SARTORELLO, FRANCESCA

SARTORELLO, FRANCESCA  

Risultati 1 - 20 di 30 (tempo di esecuzione: 0.016 secondi).
Titolo Data di pubblicazione Autore(i) Rivista Serie Titolo libro
Which assay is the most suitable to investigate von Willebrand factor functional activity? 1999 CASONATO, SANDRAPONTARA, ELENABERTOMORO, ANTONELLASARTORELLO, FRANCESCAGIROLAMI, ANTONIO THROMBOSIS AND HAEMOSTASIS - -
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 - -
Plasma and platelet von Willebrand factor abnormalities in patients with uremia: lack of correlation with uremic bleeding. 2001 CASONATO, SANDRAPONTARA, ELENASARTORELLO, FRANCESCAGIROLAMI, ANTONIO + CLINICAL AND APPLIED THROMBOSIS-HEMOSTASIS - -
Von Willebrand factor collagen binding activity in the diagnosis of von Willebrand disease: an alternative to ristocetin co-factor activity? 2001 CASONATO, SANDRAPONTARA, ELENABERTOMORO, ANTONELLASARTORELLO, FRANCESCAGIROLAMI, ANTONIO + BRITISH JOURNAL OF HAEMATOLOGY - -
Type 2M von Willebrand disease variant characterized by abnormal von willebrand factor multimerization. 2001 CASONATO, SANDRAPONTARA, ELENASARTORELLO, FRANCESCABERTOMORO, ANTONELLAGIROLAMI, ANTONIO + JOURNAL OF LABORATORY AND CLINICAL MEDICINE - -
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 - -
Reduced von Willebrand factor survival in type Vicenza von Willebrand disease. 2002 CASONATO, SANDRAPONTARA, ELENASARTORELLO, FRANCESCAPADRINI, ROBERTOGIROLAMI, ANTONIO + BLOOD - -
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 - -
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 - -
Haplotypes of Von Willebrand factor promoter predict thrombotic risk in Cushing's syndrome 2006 DAIDONE, VIVIANASARTORELLO, FRANCESCAALBIGER, NORA MARIA ELVIRAMANTERO, FRANCOPAGNAN, ANTONIOCASONATO, SANDRASCARONI, CARLA - - NA
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 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 - -
Identifying carriers of type 2N von Willebrand disease: procedures and significance. 2007 CASONATO, SANDRAPONTARA, ELENASARTORELLO, FRANCESCABERTOMORO, ANTONELLAGALLINARO, LISAPAGNAN, ANTONIO + CLINICAL AND APPLIED THROMBOSIS-HEMOSTASIS - -
Multiple von Willebrand factor mutations in patients with recessive type 1 von Willebrand disease. 2007 CASONATO, SANDRAGALLINARO, LISAPONTARA, ELENASARTORELLO, FRANCESCADAIDONE, VIVIANAPAGNAN, ANTONIO + THROMBOSIS RESEARCH - -
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 - -
von Willebrand factor propeptide makes it easy to identify the shorter von Willebrand factor survival in patients with type 1 and type Vicenza von Willebrand disease. 2008 GALLINARO, LISAPONTARA, ELENASARTORELLO, FRANCESCADAIDONE, VIVIANAPADRINI, ROBERTOPAGNAN, ANTONIOCASONATO, SANDRA + BRITISH JOURNAL OF HAEMATOLOGY - -
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 - -
Microsatellite (GT)(n) repeats and SNPs in the von Willebrand factor gene promoter do not influence circulating von Willebrand factor levels under normal conditions. 2009 DAIDONE, VIVIANAPONTARA, ELENASARTORELLO, FRANCESCAGALLINARO, LISASCARONI, CARLAPAGNAN, ANTONIOCASONATO, SANDRA + THROMBOSIS AND HAEMOSTASIS - -
Type 1 von Willebrand disease due to reduced von Willebrand factor synthesis and/or survival: observations from a case series. 2010 CASONATO, SANDRAGALLINARO, LISASARTORELLO, FRANCESCAPONTARA, ELENAPADRINI, ROBERTOBERTOMORO, ANTONELLADAIDONE, VIVIANAPAGNAN, ANTONIO + TRANSLATIONAL RESEARCH - -
Higher and lower active circulating VWF levels: different facets of von Willebrand disease 2015 CASONATO, SANDRAPONTARA, ELENAMORPURGO, MARGHERITASARTORELLO, FRANCESCADAIDONE, VIVIANA + BRITISH JOURNAL OF HAEMATOLOGY - -