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Elisa Fermo

Showing results (31-40 of 93) with videos related to

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Prenatal Diagnosis|December 28, 2006
Prenatal diagnosis for a novel homozygous mutation in PKLR gene in an Indian familyNeerja Gupta, Paola Bianchi, Elisa Fermo, et al.
Annals of Hematology|September 6, 2016
CD18 promoter methylation is associated with a higher risk of thrombotic complications in primary myelofibrosisClaudia Augello, Daniele Cattaneo, Cristina Bucelli, et al.
Blood Cells, Molecules & Diseases|March 18, 2008
Recessive hereditary methemoglobinemia: two novel mutations in the NADH-cytochrome b5 reductase geneElisa Fermo, Paola Bianchi, Cristina Vercellati, et al.
Frontiers in Physiology|August 29, 2022
Effect of primary lesions in cytoskeleton proteins on red cell membrane stability in patients with hereditary spherocytosisCristina Vercellati, Anna Paola Marcello, Bruno Fattizzo, et al.
Haematologica|November 8, 2011
Diagnostic power of laboratory tests for hereditary spherocytosis: a comparison study in 150 patients grouped according to molecular and clinical characteristicsPaola Bianchi, Elisa Fermo, Cristina Vercellati, et al.
Haematologica|July 22, 2008
Clinical and hematologic features of 300 patients affected by hereditary spherocytosis grouped according to the type of the membrane protein defectMariagabriella Mariani, Wilma Barcellini, Cristina Vercellati, et al.
Blood|December 18, 2004
Functional analysis of pyrimidine 5'-nucleotidase mutants causing nonspherocytic hemolytic anemiaLaurent R Chiarelli, Paola Bianchi, Elisa Fermo, et al.
Journal of Pediatric Hematology/Oncology|July 21, 2018
A New Variant of PKLR Gene Associated With Mild Hemolysis may be Responsible for the Misdiagnosis in Pyruvate Kinase DeficiencySultan Aydin Köker, Yeşim Oymak, Paola Bianchi, et al.
Blood Transfusion = Trasfusione Del Sangue|January 22, 2011
Hereditary red cell membrane defects: diagnostic and clinical aspectsWilma Barcellini, Paola Bianchi, Elisa Fermo, et al.
Frontiers in Oncology|May 21, 2019
The Role of New Technologies in Myeloproliferative NeoplasmsGiuseppe A Palumbo, Stefania Stella, Maria Stella Pennisi, et al.
Pageof 10

Showing results (31-40 of 93) with videos related to

Sort By:
Pageof 10
Prenatal Diagnosis|December 28, 2006
Prenatal diagnosis for a novel homozygous mutation in PKLR gene in an Indian familyNeerja Gupta, Paola Bianchi, Elisa Fermo, et al.
Annals of Hematology|September 6, 2016
CD18 promoter methylation is associated with a higher risk of thrombotic complications in primary myelofibrosisClaudia Augello, Daniele Cattaneo, Cristina Bucelli, et al.
Blood Cells, Molecules & Diseases|March 18, 2008
Recessive hereditary methemoglobinemia: two novel mutations in the NADH-cytochrome b5 reductase geneElisa Fermo, Paola Bianchi, Cristina Vercellati, et al.
Frontiers in Physiology|August 29, 2022
Effect of primary lesions in cytoskeleton proteins on red cell membrane stability in patients with hereditary spherocytosisCristina Vercellati, Anna Paola Marcello, Bruno Fattizzo, et al.
Haematologica|November 8, 2011
Diagnostic power of laboratory tests for hereditary spherocytosis: a comparison study in 150 patients grouped according to molecular and clinical characteristicsPaola Bianchi, Elisa Fermo, Cristina Vercellati, et al.
Haematologica|July 22, 2008
Clinical and hematologic features of 300 patients affected by hereditary spherocytosis grouped according to the type of the membrane protein defectMariagabriella Mariani, Wilma Barcellini, Cristina Vercellati, et al.
Blood|December 18, 2004
Functional analysis of pyrimidine 5'-nucleotidase mutants causing nonspherocytic hemolytic anemiaLaurent R Chiarelli, Paola Bianchi, Elisa Fermo, et al.
Journal of Pediatric Hematology/Oncology|July 21, 2018
A New Variant of PKLR Gene Associated With Mild Hemolysis may be Responsible for the Misdiagnosis in Pyruvate Kinase DeficiencySultan Aydin Köker, Yeşim Oymak, Paola Bianchi, et al.
Blood Transfusion = Trasfusione Del Sangue|January 22, 2011
Hereditary red cell membrane defects: diagnostic and clinical aspectsWilma Barcellini, Paola Bianchi, Elisa Fermo, et al.
Frontiers in Oncology|May 21, 2019
The Role of New Technologies in Myeloproliferative NeoplasmsGiuseppe A Palumbo, Stefania Stella, Maria Stella Pennisi, et al.
Pageof 10