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Elisa Fermo

Showing results (51-60 of 93) with videos related to

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Blood Advances|September 1, 2021
Mechanistic ion channel interactions in red cells of patients with Gárdos channelopathyJulia Jansen, Min Qiao, Laura Hertz, et al.
British Journal of Haematology|March 12, 2022
Changing trends of splenectomy in hereditary spherocytosis: The experience of a reference Centre in the last 40 yearsCristina Vercellati, Anna Zaninoni, Anna P Marcello, et al.
Haematologica|September 22, 2018
A novel gain-of-function mutation of Piezo1 is functionally affirmed in red blood cells by high-throughput patch clampMaria G Rotordam, Elisa Fermo, Nadine Becker, et al.
Plos Computational Biology|May 13, 2021
Red blood cell phenotyping from 3D confocal images using artificial neural networksGreta Simionato, Konrad Hinkelmann, Revaz Chachanidze, et al.
Pediatric Blood & Cancer|May 3, 2023
Severe hemolytic anemia in a newborn: Look out for rare Gardos channelopathies due to KCNN4 mutationVania Munaretto, Maddalena Martella, Samuela Francescato, et al.
American Journal of Hematology|February 18, 2026
Characterization of a Newly Discovered Non-Coding Variant in the EPO Gene Identified in Two Unrelated Italian Pedigrees With ErythrocytosisBarbara Mora, Valentina Bellani, Daniela Pietra, et al.
Scientific Reports|March 13, 2026
Rheological and biochemical comparison of cord and adult blood red cells for transfusion applicationsLarysa Mykhailova, Cristina Vercellati, Tiziana Montemurro, et al.
British Journal of Haematology|June 15, 2005
Red cell pyruvate kinase deficiency: 17 new mutations of the PK-LR geneElisa Fermo, Paola Bianchi, Laurent R Chiarelli, et al.
Leukemia Research|October 2, 2013
Increased prevalence of autoimmune phenomena in myelofibrosis: relationship with clinical and morphological characteristics, and with immunoregulatory cytokine patternsWilma Barcellini, Alessandra Iurlo, Tommaso Radice, et al.
Frontiers in Physiology|December 7, 2020
A Novel ALAS2 Missense Mutation in Two Brothers With Iron Overload and Associated Alterations in Serum Hepcidin/Erythroferrone LevelsAcaynne Lira Zidanes, Giacomo Marchi, Fabiana Busti, et al.
Pageof 10

Showing results (51-60 of 93) with videos related to

Sort By:
Pageof 10
Blood Advances|September 1, 2021
Mechanistic ion channel interactions in red cells of patients with Gárdos channelopathyJulia Jansen, Min Qiao, Laura Hertz, et al.
British Journal of Haematology|March 12, 2022
Changing trends of splenectomy in hereditary spherocytosis: The experience of a reference Centre in the last 40 yearsCristina Vercellati, Anna Zaninoni, Anna P Marcello, et al.
Haematologica|September 22, 2018
A novel gain-of-function mutation of Piezo1 is functionally affirmed in red blood cells by high-throughput patch clampMaria G Rotordam, Elisa Fermo, Nadine Becker, et al.
Plos Computational Biology|May 13, 2021
Red blood cell phenotyping from 3D confocal images using artificial neural networksGreta Simionato, Konrad Hinkelmann, Revaz Chachanidze, et al.
Pediatric Blood & Cancer|May 3, 2023
Severe hemolytic anemia in a newborn: Look out for rare Gardos channelopathies due to KCNN4 mutationVania Munaretto, Maddalena Martella, Samuela Francescato, et al.
American Journal of Hematology|February 18, 2026
Characterization of a Newly Discovered Non-Coding Variant in the EPO Gene Identified in Two Unrelated Italian Pedigrees With ErythrocytosisBarbara Mora, Valentina Bellani, Daniela Pietra, et al.
Scientific Reports|March 13, 2026
Rheological and biochemical comparison of cord and adult blood red cells for transfusion applicationsLarysa Mykhailova, Cristina Vercellati, Tiziana Montemurro, et al.
British Journal of Haematology|June 15, 2005
Red cell pyruvate kinase deficiency: 17 new mutations of the PK-LR geneElisa Fermo, Paola Bianchi, Laurent R Chiarelli, et al.
Leukemia Research|October 2, 2013
Increased prevalence of autoimmune phenomena in myelofibrosis: relationship with clinical and morphological characteristics, and with immunoregulatory cytokine patternsWilma Barcellini, Alessandra Iurlo, Tommaso Radice, et al.
Frontiers in Physiology|December 7, 2020
A Novel ALAS2 Missense Mutation in Two Brothers With Iron Overload and Associated Alterations in Serum Hepcidin/Erythroferrone LevelsAcaynne Lira Zidanes, Giacomo Marchi, Fabiana Busti, et al.
Pageof 10