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N P Anagnou

Showing results (1-10 of 54) with videos related to

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Blood|April 1, 1980
Glycerol-3-phosphate dehydrogenase activity in the red cells of patients with thalassemiaP Fessas, N P Anagnou, D Loukopoulos
Human Genetics|September 1, 1997
Molecular cloning of the breakpoints of the hereditary persistence of fetal hemoglobin type-6 (HPFH-6) deletion and sequence analysis of the novel juxtaposed region from the 3' end of the beta-globin gene clusterT Kosteas, A Palena, N P Anagnou
Haematologia|January 1, 1991
Recurrent attacks of hemolytic uremic syndromeN P Anagnou, N Papanicolaou, P Fessas
Blood|September 1, 1988
Laotian (delta beta) (0)-thalassemia: molecular characterization of a novel deletion associated with increased production of fetal hemoglobinJ W Zhang, G Stamatoyannopoulos, N P Anagnou
American Journal of Hematology|December 1, 1990
Developmental and inducible patterns of human theta 1-globin gene expression in embryonic/fetal and adult erythroid cellsA Mamalaki, N P Anagnou, N K Moschonas
Current Molecular Medicine|July 20, 2013
Towards more successful gene therapy clinical trials for β-thalassemiaE Drakopoulou, E Papanikolaou, M Georgomanoli, et al.
Haematologia|January 1, 1990
Defective CSA-dependent granulopoiesis in patients with chronic drug-induced neutropeniaG Eliopoulos, J Meletis, P Fessas, et al.
Blood|April 1, 1984
Advances in thalassemia researchA W Nienhuis, N P Anagnou, T J Ley
American Journal of Clinical Pathology|March 1, 1988
Myelodysplastic syndrome with acquired hemoglobin H disease. Evolution through megakaryoblastic transformation into myelofibrosisS L Abbondanzo, N P Anagnou, R A Sacher
Blood|June 15, 1994
Eastern European (delta beta) zero-thalassemia: molecular characterization of a novel 9.1-kb deletion resulting in high levels of fetal hemoglobin in the adultA Palena, A Blau, G Stamatoyannopoulos, et al.
Pageof 6

Showing results (1-10 of 54) with videos related to

Sort By:
Pageof 6
Blood|April 1, 1980
Glycerol-3-phosphate dehydrogenase activity in the red cells of patients with thalassemiaP Fessas, N P Anagnou, D Loukopoulos
Human Genetics|September 1, 1997
Molecular cloning of the breakpoints of the hereditary persistence of fetal hemoglobin type-6 (HPFH-6) deletion and sequence analysis of the novel juxtaposed region from the 3' end of the beta-globin gene clusterT Kosteas, A Palena, N P Anagnou
Haematologia|January 1, 1991
Recurrent attacks of hemolytic uremic syndromeN P Anagnou, N Papanicolaou, P Fessas
Blood|September 1, 1988
Laotian (delta beta) (0)-thalassemia: molecular characterization of a novel deletion associated with increased production of fetal hemoglobinJ W Zhang, G Stamatoyannopoulos, N P Anagnou
American Journal of Hematology|December 1, 1990
Developmental and inducible patterns of human theta 1-globin gene expression in embryonic/fetal and adult erythroid cellsA Mamalaki, N P Anagnou, N K Moschonas
Current Molecular Medicine|July 20, 2013
Towards more successful gene therapy clinical trials for β-thalassemiaE Drakopoulou, E Papanikolaou, M Georgomanoli, et al.
Haematologia|January 1, 1990
Defective CSA-dependent granulopoiesis in patients with chronic drug-induced neutropeniaG Eliopoulos, J Meletis, P Fessas, et al.
Blood|April 1, 1984
Advances in thalassemia researchA W Nienhuis, N P Anagnou, T J Ley
American Journal of Clinical Pathology|March 1, 1988
Myelodysplastic syndrome with acquired hemoglobin H disease. Evolution through megakaryoblastic transformation into myelofibrosisS L Abbondanzo, N P Anagnou, R A Sacher
Blood|June 15, 1994
Eastern European (delta beta) zero-thalassemia: molecular characterization of a novel 9.1-kb deletion resulting in high levels of fetal hemoglobin in the adultA Palena, A Blau, G Stamatoyannopoulos, et al.
Pageof 6