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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: scianguetta s. 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.
Early-onset central diabetes insipidus is associated with de novo arginine vasopressin-neurophysin II or Wolfram syndrome 1 gene mutations.
Perrotta S, Di Iorgi N, Ragione FD, Scianguetta S, Borriello A, Allegri AE, Ferraro M, Santoro C, Napoli F, Calcagno A, Giaccardi M, Cappa M, Salerno MC, Cozzolino D, Maghnie M. Perrotta S, et al. Among authors: scianguetta s. Eur J Endocrinol. 2015 Apr;172(4):461-72. doi: 10.1530/EJE-14-0942. Eur J Endocrinol. 2015. PMID: 25740874
Iron overload enhances human mesenchymal stromal cell growth and hampers matrix calcification.
Borriello A, Caldarelli I, Speranza MC, Scianguetta S, Tramontano A, Bencivenga D, Stampone E, Negri A, Nobili B, Locatelli F, Perrotta S, Oliva A, Della Ragione F. Borriello A, et al. Among authors: scianguetta s. Biochim Biophys Acta. 2016 Jun;1860(6):1211-23. doi: 10.1016/j.bbagen.2016.01.025. Epub 2016 Feb 3. Biochim Biophys Acta. 2016. PMID: 26850692
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: scianguetta s. 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.
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: scianguetta s. Eur J Endocrinol. 2019 Sep;181(3):233-244. doi: 10.1530/EJE-19-0299. Eur J Endocrinol. 2019. PMID: 31238300 Free 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: scianguetta s. N Engl J Med. 2020 Feb 27;382(9):835-844. doi: 10.1056/NEJMoa1907362. N Engl J Med. 2020. PMID: 32101665
A Phase 3 Trial of Luspatercept in Patients with Transfusion-Dependent β-Thalassemia.
Cappellini MD, Viprakasit V, Taher AT, Georgiev P, Kuo KHM, Coates T, Voskaridou E, Liew HK, Pazgal-Kobrowski I, Forni GL, Perrotta S, Khelif A, Lal A, Kattamis A, Vlachaki E, Origa R, Aydinok Y, Bejaoui M, Ho PJ, Chew LP, Bee PC, Lim SM, Lu MY, Tantiworawit A, Ganeva P, Gercheva L, Shah F, Neufeld EJ, Thompson A, Laadem A, Shetty JK, Zou J, Zhang J, Miteva D, Zinger T, Linde PG, Sherman ML, Hermine O, Porter J, Piga A; BELIEVE Investigators. Cappellini MD, et al. N Engl J Med. 2020 Mar 26;382(13):1219-1231. doi: 10.1056/NEJMoa1910182. N Engl J Med. 2020. PMID: 32212518 Clinical Trial.
25 results