PONTARA, ELENA
PONTARA, ELENA
A common ancestor more than 10,000 years old for patients with R854Q-related type 2N von Willebrand's disease in Italy.
2013 Casonato, Sandra; Daidone, Viviana; Barbon, G; Pontara, Elena; Di Pasquale, I; Gallinaro, Lisa; Marullo, L; Bertorelle, G.
A Machine-Learning Model for the Prognostic Role of C-Reactive Protein in Myocarditis
2022 Baritussio, A.; Cheng, C. Y.; Lorenzoni, G.; Basso, C.; Rizzo, S.; De Gaspari, M.; Fachin, F.; Giordani, A. S.; Ocagli, H.; Pontara, E.; Cattini, M. G. P.; Bison, E.; Gallo, N.; Plebani, M.; Tarantini, G.; Iliceto, S.; Gregori, D.; Marcolongo, R.; Caforio, A. L. P.
A new L1446P mutation is responsible for impaired von Willebrand factor synthesis, structure, and function.
2004 Casonato, Sandra; Cattini, Mg; Soldera, C; Marcato, Stefania; Sartorello, Francesca; Pontara, Elena; Pagnan, Antonio
A new variant of von Willebrand's disease (type I Padua): doublet-organized plasma von Willebrand factor oligomers in the presence of all size multimers.
1994 Casonato, Sandra; Pontara, Elena; Dannhäuser, D; Bertomoro, Antonella; Sartori, Mt; Girolami, Antonio
A novel von Willebrand factor mutation (11372S) associated with type 2B-like von Willebrand disease: An elusive phenotype and a difficult diagnosis
2007 Casonato, Sandra; Sartorello, Francesca; Pontara, Elena; Gallinaro, Lisa; Bertomoro, Antonella; Cattini, Mg; Daidone, Viviana; Szukowska, M; Pagnan, Antonio
A shorter von Willebrand factor survival in O blood group subjects explains how ABO determinants influence plasma von Willebrand factor
2008 Gallinaro, Lisa; Cattini, Mg; Sztukowska, Maryta; Padrini, Roberto; Sartorello, Francesca; Pontara, Elena; Bertomoro, Antonella; Daidone, Viviana; Pagnan, Antonio; Casonato, Sandra
Abnormal collagen binding activity of 2A von Willebrand factor: evidence that the defect depends only on the lack of large multimers.
1997 Casonato, Sandra; Pontara, Elena; Bertomoro, Antonella; Zucchetto, S; Zerbinati, P; Girolami, Antonio
Abnormalities of von Willebrand factor are also part of the prothrombotic state of Cushing's syndrome.
1999 Casonato, Sandra; Pontara, Elena; Boscaro, Marco; Sonino, Nicoletta; Sartorello, Francesca; Ferasin, S.; Girolami, Antonio
Abnormally large von Willebrand factor multimers in Henoch-Schönlein purpura.
1996 Casonato, Sandra; Pontara, Elena; Bertomoro, Antonella; Ossi, Elena; Vincenti, M; Girolami, Antonio; Borsatti, A; Bertaglia, Giselda
Acquired factor VIII:C inhibitor in a patient with Sjögren's syndrome: successful treatment with steroid and immunosuppressive therapy.
1994 Dannhäuser, D; Casonato, Sandra; Pietrogrande, F; Pontara, Elena; Bertomoro, Antonella; Zerbinati, P; Girolami, Antonio
An apparent silent nucleotide substitution (c.7056C>T) in the von Willebrand factor gene is responsible for type 1 von Willebrand disease.
2011 Daidone, Viviana; Gallinaro, Lisa; Cattini, Mg; Pontara, Elena; Bertomoro, Antonella; Pagnan, Antonio; Casonato, Sandra
An Arg760Cys mutation in the consensus sequence of the von Willebrand factor propeptide cleavage site is responsible for a new von Willebrand disease variant.
2003 Casonato, Sandra; Sartorello, Francesca; Cattini, Mg; Pontara, Elena; Soldera, C; Bertomoro, Antonella; Girolami, Antonio
Anti-phosphatidyl-serine/prothrombin antibodies (aPS/PT) in isolated lupus anticoagulant (LA): is their presence linked to dual test positivity?
2021 Tonello, Marta; Bison, Elisa; Cattini, Maria Grazia; Pontara, Elena; Iaccarino, Luca; Denas, Gentian; Cheng, Chunyan; Pengo, Vittorio
C2362F mutation gives rise to an ADAMTS13-resistant von Willebrand factor
2013 Casonato, Sandra; Pontara, Elena; Battiston, M; Morpurgo, Margherita; PELOSO CATTINI, MARIA GRAZIA; Casarin, Elisabetta; Saga, G; Daidone, Viviana; De Marco, L.
Cellular Immunology of Myocarditis: Lights and Shades—A Literature Review
2024 Vicenzetto, C.; Giordani, A. S.; Menghi, C.; Baritussio, A.; Scognamiglio, F.; Pontara, E.; Bison, E.; Peloso-Cattini, M. G.; Marcolongo, R.; Caforio, A. L. P.
Combined exon skipping and cryptic splice activation as a new molecular mechanism for recessive type 1 von Willebrand disease.
2006 Gallinaro, Lisa; Sartorello, Francesca; Pontara, Elena; Cattini, Mg; Bertomoro, Antonella; Bartoloni, L; Pagnan, Antonio; Casonato, Sandra
Combined haemophilia A and type I von Willebrand's disease: a family study including an evaluation of the effects of DDAVP infusion.
1993 Casonato, Sandra; Pontara, Elena; Boscaro, Marco; Dannhauser, D; Sartori, Mt; Girolami, Antonio
Combined hemophilia A and type 2 von Willebrand's disease: defect of both factor VIII level and factor VIII binding capacity of von Willebrand factor.
2001 Casonato, Sandra; Pontara, Elena; Sartorello, Francesca; Gemmati, D; Cattini, Mg; Girolami, Antonio
Combined partial exon skipping and cryptic splice site activation as a new molecular mechanism for recessive type 1 von Willebrand disease.
2006 Gallinaro, Lisa; Sartorello, Francesca; Pontara, Elena; Cattini, Mg; Bertomoro, Antonella; Bartoloni, L; Pagnan, Antonio; Casonato, Sandra
Contraceptive pills induce an improvement in congenital hypoplasminogenemia in two unrelated patients with ligneous conjunctivitis.
2003 Teresa Sartori, M; Saggiorato, Graziella; Pellati, D; Casonato, Sandra; Spiezia, L; Pontara, Elena; Gavasso, S; Girolami, Antonio