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Elisa Fermo

Showing results (1-10 of 93) with videos related to

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Haematologica|October 15, 2020
Molecular heterogeneity of pyruvate kinase deficiencyPaola Bianchi, Elisa Fermo
Expert Review of Hematology|February 5, 2021
Screening tools for hereditary hemolytic anemia: new concepts and strategiesElisa Fermo, Cristina Vercellati, Paola Bianchi
Annals of Translational Medicine|May 2, 2020
How will next generation sequencing (NGS) improve the diagnosis of congenital hemolytic anemia?Paola Bianchi, Cristina Vercellati, Elisa Fermo
Haematologica|June 7, 2007
Pyruvate kinase deficiencyAlberto Zanella, Paola Bianchi, Elisa Fermo
British Journal of Haematology|April 14, 2006
Hereditary pyrimidine 5'-nucleotidase deficiency: from genetics to clinical manifestationsAlberto Zanella, Paola Bianchi, Elisa Fermo, et al.
British Journal of Haematology|June 29, 2005
Red cell pyruvate kinase deficiency: molecular and clinical aspectsAlberto Zanella, Elisa Fermo, Paola Bianchi, et al.
Hematology (Amsterdam, Netherlands)|March 9, 2006
Hereditary erythrocyte pyrimidine 5'-nucleotidase deficiency: a biochemical, genetic and clinical overviewLaurent R Chiarelli, Elisa Fermo, Alberto Zanella, et al.
Human Pathology|January 21, 2014
Chromosome 7q31.1 deletion in myeloid neoplasmsPasquale Tripputi, Paola Bianchi, Elisa Fermo, et al.
Leukemia Research|October 27, 2006
HIC gene, a candidate suppressor gene within a minimal region of loss at 7q31.1 in myeloid neoplasmsDaniela Cigognini, Gianmarco Corneo, Elisa Fermo, et al.
Orphanet Journal of Rare Diseases|December 20, 2024
Diagnosis of Diamond-Blackfan anemia in adulthood: case series and review of the literatureFrancesco Versino, Paola Bianchi, Elisa Fermo, et al.
Pageof 10

Showing results (1-10 of 93) with videos related to

Sort By:
Pageof 10
Haematologica|October 15, 2020
Molecular heterogeneity of pyruvate kinase deficiencyPaola Bianchi, Elisa Fermo
Expert Review of Hematology|February 5, 2021
Screening tools for hereditary hemolytic anemia: new concepts and strategiesElisa Fermo, Cristina Vercellati, Paola Bianchi
Annals of Translational Medicine|May 2, 2020
How will next generation sequencing (NGS) improve the diagnosis of congenital hemolytic anemia?Paola Bianchi, Cristina Vercellati, Elisa Fermo
Haematologica|June 7, 2007
Pyruvate kinase deficiencyAlberto Zanella, Paola Bianchi, Elisa Fermo
British Journal of Haematology|April 14, 2006
Hereditary pyrimidine 5'-nucleotidase deficiency: from genetics to clinical manifestationsAlberto Zanella, Paola Bianchi, Elisa Fermo, et al.
British Journal of Haematology|June 29, 2005
Red cell pyruvate kinase deficiency: molecular and clinical aspectsAlberto Zanella, Elisa Fermo, Paola Bianchi, et al.
Hematology (Amsterdam, Netherlands)|March 9, 2006
Hereditary erythrocyte pyrimidine 5'-nucleotidase deficiency: a biochemical, genetic and clinical overviewLaurent R Chiarelli, Elisa Fermo, Alberto Zanella, et al.
Human Pathology|January 21, 2014
Chromosome 7q31.1 deletion in myeloid neoplasmsPasquale Tripputi, Paola Bianchi, Elisa Fermo, et al.
Leukemia Research|October 27, 2006
HIC gene, a candidate suppressor gene within a minimal region of loss at 7q31.1 in myeloid neoplasmsDaniela Cigognini, Gianmarco Corneo, Elisa Fermo, et al.
Orphanet Journal of Rare Diseases|December 20, 2024
Diagnosis of Diamond-Blackfan anemia in adulthood: case series and review of the literatureFrancesco Versino, Paola Bianchi, Elisa Fermo, et al.
Pageof 10