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

Year Number of Results
2002 5
2003 8
2005 6
2006 5
2007 3
2008 6
2009 5
2010 8
2011 13
2012 3
2013 6
2014 13
2015 7
2016 6
2017 9
2018 13
2019 25
2020 13
2021 21
2022 15
2023 11

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173 results

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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
Mitapivat versus Placebo for Pyruvate Kinase Deficiency.
Al-Samkari H, Galactéros F, Glenthøj A, Rothman JA, Andres O, Grace RF, Morado-Arias M, Layton DM, Onodera K, Verhovsek M, Barcellini W, Chonat S, Judge MP, Zagadailov E, Xu R, Hawkins P, Beynon V, Gheuens S, van Beers EJ; ACTIVATE Investigators. Al-Samkari H, et al. N Engl J Med. 2022 Apr 14;386(15):1432-1442. doi: 10.1056/NEJMoa2116634. N Engl J Med. 2022. PMID: 35417638 Clinical Trial.
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.
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.
Luspatercept for the treatment of anaemia in non-transfusion-dependent β-thalassaemia (BEYOND): a phase 2, randomised, double-blind, multicentre, placebo-controlled trial.
Taher AT, Cappellini MD, Kattamis A, Voskaridou E, Perrotta S, Piga AG, Filosa A, Porter JB, Coates TD, Forni GL, Thompson AA, Tartaglione I, Musallam KM, Backstrom JT, Esposito O, Giuseppi AC, Kuo WL, Miteva D, Lord-Bessen J, Yucel A, Zinger T, Shetty JK, Viprakasit V; BEYOND Investigators. Taher AT, et al. Among authors: perrotta s. Lancet Haematol. 2022 Oct;9(10):e733-e744. doi: 10.1016/S2352-3026(22)00208-3. Epub 2022 Aug 22. Lancet Haematol. 2022. PMID: 36007538 Clinical Trial.
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
Nineteen-month-old girl with persistent fever.
Marzuillo P, Guarino S, Casale M, Di Sessa A, Golino R, D'Angelo V, Menna G, Rossi F, Miraglia Del Giudice E, Perrotta S. Marzuillo P, et al. Among authors: perrotta s. Arch Dis Child Educ Pract Ed. 2020 Oct;105(5):308-310. doi: 10.1136/archdischild-2018-316493. Epub 2019 Feb 23. Arch Dis Child Educ Pract Ed. 2020. PMID: 30798252 No abstract available.
173 results