Zobrazeno 1 - 10
of 33
pro vyhledávání: '"Berardino, Pollio"'
Autor:
Cristina Olgasi, Chiara Borsotti, Simone Merlin, Thorsten Bergmann, Patrick Bittorf, Adeolu Badi Adewoye, Nicholas Wragg, Kelcey Patterson, Andrea Calabria, Fabrizio Benedicenti, Alessia Cucci, Alessandra Borchiellini, Berardino Pollio, Eugenio Montini, Delfina M. Mazzuca, Martin Zierau, Alexandra Stolzing, Philip.M. Toleikis, Joris Braspenning, Antonia Follenzi
Publikováno v:
Molecular Therapy: Methods & Clinical Development, Vol 23, Iss , Pp 551-566 (2021)
Hemophilia A (HA) is a rare bleeding disorder caused by deficiency/dysfunction of the FVIII protein. As current therapies based on frequent FVIII infusions are not a definitive cure, long-term expression of FVIII in endothelial cells through lentivir
Externí odkaz:
https://doaj.org/article/7a58ac952d7247cb827b394f9103e931
Autor:
Annarita Tagliaferri, Angelo Claudio Molinari, Flora Peyvandi, Antonio Coppola, Francesco Demartis, Chiara Biasoli, Alessandra Borchiellini, Dorina Cultrera, Raimondo De Cristofaro, Filomena Daniele, Paola Giordano, Emanuela Marchesini, Maurizio Margaglione, Renato Marino, Berardino Pollio, Paolo Radossi, Cristina Santoro, Rita Carlotta Santoro, Sergio Siragusa, Gianluca Sottilotta, Alberto Tosetto, Lydia Piscitelli, Maria Rosaria Villa, Ezio Zanon, Adele Finardi, Irene Schiavetti, Daniella Vaccari, Giancarlo Castaman
Publikováno v:
Haemophilia. 29:135-144
Introduction: Factor IX replacement therapy is used for treatment and prophylaxis of bleeding in haemophilia B. rIX-FP is an extended half-life albumin-fusion protein, which, in clinical studies, has demonstrated prolonged dosing intervals up to 21 d
Autor:
Patrizia Tessiatore, Riccardo Guanà, Salvatore Garofalo, Riccardo Lemini, Valentina Marchese, Berardino Pollio, Fabrizio Gennari
Publikováno v:
Pediatrics and Neonatology, Vol 61, Iss 4, Pp 455-456 (2020)
Externí odkaz:
https://doaj.org/article/22405a0675c04d88ab1a094d99b3a7e4
Autor:
Giancarlo Castaman, Flora Peyvandi, Raimondo De Cristofaro, Berardino Pollio, Dario M. N. Di Minno
Hemophilia A (HA) is an inherited X-linked bleeding disorder, caused by the deficiency of coagulation factor VIII (FVIII), with variable clinical phenotypes [...]
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d84cfc185ea8c5819fbe5e64ade8928b
https://hdl.handle.net/11588/915306
https://hdl.handle.net/11588/915306
Autor:
Berardino, Pollio, Irene, Ricca, Cristina, Dainese, Federica, Valeri, Alessandra, Valpreda, Claudia, Linari, Alessandra, Borchiellini
Publikováno v:
Acta bio-medica : Atenei Parmensis. 93(5)
Haemophilia and von Willebrand disease are the bleeding disorders most frequently encountered in the emergency department (ED), that are often the first point of contact for patients. Evidence suggests that management in the ED is currently suboptima
Autor:
Ezio, Zanon, Samantha, Pasca, Gianluca, Sottilotta, Angelo C, Molinari, Antonietta, Ferretti, Patrizia, Di Gregorio, Berardino, Pollio, Michele, Pizzuti, Lucia Dora, Notarangelo, Chiara, Biasoli, Piergiorgio, Cojutti, Federico, Pea, Paolo, Simioni, Flora, Peyvandi
Publikováno v:
Blood transfusion = Trasfusione del sangue.
Congenital factor XIII (FXIII) deficiency is a rare coagulation disorder characterized by muscular or mucocutaneous bleeding with life-threatening intracranial hemorrhages (ICHs), especially in cases with severe disease. The best treatment is the use
Autor:
Giovanni Del Borrello, Carlo Scolfaro, Giulia Pruccoli, Claudia Linari, Marco Denina, Federica Mignone, Isaac Giraudo, Manuela Spadea, Silvia Garazzino, Paola Saracco, Berardino Pollio, Claudia Bondone
Publikováno v:
Journal of Thrombosis and Haemostasis
Multiple investigators have described an increased incidence of thromboembolic events in SARS-CoV-2-infected individuals. Data concerning hemostatic complications in children hospitalized for COVID-19/multisystem inflammatory syndrome in children (MI
Autor:
Ezio Zanon, Samantha Pasca, Francesco Demartis, Annarita Tagliaferri, Cristina Santoro, Isabella Cantori, Angelo Claudio Molinari, Chiara Biasoli, Antonio Coppola, Matteo Luciani, Gianluca Sottilotta, Irene Ricca, Berardino Pollio, Alessandra Borchiellini, Alberto Tosetto, Flora Peyvandi, Anna Chiara Frigo, Paolo Simioni
Publikováno v:
Journal of Clinical Medicine; Volume 11; Issue 7; Pages: 1969
Background: Intracranial hemorrhage (ICH) is a highly serious event in patients with haemophilia (PWH) which leads to disability and in some cases to death. ICH occurs among all ages but is particularly frequent in newborns. Aim: The primary aim was
Autor:
Cristina Santoro, Antonietta Ferretti, Angiola Rocino, Paola Giordano, Angelo Claudio Molinari, Michele Schiavulli, Berardino Pollio, Ezio Zanon, Giuseppe Malcangi, Maurizio Margaglione, Matteo Luciani, Giancarlo Castaman, Giulio Feola, Alessandra Borchiellini
Publikováno v:
Journal of thrombosis and thrombolysis. 53(4)
rVIII-SingleChain is indicated for treatment and prophylaxis of bleeding in patients with haemophilia A (HA). The safety and efficacy of rVIII-SingleChain have previously been shown in the AFFINITY clinical trial programme. This survey evaluated clin
Autor:
Matteo Luciani, Anna Maria Testi, Concetta Micalizzi, Silvio Tafuri, Carmelo Rizzari, Nicola Santoro, Maria C. Putti, Caterina Consarino, Paola Giordano, Berardino Pollio, Antonella Colombini, Lucia Dora Notarangelo, Elena Mastrodicasa, Paola Carmela Corallo, Fara Petruzziello, Fiorina Casale, Rosa M. Mura, Daniela Onofrillo, Francesco De Leonardis, Paola Saracco, Massimo Grassi
Publikováno v:
Journal of Pediatric Hematology/Oncology. 41:275-279
Objective of the Study:In this study we aimed to retrospectively evaluate how centers, belonging to the Associazione Italiana Ematologia e Oncologia Pediatrica (AIEOP), manage severe acquired hypofibrinogenemia in children with acute lymphoblastic le