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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1991 2
1992 3
1993 4
1994 6
1995 5
1996 4
1997 6
1998 8
1999 10
2000 7
2001 10
2002 7
2003 9
2005 8
2006 6
2007 4
2008 11
2009 13
2010 12
2011 18
2012 5
2013 11
2014 18
2015 12
2016 16
2017 15
2018 16
2019 29
2020 18
2021 23
2022 13
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Search Results

292 results
Results by year
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Page 1
Hereditary spherocytosis.
Perrotta S, Gallagher PG, Mohandas N. Perrotta S, et al. Lancet. 2008 Oct 18;372(9647):1411-26. doi: 10.1016/S0140-6736(08)61588-3. Lancet. 2008. PMID: 18940465
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. Among authors: perrotta s. N Engl J Med. 2020 Mar 26;382(13):1219-1231. doi: 10.1056/NEJMoa1910182. N Engl J Med. 2020. PMID: 32212518 Clinical Trial.
Luspatercept improves hemoglobin levels and blood transfusion requirements in a study of patients with β-thalassemia.
Piga A, Perrotta S, Gamberini MR, Voskaridou E, Melpignano A, Filosa A, Caruso V, Pietrangelo A, Longo F, Tartaglione I, Borgna-Pignatti C, Zhang X, Laadem A, Sherman ML, Attie KM. Piga A, et al. Among authors: perrotta s. Blood. 2019 Mar 21;133(12):1279-1289. doi: 10.1182/blood-2018-10-879247. Epub 2019 Jan 7. Blood. 2019. PMID: 30617198 Free PMC article. Clinical Trial.
Clinical and Genetic Findings in Children with Neurofibromatosis Type 1, Legius Syndrome, and Other Related Neurocutaneous Disorders.
Giugliano T, Santoro C, Torella A, Del Vecchio Blanco F, Grandone A, Onore ME, Melone MAB, Straccia G, Melis D, Piccolo V, Limongelli G, Buono S, Perrotta S, Nigro V, Piluso G. Giugliano T, et al. Among authors: perrotta s. Genes (Basel). 2019 Jul 31;10(8):580. doi: 10.3390/genes10080580. Genes (Basel). 2019. PMID: 31370276 Free PMC article.
Mutations affecting the secretory COPII coat component SEC23B cause congenital dyserythropoietic anemia type II.
Schwarz K, Iolascon A, Verissimo F, Trede NS, Horsley W, Chen W, Paw BH, Hopfner KP, Holzmann K, Russo R, Esposito MR, Spano D, De Falco L, Heinrich K, Joggerst B, Rojewski MT, Perrotta S, Denecke J, Pannicke U, Delaunay J, Pepperkok R, Heimpel H. Schwarz K, et al. Among authors: perrotta s. Nat Genet. 2009 Aug;41(8):936-40. doi: 10.1038/ng.405. Epub 2009 Jun 28. Nat Genet. 2009. PMID: 19561605 Free article.
Hearing Loss in Beta-Thalassemia: Systematic Review.
Tartaglione I, Carfora R, Brotto D, Barillari MR, Costa G, Perrotta S, Manara R. Tartaglione I, et al. Among authors: perrotta s. J Clin Med. 2021 Dec 25;11(1):102. doi: 10.3390/jcm11010102. J Clin Med. 2021. PMID: 35011846 Free PMC article. Review.
Effects of Iron Chelation in Osteosarcoma.
Argenziano M, Di Paola A, Tortora C, Di Pinto D, Pota E, Di Martino M, Perrotta S, Rossi F, Punzo F. Argenziano M, et al. Among authors: perrotta s. Curr Cancer Drug Targets. 2021;21(5):443-455. doi: 10.2174/1568009620666201230090531. Curr Cancer Drug Targets. 2021. PMID: 33380300
Pulmonary artery dissection.
Perrotta S, Lentini S. Perrotta S, et al. J Card Surg. 2015 May;30(5):442-7. doi: 10.1111/jocs.12529. Epub 2015 Feb 27. J Card Surg. 2015. PMID: 25728535 Review.
Auditory cortex hypoperfusion: a metabolic hallmark in Beta Thalassemia.
Manara R, Ponticorvo S, Perrotta S, Barillari MR, Costa G, Brotto D, Di Concilio R, Ciancio A, De Michele E, Carafa PA, Canna A, Russo AG, Troisi D, Caiazza M, Ammendola F, Roberti D, Santoro C, Picariello S, Valentino MS, Inserra E, Carfora R, Cirillo M, Raimo S, Santangelo G, di Salle F, Esposito F, Tartaglione I. Manara R, et al. Among authors: perrotta s. Orphanet J Rare Dis. 2021 Aug 5;16(1):349. doi: 10.1186/s13023-021-01969-0. Orphanet J Rare Dis. 2021. PMID: 34353346 Free PMC article.
292 results