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Blood Advances
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September 1, 2021
Mechanistic ion channel interactions in red cells of patients with Gárdos channelopathy
Julia 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 years
Cristina 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 clamp
Maria 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 networks
Greta 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 mutation
Vania 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 Erythrocytosis
Barbara 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 applications
Larysa 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 gene
Elisa 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 patterns
Wilma 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 Levels
Acaynne Lira Zidanes, Giacomo Marchi, Fabiana Busti, et al.
Page
of 10
Search research articles
Search
Showing results (51-60 of 93) with videos related to
Sort By:
Page
of 10
Blood Advances
|
September 1, 2021
Mechanistic ion channel interactions in red cells of patients with Gárdos channelopathy
Julia 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 years
Cristina 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 clamp
Maria 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 networks
Greta 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 mutation
Vania 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 Erythrocytosis
Barbara 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 applications
Larysa 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 gene
Elisa 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 patterns
Wilma 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 Levels
Acaynne Lira Zidanes, Giacomo Marchi, Fabiana Busti, et al.
Page
of 10