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Page 1
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: roberti d. 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.
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: roberti d. 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.
Hereditary hypochromic microcytic anemia associated with loss-of-function DMT1 gene mutations and absence of liver iron overload.
Casale M, Borriello A, Scianguetta S, Roberti D, Caiazza M, Bencivenga D, Tartaglione I, Ladogana S, Maruzzi M, Della Ragione F, Perrotta S. Casale M, et al. Among authors: roberti d. Am J Hematol. 2018 Mar;93(3):E58-E60. doi: 10.1002/ajh.24988. Epub 2017 Dec 8. Am J Hematol. 2018. PMID: 29178181 Free article. No abstract available.
No increased cerebrovascular involvement in adult beta-thalassemia by advanced MRI analyses.
Russo AG, Ponticorvo S, Tartaglione I, Caiazza M, Roberti D, Elefante A, Casale M, Di Concilio R, Ciancio A, De Michele E, Canna A, Cirillo M, Perrotta S, Esposito F, Manara R. Russo AG, et al. Among authors: roberti d. Blood Cells Mol Dis. 2019 Sep;78:9-13. doi: 10.1016/j.bcmd.2019.05.001. Epub 2019 May 2. Blood Cells Mol Dis. 2019. PMID: 31102961
Familial neurohypophyseal diabetes insipidus in 13 kindreds and 2 novel mutations in the vasopressin gene.
Patti G, Scianguetta S, Roberti D, Di Mascio A, Balsamo A, Brugnara M, Cappa M, Casale M, Cavarzere P, Cipriani S, Corbetta S, Gaudino R, Iughetti L, Martini L, Napoli F, Peri A, Salerno MC, Salerno R, Passeri E, Maghnie M, Perrotta S, Di Iorgi N. Patti G, et al. Among authors: roberti d. Eur J Endocrinol. 2019 Sep;181(3):233-244. doi: 10.1530/EJE-19-0299. Eur J Endocrinol. 2019. PMID: 31238300 Free article.
Headache in beta-thalassemia: An Italian multicenter clinical, conventional MRI and MR-angiography case-control study.
Tartaglione I, Caiazza M, Di Concilio R, Ciancio A, De Michele E, Maietta C, Valentino MS, Russo C, Roberti D, Casale M, Elefante A, Femina G, Esposito F, Ponticorvo S, Russo AG, Canna A, Ermani M, Cirillo M, Perrotta S, Manara R. Tartaglione I, et al. Among authors: roberti d. Blood Cells Mol Dis. 2020 Mar;81:102403. doi: 10.1016/j.bcmd.2019.102403. Epub 2019 Dec 31. Blood Cells Mol Dis. 2020. PMID: 31918383
Asymptomatic intracranial aneurysms in beta-thalassemia: a three-year follow-up report.
Manara R, Caiazza M, Di Concilio R, Ciancio A, De Michele E, Maietta C, Capalbo D, Russo C, Roberti D, Casale M, Elefante A, Esposito F, Ponticorvo S, Russo AG, Canna A, Cirillo M, Perrotta S, Tartaglione I. Manara R, et al. Among authors: roberti d. Orphanet J Rare Dis. 2020 Jan 20;15(1):21. doi: 10.1186/s13023-020-1302-3. Orphanet J Rare Dis. 2020. PMID: 31959195 Free PMC article.
Effects of Germline VHL Deficiency on Growth, Metabolism, and Mitochondria.
Perrotta S, Roberti D, Bencivenga D, Corsetto P, O'Brien KA, Caiazza M, Stampone E, Allison L, Fleck RA, Scianguetta S, Tartaglione I, Robbins PA, Casale M, West JA, Franzini-Armstrong C, Griffin JL, Rizzo AM, Sinisi AA, Murray AJ, Borriello A, Formenti F, Della Ragione F. Perrotta S, et al. Among authors: roberti d. N Engl J Med. 2020 Feb 27;382(9):835-844. doi: 10.1056/NEJMoa1907362. N Engl J Med. 2020. PMID: 32101665
56 results