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Elisa Fermo

Showing results (41-50 of 93) with videos related to

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Haematologica|March 18, 2014
Imatinib and ruxolitinib association: first experience in two patientsAlessandra Iurlo, Umberto Gianelli, Davide Rapezzi, et al.
Haematologica|September 8, 2006
Two new mutations of the P5'N-1 gene found in Italian patients with hereditary hemolytic anemia: the molecular basis of the red cell enzyme disorderLaurent R Chiarelli, Elisa Fermo, Patrizia Abrusci, et al.
British Journal of Haematology|August 22, 2003
Molecular characterization of six unrelated Italian patients affected by pyrimidine 5'-nucleotidase deficiencyPaola Bianchi, Elisa Fermo, Fiorella Alfinito, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|April 8, 2010
RAS mutations contribute to evolution of chronic myelomonocytic leukemia to the proliferative variantClara Ricci, Elisa Fermo, Stefania Corti, et al.
Frontiers in Physiology|May 15, 2018
Use of Laser Assisted Optical Rotational Cell Analyzer (LoRRca MaxSis) in the Diagnosis of RBC Membrane Disorders, Enzyme Defects, and Congenital Dyserythropoietic Anemias: A Monocentric Study on 202 PatientsAnna Zaninoni, Elisa Fermo, Cristina Vercellati, et al.
Journal of Pediatric Hematology/Oncology|April 6, 2019
A New Homozygous Mutation (c.393-394del TA/c.393-394del TA) in the NT5C3 Gene Associated With Pyrimidine-5'-Nucleotidase Deficiency: A Case ReportSultan A Köker, Yeşim Oymak, Paola Bianchi, et al.
Pediatric Blood & Cancer|April 14, 2023
Overhydrated hereditary stomatocytosis: A rare cause of familiar persistent macrocytosis due to SLC4A1 variantsAnna Paola Marcello, Camilla Visconti, Cristina Vercellati, et al.
British Journal of Haematology|August 11, 2023
When alpha spectrin null alleles meet low expression alpha spectrin polymorphismsElisa Fermo, Anna Zaninoni, Cristina Vercellati, et al.
Human Mutation|July 22, 2009
Congenital dyserythropoietic anemia type II (CDAII) is caused by mutations in the SEC23B genePaola Bianchi, Elisa Fermo, Cristina Vercellati, et al.
Blood Cells, Molecules & Diseases|April 13, 2010
CDAII presenting as hydrops foetalis: molecular characterization of two casesElisa Fermo, Paola Bianchi, Lucia Dora Notarangelo, et al.
Pageof 10

Showing results (41-50 of 93) with videos related to

Sort By:
Pageof 10
Haematologica|March 18, 2014
Imatinib and ruxolitinib association: first experience in two patientsAlessandra Iurlo, Umberto Gianelli, Davide Rapezzi, et al.
Haematologica|September 8, 2006
Two new mutations of the P5'N-1 gene found in Italian patients with hereditary hemolytic anemia: the molecular basis of the red cell enzyme disorderLaurent R Chiarelli, Elisa Fermo, Patrizia Abrusci, et al.
British Journal of Haematology|August 22, 2003
Molecular characterization of six unrelated Italian patients affected by pyrimidine 5'-nucleotidase deficiencyPaola Bianchi, Elisa Fermo, Fiorella Alfinito, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|April 8, 2010
RAS mutations contribute to evolution of chronic myelomonocytic leukemia to the proliferative variantClara Ricci, Elisa Fermo, Stefania Corti, et al.
Frontiers in Physiology|May 15, 2018
Use of Laser Assisted Optical Rotational Cell Analyzer (LoRRca MaxSis) in the Diagnosis of RBC Membrane Disorders, Enzyme Defects, and Congenital Dyserythropoietic Anemias: A Monocentric Study on 202 PatientsAnna Zaninoni, Elisa Fermo, Cristina Vercellati, et al.
Journal of Pediatric Hematology/Oncology|April 6, 2019
A New Homozygous Mutation (c.393-394del TA/c.393-394del TA) in the NT5C3 Gene Associated With Pyrimidine-5'-Nucleotidase Deficiency: A Case ReportSultan A Köker, Yeşim Oymak, Paola Bianchi, et al.
Pediatric Blood & Cancer|April 14, 2023
Overhydrated hereditary stomatocytosis: A rare cause of familiar persistent macrocytosis due to SLC4A1 variantsAnna Paola Marcello, Camilla Visconti, Cristina Vercellati, et al.
British Journal of Haematology|August 11, 2023
When alpha spectrin null alleles meet low expression alpha spectrin polymorphismsElisa Fermo, Anna Zaninoni, Cristina Vercellati, et al.
Human Mutation|July 22, 2009
Congenital dyserythropoietic anemia type II (CDAII) is caused by mutations in the SEC23B genePaola Bianchi, Elisa Fermo, Cristina Vercellati, et al.
Blood Cells, Molecules & Diseases|April 13, 2010
CDAII presenting as hydrops foetalis: molecular characterization of two casesElisa Fermo, Paola Bianchi, Lucia Dora Notarangelo, et al.
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