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Silverio Perrotta

Showing results (161-170 of 200) with videos related to

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Plos One|August 12, 2010
EPO receptor gain-of-function causes hereditary polycythemia, alters CD34 cell differentiation and increases circulating endothelial precursorsSilverio Perrotta, Valeria Cucciolla, Marcella Ferraro, et al.
Cancer|March 14, 2023
Reply to "Hepatocellular carcinoma in thalassemia and other hemoglobinopathies"Raffaella Origa, Barbara Gianesin, Filomena Longo, et al.
American Journal of Hematology|March 7, 2017
Recombinant erythropoietin vs. blood transfusion care in infants with hereditary spherocytosis: a retrospective cohort study of A.I.E.O.P. patients (Associazione Italiana Emato-Oncologia Pediatrica)Piero Farruggia, Giuseppe Puccio, Ugo Ramenghi, et al.
Journal of Racial and Ethnic Health Disparities|May 18, 2020
An Analysis of Racial and Ethnic Backgrounds Within the CASiRe International Cohort of Sickle Cell Disease Patients: Implications for Disease Phenotype and Clinical ResearchAndrew D Campbell, Raffaella Colombatti, Biree Andemariam, et al.
European Journal of Endocrinology|June 26, 2019
Familial neurohypophyseal diabetes insipidus in 13 kindreds and 2 novel mutations in the vasopressin geneGiuseppa Patti, Saverio Scianguetta, Domenico Roberti, et al.
American Journal of Hematology|March 5, 2023
Inflammatory and senescence-associated mediators affect the persistence of humoral response to COVID-19 mRNA vaccination in transfusion-dependent beta-thalassemic patientsVeronica Bordoni, Maddalena Casale, Valeria Maria Pinto, et al.
Haematologica|September 22, 2011
Clinical and laboratory features of 103 patients from 42 Italian families with inherited thrombocytopenia derived from the monoallelic Ala156Val mutation of GPIbα (Bolzano mutation)Patrizia Noris, Silverio Perrotta, Roberta Bottega, et al.
Orphanet Journal of Rare Diseases|June 1, 2019
Current challenges in the management of patients with sickle cell disease - A report of the Italian experienceGiovanna Russo, Lucia De Franceschi, Raffaella Colombatti, et al.
Blood|April 7, 2011
Mutations in ANKRD26 are responsible for a frequent form of inherited thrombocytopenia: analysis of 78 patients from 21 familiesPatrizia Noris, Silverio Perrotta, Marco Seri, et al.
Cancer|November 2, 2022
Incidence of cancer and related deaths in hemoglobinopathies: A follow-up of 4631 patients between 1970 and 2021Raffaella Origa, Barbara Gianesin, Filomena Longo, et al.
Pageof 20

Showing results (161-170 of 200) with videos related to

Sort By:
Pageof 20
Plos One|August 12, 2010
EPO receptor gain-of-function causes hereditary polycythemia, alters CD34 cell differentiation and increases circulating endothelial precursorsSilverio Perrotta, Valeria Cucciolla, Marcella Ferraro, et al.
Cancer|March 14, 2023
Reply to "Hepatocellular carcinoma in thalassemia and other hemoglobinopathies"Raffaella Origa, Barbara Gianesin, Filomena Longo, et al.
American Journal of Hematology|March 7, 2017
Recombinant erythropoietin vs. blood transfusion care in infants with hereditary spherocytosis: a retrospective cohort study of A.I.E.O.P. patients (Associazione Italiana Emato-Oncologia Pediatrica)Piero Farruggia, Giuseppe Puccio, Ugo Ramenghi, et al.
Journal of Racial and Ethnic Health Disparities|May 18, 2020
An Analysis of Racial and Ethnic Backgrounds Within the CASiRe International Cohort of Sickle Cell Disease Patients: Implications for Disease Phenotype and Clinical ResearchAndrew D Campbell, Raffaella Colombatti, Biree Andemariam, et al.
European Journal of Endocrinology|June 26, 2019
Familial neurohypophyseal diabetes insipidus in 13 kindreds and 2 novel mutations in the vasopressin geneGiuseppa Patti, Saverio Scianguetta, Domenico Roberti, et al.
American Journal of Hematology|March 5, 2023
Inflammatory and senescence-associated mediators affect the persistence of humoral response to COVID-19 mRNA vaccination in transfusion-dependent beta-thalassemic patientsVeronica Bordoni, Maddalena Casale, Valeria Maria Pinto, et al.
Haematologica|September 22, 2011
Clinical and laboratory features of 103 patients from 42 Italian families with inherited thrombocytopenia derived from the monoallelic Ala156Val mutation of GPIbα (Bolzano mutation)Patrizia Noris, Silverio Perrotta, Roberta Bottega, et al.
Orphanet Journal of Rare Diseases|June 1, 2019
Current challenges in the management of patients with sickle cell disease - A report of the Italian experienceGiovanna Russo, Lucia De Franceschi, Raffaella Colombatti, et al.
Blood|April 7, 2011
Mutations in ANKRD26 are responsible for a frequent form of inherited thrombocytopenia: analysis of 78 patients from 21 familiesPatrizia Noris, Silverio Perrotta, Marco Seri, et al.
Cancer|November 2, 2022
Incidence of cancer and related deaths in hemoglobinopathies: A follow-up of 4631 patients between 1970 and 2021Raffaella Origa, Barbara Gianesin, Filomena Longo, et al.
Pageof 20