PERROTTA, Silverio

PERROTTA, Silverio  

Dipartimento della Donna, del Bambino e di Chirurgia Generale e Specialistica  

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4.2 Nippon mutation in a non-Japanese patient with hereditary spherocytosis [3] 1-gen-1999 Perrotta, Silverio; Iolascon, A; Polito, R; D'Urzo, G; Conte, Ml; MIRAGLIA DEL GIUDICE, Emanuele
A 23-month-old girl with chronic seborrhoeic' dermatitis, dehydration and failure to thrive 1-gen-2019 Marzuillo, Pierluigi; Grandone, Anna; Guarino, Stefano; Apicella, Andrea; Panarese, Iacopo; Picciano, Ludovica; Fedele, Maria Cristina; Palladino, Federica; Perrotta, Silverio; Miraglia Del Giudice, Emanuele
A cancer-associated CDKN1B mutation induces p27 phosphorylation on a novel residue: a new mechanism for tumor suppressor loss-of-function 1-gen-2021 Bencivenga, Debora; Stampone, Emanuela; Aulitto, Arianna; Tramontano, Annunziata; Barone, Clementina; Negri, Aide; Roberti, Domenico; Perrotta, Silverio; Della Ragione, Fulvio; Borriello, Adriana
A deletional frameshift mutation in spectrin beta-gene associated with hereditary elliptocytosis in spectrin Napoli 1-gen-1994 Wilmotte, R; MIRAGLIA DEL GIUDICE, Emanuele; Marechal, J; Perrotta, Silverio; DE MATTIA, D; Delaunay, J; Iolascon, A.
A genome search for primary vesicoureteral reflux shows further evidence for genetic heterogeneity 1-gen-2008 Conte, Ml; BERTOLI AVELLA, Am; DE GRAAF, Bm; Punzo, F; Lama, G; LA MANNA, A; Grassia, C; Rambaldi, Pier Francesco; Oostra, Ba; Perrotta, Silverio
A mutation in the acyl-coenzyme A binding domain-containing protein 5 gene (ACBD5 ) identified in autosomal dominant thrombocytopenia 1-gen-2010 Punzo, F; Mientjes, Ej; Rohe, Cf; Scianguetta, S; Amendola, G; Oostra, Ba; BERTOLI AVELLA, Am; Perrotta, Silverio
A Novel 12q13.2-q13.3 Microdeletion Syndrome With Combined Features of Diamond Blackfan Anemia, Pierre Robin Sequence and Klippel Feil Deformity 1-gen-2018 Roberti, Domenico; Conforti, Renata; Giugliano, Teresa; Brogna, Barbara; Tartaglione, Immacolata; Casale, Maddalena; Piluso, Giulio; Perrotta, Silverio
A novel MEIS2 mutation explains the complex phenotype in a boy with a typical NF1 microdeletion syndrome 1-gen-2021 Santoro, Claudia; Riccio, Simona; Palladino, Federica; Aliberti, Ferdinando; Carotenuto, Marco; Zanobio, Mariateresa; Peduto, Cristina; Nigro, Vincenzo; Perrotta, Silverio; Piluso, Giulio
A phase 3 study of deferasirox (ICL670), a once-daily oral iron chelator, in patients with beta-thalassemia. 1-gen-2006 Cappellini, M.; Cohen, A.; Piga, A.; Bejaoui, M.; Perrotta, Silverio; Agaoglu, L.; Aydinok, Y.; Kattamis, A.; Kilinc, Y.; Porter, J.; Capra, M.; Galanello, R.; Fattoum, S.; Drelichman, G.; Magnano, C.; Verissimo, M.; ATHANASSIOU METAXA, M.; Giardina, P.; KOURAKLI SYMEONIDIS, A.; JANKA SCHAUB, G.; Coates, T.; Vermylen, C.; Ollivieri, N.; Thuret, I.; Opitz, H.; RESSAYRE DJAFFER, C.; Marks, P.; Alberti, D.
A phase 3 trial of luspatercept in patients with transfusion-dependent β-thalassemia 1-gen-2020 Domenica Cappellini, M.; Viprakasit, V.; Taher, A. T.; Georgiev, P.; Kuo, K. H. M.; Coates, T.; Voskaridou, E.; Liew, H. -K.; Pazgal-Kobrowski, I.; Forni, G. L.; Perrotta, S.; Khelif, A.; Lal, A.; Kattamis, A.; Vlachaki, E.; Origa, R.; Aydinok, Y.; Bejaoui, M.; Joy Ho, P.; Chew, L. -P.; Bee, P. -C.; Lim, S. -M.; Lu, M. -Y.; Tantiworawit, A.; Ganeva, P.; Gercheva, L.; Shah, F.; Neufeld, E. J.; Thompson, A.; Laadem, A.; Shetty, J. K.; Zou, J.; Zhang, J.; Miteva, D.; Zinger, T.; Linde, P. G.; Sherman, M. L.; Hermine, O.; Porter, J.; Piga, A.
