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A Stamoulakatou

Showing results (1-10 of 20) with videos related to

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The Hematology Journal : the Official Journal of the European Haematology Association|March 29, 2002
Increased erythropoietin level induced by hydroxyurea treatment of sickle cell patientsI Papassotiriou, E Voskaridou, A Stamoulakatou, et al.
Pediatric Hematology and Oncology|July 1, 1997
Tissue oxygenation in patients with hemoglobinopathy HI Papassotiriou, E Kanavakis, A Stamoulakatou, et al.
Pediatric Hematology and Oncology|September 17, 2005
Glucose-6-phosphate dehydrogenase deficiency and Gilbert syndrome: a gene interaction underlies severe jaundice without severe hemolysisP Nicolaidou, S Kostaridou, A Mavri, et al.
Haematologica|July 17, 2001
Valproic acid, trichostatin and their combination with hemin preferentially enhance gamma-globin gene expression in human erythroid liquid culturesP Marianna, P Kollia, S Akel, et al.
Journal of Pediatric Hematology/Oncology|December 18, 1998
Erythroid marrow activity and hemoglobin H levels in hemoglobin H diseaseI Papassotiriou, J Traeger-Synodinos, E Kanavakis, et al.
Haematologica|April 28, 2001
Erythroid marrow activity and functional anemia in patients with the rare interaction of a single functional a-globin and beta-globin geneJ Traeger-Synodinos, I Papassotiriou, C Vrettou, et al.
Blood Cells, Molecules & Diseases|October 24, 2000
Distinct phenotypic expression associated with a new hyperunstable alpha globin variant (Hb heraklion, alpha1cd37(C2)Pro>0): comparison to other alpha-thalassemic hemoglobinopathiesJ Traeger-Synodinos, I Papassotiriou, A Metaxotou-Mavrommati, et al.
Hemoglobin|September 18, 1999
Rapid and accurate quantitation of Hb Bart's and Hb H using weak cation exchange high performance liquid chromatography: correlation with the alpha-thalassemia genotypeI Papassotiriou, J Traeger-Synodinos, C Vlachou, et al.
European Journal of Clinical Nutrition|July 1, 2004
Effect of iron supplementation on cognition in Greek preschoolersE Metallinos-Katsaras, E Valassi-Adam, K G Dewey, et al.
Hemoglobin|November 24, 1999
Interaction of an alpha(+)-thalassemia deletion with either a highly unstable alpha-globin variant (alpha2, codon 59, GGC-->GAC) or a nondeletional alpha-thalassemia mutation (AATAAA-->AATAAG): comparison of phenotypes illustrating "dominant" alpha-thalassemiaJ Traeger-Synodinos, A Metaxotou-Mavrommati, M Karagiorga, et al.
Pageof 2

Showing results (1-10 of 20) with videos related to

Sort By:
Pageof 2
The Hematology Journal : the Official Journal of the European Haematology Association|March 29, 2002
Increased erythropoietin level induced by hydroxyurea treatment of sickle cell patientsI Papassotiriou, E Voskaridou, A Stamoulakatou, et al.
Pediatric Hematology and Oncology|July 1, 1997
Tissue oxygenation in patients with hemoglobinopathy HI Papassotiriou, E Kanavakis, A Stamoulakatou, et al.
Pediatric Hematology and Oncology|September 17, 2005
Glucose-6-phosphate dehydrogenase deficiency and Gilbert syndrome: a gene interaction underlies severe jaundice without severe hemolysisP Nicolaidou, S Kostaridou, A Mavri, et al.
Haematologica|July 17, 2001
Valproic acid, trichostatin and their combination with hemin preferentially enhance gamma-globin gene expression in human erythroid liquid culturesP Marianna, P Kollia, S Akel, et al.
Journal of Pediatric Hematology/Oncology|December 18, 1998
Erythroid marrow activity and hemoglobin H levels in hemoglobin H diseaseI Papassotiriou, J Traeger-Synodinos, E Kanavakis, et al.
Haematologica|April 28, 2001
Erythroid marrow activity and functional anemia in patients with the rare interaction of a single functional a-globin and beta-globin geneJ Traeger-Synodinos, I Papassotiriou, C Vrettou, et al.
Blood Cells, Molecules & Diseases|October 24, 2000
Distinct phenotypic expression associated with a new hyperunstable alpha globin variant (Hb heraklion, alpha1cd37(C2)Pro>0): comparison to other alpha-thalassemic hemoglobinopathiesJ Traeger-Synodinos, I Papassotiriou, A Metaxotou-Mavrommati, et al.
Hemoglobin|September 18, 1999
Rapid and accurate quantitation of Hb Bart's and Hb H using weak cation exchange high performance liquid chromatography: correlation with the alpha-thalassemia genotypeI Papassotiriou, J Traeger-Synodinos, C Vlachou, et al.
European Journal of Clinical Nutrition|July 1, 2004
Effect of iron supplementation on cognition in Greek preschoolersE Metallinos-Katsaras, E Valassi-Adam, K G Dewey, et al.
Hemoglobin|November 24, 1999
Interaction of an alpha(+)-thalassemia deletion with either a highly unstable alpha-globin variant (alpha2, codon 59, GGC-->GAC) or a nondeletional alpha-thalassemia mutation (AATAAA-->AATAAG): comparison of phenotypes illustrating "dominant" alpha-thalassemiaJ Traeger-Synodinos, A Metaxotou-Mavrommati, M Karagiorga, et al.
Pageof 2