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A Hemodynamic Study of Pulmonary Hypertension in Sickle Cell Disease

The New England journal of medicine, 2011-07, Vol.365 (1), p.44-53

2011

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Hemolytic transfusion reactions in sickle cell disease: underappreciated and potentially fatal

Haematologica (Roma), 2020-03, Vol.105 (3), p.539

2020

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Epidemiology and disease burden of sickle cell disease in France: A descriptive study based on a French nationwide claim database

PloS one, 2021-07, Vol.16 (7), p.e0253986-e0253986

2021

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Delayed hemolytic transfusion reaction in adult sickle‐cell disease: presentations, outcomes, and treatments of 99 referral center episodes

American journal of hematology, 2016-10, Vol.91 (10), p.989-994

2016

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Decreased risk of underdosing with continuous infusion versus intermittent administration of cefotaxime in patients with sickle cell disease and acute chest syndrome

PloS one, 2024-04, Vol.19 (4), p.e0302298-e0302298

2024

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A study of 28 pregnant women with sickle cell disease and COVID-19: elevated maternal and fetal morbidity rates

Haematologica (Roma), 2024-05, Vol.109 (5), p.1562

2024

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Sickle cell disease induces resistance to cutaneous carcinogenesis

Orphanet journal of rare diseases, 2020-03, Vol.15 (1), p.66-5, Article 66

2020

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Anti-C5 antibody treatment for delayed hemolytic transfusion reactions in sickle cell disease

Haematologica (Roma), 2020-11, Vol.105 (11), p.2694

2020

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PB2505: THERAPEUTIC PHLEBOTOMY INSTANTLY AFFECTS BLOOD PARAMETERS AND VISCOCITY IN SICKLE CELL DISEASE PATIENTS

HemaSphere, 2023-08, Vol.7 (S3), p.e69597f7-n/a

2023

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Pulmonary Hypertension and Cor Pulmonale during Severe Acute Chest Syndrome in Sickle Cell Disease

American journal of respiratory and critical care medicine, 2008-03, Vol.177 (6), p.646-653

2008

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Outcomes of Pregnancy in Sickle Cell Disease Patients: Results from the Prospective ESCORT-HU Cohort Study

Biomedicines, 2023-02, Vol.11 (2), p.597

2023

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Is chest X‐ray still relevant for acute chest syndrome diagnosis?

Health science reports, 2024-05, Vol.7 (5), p.e2053-n/a

2024

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P1438: L‐GLUTAMINE: A NOVEL AND EFFECTIVE THERAPEUTIC TOOL FOR VOC REDUCTION IN SCD

HemaSphere, 2023-08, Vol.7 (S3), p.e73462e7-n/a

2023

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Characteristics of Moyamoya Syndrome in Sickle-Cell Disease by Magnetic Resonance Angiography: An Adult-Cohort Study

Frontiers in neurology, 2019, Vol.10, p.15-15

2019

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Case Report of Myelodysplastic Syndrome in a Sickle-Cell Disease Patient Treated with Hydroxyurea and Literature Review

Biomedicines, 2022-12, Vol.10 (12), p.3201

2022

Volltextzugriff (PDF)

Magnetic Resonance Imaging Assessment of Kidney Oxygenation and Perfusion During Sickle Cell Vaso-occlusive Crises

American journal of kidney diseases, 2017-01, Vol.69 (1), p.51-59

2017

Volltextzugriff (PDF)

ADAMTS13 and von Willebrand factor assessment in steady state and acute vaso‐occlusive crisis of sickle cell disease

Research and practice in thrombosis and haemostasis, 2021-01, Vol.5 (1), p.197-203

2021

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Spectrum of adult Parvovirus B19 infection according to the underlying predisposing condition and proposals for clinical practice

British journal of haematology, 2015-07, Vol.170 (2), p.192-199

2015

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Thromboprophylaxis Reduced Venous Thromboembolism in Sickle Cell Patients with Central Venous Access Devices: A Retrospective Cohort Study

