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Serge Pissard

Showing results (21-30 of 63) with videos related to

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Annales De Biologie Clinique|November 17, 2016
Clinical and biological specificity of beta-thalassemia intermedia: a case reportJean-Maxime Girard, Guillaume Drevin, Jean-François Brasme, et al.
The Journal of Pediatrics|March 27, 2007
Pyruvate kinase (PK) deficiency in newborns: the pitfalls of diagnosisSerge Pissard, Mariane de Montalembert, Dora Bachir, et al.
American Journal of Hematology|August 1, 2007
A novel mutation of the beta-globin gene promoter (-102 C>A) and pitfalls in family screeningPatricia Aguilar-Martinez, Eric Jourdan, Sophie Brun, et al.
Transfusion|September 21, 2007
Decreased transfusion needs associated with hydroxyurea therapy in Algerian patients with thalassemia major or intermediaMohamed Bradai, Serge Pissard, Mohand Tayeb Abad, et al.
Hemoglobin|July 21, 2010
Identification of a new mutation on the beta-globin gene: codons 8/9 (+AGAA); GAG.AAG.TCT(Glu-Lys-Ser)>GAG. AAAGAAG, in a patient from the north of France with a phenotype of beta-thalassemia minorAnne France Georgel, Claude Méreau, Christophe Willekens, et al.
Haematologica|July 18, 2012
Estimation of the difference in HbF expression due to loss of the 5' δ-globin BCL11A binding regionElyes Slim Ghedira, Laure Lecerf, Emmanuelle Faubert, et al.
European Journal of Haematology|December 5, 2012
A novel epsilon gamma delta beta thalassemia presenting with pregnancy complications and severe neonatal anemiaHanna Shalev, Daniela Landau, Serge Pissard, et al.
BMC Pediatrics|June 22, 2020
High fetal hemoglobin level is associated with increased risk of cerebral vasculopathy in children with sickle cell disease in MayotteAbdourahim Chamouine, Thoueiba Saandi, Mathias Muszlak, et al.
Hematology (Amsterdam, Netherlands)|December 6, 2008
Sickle cell disease in a carrier with pyruvate kinase deficiencyNazeer Alli, Marius Coetzee, Vernon Louw, et al.
Hemoglobin|September 16, 2014
Characterization of two unique α-globin gene cluster deletions causing α-thalassemia in Israeli ArabsOded Gilad, Orly Dgany, Sharon Noy-Lotan, et al.
Pageof 7

Showing results (21-30 of 63) with videos related to

Sort By:
Pageof 7
Annales De Biologie Clinique|November 17, 2016
Clinical and biological specificity of beta-thalassemia intermedia: a case reportJean-Maxime Girard, Guillaume Drevin, Jean-François Brasme, et al.
The Journal of Pediatrics|March 27, 2007
Pyruvate kinase (PK) deficiency in newborns: the pitfalls of diagnosisSerge Pissard, Mariane de Montalembert, Dora Bachir, et al.
American Journal of Hematology|August 1, 2007
A novel mutation of the beta-globin gene promoter (-102 C>A) and pitfalls in family screeningPatricia Aguilar-Martinez, Eric Jourdan, Sophie Brun, et al.
Transfusion|September 21, 2007
Decreased transfusion needs associated with hydroxyurea therapy in Algerian patients with thalassemia major or intermediaMohamed Bradai, Serge Pissard, Mohand Tayeb Abad, et al.
Hemoglobin|July 21, 2010
Identification of a new mutation on the beta-globin gene: codons 8/9 (+AGAA); GAG.AAG.TCT(Glu-Lys-Ser)>GAG. AAAGAAG, in a patient from the north of France with a phenotype of beta-thalassemia minorAnne France Georgel, Claude Méreau, Christophe Willekens, et al.
Haematologica|July 18, 2012
Estimation of the difference in HbF expression due to loss of the 5' δ-globin BCL11A binding regionElyes Slim Ghedira, Laure Lecerf, Emmanuelle Faubert, et al.
European Journal of Haematology|December 5, 2012
A novel epsilon gamma delta beta thalassemia presenting with pregnancy complications and severe neonatal anemiaHanna Shalev, Daniela Landau, Serge Pissard, et al.
BMC Pediatrics|June 22, 2020
High fetal hemoglobin level is associated with increased risk of cerebral vasculopathy in children with sickle cell disease in MayotteAbdourahim Chamouine, Thoueiba Saandi, Mathias Muszlak, et al.
Hematology (Amsterdam, Netherlands)|December 6, 2008
Sickle cell disease in a carrier with pyruvate kinase deficiencyNazeer Alli, Marius Coetzee, Vernon Louw, et al.
Hemoglobin|September 16, 2014
Characterization of two unique α-globin gene cluster deletions causing α-thalassemia in Israeli ArabsOded Gilad, Orly Dgany, Sharon Noy-Lotan, et al.
Pageof 7