D. Bachir

发表

Rare RHCE phenotypes in black individuals of Afro-Caribbean origin: identification and transfusion safety.

F. Noizat‐Pirenne, Ketty Lee, P. Pennec, 2002, Blood.

Gerbich reactivity in 4.1(—) hereditary elliptocytosis and protein 4.1 level in blood group Gerbich deficiency

D. Bachir, J. Cartron, J. Delaunay, 1987, British journal of haematology.

Oral magnesium supplements reduce erythrocyte dehydration in patients with sickle cell disease.

O. Platt, S. Alper, L. De Franceschi, 1997, The Journal of clinical investigation.

Preventive treatment of priapism in sickle cell disease with oral and self-administered intracavernous injection of etilefrine.

D. Bachir, F. Galactéros, R. Virag, 1996, Urology.

A hemodynamic study of pulmonary hypertension in sickle cell disease.

L. Savale, G. Simonneau, D. O’Callaghan, 2011, The New England journal of medicine.

Characteristics and outcome of connective tissue diseases in patients with sickle-cell disease: report of 30 cases.

D. Bachir, F. Galactéros, M. Michel, 2008, Seminars in arthritis and rheumatism.

Genetic and hematological studies in a group of 114 adult patients with SC sickle cell disease

F. Roudot-thoraval, D. Bachir, H. Wajcman, 1998, American journal of hematology.

Factors associated with dyspnea in adult patients with sickle cell disease.

C. Delclaux, J. Monin, D. Bachir, 2005, Chest.

Aggregation of mononuclear and red blood cells through an alpha4beta1-Lu/basal cell adhesion molecule interaction in sickle cell disease

D. Bachir, Y. Colin, F. Galactéros, 2019 .

Aggregation of mononuclear and red blood cells through an α4β1-Lu/basal cell adhesion molecule interaction in sickle cell disease

O. Renaud, D. Bachir, Y. Colin, 2010, Haematologica.

Aggregation of mononuclear and red blood cells through α 4 β 1-Lu / BCAM interaction in sickle cell disease

O. Renaud, D. Bachir, Y. Colin, 2010 .

Estimation of the difference in HbF expression due to loss of the 5 ' d-globin BCL 11 A binding region by Elyes

D. Bachir, F. Galactéros, K. Moradkhani, 2012 .

MRI features of intrahepatic extramedullary haematopoiesis in sickle cell anaemia

A. Luciani, A. Rahmouni, D. Bachir, 2006, Cancer imaging : the official publication of the International Cancer Imaging Society.

Two French Caucasian Families with Dominant Thalassemia-Like Phenotypes Due to Hyper Unstable Hemoglobin Variants: Hb Sainte Seve [Codon 118 (− T)] and Codon 127 [CAG→TAG (Gln→Stop])

D. Bachir, H. Wajcman, F. Galactéros, 2005, Hemoglobin.

[Sickle-cell retinopathy: Retrospective study of 730 patients followed in a referral center].

E. Souied, D. Bachir, F. Galactéros, 2012, Journal francais d'ophtalmologie.

Endothelial dysfunction in patients with sickle cell disease is related to selective impairment of shear stress-mediated vasodilation.

G. Pelle, D. Bachir, F. Galactéros, 2001, Blood.

Resveratrol, a natural dietary phytoalexin, possesses similar properties to hydroxyurea towards erythroid differentiation

P. Romeo, D. Bachir, F. Galactéros, 2001, British journal of haematology.

Bronchoalveolar lavage in adult sickle cell patients with acute chest syndrome: value for diagnostic assessment of fat embolism.

A. Rahmouni, C. Brun-Buisson, F. Lebargy, 1996, American journal of respiratory and critical care medicine.

Patterns of mortality in sickle cell disease in adults in France and England.

F. Roudot-thoraval, D. Bachir, F. Galactéros, 2002, The hematology journal : the official journal of the European Haematology Association.

Transplantation for liver failure in patients with sickle cell disease: Challenging but feasible

J. Calderaro, A. Mallat, E. Zafrani, 2011, Liver transplantation : official publication of the American Association for the Study of Liver Diseases and the International Liver Transplantation Society.

Early intermittent noninvasive ventilation for acute chest syndrome in adults with sickle cell disease: a pilot study

L. Brochard, D. Bachir, F. Galactéros, 2010, Intensive Care Medicine.

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

B. Pégourié, T. Leblanc, C. Berger, 2010, Haematologica.

Induced sputum versus bronchoalveolar lavage during acute chest syndrome in sickle cell disease.

