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Jacques Elion

Showing results (41-50 of 69) with videos related to

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Hematology (Amsterdam, Netherlands)|February 24, 2017
Haemoglobin F, A2, and S levels in subjects with or without sickle cell trait in south-eastern GabonLandry-Erik Mombo, Gaël Mabioko-Mbembo, Roland-Fabrice Kassa-Kassa, et al.
Haematologica|February 14, 2013
Fetal hemoglobin and hydroxycarbamide moduate both plasma concentration and cellular origin of circulating microparticles in sickle cell anemia childrenDanitza Nébor, Marc Romana, Raoul Santiago, et al.
Blood Cells, Molecules & Diseases|September 14, 2010
Strong association between a new marker of hemolysis and glomerulopathy in sickle cell anemiaMicheline Maier-Redelsperger, Pierre Lévy, François Lionnet, et al.
American Journal of Hematology|June 30, 2004
Angiotensinogen gene associated polymorphisms and risk of stroke in sickle cell anemia: Additional data supporting an associationMarc Romana, Jean-Pierre Diara, Lydia Doumbo, et al.
Scientific Reports|May 5, 2017
Heterozygous HbAC but not HbAS is associated with higher newborn birthweight among women with pregnancy-associated malariaMarilou Tétard, Jacqueline Milet, Sébastien Dechavanne, et al.
Annales De Biologie Clinique|July 24, 2010
[Flowcharts for the diagnosis and the molecular characterization of hemoglobinopathies]Patricia Aguilar-Martinez, Catherine Badens, Nathalie Bonello-Palot, et al.
British Journal of Haematology|October 15, 2013
Impact of glucose-6-phosphate dehydrogenase deficiency on sickle cell anaemia expression in infancy and early childhood: a prospective studyMalika Benkerrou, Corinne Alberti, Nathalie Couque, et al.
British Journal of Haematology|November 24, 2018
New insights into red cell rheology and adhesion in patients with sickle cell anaemia during vaso-occlusive crisesClaudine Lapoumeroulie, Philippe Connes, Sara El Hoss, et al.
Human Pathology|January 26, 2005
The placental-umbilical unit in sickle cell disease pregnancy: a model for studying in vivo functional adjustments to hypoxia in humansPaul Trampont, Martine Roudier, Anne-Marie Andrea, et al.
Plos One|May 5, 2016
Men with Sickle Cell Anemia and Priapism Exhibit Increased Hemolytic Rate, Decreased Red Blood Cell Deformability and Increased Red Blood Cell Aggregate StrengthKizzy-Clara Cita, Laurent Brureau, Nathalie Lemonne, et al.
Pageof 7

Showing results (41-50 of 69) with videos related to

Sort By:
Pageof 7
Hematology (Amsterdam, Netherlands)|February 24, 2017
Haemoglobin F, A2, and S levels in subjects with or without sickle cell trait in south-eastern GabonLandry-Erik Mombo, Gaël Mabioko-Mbembo, Roland-Fabrice Kassa-Kassa, et al.
Haematologica|February 14, 2013
Fetal hemoglobin and hydroxycarbamide moduate both plasma concentration and cellular origin of circulating microparticles in sickle cell anemia childrenDanitza Nébor, Marc Romana, Raoul Santiago, et al.
Blood Cells, Molecules & Diseases|September 14, 2010
Strong association between a new marker of hemolysis and glomerulopathy in sickle cell anemiaMicheline Maier-Redelsperger, Pierre Lévy, François Lionnet, et al.
American Journal of Hematology|June 30, 2004
Angiotensinogen gene associated polymorphisms and risk of stroke in sickle cell anemia: Additional data supporting an associationMarc Romana, Jean-Pierre Diara, Lydia Doumbo, et al.
Scientific Reports|May 5, 2017
Heterozygous HbAC but not HbAS is associated with higher newborn birthweight among women with pregnancy-associated malariaMarilou Tétard, Jacqueline Milet, Sébastien Dechavanne, et al.
Annales De Biologie Clinique|July 24, 2010
[Flowcharts for the diagnosis and the molecular characterization of hemoglobinopathies]Patricia Aguilar-Martinez, Catherine Badens, Nathalie Bonello-Palot, et al.
British Journal of Haematology|October 15, 2013
Impact of glucose-6-phosphate dehydrogenase deficiency on sickle cell anaemia expression in infancy and early childhood: a prospective studyMalika Benkerrou, Corinne Alberti, Nathalie Couque, et al.
British Journal of Haematology|November 24, 2018
New insights into red cell rheology and adhesion in patients with sickle cell anaemia during vaso-occlusive crisesClaudine Lapoumeroulie, Philippe Connes, Sara El Hoss, et al.
Human Pathology|January 26, 2005
The placental-umbilical unit in sickle cell disease pregnancy: a model for studying in vivo functional adjustments to hypoxia in humansPaul Trampont, Martine Roudier, Anne-Marie Andrea, et al.
Plos One|May 5, 2016
Men with Sickle Cell Anemia and Priapism Exhibit Increased Hemolytic Rate, Decreased Red Blood Cell Deformability and Increased Red Blood Cell Aggregate StrengthKizzy-Clara Cita, Laurent Brureau, Nathalie Lemonne, et al.
Pageof 7