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Véronique Picard

Showing results (1-10 of 49) with videos related to

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Seminars in Hematology|September 26, 2015
Non-immune Hemolysis: Diagnostic ConsiderationsPhotis Beris, Véronique Picard
American Journal of Hematology|November 15, 2023
Elevated MCHC reveals a Southeast Asian OvalocytosisMaïssa Souissi, Sylvie Daliphard, Véronique Picard, et al.
Clinical Case Reports|August 15, 2015
Infantile pyknocytosis, a rare cause of hemolytic anemia in newborns: report of two cases in twin girls and literature overviewMohamad El Nabouch, Iarolalao Rakotoharinandrasana, Alexis Ndayikeza, et al.
British Journal of Haematology|June 9, 2020
Previously misdiagnosed red cell membrane disorder and familial consequencesDelphine Gérard, Sophie Bourin, Aurélie Phulpin, et al.
Clinical Genetics|August 28, 2022
A Gardos channelopathy associated with nonimmune hydrops and fetal lossLeïla Ghesh, Thomas Besnard, Madeleine Joubert, et al.
Medecine Sciences : M/S|November 15, 2006
[Coagulation factor mutations and thrombosis]Martine Aiach, Martine Alhenc-Gelas, Delphine Borgel, et al.
European Journal of Pharmaceutical Sciences : Official Journal of the European Federation for Pharmaceutical Sciences|November 3, 2005
Interactions between the dopamine agonist, bromocriptine and the efflux protein, P-glycoprotein at the blood-brain barrier in the mouseSarah Vautier, Lucette Lacomblez, Hélène Chacun, et al.
Blood|September 21, 2007
Antithrombin Cambridge II (A384S): prevalence in patients of the Paris Thrombosis Study (PATHROS)Véronique Picard, Isabelle Présot, Pierre-Yves Scarabin, et al.
Haematologica|December 4, 2012
Testing for hereditary spherocytosis: a French experienceCaroline Mayeur-Rousse, Mélanie Gentil, Jérémie Botton, et al.
Thrombosis and Haemostasis|March 17, 2017
Thrombotic risk according to SERPINC1 genotype in a large cohort of subjects with antithrombin inherited deficiencyMartine Alhenc-Gelas, Genevieve Plu-Bureau, Justine Hugon-Rodin, et al.
Pageof 5

Showing results (1-10 of 49) with videos related to

Sort By:
Pageof 5
Seminars in Hematology|September 26, 2015
Non-immune Hemolysis: Diagnostic ConsiderationsPhotis Beris, Véronique Picard
American Journal of Hematology|November 15, 2023
Elevated MCHC reveals a Southeast Asian OvalocytosisMaïssa Souissi, Sylvie Daliphard, Véronique Picard, et al.
Clinical Case Reports|August 15, 2015
Infantile pyknocytosis, a rare cause of hemolytic anemia in newborns: report of two cases in twin girls and literature overviewMohamad El Nabouch, Iarolalao Rakotoharinandrasana, Alexis Ndayikeza, et al.
British Journal of Haematology|June 9, 2020
Previously misdiagnosed red cell membrane disorder and familial consequencesDelphine Gérard, Sophie Bourin, Aurélie Phulpin, et al.
Clinical Genetics|August 28, 2022
A Gardos channelopathy associated with nonimmune hydrops and fetal lossLeïla Ghesh, Thomas Besnard, Madeleine Joubert, et al.
Medecine Sciences : M/S|November 15, 2006
[Coagulation factor mutations and thrombosis]Martine Aiach, Martine Alhenc-Gelas, Delphine Borgel, et al.
European Journal of Pharmaceutical Sciences : Official Journal of the European Federation for Pharmaceutical Sciences|November 3, 2005
Interactions between the dopamine agonist, bromocriptine and the efflux protein, P-glycoprotein at the blood-brain barrier in the mouseSarah Vautier, Lucette Lacomblez, Hélène Chacun, et al.
Blood|September 21, 2007
Antithrombin Cambridge II (A384S): prevalence in patients of the Paris Thrombosis Study (PATHROS)Véronique Picard, Isabelle Présot, Pierre-Yves Scarabin, et al.
Haematologica|December 4, 2012
Testing for hereditary spherocytosis: a French experienceCaroline Mayeur-Rousse, Mélanie Gentil, Jérémie Botton, et al.
Thrombosis and Haemostasis|March 17, 2017
Thrombotic risk according to SERPINC1 genotype in a large cohort of subjects with antithrombin inherited deficiencyMartine Alhenc-Gelas, Genevieve Plu-Bureau, Justine Hugon-Rodin, et al.
Pageof 5