L. Brochard, B. Housset, D. Bachir, 2003, American journal of respiratory and critical care medicine.

Decreased sickle red blood cell adhesion to laminin by hydroxyurea is associated with inhibition of Lu/BCAM protein phosphorylation.

D. Bachir, Y. Colin, F. Galactéros, 2010, Blood.

CD36 deficiency is frequent and can cause platelet immunization in Africans

N. Debili, P. Bierling, D. Bachir, 1999, Transfusion.

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

C. Rieux, F. Pirenne, D. Bachir, 2016, American journal of hematology.

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

D. Bachir, F. Galactéros, P. Girard, 2011, Orphanet journal of rare diseases.

Preliminary report of a toxicity study of hydroxyurea in sickle cell disease

D. Bachir, M. Montalembert, M. de Montalembert, 1999, Archives of disease in childhood.

The natural history of asymptomatic osteonecrosis of the femoral head in adults with sickle cell disease.

D. Bachir, F. Galactéros, P. Hernigou, 2006, The Journal of bone and joint surgery. American volume.

[Study of 206 transfused sickle cell disease patients: immunization, transfusion safety and red blood cell supply].

P. Bierling, F. Noizat‐Pirenne, D. Bachir, 2008, Transfusion clinique et biologique : journal de la Societe francaise de transfusion sanguine.

Prevalence and Mechanism of Pulmonary Hypertension in Sickle Cell Disease: A Prospective Multicentre French Study.

L. Savale, G. Simonneau, D. Bachir, 2009, ATS 2009.

Delayed hemolytic transfusion reaction in sickle cell disease patients: evidence of an emerging syndrome with suicidal red blood cell death

P. Bierling, F. Noizat‐Pirenne, D. Bachir, 2009, Transfusion.

Frozen Blood and Transfusion‐Transmitted Hepatitis C Virus

D. Bachir, F. Galactéros, F. Bernaudin, 1993, Vox sanguinis.

Cerebrovascular accidents in sickle cell disease. Risk factors and blood transfusion influence

D. Bachir, F. Galactéros, M. Montalembert, 1993, European Journal of Pediatrics.

Estimation of the difference in HbF expression due to loss of the 5' δ-globin BCL11A binding region

D. Bachir, F. Galactéros, K. Moradkhani, 2013, Haematologica.

Kinetic alterations of the red cell membrane phosphatase in α‐ and β‐Thalassemia

D. Bachir, J. Delaunay, N. Alloisio, 1982 .

Pulmonary fat embolism after prostaglandin infusion in sickle cell disease with fatal outcome despite exchange blood transfusion

J. Dhainaut, D. Bachir, J. Dhainaut, 1993, American journal of hematology.

Aplastic crisis due to extensive bone marrow necrosis and human parvovirus infection in sickle cell disease.

D. Bachir, F. Galactéros, A. Schaeffer, 1991, The American journal of medicine.

Increased in vivo production of thromboxane in patients with sickle cell disease is accompanied by an impairment of platelet functions to the thromboxane A2 agonist U46619.

J. Maclouf, D. Bachir, F. Galactéros, 1993, Arteriosclerosis and thrombosis : a journal of vascular biology.

Vascular lesions of the liver in sickle cell disease. A clinicopathological study in 26 living patients.

D. Dhumeaux, E. Zafrani, D. Bachir, 1995, Archives of pathology & laboratory medicine.

The Natural History of Symptomatic Osteonecrosis in Adults with Sickle-Cell Disease

D. Bachir, F. Galactéros, P. Hernigou, 2003, The Journal of bone and joint surgery. American volume.

Avascular necrosis of the femoral head in sickle-cell disease. Treatment of collapse by the injection of acrylic cement.

D. Bachir, F. Galactéros, P. Hernigou, 1993, The Journal of bone and joint surgery. British volume.

AVASCULAR NECROSIS OF THE FEMORAL HEAD IN SICKLE-CELL DISEASE

D. Bachir, F. Galactéros, P. Hernigou, 1993 .

Deformities of the hip in adults who have sickle-cell disease and had avascular necrosis in childhood. A natural history of fifty-two patients.

D. Bachir, F. Galactéros, D. Goutallier, 1991, The Journal of bone and joint surgery. American volume.

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

P. Jouannet, D. Bachir, F. Galactéros, 2008, Haematologica.

K+ efflux in deoxygenated sickle cells in the presence or absence of DIOA, a specific inhibitor of the [K+, Cl‐] cotransport system

O. Olivieri, D. Bachir, Y. Beuzard, 1991, British journal of haematology.

The involvement of the Ca-dependent K channel and of the KCl co-transport in sickle cell dehydration during cyclic deoxygenation.

