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Seminars in Hematology
|
September 26, 2015
Non-immune Hemolysis: Diagnostic Considerations
Photis Beris, Véronique Picard
American Journal of Hematology
|
November 15, 2023
Elevated MCHC reveals a Southeast Asian Ovalocytosis
Maïssa 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 overview
Mohamad El Nabouch, Iarolalao Rakotoharinandrasana, Alexis Ndayikeza, et al.
British Journal of Haematology
|
June 9, 2020
Previously misdiagnosed red cell membrane disorder and familial consequences
Delphine Gérard, Sophie Bourin, Aurélie Phulpin, et al.
Clinical Genetics
|
August 28, 2022
A Gardos channelopathy associated with nonimmune hydrops and fetal loss
Leïla 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 mouse
Sarah 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 experience
Caroline 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 deficiency
Martine Alhenc-Gelas, Genevieve Plu-Bureau, Justine Hugon-Rodin, et al.
Page
of 5
Search research articles
Search
Showing results (1-10 of 49) with videos related to
Sort By:
Page
of 5
Seminars in Hematology
|
September 26, 2015
Non-immune Hemolysis: Diagnostic Considerations
Photis Beris, Véronique Picard
American Journal of Hematology
|
November 15, 2023
Elevated MCHC reveals a Southeast Asian Ovalocytosis
Maïssa 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 overview
Mohamad El Nabouch, Iarolalao Rakotoharinandrasana, Alexis Ndayikeza, et al.
British Journal of Haematology
|
June 9, 2020
Previously misdiagnosed red cell membrane disorder and familial consequences
Delphine Gérard, Sophie Bourin, Aurélie Phulpin, et al.
Clinical Genetics
|
August 28, 2022
A Gardos channelopathy associated with nonimmune hydrops and fetal loss
Leïla 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 mouse
Sarah 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 experience
Caroline 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 deficiency
Martine Alhenc-Gelas, Genevieve Plu-Bureau, Justine Hugon-Rodin, et al.
Page
of 5