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Elisa Fermo

Showing results (11-20 of 93) with videos related to

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Clinical Pediatrics|March 5, 2024
Recessive Hereditary Methemoglobinemia Type II in a Microcephalic InfantTugba Belgemen-Ozer, Kursat Bora Carman, Paola Bianchi, et al.
Blood Reviews|March 16, 2007
Pyruvate kinase deficiency: the genotype-phenotype associationAlberto Zanella, Elisa Fermo, Paola Bianchi, et al.
European Journal of Internal Medicine|May 23, 2017
Paroxysmal nocturnal hemoglobinuria with spontaneous clinical remissionValeria Ferla, Anna Zaninoni, Bruno Fattizzo, et al.
American Journal of Hematology|August 13, 2004
Clinical and molecular aspects of 23 patients affected by paroxysmal nocturnal hemoglobinuriaCarla Boschetti, Elisa Fermo, Paola Bianchi, et al.
Annals of Hematology|November 8, 2014
Molecular analyses in the diagnosis of myeloproliferative neoplasm-related splanchnic vein thrombosisAlessandra Iurlo, Daniele Cattaneo, Umberto Gianelli, et al.
Frontiers in Immunology|July 14, 2020
Congenital Hemolytic Anemias: Is There a Role for the Immune System?Anna Zaninoni, Elisa Fermo, Cristina Vercellati, et al.
Clinical Laboratory|June 4, 2013
A case of hereditary spherocytosis misdiagnosed as pyruvate kinase deficient hemolytic anemiaCristina Vercellati, Anna Paola Marcello, Elisa Fermo, et al.
Annals of Hematology|June 18, 2015
Clinical and morphologic features in five post-polycythemic myelofibrosis patients treated with ruxolitinibAlessandra Iurlo, Daniele Cattaneo, Leonardo Boiocchi, et al.
Blood Cells, Molecules & Diseases|May 24, 2008
Molecular basis of pyrimidine 5'-nucleotidase deficiency caused by 3 newly identified missense mutations (c.187T>C, c.469G>C and c.740T>C) and a tabulation of known mutationsLaurent R Chiarelli, Simone M Morera, Alessandro Galizzi, et al.
Pediatrics|March 3, 2010
A novel missense mutation in MVK associated with MK deficiency and dyserythropoietic anemiaAyman Samkari, Arturo Borzutzky, Elisa Fermo, et al.
Pageof 10

Showing results (11-20 of 93) with videos related to

Sort By:
Pageof 10
Clinical Pediatrics|March 5, 2024
Recessive Hereditary Methemoglobinemia Type II in a Microcephalic InfantTugba Belgemen-Ozer, Kursat Bora Carman, Paola Bianchi, et al.
Blood Reviews|March 16, 2007
Pyruvate kinase deficiency: the genotype-phenotype associationAlberto Zanella, Elisa Fermo, Paola Bianchi, et al.
European Journal of Internal Medicine|May 23, 2017
Paroxysmal nocturnal hemoglobinuria with spontaneous clinical remissionValeria Ferla, Anna Zaninoni, Bruno Fattizzo, et al.
American Journal of Hematology|August 13, 2004
Clinical and molecular aspects of 23 patients affected by paroxysmal nocturnal hemoglobinuriaCarla Boschetti, Elisa Fermo, Paola Bianchi, et al.
Annals of Hematology|November 8, 2014
Molecular analyses in the diagnosis of myeloproliferative neoplasm-related splanchnic vein thrombosisAlessandra Iurlo, Daniele Cattaneo, Umberto Gianelli, et al.
Frontiers in Immunology|July 14, 2020
Congenital Hemolytic Anemias: Is There a Role for the Immune System?Anna Zaninoni, Elisa Fermo, Cristina Vercellati, et al.
Clinical Laboratory|June 4, 2013
A case of hereditary spherocytosis misdiagnosed as pyruvate kinase deficient hemolytic anemiaCristina Vercellati, Anna Paola Marcello, Elisa Fermo, et al.
Annals of Hematology|June 18, 2015
Clinical and morphologic features in five post-polycythemic myelofibrosis patients treated with ruxolitinibAlessandra Iurlo, Daniele Cattaneo, Leonardo Boiocchi, et al.
Blood Cells, Molecules & Diseases|May 24, 2008
Molecular basis of pyrimidine 5'-nucleotidase deficiency caused by 3 newly identified missense mutations (c.187T>C, c.469G>C and c.740T>C) and a tabulation of known mutationsLaurent R Chiarelli, Simone M Morera, Alessandro Galizzi, et al.
Pediatrics|March 3, 2010
A novel missense mutation in MVK associated with MK deficiency and dyserythropoietic anemiaAyman Samkari, Arturo Borzutzky, Elisa Fermo, et al.
Pageof 10