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Risk factors for mortality in adult patients with sickle cell disease: a meta-analysis of studies in North America and Europe

Haematologica (Roma), 2017-04, Vol.102 (4), p.626-636

2017

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Potential of cell tracking velocimetry as an economical and portable hematology analyzer

Scientific reports, 2022-02, Vol.12 (1), p.1692-1692, Article 1692

2022

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The Evolving Landscape of Drug Therapies for Sickle Cell Disease

Hematology/oncology clinics of North America, 2022-12, Vol.36 (6), p.1285-1312

2022

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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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Real-world characteristics of patients with sickle cell disease who initiated crizanlizumab therapy

Current medical research and opinion, 2023-04, Vol.39 (4), p.555-565

2023

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Persistent albuminuria and chronic kidney disease in adults with sickle cell anaemia: Results from a multicenter natural history study

British journal of haematology, 2024-07, Vol.205 (3), p.1159-1169

2024

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Hypoxia in sickle cell disease due to right to left shunting

American journal of hematology, 2019-02, Vol.94 (2), p.E53-E55

2019

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Elevated tricuspid regurgitation velocity is associated with increased adverse haematologic events during pregnancy in women with sickle cell disease

British journal of haematology, 2022-06, Vol.197 (6), p.795-801

2022

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Association of biomarkers of endothelial function, coagulation activation and kidney injury with persistent albuminuria in sickle cell anaemia

British journal of haematology, 2024-09

2024

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Gaps in the diagnosis and management of iron overload in sickle cell disease: a ‘real‐world’ report from the GRNDaD registry

British journal of haematology, 2021-12, Vol.195 (5), p.e157-e160

2021

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Human papillomavirus in metastatic squamous carcinoma from unknown primaries in the head and neck: A retrospective 7 year study

Experimental and molecular pathology, 2009-10, Vol.87 (2), p.94-98

2009

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Hydroxyurea is associated with lower prevalence of albuminuria in adults with sickle cell disease

Nephrology, dialysis, transplantation, 2014-06, Vol.29 (6), p.1211-1218

2014

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Building access to care in adult sickle cell disease: defining models of care, essential components, and economic aspects

Blood advances, 2020-08, Vol.4 (16), p.3804-3813

2020

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Pure white cell aplasia in a patient with thymic carcinoma

Blood, 2013-08, Vol.122 (8), p.1340-1340

2013

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Long‐term biological effects in sickle cell disease: insights from a post‐crizanlizumab study

British journal of haematology, 2021-11, Vol.195 (4), p.e150-e153

2021

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Venous thromboembolism prophylaxis practices for patients with sickle cell disease prior to and during the COVID-19 pandemic

Blood coagulation & fibrinolysis, 2023-12, Vol.34 (8), p.471-477

2023

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Alloimmunization is associated with older age of transfused red blood cells in sickle cell disease

American journal of hematology, 2015-08, Vol.90 (8), p.691-695

2015

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Advances in new drug therapies for the management of sickle cell disease

Expert opinion on orphan drugs, 2018-01, Vol.6 (5), p.329-343

2018

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The acute chest syndrome of sickle cell disease

Expert opinion on pharmacotherapy, 2013-06, Vol.14 (8), p.991-999

2013

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A pilot study of eptifibatide for treatment of acute pain episodes in sickle cell disease

Thrombosis research, 2013-09, Vol.132 (3), p.341-345

2013

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Longitudinal study of echocardiography‐derived tricuspid regurgitant jet velocity in sickle cell disease

British journal of haematology, 2013-09, Vol.162 (6), p.836-841

2013

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Decades after the cooperative study: A re-examination of systemic blood pressure in sickle cell disease

American journal of hematology, 2012-10, Vol.87 (10), p.E65-E68

2012

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Computed tomography angiogram in diagnosis of Churg-Strauss vasculitis

Journal of rheumatology, 2009-12, Vol.36 (12), p.2851-2852

2009

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Magnetic Fractionation of Red Blood Cells Based on Oxygen Saturation in Sickle Cell Disease

Blood, 2022-11, Vol.140 (Supplement 1), p.8560-8561

2022

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Risk factors for mortality in adult patients with sickle cell disease: a meta-analysis of studies in North America and Europe

Potential of cell tracking velocimetry as an economical and portable hematology analyzer

The Evolving Landscape of Drug Therapies for Sickle Cell Disease

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

Real-world characteristics of patients with sickle cell disease who initiated crizanlizumab therapy

Persistent albuminuria and chronic kidney disease in adults with sickle cell anaemia: Results from a multicenter natural history study

Hypoxia in sickle cell disease due to right to left shunting

Elevated tricuspid regurgitation velocity is associated with increased adverse haematologic events during pregnancy in women with sickle cell disease

Association of biomarkers of endothelial function, coagulation activation and kidney injury with persistent albuminuria in sickle cell anaemia

Gaps in the diagnosis and management of iron overload in sickle cell disease: a ‘real‐world’ report from the GRNDaD registry

Human papillomavirus in metastatic squamous carcinoma from unknown primaries in the head and neck: A retrospective 7 year study

Hydroxyurea is associated with lower prevalence of albuminuria in adults with sickle cell disease

Building access to care in adult sickle cell disease: defining models of care, essential components, and economic aspects

Pure white cell aplasia in a patient with thymic carcinoma

Long‐term biological effects in sickle cell disease: insights from a post‐crizanlizumab study

Venous thromboembolism prophylaxis practices for patients with sickle cell disease prior to and during the COVID-19 pandemic

Alloimmunization is associated with older age of transfused red blood cells in sickle cell disease

Advances in new drug therapies for the management of sickle cell disease

The acute chest syndrome of sickle cell disease

Riociguat in patients with sickle cell disease and hypertension or proteinuria (STERIO-SCD): a randomised, double-blind, placebo controlled, phase 1–2 trial

A pilot study of eptifibatide for treatment of acute pain episodes in sickle cell disease

Longitudinal study of echocardiography‐derived tricuspid regurgitant jet velocity in sickle cell disease

Decades after the cooperative study: A re-examination of systemic blood pressure in sickle cell disease

Computed tomography angiogram in diagnosis of Churg-Strauss vasculitis

Magnetic Fractionation of Red Blood Cells Based on Oxygen Saturation in Sickle Cell Disease

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