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D Bachir

Showing results (21-30 of 70) with videos related to

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Nouvelle Revue Francaise D'Hematologie|January 1, 1990
Congenital sideroblastic anemia without clinical iron overload. A case reportJ M Pignon, J Breton-Gorius, D Bachir, et al.
Biochimica Et Biophysica Acta|February 22, 1994
The involvement of the Ca-dependent K channel and of the KCl co-transport in sickle cell dehydration during cyclic deoxygenationM Apovo, Y Beuzard, F Galacteros, et al.
Chirurgie; Memoires De L'Academie De Chirurgie|January 1, 1997
[Ambulatory treatment and prevention of priapism using alpha-agonists. Apropos of 172 cases]R Virag, D Bachir, J Floresco, et al.
European Journal of Pediatrics|March 1, 1993
Cerebrovascular accidents in sickle cell disease. Risk factors and blood transfusion influence. French Study Group on Sickle Cell DiseaseM de Montalembert, P Beauvais, D Bachir, et al.
Transfusion Clinique Et Biologique : Journal De La Societe Francaise De Transfusion Sanguine|March 27, 2019
Delayed hemolytic transfusion reaction in the French hemovigilance systemC Rieux, G Brittenham, D Bachir, et al.
The European Respiratory Journal|December 24, 1998
Pulmonary function in sickle cell disease with or without acute chest syndromeF Santoli, F Zerah, N Vasile, et al.
Presse Medicale (Paris, France : 1983)|February 22, 2000
[Fatal multiple organ failure in a homozygous sickle cell patient]E Vanhille, B Mégarbane, O Axler, et al.
Biochimica Et Biophysica Acta|June 11, 1985
Red cell membrane sialoglycoprotein beta in homozygous and heterozygous 4.1(-) hereditary elliptocytosisN Alloisio, L Morlé, D Bachir, et al.
Revue De Chirurgie Orthopedique Et Reparatrice De L'Appareil Moteur|January 28, 2005
[Total hip arthroplasty for the treatment of septic hip arthritis in adults with sickle-cell disease]P Hernigou, T Odent, O Manicom, et al.
Acta Haematologica|January 1, 1981
Hemoglobin Bart's in Northern AlgeriaT Henni, D Bachir, P Tabone, et al.
Pageof 7

Showing results (21-30 of 70) with videos related to

Sort By:
Pageof 7
Nouvelle Revue Francaise D'Hematologie|January 1, 1990
Congenital sideroblastic anemia without clinical iron overload. A case reportJ M Pignon, J Breton-Gorius, D Bachir, et al.
Biochimica Et Biophysica Acta|February 22, 1994
The involvement of the Ca-dependent K channel and of the KCl co-transport in sickle cell dehydration during cyclic deoxygenationM Apovo, Y Beuzard, F Galacteros, et al.
Chirurgie; Memoires De L'Academie De Chirurgie|January 1, 1997
[Ambulatory treatment and prevention of priapism using alpha-agonists. Apropos of 172 cases]R Virag, D Bachir, J Floresco, et al.
European Journal of Pediatrics|March 1, 1993
Cerebrovascular accidents in sickle cell disease. Risk factors and blood transfusion influence. French Study Group on Sickle Cell DiseaseM de Montalembert, P Beauvais, D Bachir, et al.
Transfusion Clinique Et Biologique : Journal De La Societe Francaise De Transfusion Sanguine|March 27, 2019
Delayed hemolytic transfusion reaction in the French hemovigilance systemC Rieux, G Brittenham, D Bachir, et al.
The European Respiratory Journal|December 24, 1998
Pulmonary function in sickle cell disease with or without acute chest syndromeF Santoli, F Zerah, N Vasile, et al.
Presse Medicale (Paris, France : 1983)|February 22, 2000
[Fatal multiple organ failure in a homozygous sickle cell patient]E Vanhille, B Mégarbane, O Axler, et al.
Biochimica Et Biophysica Acta|June 11, 1985
Red cell membrane sialoglycoprotein beta in homozygous and heterozygous 4.1(-) hereditary elliptocytosisN Alloisio, L Morlé, D Bachir, et al.
Revue De Chirurgie Orthopedique Et Reparatrice De L'Appareil Moteur|January 28, 2005
[Total hip arthroplasty for the treatment of septic hip arthritis in adults with sickle-cell disease]P Hernigou, T Odent, O Manicom, et al.
Acta Haematologica|January 1, 1981
Hemoglobin Bart's in Northern AlgeriaT Henni, D Bachir, P Tabone, et al.
Pageof 7