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Long-term improvement in cardiac magnetic resonance in β-thalassemia major patients treated with deferasirox extends to patients with abnormal baseline cardiac function.
Casale M, Filosa A, Ragozzino A, Amendola G, Roberti D, Tartaglione I, De Michele E, Cozzolino D, Rispoli G, Palmieri F, Pugliese U, Scianguetta S, Signoriello G, Musallam KM, Perrotta S. Casale M, et al. Among authors: amendola g. Am J Hematol. 2019 Mar;94(3):312-318. doi: 10.1002/ajh.25370. Epub 2018 Dec 11. Am J Hematol. 2019. PMID: 30489651 Free article.
Endocrine function and bone disease during long-term chelation therapy with deferasirox in patients with β-thalassemia major.
Casale M, Citarella S, Filosa A, De Michele E, Palmieri F, Ragozzino A, Amendola G, Pugliese U, Tartaglione I, Della Rocca F, Cinque P, Nobili B, Perrotta S. Casale M, et al. Among authors: amendola g. Am J Hematol. 2014 Dec;89(12):1102-6. doi: 10.1002/ajh.23844. Epub 2014 Sep 26. Am J Hematol. 2014. PMID: 25197009 Free article. Clinical Trial.
No evidence of increased cerebrovascular involvement in adult neurologically-asymptomatic β-Thalassaemia. A multicentre multimodal magnetic resonance study.
Tartaglione I, Russo C, Elefante A, Caiazza M, Casale M, Di Concilio R, Ciancio A, De Michele E, Amendola G, Gritti P, Carafa PA, Ferrantino T, Centanni A, Ippolito N, Caserta V, Oliveto T, Granato I, Femina G, Esposito F, Ponticorvo S, Russo AG, Canna A, Ermani M, Cirillo M, Perrotta S, Manara R. Tartaglione I, et al. Among authors: amendola g. Br J Haematol. 2019 May;185(4):733-742. doi: 10.1111/bjh.15834. Epub 2019 Mar 5. Br J Haematol. 2019. PMID: 30836432 Free article.
EPO receptor gain-of-function causes hereditary polycythemia, alters CD34 cell differentiation and increases circulating endothelial precursors.
Perrotta S, Cucciolla V, Ferraro M, Ronzoni L, Tramontano A, Rossi F, Scudieri AC, Borriello A, Roberti D, Nobili B, Cappellini MD, Oliva A, Amendola G, Migliaccio AR, Mancuso P, Martin-Padura I, Bertolini F, Yoon D, Prchal JT, Della Ragione F. Perrotta S, et al. Among authors: amendola g. PLoS One. 2010 Aug 5;5(8):e12015. doi: 10.1371/journal.pone.0012015. PLoS One. 2010. Retraction in: PLoS One. 2020 Mar 4;15(3):e0230279. doi: 10.1371/journal.pone.0230279. PMID: 20700488 Free PMC article. Retracted.
Mutations in ANKRD26 are responsible for a frequent form of inherited thrombocytopenia: analysis of 78 patients from 21 families.
Noris P, Perrotta S, Seri M, Pecci A, Gnan C, Loffredo G, Pujol-Moix N, Zecca M, Scognamiglio F, De Rocco D, Punzo F, Melazzini F, Scianguetta S, Casale M, Marconi C, Pippucci T, Amendola G, Notarangelo LD, Klersy C, Civaschi E, Balduini CL, Savoia A. Noris P, et al. Among authors: amendola g. Blood. 2011 Jun 16;117(24):6673-80. doi: 10.1182/blood-2011-02-336537. Epub 2011 Apr 5. Blood. 2011. PMID: 21467542 Free article.
97 results