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Elisa Fermo

Showing results (61-70 of 93) with videos related to

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British Journal of Haematology|March 15, 2018
Transduction with BBF2H7/CREB3L2 upregulates SEC23A protein in erythroblasts and partially corrects the hypo-glycosylation phenotype associated with CDAIIStéphanie Pellegrin, Katy L Haydn-Smith, Lea A Hampton-O'Neil, et al.
Case Reports in Hematology|April 4, 2017
Hereditary Xerocytosis due to Mutations in <i>PIEZO1</i> Gene Associated with Heterozygous Pyruvate Kinase Deficiency and Beta-Thalassemia Trait in Two Unrelated FamiliesElisa Fermo, Cristina Vercellati, Anna Paola Marcello, et al.
Hematological Oncology|October 7, 2015
Oxidative status in treatment-naïve essential thrombocythemia: a pilot study in a single centerAlessandra Iurlo, Rachele De Giuseppe, Mariarita Sciumè, et al.
British Journal of Haematology|July 30, 2016
Analysis of a cohort of 101 CDAII patients: description of 24 new molecular variants and genotype-phenotype correlationsPaola Bianchi, Klaus Schwarz, Josef Högel, et al.
Frontiers in Physiology|June 7, 2021
Targeted Next Generation Sequencing and Diagnosis of Congenital Hemolytic Anemias: A Three Years Experience Monocentric StudyElisa Fermo, Cristina Vercellati, Anna Paola Marcello, et al.
American Journal of Clinical Pathology|August 15, 2008
The significance of bone marrow biopsy and JAK2V617F mutation in the differential diagnosis between the "early" prepolycythemic phase of polycythemia vera and essential thrombocythemiaUmberto Gianelli, Alessandra Iurlo, Claudia Vener, et al.
Frontiers in Physiology|May 29, 2019
Clinical and Molecular Spectrum of Glucose-6-Phosphate Isomerase Deficiency. Report of 12 New CasesElisa Fermo, Cristina Vercellati, Anna Paola Marcello, et al.
Scientific Reports|March 17, 2023
Evaluation of the main regulators of systemic iron homeostasis in pyruvate kinase deficiencyAnna Zaninoni, Roberta Marra, Elisa Fermo, et al.
Transfusion|August 12, 2015
Detection of red blood cell antibodies in mitogen-stimulated cultures from patients with hereditary spherocytosisAnna Zaninoni, Cristina Vercellati, Francesca G Imperiali, et al.
Molecular Genetics and Metabolism|June 19, 2012
A new variant of phosphoglycerate kinase deficiency (p.I371K) with multiple tissue involvement: molecular and functional characterizationElisa Fermo, Paola Bianchi, Laurent Roberto Chiarelli, et al.
Pageof 10

Showing results (61-70 of 93) with videos related to

Sort By:
Pageof 10
British Journal of Haematology|March 15, 2018
Transduction with BBF2H7/CREB3L2 upregulates SEC23A protein in erythroblasts and partially corrects the hypo-glycosylation phenotype associated with CDAIIStéphanie Pellegrin, Katy L Haydn-Smith, Lea A Hampton-O'Neil, et al.
Case Reports in Hematology|April 4, 2017
Hereditary Xerocytosis due to Mutations in <i>PIEZO1</i> Gene Associated with Heterozygous Pyruvate Kinase Deficiency and Beta-Thalassemia Trait in Two Unrelated FamiliesElisa Fermo, Cristina Vercellati, Anna Paola Marcello, et al.
Hematological Oncology|October 7, 2015
Oxidative status in treatment-naïve essential thrombocythemia: a pilot study in a single centerAlessandra Iurlo, Rachele De Giuseppe, Mariarita Sciumè, et al.
British Journal of Haematology|July 30, 2016
Analysis of a cohort of 101 CDAII patients: description of 24 new molecular variants and genotype-phenotype correlationsPaola Bianchi, Klaus Schwarz, Josef Högel, et al.
Frontiers in Physiology|June 7, 2021
Targeted Next Generation Sequencing and Diagnosis of Congenital Hemolytic Anemias: A Three Years Experience Monocentric StudyElisa Fermo, Cristina Vercellati, Anna Paola Marcello, et al.
American Journal of Clinical Pathology|August 15, 2008
The significance of bone marrow biopsy and JAK2V617F mutation in the differential diagnosis between the "early" prepolycythemic phase of polycythemia vera and essential thrombocythemiaUmberto Gianelli, Alessandra Iurlo, Claudia Vener, et al.
Frontiers in Physiology|May 29, 2019
Clinical and Molecular Spectrum of Glucose-6-Phosphate Isomerase Deficiency. Report of 12 New CasesElisa Fermo, Cristina Vercellati, Anna Paola Marcello, et al.
Scientific Reports|March 17, 2023
Evaluation of the main regulators of systemic iron homeostasis in pyruvate kinase deficiencyAnna Zaninoni, Roberta Marra, Elisa Fermo, et al.
Transfusion|August 12, 2015
Detection of red blood cell antibodies in mitogen-stimulated cultures from patients with hereditary spherocytosisAnna Zaninoni, Cristina Vercellati, Francesca G Imperiali, et al.
Molecular Genetics and Metabolism|June 19, 2012
A new variant of phosphoglycerate kinase deficiency (p.I371K) with multiple tissue involvement: molecular and functional characterizationElisa Fermo, Paola Bianchi, Laurent Roberto Chiarelli, et al.
Pageof 10