Search research articles
Contact Us
Filters
Showing results (21-30 of 63) with videos related to
Page
of 7
Sort By:
Annales De Biologie Clinique
|
November 17, 2016
Clinical and biological specificity of beta-thalassemia intermedia: a case report
Jean-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 diagnosis
Serge 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 screening
Patricia 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 intermedia
Mohamed 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 minor
Anne 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 region
Elyes 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 anemia
Hanna 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 Mayotte
Abdourahim Chamouine, Thoueiba Saandi, Mathias Muszlak, et al.
Hematology (Amsterdam, Netherlands)
|
December 6, 2008
Sickle cell disease in a carrier with pyruvate kinase deficiency
Nazeer 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 Arabs
Oded Gilad, Orly Dgany, Sharon Noy-Lotan, et al.
Page
of 7
Search research articles
Search
Showing results (21-30 of 63) with videos related to
Sort By:
Page
of 7
Annales De Biologie Clinique
|
November 17, 2016
Clinical and biological specificity of beta-thalassemia intermedia: a case report
Jean-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 diagnosis
Serge 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 screening
Patricia 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 intermedia
Mohamed 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 minor
Anne 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 region
Elyes 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 anemia
Hanna 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 Mayotte
Abdourahim Chamouine, Thoueiba Saandi, Mathias Muszlak, et al.
Hematology (Amsterdam, Netherlands)
|
December 6, 2008
Sickle cell disease in a carrier with pyruvate kinase deficiency
Nazeer 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 Arabs
Oded Gilad, Orly Dgany, Sharon Noy-Lotan, et al.
Page
of 7