D. Bachir, Y. Beuzard, F. Galactéros, 1994, Biochimica et biophysica acta.

Fate of α‐Hemoglobin Chains and Erythrocyte Defects in β‐Thalassemia a

D. Bachir, P. Rouyer‐Fessard, Y. Beuzard, 1990 .

No effect of CYP450 and P‐glycoprotein on hydroxyurea in vitro metabolism

D. Bachir, F. Galactéros, A. Astier, 2010, Fundamental & clinical pharmacology.

Sickle cell β‐thalassaemia compared with sickle cell anaemia in Algeria

T. Henni, D. Bachir, J. Godet, 2009 .

Clinical Follow-Up of Hydroxyurea-Treated Adults with Sickle Cell Disease

F. Roudot-thoraval, Ketty Lee, D. Bachir, 2010, Acta Haematologica.

[Acute splenic sequestration: a rare and severe complication of sickle cell anemia in adults. A case report].

D. Bachir, F. Galactéros, A. Schaeffer, 2005, La Revue de medecine interne.

Plasma and Urine Hydroxyurea Levels Might be Useful in the Management of Adult Sickle Cell Disease

D. Bachir, F. Galactéros, A. Astier, 2007, Hemoglobin.

Pharmacokinetics of hydroxyurea 1,000 mg coated breakable tablets and 500 mg capsules in pediatric and adult patients with sickle cell disease.

F. Roudot-thoraval, D. Bachir, J. Bresson, 2006, Haematologica.

Pulmonary function in sickle cell disease with or without acute chest syndrome.

G. Atlan, D. Bachir, F. Galactéros, 1998, The European respiratory journal.

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

D. Bachir, R. Girot, F. Lionnet, 2009, American journal of hematology.

Rituximab for prevention of delayed hemolytic transfusion reaction in sickle cell disease

P. Bierling, F. Noizat‐Pirenne, D. Bachir, 2007, Haematologica.

Acute chest syndrome in adults with sickle cell disease.

F. Roudot-thoraval, D. Bachir, F. Galactéros, 2000, Chest.

The nonexpression of CD36 on reticulocytes and mature red blood cells does not modify the clinical course of patients with sickle cell anemia.

P. Gane, F. Roudot-thoraval, P. Bierling, 2001, Blood.

The nonexpression of CD 36 on reticulocytes and mature red blood cells does not modify the clinical course of patients with sickle cell anemia

P. Gane, F. Roudot-thoraval, P. Bierling, 2001 .

A new sickle cell disease phenotype associating Hb S trait, severe pyruvate kinase deficiency (PK Conakry), and an α2 globin gene variant (Hb Conakry)

D. Bachir, H. Wajcman, J. Kister, 1998, British journal of haematology.

Alpha globin gene triplication in severe heterozygous beta thalassemia.

T. Henni, F. Morlé, D. Bachir, 1985, Acta haematologica.

Hemoglobin Variants and Activity of the (K'Cl-) Cotransport System in Human Erythrocytes

O. Olivieri, C. Brugnara, D. Bachir, 1992 .

Hemoglobin variants and activity of the (K+Cl-) cotransport system in human erythrocytes.

O. Olivieri, C. Brugnara, D. Bachir, 1992, Blood.

[Transfusion and alloimmunization in sickle cell anemia patients].

P. Bierling, D. Bachir, F. Galactéros, 1994, Transfusion clinique et biologique : journal de la Societe francaise de transfusion sanguine.

A study of membrane protein defects and alpha hemoglobin chains of red blood cells in human beta thalassemia.

D. Bachir, P. Rouyer‐Fessard, Y. Beuzard, 1989, The Journal of biological chemistry.

Indirect evaluation of a gene frequency: calculation of beta-thalassemia frequency in Algeria based on associated hemoglobin variants frequency.

D. Bachir, V. Nigon, M. Belhani, 1984, Human heredity.

Hemoglobin Bart's in Northern Algeria.

T. Henni, D. Bachir, P. Jurdic, 1981, Acta haematologica.

A randomized, controlled clinical trial of ketoprofen for sickle-cell disease vaso-occlusive crises in adults.

F. Roudot-thoraval, D. Bachir, F. Galactéros, 2009, Blood.

Adverse effect of hydroxyurea on spermatogenesis in patients with sickle cell anemia after 6 months of treatment.

F. Eustache, D. Bachir, F. Galactéros, 2017, Blood.

Abnormalities of the adult shoulder due to sickle cell osteonecrosis during childhood.

