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

Dominique Labie

Showing results (41-50 of 50) with videos related to

Pageof 5
Sort By:
You have reached the last page of results.This site can display upto 50 results.
Medecine Sciences : M/S|November 13, 2014
[Sickle cell disease: pneumococcus escapes prevention and adapts to the disease. Consequences on vaccine design]Dominique Labie, Jacques Elion
Medecine Sciences : M/S|May 26, 2011
[Thalassemia: therapeutic hopes carried by hepcidin]Sophie Vaulont, Dominique Labie
Medecine Sciences : M/S|February 6, 2010
[Update on RNA splicing repair: applications to beta thalassemia and other perspectives]Dominique Labie, Jean-Claude Kaplan
Medecine Sciences : M/S|May 31, 2012
[Malaria: is there a role for the iron-hepcidin axis?]Sophie Vaulont, Laurent Rénia, Dominique Labie
Blood Cells, Molecules & Diseases|June 30, 2004
Automated analysis of mature red blood cells and reticulocytes in SS and SC diseaseMicheline Maier-Redelsperger, Antoine Flahault, Maria Grazia Neonato, et al.
Hemoglobin|February 12, 2009
Molecular heterogeneity of beta-thalassemia in Algeria: how to face up to a major health problemNassima Boudrahem-Addour, Nadia Zidani, Nathalie Carion, et al.
Hemoglobin|June 20, 2013
Annotated definition of BCL11A and HMIP-2 haplotypes through the analysis of sicilian β-thalassemia patients with high levels of fetal hemoglobinMaria A Buccheri, Sonia Spina, Concetta Ruberto, et al.
Haematologica|October 14, 2003
Asymptomatic and mild beta-thalassemia in homozygotes and compound heterozygotes for the IVS2+1G-->A mutation: role of the beta-globin gene haplotypeAngela Ragusa, Silvestra Amata, Turi Lombardo, et al.
Human Immunology|March 2, 2002
Infectious complications in sickle cell disease are influenced by HLA class II allelesRyad Tamouza, Maria Grazia Neonato, Marc Busson, et al.
Human Immunology|October 27, 2007
HLA-E*0101 allele in homozygous state favors severe bacterial infections in sickle cell anemiaRyad Tamouza, Marc Busson, Catherine Fortier, et al.
Pageof 5

Showing results (41-50 of 50) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 50 results.
Medecine Sciences : M/S|November 13, 2014
[Sickle cell disease: pneumococcus escapes prevention and adapts to the disease. Consequences on vaccine design]Dominique Labie, Jacques Elion
Medecine Sciences : M/S|May 26, 2011
[Thalassemia: therapeutic hopes carried by hepcidin]Sophie Vaulont, Dominique Labie
Medecine Sciences : M/S|February 6, 2010
[Update on RNA splicing repair: applications to beta thalassemia and other perspectives]Dominique Labie, Jean-Claude Kaplan
Medecine Sciences : M/S|May 31, 2012
[Malaria: is there a role for the iron-hepcidin axis?]Sophie Vaulont, Laurent Rénia, Dominique Labie
Blood Cells, Molecules & Diseases|June 30, 2004
Automated analysis of mature red blood cells and reticulocytes in SS and SC diseaseMicheline Maier-Redelsperger, Antoine Flahault, Maria Grazia Neonato, et al.
Hemoglobin|February 12, 2009
Molecular heterogeneity of beta-thalassemia in Algeria: how to face up to a major health problemNassima Boudrahem-Addour, Nadia Zidani, Nathalie Carion, et al.
Hemoglobin|June 20, 2013
Annotated definition of BCL11A and HMIP-2 haplotypes through the analysis of sicilian β-thalassemia patients with high levels of fetal hemoglobinMaria A Buccheri, Sonia Spina, Concetta Ruberto, et al.
Haematologica|October 14, 2003
Asymptomatic and mild beta-thalassemia in homozygotes and compound heterozygotes for the IVS2+1G-->A mutation: role of the beta-globin gene haplotypeAngela Ragusa, Silvestra Amata, Turi Lombardo, et al.
Human Immunology|March 2, 2002
Infectious complications in sickle cell disease are influenced by HLA class II allelesRyad Tamouza, Maria Grazia Neonato, Marc Busson, et al.
Human Immunology|October 27, 2007
HLA-E*0101 allele in homozygous state favors severe bacterial infections in sickle cell anemiaRyad Tamouza, Marc Busson, Catherine Fortier, et al.
Pageof 5