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

Marc Romana

Showing results (21-30 of 108) with videos related to

Pageof 11
Sort By:
American Journal of Hematology|August 30, 2012
Increased blood viscosity and red blood cell aggregation in a patient with sickle cell anemia and smoldering myelomaNathalie Lemonne, Philippe Connes, Marc Romana, et al.
Plos One|January 26, 2013
Survey of Naegleria fowleri in geothermal recreational waters of Guadeloupe (French West Indies)Mirna Moussa, Johan F De Jonckheere, Jérôme Guerlotté, et al.
American Journal of Hematology|April 22, 2006
UGT1A1 polymorphism outweighs the modest effect of deletional (-3.7 kb) alpha-thalassemia on cholelithogenesis in sickle cell anemiaVicky Chaar, Lysiane Kéclard, Maryse Etienne-Julan, et al.
British Journal of Haematology|April 24, 2014
Effects of oxidative stress on red blood cell rheology in sickle cell patientsRégine Hierso, Xavier Waltz, Pierre Mora, et al.
Haematologica|February 16, 2005
Association of UGT1A1 polymorphism with prevalence and age at onset of cholelithiasis in sickle cell anemiaVicky Chaar, Lysiane Kéclard, Jean Pierre Diara, et al.
Journal of Sport and Health Science|December 14, 2020
Does endurance training improve red blood cell aging and hemorheology in moderate-trained healthy individuals?Daniel A Bizjak, Fabian Tomschi, Gunnar Bales, et al.
Hemoglobin|June 8, 2010
Phenotypic expression and origin of the rare beta-thalassemia splice site mutation HBB:c.315 + 1G>TCédrick Broquere, Karine Brudey, Cornelis L Harteveld, et al.
American Journal of Human Biology : the Official Journal of the Human Biology Council|February 8, 2008
Beta-globin gene cluster haplotypes and alpha-thalassemia in sickle cell disease patients from TrinidadAltheia Jones-Lecointe, Erskine Smith, Marc Romana, et al.
Clinical Hemorheology and Microcirculation|March 13, 2013
Exercise-related complications in sickle cell traitJulien Tripette, Marie-Dominique Hardy-Dessources, Marc Romana, et al.
Clinical Immunology (Orlando, Fla.)|March 30, 2010
Association between Duffy antigen receptor for chemokines expression and levels of inflammation markers in sickle cell anemia patientsDanitza Nebor, Marie Claude Durpes, Danielle Mougenel, et al.
Pageof 11

Showing results (21-30 of 108) with videos related to

Sort By:
Pageof 11
American Journal of Hematology|August 30, 2012
Increased blood viscosity and red blood cell aggregation in a patient with sickle cell anemia and smoldering myelomaNathalie Lemonne, Philippe Connes, Marc Romana, et al.
Plos One|January 26, 2013
Survey of Naegleria fowleri in geothermal recreational waters of Guadeloupe (French West Indies)Mirna Moussa, Johan F De Jonckheere, Jérôme Guerlotté, et al.
American Journal of Hematology|April 22, 2006
UGT1A1 polymorphism outweighs the modest effect of deletional (-3.7 kb) alpha-thalassemia on cholelithogenesis in sickle cell anemiaVicky Chaar, Lysiane Kéclard, Maryse Etienne-Julan, et al.
British Journal of Haematology|April 24, 2014
Effects of oxidative stress on red blood cell rheology in sickle cell patientsRégine Hierso, Xavier Waltz, Pierre Mora, et al.
Haematologica|February 16, 2005
Association of UGT1A1 polymorphism with prevalence and age at onset of cholelithiasis in sickle cell anemiaVicky Chaar, Lysiane Kéclard, Jean Pierre Diara, et al.
Journal of Sport and Health Science|December 14, 2020
Does endurance training improve red blood cell aging and hemorheology in moderate-trained healthy individuals?Daniel A Bizjak, Fabian Tomschi, Gunnar Bales, et al.
Hemoglobin|June 8, 2010
Phenotypic expression and origin of the rare beta-thalassemia splice site mutation HBB:c.315 + 1G>TCédrick Broquere, Karine Brudey, Cornelis L Harteveld, et al.
American Journal of Human Biology : the Official Journal of the Human Biology Council|February 8, 2008
Beta-globin gene cluster haplotypes and alpha-thalassemia in sickle cell disease patients from TrinidadAltheia Jones-Lecointe, Erskine Smith, Marc Romana, et al.
Clinical Hemorheology and Microcirculation|March 13, 2013
Exercise-related complications in sickle cell traitJulien Tripette, Marie-Dominique Hardy-Dessources, Marc Romana, et al.
Clinical Immunology (Orlando, Fla.)|March 30, 2010
Association between Duffy antigen receptor for chemokines expression and levels of inflammation markers in sickle cell anemia patientsDanitza Nebor, Marie Claude Durpes, Danielle Mougenel, et al.
Pageof 11