Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Elio Boeri"'
Autor:
Augusto B. Federici, Giancarlo Castaman, Massimo Franchini, Massimo Morfini, Ezio Zanon, Antonio Coppola, Annarita Tagliaferri, Elio Boeri, Maria Gabriella Mazzucconi, Gina Rossetti, Pier Mannuccio Mannucci
Publikováno v:
Haematologica, Vol 92, Iss 7 (2007)
Background and Objectives Plasma-derived concentrates containing von Willebrand factor and factor VIII (VWF/FVIII concentrates) are the mainstay of treatment of patients with inherited von Willebrand’s disease (VWD) who are unresponsive or have a c
Externí odkaz:
https://doaj.org/article/464a6b429be6480b92d55fede46e8826
Autor:
Gaia Savioli, Elio Boeri, Manuela Balocco, Gian Luca Forni, Massimo Costantini, Cristina Venturino, Giorgia Gollo
Publikováno v:
Patient preference and adherence
Patient Preference and Adherence, Vol 2013, Iss default, Pp 231-236 (2013)
Patient Preference and Adherence, Vol 2013, Iss default, Pp 231-236 (2013)
Giorgia Gollo,1 Gaia Savioli,2 Manuela Balocco,2 Cristina Venturino,3 Elio Boeri,4 Massimo Costantini,1 Gian Luca Forni21Regional Palliative Care Network, IRCCS AOU San Martino-IST, Genoa; 2Hematology, Center for Thalassemia, Galliera Hospital, Genoa
Autor:
Giorgio Dini, Maura Faraci, Amnon Cohen, Barbara Cappelli, Edoardo Lanino, Sandro Dallorso, Elio Boeri, Giuseppe Morreale, Francesca Scuderi
Publikováno v:
Pediatric Transplantation. 12:117-120
CEP is a rare inborn error of porphyrin-heme synthesis. Clinical manifestations can range from mild to severe and include erythrodontia, reddish-colored urine, and hemolytic anemia that can be mild or severe and may result in splenomegaly. Completely
Autor:
Maria Patrizia Bicocchi, Pier G. Mori, F. Bottini, Angelo Claudio Molinari, Maura Acquila, Camillo Rosano, Elio Boeri, Mirella Pasino, Tiziana Lanza
Publikováno v:
British Journal of Haematology. 122:810-817
Summary. We describe 18 novel mutations, unreported in the Haemophilia A mutation Databases, that have been identified in a cohort of unrelated, Italian patients affected with haemophilia A (HA). Screening of the factor VIII gene (FVIII) was performe
Publikováno v:
American journal of hematology. 84(5)
Autor:
Stefano Avanzini, Valentina Rossi, Angela Basile, Elio Boeri, Vincenzo Jasonni, G. Bisio, Giovanni Montobbio, Sara Costanzo, Caterina Asquasciati, Giovanni Rapuzzi, Alessio Pini Prato, Girolamo Mattioli
Publikováno v:
Journal of laparoendoscopicadvanced surgical techniques. Part A. 19(3)
Either "open" and laparoscopic spleen surgery in pediatric age are well known and performed with ease in children. Yet, few data regarding follow-up and outcome are discussed in the international literature.Clinical notes of all patient who underwent
Autor:
Maria Gabriella Mazzucconi, Massimo Franchini, Augusto B. Federici, Ezio Zanon, Antonio Coppola, Annarita Tagliaferri, Elio Boeri, Massimo Morfini, Pier Mannuccio Mannucci, G. Rossetti, Giancarlo Castaman
Publikováno v:
Haematologica. 92(7)
Plasma-derived concentrates containing von Willebrand factor and factor VIII (VWF/FVIII concentrates) are the mainstay of treatment of patients with inherited von Willebrand's disease (VWD) who are unresponsive or have a contraindication to desmopres
Autor:
Fabio Corsolini, Cristina Morerio, Barbara R. Migeon, Angelo Claudio Molinari, Elio Boeri, Mirella Pasino, F. Bottini, Maura Acquila, Tiziana Lanza, Maria Patrizia Bicocchi
Publikováno v:
European journal of human genetics : EJHG. 13(5)
A basic tenet of the Lyon hypothesis is that X inactivation occurs randomly with respect to parental origin of the X chromosome. Yet, nonrandom patterns of X inactivation are common - often ascertained in women who manifest recessive X-linked disorde
Autor:
Angiola Rocino, Maria Messina, Elena Santagostino, Maria Gabriella Mazzucconi, Annarita Tagliaferri, Giacomo Mancuso, Pier Mannuccio Mannucci, Elio Boeri, Maria Elisa Mancuso, Matteo Luciani
Publikováno v:
Blood. 104:37-37
In a multicenter case-control study we investigated the impact of prenatal/perinatal events and early FVIII exposure on the inhibitor risk in hemophiliacs. Patients: 102 children (age:13–196 months) with hemophilia A (FVIII≤2%) exclusively treate
Autor:
Paolo E Caffarena, Angelo Claudio Molinari, Stefano Amato, Vincenzo Lasonni, Paolo Dodero, Pier Giorgio Mori, Elio Boeri, Sebastiana Odino
Publikováno v:
Pediatric Research. 36:30A-30A
Protein C deficiency is one of the most important cause of thrombosis during early infancy and may have different ways of presentation. We have collected 11 patients, 10 with portal vein thrombosis, 1 with thrombosis of both right and left jugular ve