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Morbidity and mortality of sickle cell disease patients starting intermittent haemodialysis: a comparative cohort study with non‐ Sickle dialysis patients

British journal of haematology, 2016-07, Vol.174 (1), p.148-152

2016

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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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Arterio‐venous fistula for automated red blood cells exchange in patients with sickle cell disease: Complications and outcomes

American journal of hematology, 2017-02, Vol.92 (2), p.136-140

2017

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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

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Determinants of Hydroxychloroquine Blood Concentration Variations in Systemic Lupus Erythematosus

Arthritis & rheumatology (Hoboken, N.J.), 2015-08, Vol.67 (8), p.2176-2184

2015

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Monoclonal B-cell lymphocyte proliferation in a patient presenting with historical Whipple disease

Internal medicine journal, 2013-03, Vol.43 (3), p.338-341

2013

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Transfusion requirements and complication rate in β‐thalassemia intermedia due to heterozygous β‐globin gene mutation and triplicated α‐globin genes

European journal of haematology, 2023-11, Vol.111 (5), p.742-747

2023

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Study of Anti-Müllerian Hormone and Its Relation to the Subsequent Probability of Pregnancy in 112 Patients With Systemic Lupus Erythematosus, Exposed or Not to Cyclophosphamide

The journal of clinical endocrinology and metabolism, 2013-09, Vol.98 (9), p.3785-3792

2013

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Hydroxyurea Exposure throughout Pregnancy in Patients with Sickle-Cell Disease : 4 Case Reports from European Non-Interventional, Multicentric, Prospective Escort-HU Study

Blood, 2019-11, Vol.134 (Supplement_1), p.1027-1027

2019

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Six Months of Hydroxyurea Reduces Albuminuria in Patients with Sickle Cell Disease

Journal of the American Society of Nephrology, 2016-06, Vol.27 (6), p.1847-1853

2016

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Acute-on-chronic liver failure due to severe intrahepatic vaso-occlusion and recurrence of the intial disease: 2 major features in liver transplantation for severe sickle-cell-related hepatopathy

Journal of hepatology, 2022-07, Vol.77, p.S791-S792

2022

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Sickle-Cell Disease Patients' Attitudes Towards Their Treatment with Hydroxycarbamide

Blood, 2019-11, Vol.134 (Supplement_1), p.1013-1013

2019

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Outcomes of Pregnancies in Patients with Sickle-Cell Disease : Update from European Non-Interventional, Multicentric, Prospective Escort-HU Study

Blood, 2019-11, Vol.134 (Supplement_1), p.891-891

2019

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Haematological determinants of cardiac involvement in adults with sickle cell disease

European heart journal, 2016-04, Vol.37 (14), p.1158-1167

2016

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The liver in sickle cell disease

La Presse médicale (1983), 2023-12, Vol.52 (4), p.104212-104212, Article 104212

2023

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Clinical outcome after a totally implantable venous access port-related infection in cancer patients: a prospective study and review of the literature

Medicine (Baltimore), 2012-11, Vol.91 (6), p.309-318

2012

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99 Episodes of Delayed Hemolysis Post transfusion Reaction among Adult Patients with Sickle Cell Disease; Clinical Presentation, Prognosis, and Treatment

Blood, 2014-12, Vol.124 (21), p.4092-4092

2014

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Causes of Death in Sickle Cell Disease Adult Patients: Old and New Trends

Blood, 2014-12, Vol.124 (21), p.2715-2715

2014

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Arterio-Venous Fistula Is an Applicable Vascular Access for Erythracytapheresis in Patients with Sickle Cell Disease

Blood, 2016-12, Vol.128 (22), p.4856-4856

2016

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Monoclonal B ‐cell lymphocyte proliferation in a patient presenting with historical W hipple disease

Internal medicine journal, 2013-03, Vol.43 (3), p.338-341

2013

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Prospective Comparison of Sperm Parameters in SCD Adult Patients Before and after a 6 Months Treatment with hydroxyurea (HU)

Blood, 2012-11, Vol.120 (21), p.242-242

2012

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

Biomedicines, 2022, Vol.10 (12)

2022

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Management of acute complications in sickle cell disease

La revue du praticien, 2014-10, Vol.64 (8), p.1114

2014

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Sickle Cell Disease
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Morbidity and mortality of sickle cell disease patients starting intermittent haemodialysis: a comparative cohort study with non‐ Sickle dialysis patients

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

Arterio‐venous fistula for automated red blood cells exchange in patients with sickle cell disease: Complications and outcomes

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

Determinants of Hydroxychloroquine Blood Concentration Variations in Systemic Lupus Erythematosus

Hydroxychloroquine in systemic lupus erythematosus: results of a French multicentre controlled trial (PLUS Study)

Monoclonal B-cell lymphocyte proliferation in a patient presenting with historical Whipple disease

Transfusion requirements and complication rate in β‐thalassemia intermedia due to heterozygous β‐globin gene mutation and triplicated α‐globin genes

Moderate-intensity endurance-exercise training in patients with sickle-cell disease without severe chronic complications (EXDRE): an open-label randomised controlled trial

Study of Anti-Müllerian Hormone and Its Relation to the Subsequent Probability of Pregnancy in 112 Patients With Systemic Lupus Erythematosus, Exposed or Not to Cyclophosphamide

Hydroxyurea Exposure throughout Pregnancy in Patients with Sickle-Cell Disease : 4 Case Reports from European Non-Interventional, Multicentric, Prospective Escort-HU Study

Six Months of Hydroxyurea Reduces Albuminuria in Patients with Sickle Cell Disease

Acute-on-chronic liver failure due to severe intrahepatic vaso-occlusion and recurrence of the intial disease: 2 major features in liver transplantation for severe sickle-cell-related hepatopathy

Sickle-Cell Disease Patients' Attitudes Towards Their Treatment with Hydroxycarbamide

Outcomes of Pregnancies in Patients with Sickle-Cell Disease : Update from European Non-Interventional, Multicentric, Prospective Escort-HU Study

Haematological determinants of cardiac involvement in adults with sickle cell disease

The liver in sickle cell disease

Clinical outcome after a totally implantable venous access port-related infection in cancer patients: a prospective study and review of the literature

99 Episodes of Delayed Hemolysis Post transfusion Reaction among Adult Patients with Sickle Cell Disease; Clinical Presentation, Prognosis, and Treatment

Causes of Death in Sickle Cell Disease Adult Patients: Old and New Trends

Arterio-Venous Fistula Is an Applicable Vascular Access for Erythracytapheresis in Patients with Sickle Cell Disease

Monoclonal B ‐cell lymphocyte proliferation in a patient presenting with historical W hipple disease

Prospective Comparison of Sperm Parameters in SCD Adult Patients Before and after a 6 Months Treatment with hydroxyurea (HU)

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

Management of acute complications in sickle cell disease

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