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Serge Pissard

Showing results (51-60 of 63) with videos related to

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European Journal of Haematology|July 4, 2018
Inherited or acquired modifiers of iron status may dramatically affect the phenotype in dehydrated hereditary stomatocytosisCorentin Orvain, Lydie Da Costa, Richard Van Wijk, et al.
Blood|December 8, 2010
Pathophysiology of sickle cell disease is mirrored by the red blood cell metabolomeDhouha Darghouth, Bérengère Koehl, Geoffrey Madalinski, et al.
Cancer Research|December 18, 2003
FGFR3 and TP53 gene mutations define two distinct pathways in urothelial cell carcinoma of the bladderAshraf A Bakkar, Herve Wallerand, François Radvanyi, et al.
Human Molecular Genetics|April 10, 2014
Comprehensive functional annotation of 18 missense mutations found in suspected hemochromatosis type 4 patientsIsabelle Callebaut, Rozenn Joubrel, Serge Pissard, et al.
Blood Cells, Molecules & Diseases|April 2, 2025
Comprehensive analysis of sickle β<sup>+</sup>-thalassemia genotypes and their associated HbA levels in FranceCecilia Baltus, Stéphane Moutereau, Nathalie Couque, et al.
European Heart Journal|October 31, 2015
Haematological determinants of cardiac involvement in adults with sickle cell diseaseThibaud Damy, Diane Bodez, Anoosha Habibi, et al.
American Journal of Hematology|April 23, 2026
A Novel Plasma Heme Assay Reveals Disease Severity in Beta-Thalassemia and Sickle Cell AnemiaLaurent Kiger, Nicolas Hebert, Laura Bencheikh, et al.
Orphanet Journal of Rare Diseases|July 10, 2020
Exome sequencing for diagnosis of congenital hemolytic anemiaLamisse Mansour-Hendili, Abdelrazak Aissat, Bouchra Badaoui, et al.
Haematologica|December 7, 2014
A genetic score for the prediction of beta-thalassemia severityFabrice Danjou, Marcella Francavilla, Franco Anni, et al.
American Journal of Hematology|October 26, 2018
Addressing the diagnostic gaps in pyruvate kinase deficiency: Consensus recommendations on the diagnosis of pyruvate kinase deficiencyPaola Bianchi, Elisa Fermo, Bertil Glader, et al.
Pageof 7

Showing results (51-60 of 63) with videos related to

Sort By:
Pageof 7
European Journal of Haematology|July 4, 2018
Inherited or acquired modifiers of iron status may dramatically affect the phenotype in dehydrated hereditary stomatocytosisCorentin Orvain, Lydie Da Costa, Richard Van Wijk, et al.
Blood|December 8, 2010
Pathophysiology of sickle cell disease is mirrored by the red blood cell metabolomeDhouha Darghouth, Bérengère Koehl, Geoffrey Madalinski, et al.
Cancer Research|December 18, 2003
FGFR3 and TP53 gene mutations define two distinct pathways in urothelial cell carcinoma of the bladderAshraf A Bakkar, Herve Wallerand, François Radvanyi, et al.
Human Molecular Genetics|April 10, 2014
Comprehensive functional annotation of 18 missense mutations found in suspected hemochromatosis type 4 patientsIsabelle Callebaut, Rozenn Joubrel, Serge Pissard, et al.
Blood Cells, Molecules & Diseases|April 2, 2025
Comprehensive analysis of sickle β<sup>+</sup>-thalassemia genotypes and their associated HbA levels in FranceCecilia Baltus, Stéphane Moutereau, Nathalie Couque, et al.
European Heart Journal|October 31, 2015
Haematological determinants of cardiac involvement in adults with sickle cell diseaseThibaud Damy, Diane Bodez, Anoosha Habibi, et al.
American Journal of Hematology|April 23, 2026
A Novel Plasma Heme Assay Reveals Disease Severity in Beta-Thalassemia and Sickle Cell AnemiaLaurent Kiger, Nicolas Hebert, Laura Bencheikh, et al.
Orphanet Journal of Rare Diseases|July 10, 2020
Exome sequencing for diagnosis of congenital hemolytic anemiaLamisse Mansour-Hendili, Abdelrazak Aissat, Bouchra Badaoui, et al.
Haematologica|December 7, 2014
A genetic score for the prediction of beta-thalassemia severityFabrice Danjou, Marcella Francavilla, Franco Anni, et al.
American Journal of Hematology|October 26, 2018
Addressing the diagnostic gaps in pyruvate kinase deficiency: Consensus recommendations on the diagnosis of pyruvate kinase deficiencyPaola Bianchi, Elisa Fermo, Bertil Glader, et al.
Pageof 7