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Glomerular Hyperfiltration in Adult Sickle Cell Anemia: A Frequent Hemolysis Associated Feature

Clinical journal of the American Society of Nephrology, 2010-05, Vol.5 (5), p.756-761

2010

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Sickle cell disease, a genetic haemoglobin disease

Revue de l'infirmière, 2022-01, Vol.71 (277), p.16

Girot, Robert

2022

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Influence of sickle cell disease and treatment with hydroxyurea on sperm parameters and fertility of human males

Haematologica (Roma), 2008-07, Vol.93 (7), p.988-993

2008

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Endothelin receptor antagonism prevents hypoxia-induced mortality and morbidity in a mouse model of sickle-cell disease

The Journal of clinical investigation, 2008-05, Vol.118 (5), p.1924-1933

2008

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Complications and treatment of patients with β-thalassemia in France: results of the National Registry

Haematologica (Roma), 2010-05, Vol.95 (5), p.724-729

2010

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Steroid treatment in children with sickle-cell disease

Haematologica (Roma), 2007-03, Vol.92 (3), p.425-426

2007

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The Association of CD81 Polymorphisms with Alloimmunization in Sickle Cell Disease

Clinical & developmental immunology, 2013-01, Vol.2013, p.937846-9

2013

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An Evaluation of Three Ways of Communicating Carrier Status Results to the Parents of Children in a Neonatal Sickle Cell Screening Programme

Frontiers in pediatrics, 2020-06, Vol.8, p.300-300

2020

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Urinary endothelin-1 as a marker of renal damage in sickle cell disease

Nephrology, dialysis, transplantation, 2005-11, Vol.20 (11), p.2408-2413

2005

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Identification of new prognosis factors from the clinical and epidemiologic analysis of a registry of 229 diamond-blackfan anemia patients

Pediatric research, 1999-11, Vol.46 (5), p.553-561

1999

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Hemoglobin sickle cell disease complications: a clinical study of 179 cases

Haematologica (Roma), 2012-08, Vol.97 (8), p.1136-1141

2012

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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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Topical effectiveness of molgramostim (GM-CSF) in sickle cell leg ulcers

Dermatology (Basel), 2004-01, Vol.208 (2), p.135

2004

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Outcomes of Adult Patients With Sickle Cell Disease Admitted to the ICU: A Case Series

Critical care medicine, 2014-07, Vol.42 (7), p.1629-1639

2014

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The acceleration of the propagation phase of thrombin generation in patients with steady-state sickle cell disease is associated with circulating erythrocyte-derived microparticles

Thrombosis and haemostasis, 2012-06, Vol.107 (6), p.1044

2012

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Prophylactic laparoscopic cholecystectomy in adult sickle cell disease patients with cholelithiasis: A prospective cohort study

International journal of surgery (London, England), 2015-10, Vol.22, p.62-66

2015

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Renin‐angiotensin system blockade promotes a cardio‐renal protection in albuminuric homozygous sickle cell patients

British journal of haematology, 2017-12, Vol.179 (5), p.820-828

2017

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Persistent B19 infection in immunocompetent individuals: implications for transfusion safety

Blood, 2005-10, Vol.106 (8), p.2890-2895

2005

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Rituximab as an effective treatment of hyperhemolysis syndrome in sickle cell anemia

American journal of hematology, 2010-01, Vol.85 (1), p.91-92

2010

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High lactate dehydrogenase levels at admission for painful vaso-occlusive crisis is associated with severe outcome in adult SCD patients

Clinical biochemistry, 2012-12, Vol.45 (18), p.1578-1582

2012

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Prevalence and correlates of metabolic acidosis among patients with homozygous sickle cell disease

Clinical journal of the American Society of Nephrology, 2014-04, Vol.9 (4), p.648-653

2014

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Glomerular Hyperfiltration in Adult Sickle Cell Anemia: A Frequent Hemolysis Associated Feature

Sickle cell disease, a genetic haemoglobin disease

Influence of sickle cell disease and treatment with hydroxyurea on sperm parameters and fertility of human males

Endothelin receptor antagonism prevents hypoxia-induced mortality and morbidity in a mouse model of sickle-cell disease

Family cord blood banking for sickle cell disease: a twenty-year experience in two dedicated public cord blood banks

Complications and treatment of patients with β-thalassemia in France: results of the National Registry

Steroid treatment in children with sickle-cell disease

Prospective evaluation of patient-reported outcomes during treatment with deferasirox or deferoxamine for iron overload in patients with β-thalassemia

The Association of CD81 Polymorphisms with Alloimmunization in Sickle Cell Disease

An Evaluation of Three Ways of Communicating Carrier Status Results to the Parents of Children in a Neonatal Sickle Cell Screening Programme

Urinary endothelin-1 as a marker of renal damage in sickle cell disease

Identification of new prognosis factors from the clinical and epidemiologic analysis of a registry of 229 diamond-blackfan anemia patients

Hemoglobin sickle cell disease complications: a clinical study of 179 cases

A Hemodynamic Study of Pulmonary Hypertension in Sickle Cell Disease

Topical effectiveness of molgramostim (GM-CSF) in sickle cell leg ulcers

Outcomes of Adult Patients With Sickle Cell Disease Admitted to the ICU: A Case Series

The acceleration of the propagation phase of thrombin generation in patients with steady-state sickle cell disease is associated with circulating erythrocyte-derived microparticles

Prophylactic laparoscopic cholecystectomy in adult sickle cell disease patients with cholelithiasis: A prospective cohort study

Polymorphisms in Inflammatory Genes Modulate the Occurrence of Clinical Complications in Patients with Sickle Cell Disease

Renin‐angiotensin system blockade promotes a cardio‐renal protection in albuminuric homozygous sickle cell patients

A Polymorphism in Toll-like Receptor 2 Gene Is Associated with Occurrence of Bacterial Infections in Sickle Cell Disease Patients

Persistent B19 infection in immunocompetent individuals: implications for transfusion safety

Rituximab as an effective treatment of hyperhemolysis syndrome in sickle cell anemia

High lactate dehydrogenase levels at admission for painful vaso-occlusive crisis is associated with severe outcome in adult SCD patients

Prevalence and correlates of metabolic acidosis among patients with homozygous sickle cell disease

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