Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

D Bachir

Showing results (61-70 of 70) with videos related to

Pageof 7
Sort By:
You have reached the last page of results.This site can display upto 70 results.
British Journal of Haematology|January 1, 1987
Gerbich reactivity in 4.1 (-) hereditary elliptocytosis and protein 4.1 level in blood group Gerbich deficiencyD Sondag, N Alloisio, D Blanchard, et al.
Transfusion Clinique Et Biologique : Journal De La Societe Francaise De Transfusion Sanguine|January 1, 1994
[Transfusion and alloimmunization in sickle cell anemia patients]F Norol, J Nadjahi, D Bachir, et al.
Nouvelle Revue Francaise D'Hematologie|January 1, 1988
A case of sickle cell anemia with severe infection, transfusion inefficiency and transient sideroblastic anemiaD Bachir, Y Beuzard, C Desaint, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|August 26, 1998
Early glomerular dysfunction in patients with sickle cell anemiaF Schmitt, F Martinez, G Brillet, et al.
Transfusion|September 30, 1999
CD36 deficiency is frequent and can cause platelet immunization in AfricansK Lee, B Godeau, P Fromont, et al.
British Journal of Haematology|January 14, 1999
A new sickle cell disease phenotype associating Hb S trait, severe pyruvate kinase deficiency (PK Conakry), and an alpha2 globin gene variant (Hb Conakry)M Cohen-Solal, C Préhu, H Wajcman, et al.
Transfusion Clinique Et Biologique : Journal De La Societe Francaise De Transfusion Sanguine|November 26, 2008
[Study of 206 transfused sickle cell disease patients: immunization, transfusion safety and red blood cell supply]N Meunier, M Rodet, P Bonin, et al.
La Revue De Medecine Interne|September 28, 2015
[Symptomatic extramedullary haematopoiesis in β-thalassemia: A retrospective single centre study]F Maazoun, J Gellen Dautremer, A Boutekadjirt, et al.
American Journal of Respiratory and Critical Care Medicine|May 1, 1996
Bronchoalveolar lavage in adult sickle cell patients with acute chest syndrome: value for diagnostic assessment of fat embolismB Godeau, A Schaeffer, D Bachir, et al.
European Journal of Haematology|April 25, 2000
Iron overload in thalassaemias and genetic haemochromatosisP Aguilar-Martinez, J F Schved, C Badens, et al.
Pageof 7

Showing results (61-70 of 70) with videos related to

Sort By:
Pageof 7
You have reached the last page of results.This site can display upto 70 results.
British Journal of Haematology|January 1, 1987
Gerbich reactivity in 4.1 (-) hereditary elliptocytosis and protein 4.1 level in blood group Gerbich deficiencyD Sondag, N Alloisio, D Blanchard, et al.
Transfusion Clinique Et Biologique : Journal De La Societe Francaise De Transfusion Sanguine|January 1, 1994
[Transfusion and alloimmunization in sickle cell anemia patients]F Norol, J Nadjahi, D Bachir, et al.
Nouvelle Revue Francaise D'Hematologie|January 1, 1988
A case of sickle cell anemia with severe infection, transfusion inefficiency and transient sideroblastic anemiaD Bachir, Y Beuzard, C Desaint, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|August 26, 1998
Early glomerular dysfunction in patients with sickle cell anemiaF Schmitt, F Martinez, G Brillet, et al.
Transfusion|September 30, 1999
CD36 deficiency is frequent and can cause platelet immunization in AfricansK Lee, B Godeau, P Fromont, et al.
British Journal of Haematology|January 14, 1999
A new sickle cell disease phenotype associating Hb S trait, severe pyruvate kinase deficiency (PK Conakry), and an alpha2 globin gene variant (Hb Conakry)M Cohen-Solal, C Préhu, H Wajcman, et al.
Transfusion Clinique Et Biologique : Journal De La Societe Francaise De Transfusion Sanguine|November 26, 2008
[Study of 206 transfused sickle cell disease patients: immunization, transfusion safety and red blood cell supply]N Meunier, M Rodet, P Bonin, et al.
La Revue De Medecine Interne|September 28, 2015
[Symptomatic extramedullary haematopoiesis in β-thalassemia: A retrospective single centre study]F Maazoun, J Gellen Dautremer, A Boutekadjirt, et al.
American Journal of Respiratory and Critical Care Medicine|May 1, 1996
Bronchoalveolar lavage in adult sickle cell patients with acute chest syndrome: value for diagnostic assessment of fat embolismB Godeau, A Schaeffer, D Bachir, et al.
European Journal of Haematology|April 25, 2000
Iron overload in thalassaemias and genetic haemochromatosisP Aguilar-Martinez, J F Schved, C Badens, et al.
Pageof 7