Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Nicolina Giagu"'
Autor:
Raffaella Origa, Mario Cazzola, Elisabetta Mereu, Fabrice Danjou, Susanna Barella, Nicolina Giagu, Renzo Galanello, Dorine W. Swinkels
Publikováno v:
Haematologica, Vol 100, Iss 5 (2015)
Externí odkaz:
https://doaj.org/article/122b84939a3b4de780f9a2774292e848
Autor:
Fabrice Danjou, Zvi Ioav Cabantchik, Raffaella Origa, Paolo Moi, Michela Marcias, Susanna Barella, Elisabetta Defraia, Carlo Dessì, Maria Loreta Foschini, Nicolina Giagu, Giovan Battista Leoni, Maddalena Morittu, Renzo Galanello
Publikováno v:
Haematologica, Vol 99, Iss 3 (2014)
Externí odkaz:
https://doaj.org/article/67e5a64fac5844e1993f651439495efa
Autor:
Maria Carla Sollaino, Maria Elisabetta Paglietti, Lucia Perseu, Nicolina Giagu, Daniela Loi, Renzo Galanello
Publikováno v:
Haematologica, Vol 94, Iss 10 (2009)
Ten patients with thalassemia intermedia with variable severity and apparent simple heterozygosis for β0 39 C>T nonsense mutation were submitted to clinical, hematologic and molecular studies. The presence of an unknown molecular defect (silent β-t
Externí odkaz:
https://doaj.org/article/5abc5df829474fc4bbe431b5ba2a8f7f
Autor:
Raffaella Origa, Renzo Galanello, Tomas Ganz, Nicolina Giagu, Liliana Maccioni, Gavino Faa, Elizabeta Nemeth
Publikováno v:
Haematologica, Vol 92, Iss 5 (2007)
Background and Objectives Patients with β-thalassemia, like those with genetic hemochromatosis, develop iron overload due to increased iron absorption, and their iron burden is further exacerbated by transfusion therapy. Hepcidin, a hepatic hormone,
Externí odkaz:
https://doaj.org/article/b39c9935e3a44343b2114068eaff4acd
Autor:
Susanna Barella, Raffaella Origa, Paolo Moi, Carlo Dessì, Michela Marcias, Renzo Galanello, Elisabetta Defraia, Maria Loreta Foschini, Maddalena Morittu, Zvi Ioav Cabantchik, Giovan Battista Leoni, Fabrice Danjou, Nicolina Giagu
Publikováno v:
Haematologica. 99:e38-e40
Since the implementation of deferrioxamine for the treatment of thalassemia major, it has been customary to initiate chelation after the first 10–20 transfusions or when serum ferritin reached over 1000 mcg/L.[1][1] However, in non-chronically-tran
Autor:
Elizabeta Nemeth, Nicolina Giagu, Tomas Ganz, Renzo Galanello, Raffaella Origa, Gavino Faa, L Maccioni
Publikováno v:
Haematologica. 92:583-588
Background and Objectives Patients with β-thalassemia, like those with genetic hemochromatosis, develop iron overload due to increased iron absorption, and their iron burden is further exacerbated by transfusion therapy. Hepcidin, a hepatic hormone,
Autor:
Susanna Barella, Simona Campus, Raffaella Origa, Renzo Galanello, Patrizio Bina, Maria Carla Sollaino, L Perseu, C. Mandas, Nicolina Giagu
Publikováno v:
British Journal of Haematology. 136:326-332
In this study, 251 Sardinian patients (187 adults and 64 children) with haemoglobin (Hb) H disease were evaluated. Two-hundred and sixteen patients (86%) had the deletional type (- -/-alpha) and 36 (14%) patients had the non-deletional type (- -/alph
Publikováno v:
Blood Cells, Molecules, and Diseases. 48:121-123
Mutations in TMPRSS6 gene cause iron-refractory iron deficiency anemia, a rare autosomal recessive disorder characterized by hypochromic microcytic anemia not responsive to oral iron therapy and partially responsive to parenteral iron administration.
Autor:
Fausto Dore, Maria P. Turco, Nicola L. Liberato, Renzo Galanello, Susanna Barella, Antonio Cao, Nicolina Giagu, Giovanni Barosi, Roberta Guarnone
Publikováno v:
Blood. 83:561-565
Clinical data suggest that in 8-thalassemia-intermedia patients, higher levels of circulating fetal hemoglobin (HbF) are associated with greater disease severity at comparable degrees of anemia. We assessed the influence of the amount of circulating
Publikováno v:
Blood cells, moleculesdiseases. 48(1)
Variations at the KLF1 gene have been associated with a series of human erythroid phenotypes including the In-(Lu) phenotype, hereditary persistence of fetal hemoglobin, congenital dyserythropoietic anemia, borderline HbA2 and increased red blood cel