D. Bachir, F. Galactéros, P. Hernigou, 1998, Revue du rhumatisme.

[164 epiphyseal necroses (hips, shoulders, knees) in 55 patients with sickle cell anemia. Characteristics, epidemiologic and etiopathogenic aspects].

D. Bachir, F. Galactéros, D. Goutallier, 1989, Revue du rhumatisme et des maladies osteo-articulaires.

Improvement of microcirculation abnormalities in sickle cell patients upon buflomedil treatment.

D. Bachir, Y. Beuzard, F. Galactéros, 1993, Microvascular research.

Pyruvate kinase (PK) deficiency in newborns: the pitfalls of diagnosis.

B. Bader-Meunier, D. Bachir, H. Wajcman, 2007, The Journal of pediatrics.

Bloodstream Infection in Adults With Sickle Cell Disease: Association With Venous Catheters, Staphylococcus aureus, and Bone-Joint Infections

F. Roudot-thoraval, C. Brun-Buisson, J. Zahar, 2006, Medicine.

Severe pneumococcal sepsis and meningitis in human immunodeficiency virus-infected adults with sickle cell disease.

C. Brun-Buisson, D. Bachir, F. Galactéros, 1992, Clinical infectious diseases : an official publication of the Infectious Diseases Society of America.

Sickle‐cell disease stroke throughout life: A retrospective study in an adult referral center

D. Calvet, H. Hosseini, D. Bachir, 2014, American journal of hematology.

A Study of Membrane Protein Defects and a! Hemoglobin Chains of Red Blood Cells in Human ,8 Thalassemia*

D. Bachir, M. Garel, C. Domenget, 2001 .

Prospective Multicentric Survey On Pulmonary Hypertension (PH) in Adults with Sickle Cell Disease.

L. Savale, G. Simonneau, D. Bachir, 2009 .

The heterozygous form of 4.1(-) hereditary elliptocytosis [the 4.1(-) trait].

D. Bachir, O. Gentilhomme, N. Alloisio, 1985, Blood.

Fat emboli unleashed: an exceptional etiology of encephalitis in sickle cell disease

I. Klein, L. Bouadma, B. Régnier, 2008, Annals of Hematology.

Red cell membrane sialoglycoptein β in homozygous and heterozygous 4.1(−) hereditary elliptocytosis

D. Bachir, J. Delaunay, N. Alloisio, 1985 .

Two French Caucasian Families with Dominant Thalassemia-Like Phenotypes Due to Hyper Unstable Hemoglobin Variants: Hb Sainte Seve [Codon 118 (− T)] and Codon 127 [CAG→TAG (Gln→Stop])

D. Bachir, H. Wajcman, F. Galactéros, 2005, Hemoglobin.

Early glomerular dysfunction in patients with sickle cell anemia.

G. Choukroun, J. Grünfeld, B. Lacour, 1998, American journal of kidney diseases : the official journal of the National Kidney Foundation.

Delayed hemolytic transfusion reaction in the French hemovigilance system.

C. Rieux, G. Brittenham, D. Bachir, 2019, Transfusion clinique et biologique : journal de la Societe francaise de transfusion sanguine.

[Hip dysplasia, a complication of sickle cell anemia].

D. Bachir, F. Galactéros, P. Hernigou, 1993, Revue du rhumatisme.

[Acute aseptic arthritis in major sickle cell syndromes].

D. Bachir, F. Galactéros, A. Schaeffer, 1993, Presse medicale.

[Transfusion in sickle cell anemia].

D. Bachir, F. Galactéros, M. Bonnet-Gajdos, 1990, Presse medicale.

Successful combined heart and kidney transplantation in a patient with sickle-cell anemia.

C. Abbou, D. Bachir, P. Grimbert, 2006, The Journal of heart and lung transplantation : the official publication of the International Society for Heart Transplantation.

Socio-psychological impact of infused iron chelation therapy with deferoxamine in metropolitan France: ISOSFER study results

D. Bachir, S. Bisot-Locard, I. Thuret, 2009, Hematology.

Fate of alpha-hemoglobin chains and erythrocyte defects in beta-thalassemia.

D. Bachir, P. Rouyer‐Fessard, Y. Beuzard, 1990, Annals of the New York Academy of Sciences.

A hemodynamic study of pulmonary hypertension in sickle cell disease.

L. Savale, G. Simonneau, D. O’Callaghan, 2011, The New England journal of medicine.

[Natural history of hip necrosis in sickle cell disease. Apropos of 104 necroses].

D. Bachir, F. Galactéros, D. Goutallier, 1989, Revue de chirurgie orthopedique et reparatrice de l'appareil moteur.