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Elisa Fermo

Showing results (21-30 of 93) with videos related to

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Blood Cells, Molecules & Diseases|August 19, 2008
A case of congenital red cell pyruvate kinase deficiency associated with hereditary stomatocytosisAnna Paola Marcello, Cristina Vercellati, Elisa Fermo, et al.
Leukemia & Lymphoma|November 9, 2007
Hematological, molecular and cytokine changes after reduced intensity bone marrow transplantation for paroxysmal nocturnal hemoglobinuriaWilma Barcellini, Elisa Fermo, Francesca Guia Imperiali, et al.
Blood Cells, Molecules & Diseases|August 19, 2004
A new variant of adenylate kinase (delG138) associated with severe hemolytic anemiaElisa Fermo, Paola Bianchi, Cristina Vercellati, et al.
Journal of Pediatric Hematology/Oncology|January 9, 2018
A Case With Pyruvate Kinase Deficiency Remarkably Sensitive to HeatTekin Aksu, Neşe Yarali, Elisa Fermo, et al.
Experimental Hematology|July 31, 2007
Erythrocyte adenylate kinase deficiency: characterization of recombinant mutant forms and relationship with nonspherocytic hemolytic anemiaPatrizia Abrusci, Laurent R Chiarelli, Alessandro Galizzi, et al.
Brain & Development|July 24, 2010
Cerebellar atrophy in a child with hereditary methemoglobinemia type IICarlo Fusco, Giuliana Soncini, Daniele Frattini, et al.
Haematologica|June 15, 2004
Increased resistance of PIG-A- bone marrow progenitors to tumor necrosis factor a and interferon gamma: possible implications for the in vivo dominance of paroxysmal nocturnal hemoglobinuria clonesWilma Barcellini, Elisa Fermo, Francesca Guia Imperiali, et al.
Journal of Pediatric Hematology/Oncology|May 31, 2018
Identification of a Novel Mutation in the SEC23B Gene Associated With Congenital Dyserythropoietic Anemia Type II Through the Use of Next-generation Sequencing Panel in an Undiagnosed Case of Nonimmune Hereditary Hemolytic AnemiaSultan Aydin Koker, Tuba H Karapinar, Yeşim Oymak, et al.
European Journal of Haematology|April 9, 2010
Triose phosphate isomerase deficiency associated with two novel mutations in TPI geneElisa Fermo, Paola Bianchi, Cristina Vercellati, et al.
Plos One|February 21, 2012
Molecular insights on pathogenic effects of mutations causing phosphoglycerate kinase deficiencyLaurent R Chiarelli, Simone M Morera, Paola Bianchi, et al.
Pageof 10

Showing results (21-30 of 93) with videos related to

Sort By:
Pageof 10
Blood Cells, Molecules & Diseases|August 19, 2008
A case of congenital red cell pyruvate kinase deficiency associated with hereditary stomatocytosisAnna Paola Marcello, Cristina Vercellati, Elisa Fermo, et al.
Leukemia & Lymphoma|November 9, 2007
Hematological, molecular and cytokine changes after reduced intensity bone marrow transplantation for paroxysmal nocturnal hemoglobinuriaWilma Barcellini, Elisa Fermo, Francesca Guia Imperiali, et al.
Blood Cells, Molecules & Diseases|August 19, 2004
A new variant of adenylate kinase (delG138) associated with severe hemolytic anemiaElisa Fermo, Paola Bianchi, Cristina Vercellati, et al.
Journal of Pediatric Hematology/Oncology|January 9, 2018
A Case With Pyruvate Kinase Deficiency Remarkably Sensitive to HeatTekin Aksu, Neşe Yarali, Elisa Fermo, et al.
Experimental Hematology|July 31, 2007
Erythrocyte adenylate kinase deficiency: characterization of recombinant mutant forms and relationship with nonspherocytic hemolytic anemiaPatrizia Abrusci, Laurent R Chiarelli, Alessandro Galizzi, et al.
Brain & Development|July 24, 2010
Cerebellar atrophy in a child with hereditary methemoglobinemia type IICarlo Fusco, Giuliana Soncini, Daniele Frattini, et al.
Haematologica|June 15, 2004
Increased resistance of PIG-A- bone marrow progenitors to tumor necrosis factor a and interferon gamma: possible implications for the in vivo dominance of paroxysmal nocturnal hemoglobinuria clonesWilma Barcellini, Elisa Fermo, Francesca Guia Imperiali, et al.
Journal of Pediatric Hematology/Oncology|May 31, 2018
Identification of a Novel Mutation in the SEC23B Gene Associated With Congenital Dyserythropoietic Anemia Type II Through the Use of Next-generation Sequencing Panel in an Undiagnosed Case of Nonimmune Hereditary Hemolytic AnemiaSultan Aydin Koker, Tuba H Karapinar, Yeşim Oymak, et al.
European Journal of Haematology|April 9, 2010
Triose phosphate isomerase deficiency associated with two novel mutations in TPI geneElisa Fermo, Paola Bianchi, Cristina Vercellati, et al.
Plos One|February 21, 2012
Molecular insights on pathogenic effects of mutations causing phosphoglycerate kinase deficiencyLaurent R Chiarelli, Simone M Morera, Paola Bianchi, et al.
Pageof 10