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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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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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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.1044-1052

2012

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Maternal mortality among women with sickle-cell disease in France, 1996–2009

European journal of obstetrics & gynecology and reproductive biology, 2015-11, Vol.194, p.183-188

2015

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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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Sickle cell leg ulcers: a frequently disabling complication and a marker of severity

British journal of dermatology (1951), 2008-02, Vol.158 (2), p.339-344

2008

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The risk of going abroad in sickle cell disease: a study of 148 adults

Transactions of the Royal Society of Tropical Medicine and Hygiene, 2011-06, Vol.105 (6), p.310-314

2011

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Sickle cell disease: from childhood to adult age

Archives de pédiatrie : organe officiel de la Société française de pédiatrie, 2007-06, Vol.14 (6), p.605-606

2007

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Complete or partial seroreversion in immunocompetent individuals after self-limited HCV infection: consequences for transfusion

Transfusion (Philadelphia, Pa.), 2004-03, Vol.44 (3), p.343-348

2004

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Infectious complications in sickle cell disease are influenced by HLA class II alleles

Human immunology, 2002-03, Vol.63 (3), p.194-199

2002

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The impact of screening sickle-cell carriers in the general population. A retrospective study in the Paris screening center

Revue d'épidémiologie et de santé publique, 2015-04, Vol.63 (2), p.77-84

2015

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Natural history of the TT virus infection through follow-up of TTV DNA-positive multiple-transfused patients

Blood, 2000, Vol.95 (1), p.347-351

2000

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Incidence of G20210A mutation in severe vaso-occlusive events complicating sickle cell anemia

Blood coagulation & fibrinolysis, 1999-03, Vol.10 (2), p.111-112

1999

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Partial splenectomy in homozygous beta thalassaemia

Archives of disease in childhood, 1990-03, Vol.65 (3), p.304-307

1990

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No evidence for a defect in growth hormone binding to liver membranes in thalassemia major

The journal of clinical endocrinology and metabolism, 1989, Vol.68 (1), p.94-98

1989

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Human T-cell lymphotropic virus type I and II DNA amplification in seropositive and seronegative at-risk individuals

Transfusion (Philadelphia, Pa.), 1993-02, Vol.33 (2), p.106-110

1993

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Red cell kinetics in thalassaemia intermedia: its use for a prospective prognosis

British journal of haematology, 1985-03, Vol.59 (3), p.533-539

1985

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Three-year follow-up of hydroxyurea treatment in severely ill children with sickle cell disease. The French Study Group on Sickle Cell Disease

Journal of pediatric hematology/oncology, 1997-07, Vol.19 (4), p.313

1997

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Prevention and treatment of erectile disorders in sickle cell disease

La revue de medecine interne, 1997, Vol.18 Suppl 1, p.46s

1997

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Cerebrovascular accidents in sickle cell disease. Risk factors and blood transfusion influence. French Study Group on Sickle Cell Disease

European journal of pediatrics, 1993-03, Vol.152 (3), p.201-204

1993

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Lymphadenopathy syndrome in two thalassemic patients after LAV contamination by blood transfusion

The New England journal of medicine, 1985-03, Vol.312 (10), p.648-649

1985

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Hepatitis C associated with Guillain-Barré syndrome

Liver (Copenhagen), 1998-02, Vol.18 (1), p.49-51

1998

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Iron chelation in children

Annales de pediatrie, 1989-10, Vol.36 (8), p.533

1989

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Treatment of homozygote beta thalassemia in Algiers. A 5-year follow-up of 66 patients

La Presse médicale (1983), 1989-05, Vol.18 (20), p.1010-1013

1989

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

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

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

Maternal mortality among women with sickle-cell disease in France, 1996–2009

Persistent B19 infection in immunocompetent individuals: implications for transfusion safety

Sickle cell leg ulcers: a frequently disabling complication and a marker of severity

Polymorphisms in Inflammatory Genes Modulate Clinical Complications in Patients With Sickle Cell Disease

The risk of going abroad in sickle cell disease: a study of 148 adults

Sickle cell disease: from childhood to adult age

Complete or partial seroreversion in immunocompetent individuals after self-limited HCV infection: consequences for transfusion

Infectious complications in sickle cell disease are influenced by HLA class II alleles

The impact of screening sickle-cell carriers in the general population. A retrospective study in the Paris screening center

Natural history of the TT virus infection through follow-up of TTV DNA-positive multiple-transfused patients

Incidence of G20210A mutation in severe vaso-occlusive events complicating sickle cell anemia

Partial splenectomy in homozygous beta thalassaemia

No evidence for a defect in growth hormone binding to liver membranes in thalassemia major

Human T-cell lymphotropic virus type I and II DNA amplification in seropositive and seronegative at-risk individuals

Red cell kinetics in thalassaemia intermedia: its use for a prospective prognosis

Three-year follow-up of hydroxyurea treatment in severely ill children with sickle cell disease. The French Study Group on Sickle Cell Disease

Prevention and treatment of erectile disorders in sickle cell disease

Cerebrovascular accidents in sickle cell disease. Risk factors and blood transfusion influence. French Study Group on Sickle Cell Disease

Lymphadenopathy syndrome in two thalassemic patients after LAV contamination by blood transfusion

Hepatitis C associated with Guillain-Barré syndrome

Iron chelation in children

Treatment of homozygote beta thalassemia in Algiers. A 5-year follow-up of 66 patients

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