related Outcomes in Adults and Children With Sickle Cell Disease: A Multivariable Analysis of the GRNDaD Multicenter Registry

A mobile app offering distractions and tips to cope with cigarette craving: a qualitative study

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