Journal of clinical medicine, 2022-02, Vol.11 (5), p.1193

2022

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Score Predicting Acute Chest Syndrome During Vaso-occlusive Crises in Adult Sickle-cell Disease Patients

EBioMedicine, 2016-08, Vol.10 (C), p.305-311

2016

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How to avoid the problem of erythrocyte alloimmunization in sickle cell disease

Hematology, 2021-12, Vol.2021 (1), p.689-695

2021

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Procalcitonin to Reduce Antibiotic Exposure during Acute Chest Syndrome in Adult Patients with Sickle-Cell Disease

Journal of clinical medicine, 2020-11, Vol.9 (11), p.3718

2020

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Managing pregnancy in patients with sickle cell disease from a transfusion perspective

Hematology, 2023-12, Vol.2023 (1), p.640

2023

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Population pharmacokinetics and pharmacodynamics of hydroxyurea in sickle cell anemia patients, a basis for optimizing the dosing regimen

Orphanet journal of rare diseases, 2011-05, Vol.6 (1), p.30-30, Article 30

2011

Volltextzugriff (PDF)

Factors Associated With Dyspnea in Adult Patients With Sickle Cell Disease

Chest, 2005-11, Vol.128 (5), p.3336-3344

2005

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A Hemodynamic Study of Pulmonary Hypertension in Sickle Cell Disease

Hemolytic transfusion reactions in sickle cell disease: underappreciated and potentially fatal

Epidemiology and disease burden of sickle cell disease in France: A descriptive study based on a French nationwide claim database

Delayed hemolytic transfusion reaction in adult sickle‐cell disease: presentations, outcomes, and treatments of 99 referral center episodes

Decreased risk of underdosing with continuous infusion versus intermittent administration of cefotaxime in patients with sickle cell disease and acute chest syndrome

A study of 28 pregnant women with sickle cell disease and COVID-19: elevated maternal and fetal morbidity rates

Sickle cell disease induces resistance to cutaneous carcinogenesis

Anti-C5 antibody treatment for delayed hemolytic transfusion reactions in sickle cell disease

PB2505: THERAPEUTIC PHLEBOTOMY INSTANTLY AFFECTS BLOOD PARAMETERS AND VISCOCITY IN SICKLE CELL DISEASE PATIENTS

Pulmonary Hypertension and Cor Pulmonale during Severe Acute Chest Syndrome in Sickle Cell Disease

Outcomes of Pregnancy in Sickle Cell Disease Patients: Results from the Prospective ESCORT-HU Cohort Study

Is chest X‐ray still relevant for acute chest syndrome diagnosis?

P1438: L‐GLUTAMINE: A NOVEL AND EFFECTIVE THERAPEUTIC TOOL FOR VOC REDUCTION IN SCD

Characteristics of Moyamoya Syndrome in Sickle-Cell Disease by Magnetic Resonance Angiography: An Adult-Cohort Study

Case Report of Myelodysplastic Syndrome in a Sickle-Cell Disease Patient Treated with Hydroxyurea and Literature Review

Magnetic Resonance Imaging Assessment of Kidney Oxygenation and Perfusion During Sickle Cell Vaso-occlusive Crises

ADAMTS13 and von Willebrand factor assessment in steady state and acute vaso‐occlusive crisis of sickle cell disease

Spectrum of adult Parvovirus B19 infection according to the underlying predisposing condition and proposals for clinical practice

Thromboprophylaxis Reduced Venous Thromboembolism in Sickle Cell Patients with Central Venous Access Devices: A Retrospective Cohort Study

Score Predicting Acute Chest Syndrome During Vaso-occlusive Crises in Adult Sickle-cell Disease Patients

How to avoid the problem of erythrocyte alloimmunization in sickle cell disease

Procalcitonin to Reduce Antibiotic Exposure during Acute Chest Syndrome in Adult Patients with Sickle-Cell Disease

Managing pregnancy in patients with sickle cell disease from a transfusion perspective

Population pharmacokinetics and pharmacodynamics of hydroxyurea in sickle cell anemia patients, a basis for optimizing the dosing regimen

Factors Associated With Dyspnea in Adult Patients With Sickle Cell Disease

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