A rapid method for the detection of alpha I/65 hereditary elliptocytosis 1-gen-1993 Iolascon, A; MIRAGLIA DEL GIUDICE, Emanuele; Perrotta, Silverio; Pinto, L; Cutillo, S.
A study of the geographic distribution and associated risk factors of leg ulcers within an international cohort of sickle cell disease patients: the CASiRe group analysis 1-gen-2020 Antwi-Boasiako, C.; Andemariam, B.; Colombatti, R.; Asare, E. V.; Strunk, C.; Piccone, C. M.; Manwani, D.; Boruchov, D.; Farooq, F.; Urbonya, R.; Wilson, S.; Boatemaa, G. D.; Perrotta, S.; Sainati, L.; Rivers, A.; Rao, S.; Zempsky, W.; Ekem, I.; Sey, F.; Segbefia, C.; Inusa, B.; Tartaglione, I.; Campbell, A. D.
Abbreviated breast magnetic resonance imaging (FAST-MRI): A novel approach to breast cancer screening in patients with previous Hodgkin lymphoma 1-gen-2019 Indolfi, C; Cappabianca, S; Rossi, F; Perrotta, S; Procaccini, E; Pota, E; Martino, Md; Pinto, Dd; Casale, F; Indolfi, P.
Abnormalities of erythrocyte glycoconjugates are identical in two families with congenital dyserythropoietic anemia type II with different chromosomal localizations of the disease gene 1-gen-2007 Zdebska, E; Iolascon, A; Spychalska, J; Perrotta, Silverio; Lanzara, C; SMOLENSKA SYM, G; Koscielak, J.
Absence of blood donors’ anti-SARS-CoV-2 antibodies in pre-storage leukoreduced red blood cell units indicates no role of passive immunity for blood recipients 1-gen-2024 Casale, M.; Di Girolamo, M. G.; Di Maio, N.; Tomeo, R.; Iengo, M.; Scianguetta, S.; Palma, T.; Porcelli, F.; Misso, S.; Perrotta, S.
Absence of CYCS mutations in a large Italian cohort of patients with inherited thrombocytopenias of unknown origin 1-gen-2009 Savoia, A; Noris, P; Perrotta, Silverio; Punzo, F; Rocco, Dd; Oostra, Ba; Balduini, Cl
Acute events in children with sickle cell disease in Italy during the COVID-19 pandemic: useful lessons learned 1-gen-2021 Munaretto, V.; Voi, V.; Palazzi, G.; Notarangelo, L. D.; Corti, P.; Baretta, V.; Casale, M.; Barone, A.; Cuzzubbo, D.; Samperi, P.; Tripodi, S.; Giona, F.; Miano, M.; Nocerino, A.; Del Vecchio, G. C.; Piccolo, C.; Sau, A.; Filippini, B.; Casciana, M. L.; Arcioni, F.; Migliavacca, M.; Saracco, P.; Gorio, C.; Cesaro, S.; Perrotta, S.; Zecca, M.; Giordano, P.; Fasoli, S.; Coppadoro, B.; Russo, G.; Sainati, L.; Colombatti, R.
Acute kidney injury in children hospitalized for acute gastroenteritis: prevalence and risk factors 1-gen-2021 Marzuillo, Pierluigi; Baldascino, Maria; Guarino, Stefano; Perrotta, Silverio; Miraglia Del Giudice, Emanuele; Nunziata, Felice
Age of first pain crisis and associated complications in the CASiRe international sickle cell disease cohort 1-gen-2021 Tartaglione, I.; Strunk, C.; Antwi-Boasiako, C.; Andemariam, B.; Colombatti, R.; Asare, E. V.; Piccone, C. M.; Manwani, D.; Boruchov, D.; Tavernier, F.; Farooq, F.; Akatue, S.; Oteng, B.; Urbonya, R.; Wilson, S.; Owda, A.; Bamfo, R.; Boatemaa, G. D.; Rao, S.; Zempsky, W.; Sey, F.; Inusa, B. P.; Perrotta, S.; Segbefia, C.; Campbell, A. D.
Alpha I/65 hereditary elliptocytosis in southern Italy: evidence for an African origin 1-gen-1992 MIRAGLIA DEL GIUDICE, Emanuele; Ducluzeau, Mt; Alloisio, N; Wilmotte, R; Delaunay, J; Perrotta, Silverio; Cutillo, S; Iolascon, A.