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Haematologica
|
August 6, 2002
Inherited thrombocytopenias: from genes to therapy
Carlo L Balduini, Achille Iolascon, Anna Savoia
Haematologica
|
October 16, 2012
Clinical aspects and pathogenesis of congenital dyserythropoietic anemias: from morphology to molecular approach
Achille Iolascon, Maria Rosaria Esposito, Roberta Russo
Blood
|
August 14, 2013
Congenital dyserythropoietic anemias: molecular insights and diagnostic approach
Achille Iolascon, Hermann Heimpel, Anders Wahlin, et al.
American Journal of Hematology
|
October 4, 2017
Hereditary stomatocytosis: An underdiagnosed condition
Immacolata Andolfo, Roberta Russo, Antonella Gambale, et al.
Expert Review of Hematology
|
December 15, 2015
Diagnosis and management of congenital dyserythropoietic anemias
Antonella Gambale, Achille Iolascon, Immacolata Andolfo, et al.
European Journal of Clinical Pharmacology
|
November 12, 2010
Pediatric pharmacogenetic and pharmacogenomic studies: the current state and future perspectives
Roberta Russo, Mario Capasso, Paolo Paolucci, et al.
Blood
|
September 25, 2003
Congenital dyserythropoietic anemia type II in human patients is not due to mutations in the erythroid anion exchanger 1
Silverio Perrotta, Lucio Luzzatto, Massimo Carella, et al.
Haematologica
|
November 2, 2016
New insights on hereditary erythrocyte membrane defects
Immacolata Andolfo, Roberta Russo, Antonella Gambale, et al.
Haematologica
|
February 12, 2002
Proliferate and survive: cell division cycle and apoptosis in human neuroblastoma
Adriana Borriello, Roberta Roberto, Fulvio Della Ragione, et al.
Hematology. American Society of Hematology. Education Program
|
December 4, 2020
Inherited microcytic anemias
Maria Domenica Cappellini, Roberta Russo, Immacolata Andolfo, et al.
Page
of 29
Search research articles
Search
Showing results (21-30 of 290) with videos related to
Sort By:
Page
of 29
Haematologica
|
August 6, 2002
Inherited thrombocytopenias: from genes to therapy
Carlo L Balduini, Achille Iolascon, Anna Savoia
Haematologica
|
October 16, 2012
Clinical aspects and pathogenesis of congenital dyserythropoietic anemias: from morphology to molecular approach
Achille Iolascon, Maria Rosaria Esposito, Roberta Russo
Blood
|
August 14, 2013
Congenital dyserythropoietic anemias: molecular insights and diagnostic approach
Achille Iolascon, Hermann Heimpel, Anders Wahlin, et al.
American Journal of Hematology
|
October 4, 2017
Hereditary stomatocytosis: An underdiagnosed condition
Immacolata Andolfo, Roberta Russo, Antonella Gambale, et al.
Expert Review of Hematology
|
December 15, 2015
Diagnosis and management of congenital dyserythropoietic anemias
Antonella Gambale, Achille Iolascon, Immacolata Andolfo, et al.
European Journal of Clinical Pharmacology
|
November 12, 2010
Pediatric pharmacogenetic and pharmacogenomic studies: the current state and future perspectives
Roberta Russo, Mario Capasso, Paolo Paolucci, et al.
Blood
|
September 25, 2003
Congenital dyserythropoietic anemia type II in human patients is not due to mutations in the erythroid anion exchanger 1
Silverio Perrotta, Lucio Luzzatto, Massimo Carella, et al.
Haematologica
|
November 2, 2016
New insights on hereditary erythrocyte membrane defects
Immacolata Andolfo, Roberta Russo, Antonella Gambale, et al.
Haematologica
|
February 12, 2002
Proliferate and survive: cell division cycle and apoptosis in human neuroblastoma
Adriana Borriello, Roberta Roberto, Fulvio Della Ragione, et al.
Hematology. American Society of Hematology. Education Program
|
December 4, 2020
Inherited microcytic anemias
Maria Domenica Cappellini, Roberta Russo, Immacolata Andolfo, et al.
Page
of 29