PONTARA, ELENA

PONTARA, ELENA  

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Risultati 1 - 20 di 69 (tempo di esecuzione: 0.048 secondi).
Titolo Data di pubblicazione Autori Rivista Serie Titolo libro
A common ancestor more than 10,000 years old for patients with R854Q-related type 2N von Willebrand's disease in Italy. 2013 CASONATO, SANDRADAIDONE, VIVIANAPONTARA, ELENAGALLINARO, LISA + HAEMATOLOGICA - -
A Machine-Learning Model for the Prognostic Role of C-Reactive Protein in Myocarditis 2022 Baritussio A.Lorenzoni G.Basso C.Rizzo S.De Gaspari M.Giordani A. S.Ocagli H.Pontara E.Bison E.Gallo N.Plebani M.Tarantini G.Iliceto S.Gregori D.Caforio A. L. P. + JOURNAL OF CLINICAL MEDICINE - -
A new L1446P mutation is responsible for impaired von Willebrand factor synthesis, structure, and function. 2004 CASONATO, SANDRAMARCATO, STEFANIASARTORELLO, FRANCESCAPONTARA, ELENAPAGNAN, ANTONIO + JOURNAL OF LABORATORY AND CLINICAL MEDICINE - -
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, SANDRAPONTARA, ELENABERTOMORO, ANTONELLAGIROLAMI, ANTONIO + HAEMATOLOGIA - -
A novel von Willebrand factor mutation (11372S) associated with type 2B-like von Willebrand disease: An elusive phenotype and a difficult diagnosis 2007 CASONATO, SANDRASARTORELLO, FRANCESCAPONTARA, ELENAGALLINARO, LISABERTOMORO, ANTONELLADAIDONE, VIVIANAPAGNAN, ANTONIO + THROMBOSIS AND HAEMOSTASIS - -
A shorter von Willebrand factor survival in O blood group subjects explains how ABO determinants influence plasma von Willebrand factor 2008 SZTUKOWSKA, MARYTAPADRINI, ROBERTOSARTORELLO, FRANCESCAPONTARA, ELENABERTOMORO, ANTONELLADAIDONE, VIVIANAPAGNAN, ANTONIOCASONATO, SANDRA + BLOOD - -
Abnormal collagen binding activity of 2A von Willebrand factor: evidence that the defect depends only on the lack of large multimers. 1997 CASONATO, SANDRAPONTARA, ELENABERTOMORO, ANTONELLAGIROLAMI, ANTONIO + JOURNAL OF LABORATORY AND CLINICAL MEDICINE - -
Abnormalities of von Willebrand factor are also part of the prothrombotic state of Cushing's syndrome. 1999 CASONATO, SANDRAPONTARA, ELENABOSCARO, MARCOSONINO, NICOLETTASARTORELLO, FRANCESCAGIROLAMI, ANTONIO + BLOOD COAGULATION & FIBRINOLYSIS - -
Abnormally large von Willebrand factor multimers in Henoch-Schönlein purpura. 1996 CASONATO, SANDRAPONTARA, ELENABERTOMORO, ANTONELLAOSSI, ELENAGIROLAMI, ANTONIOBERTAGLIA, GISELDA + AMERICAN JOURNAL OF HEMATOLOGY - -
Acquired factor VIII:C inhibitor in a patient with Sjögren's syndrome: successful treatment with steroid and immunosuppressive therapy. 1994 CASONATO, SANDRAPONTARA, ELENABERTOMORO, ANTONELLAGIROLAMI, ANTONIO + ACTA HAEMATOLOGICA - -
An apparent silent nucleotide substitution (c.7056C>T) in the von Willebrand factor gene is responsible for type 1 von Willebrand disease. 2011 DAIDONE, VIVIANAGALLINARO, LISAPONTARA, ELENABERTOMORO, ANTONELLAPAGNAN, ANTONIOCASONATO, SANDRA + HAEMATOLOGICA - -
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, SANDRASARTORELLO, FRANCESCAPONTARA, ELENABERTOMORO, ANTONELLAGIROLAMI, ANTONIO + BLOOD - -
Anti-phosphatidyl-serine/prothrombin antibodies (aPS/PT) in isolated lupus anticoagulant (LA): is their presence linked to dual test positivity? 2021 Tonello, MartaBison, ElisaCattini, Maria GraziaPontara, ElenaIaccarino, LucaCheng, Chunyan + CLINICAL CHEMISTRY AND LABORATORY MEDICINE - -
C2362F mutation gives rise to an ADAMTS13-resistant von Willebrand factor 2013 CASONATO, SANDRAPONTARA, ELENAMORPURGO, MARGHERITAPELOSO CATTINI, MARIA GRAZIACASARIN, ELISABETTADAIDONE, VIVIANA + THROMBOSIS AND HAEMOSTASIS - -
Combined exon skipping and cryptic splice activation as a new molecular mechanism for recessive type 1 von Willebrand disease. 2006 GALLINARO, LISASARTORELLO, FRANCESCAPONTARA, ELENABERTOMORO, ANTONELLAPAGNAN, ANTONIOCASONATO, SANDRA + THROMBOSIS AND HAEMOSTASIS - -
Combined haemophilia A and type I von Willebrand's disease: a family study including an evaluation of the effects of DDAVP infusion. 1993 CASONATO, SANDRAPONTARA, ELENABOSCARO, MARCOGIROLAMI, ANTONIO + HAEMATOLOGIA - -
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, SANDRAPONTARA, ELENASARTORELLO, FRANCESCAGIROLAMI, ANTONIO + HAEMATOLOGICA - -
Combined partial exon skipping and cryptic splice site activation as a new molecular mechanism for recessive type 1 von Willebrand disease. 2006 GALLINARO, LISASARTORELLO, FRANCESCAPONTARA, ELENABERTOMORO, ANTONELLAPAGNAN, ANTONIOCASONATO, SANDRA + THROMBOSIS AND HAEMOSTASIS - -
Contraceptive pills induce an improvement in congenital hypoplasminogenemia in two unrelated patients with ligneous conjunctivitis. 2003 SAGGIORATO, GRAZIELLACASONATO, SANDRASpiezia LPONTARA, ELENAGIROLAMI, ANTONIO + THROMBOSIS AND HAEMOSTASIS - -
DDAVP infusion in haemophilia A carriers: different behaviour of plasma factor VIII and von Willebrand factor. 1996 CASONATO, SANDRAPONTARA, ELENABERTOMORO, ANTONELLAGIROLAMI, ANTONIO + BLOOD COAGULATION & FIBRINOLYSIS - -