Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Laura Maffei"'
Autor:
Sara Massimi, Marco Gabbianelli, Brigitta Buttari, Laura Maffei, Elisabetta Profumo, Patrizia Caprari, Francesco Sorrentino, Rachele Riganò
Publikováno v:
Annals of hematology. 99(10)
β-Thalassemia is an inherited single gene disorder related to reduced synthesis of the β-globin chain of hemoglobin. Patients with β-thalassemia present variable clinical severity ranging from asymptomatic trait to severe transfusion-dependent ane
Autor:
Francesco Sorrentino, Rocco Rago, Maurizio Poggi, Laura Maffei, Elisabetta Abruzzese, Donatella Dell'Anna, Lorenza Torti, Stefano Aureli, Giovanni Loyola, Paolo de Fabritiis
Publikováno v:
Blood. 136:22-23
Introduction Major thalassemia (TM) and sickle cell disease (SCD), two common genetic hemoglobinopathies, were often fatal 50 years ago. Novel therapeutic and diagnostic methods are increasing lifespan and quality of life. Recent advances in iron che
Autor:
Elisabetta Abruzzese, Rossella Miceli, Francesco Sorrentino, Paolo de Fabritiis, Laura Maffei, Lorenza Torti
Publikováno v:
Mediterranean Journal of Hematology and Infectious Diseases. 12:e2020052
Not required for Letters
Autor:
Vincenzo Toscano, Anna Losardo, Maurizio Poggi, Filomena Terlizzi, Francesco Sorrentino, Francesco Equitani, Carmine Daniele, Maria Paola Smacchia, maria Rita Guitarrini, Methap Pasin, Pellegrina Pugliese, Salvatore Monti, Laura Maffei
Publikováno v:
Annals of hematology. 95(5)
In this study, we compared the long-term effects of different iron chelation regimens (deferoxamine, deferiprone, deferoxamine + deferiprone, and deferasirox) in preventing or reversing endocrinopathy (diabetes mellitus, hypothyroidism, or hypogonadi
Autor:
Christina Cox, A Bruno, Laura Maffei, Francesco Buccisano, Giuseppe Papa, Roberto Stasi, Anna Tamburini, Adriano Venditti, G Aronica, G Del Poeta
Publikováno v:
Blood. 87:418-420
Autor:
Guido Modiano, I Bianco, Mauro Mezzabotta, Paola Di Biagio, Laura Maffei, Lerone M, Enrica Foglietta, D Ponzini, Antonio Amato, Maria Pia Cappabianca, Silvana Rinaldi, Paola Grisanti, Carmelo D'asero, Fabrizio Mastropietro
Publikováno v:
BMC Blood Disorders
BMC Blood Disorders, Vol 2, Iss 1, p 2 (2002)
BMC Blood Disorders, Vol 2, Iss 1, p 2 (2002)
Background The thalassemic syndromes originate from mutations of the globin genes that cause, besides the characteristic clinical picture, also an increased Hb F amount. It is not yet clear if there are more factors, besides the beta globin genotype,
Publikováno v:
Annals of hematology. 73(6)
In some patients compliance to subcutaneous desferrioxamine therapy is reduced because of allergic symptoms. Effective drug desensitization consists of bringing patients to tolerate the same mode of administration. We evaluated three thalassemic pati
Autor:
Sergio Amadori, Laura Maffei, Anna Tamburini, Francesco Buccisano, Adriano Venditti, Roberto Stasi, G Aronica, G Del Poeta, Gaspare Adorno, Maria Christina Cox, Giuseppe Papa, Mario Masi, Maria Domenica Simone, Antonio Bruno, Maurizio Tribalto
FAB proposals for the diagnosis of AML-M0 represent the formal recognition of a distinct entity which has been described over the past few years by several authors and called minimally differentiated acute myeloid leukemia. By definition, AML-M0 incl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f41b613cd3881fdaedc202313950941b
https://hdl.handle.net/2108/50998
https://hdl.handle.net/2108/50998
Autor:
Francesco Buccisano, Adriano Venditti, Giovanni Del Poeta, G Aronica, Laura Maffei, M. Domenica Simone, Anna Tamburini, Sergio Amadori, M. Christina Cox-Froncillo, Antonio Bruno, Giuseppe Papa
Publikováno v:
Blood. 89:345-345
To the Editor: We read with interest the recent letter by Cuneo et al,[1][1] which raises important issues about the diagnosis and classification of acute myeloid leukemia (AML)-M0 and its relation with AML-M1. The authors point out the very high inc