SARTORELLO, FRANCESCA

SARTORELLO, FRANCESCA  

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Risultati 1 - 20 di 26 (tempo di esecuzione: 0.032 secondi).
Titolo Data di pubblicazione Autori Rivista Serie Titolo libro
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 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 - -
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 - -
Absence of hypercoagulability after nCoV-19 vaccination: An observational pilot study 2021 Campello, ElenaSimion, ChiaraBulato, CristianaRadu, Claudia MGavasso, SabrinaSartorello, FrancescaSaggiorato, GraziellaSpiezia, LucaSimioni, Paolo + THROMBOSIS RESEARCH - -
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 - -
Assessing Clinically Meaningful Hypercoagulability after COVID-19 Vaccination: A Longitudinal Study 2022 Campello, ElenaBulato, CristianaSimion, ChiaraSpiezia, LucaRadu, Claudia MariaGavasso, SabrinaSartorello, FrancescaSaggiorato, GraziellaTormene, DanielaSimioni, Paolo + THROMBOSIS AND HAEMOSTASIS - -
Association between ABO blood group and bleeding phenotype in patients with mild rare bleeding disorders 2018 Spiezia, LucaCampello, ElenaTURATTI, GIACOMOSIMION, CHIARAGavasso, SabrinaSaggiorato, GraziellaSartorello, FrancescaSimioni, Paolo + HAEMOPHILIA - -
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 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 - -
Endocytosis of exogenous factor V by ex-vivo differentiated megakaryocytes from patients with severe parahaemophilia 2016 Radu, Claudia M.Spiezia, LucaBulato, CristianaGavasso, SabrinaCampello, ElenaSartorello, FrancescaSimioni, Paolo + BRITISH JOURNAL OF HAEMATOLOGY - -
Higher and lower active circulating VWF levels: different facets of von Willebrand disease 2015 CASONATO, SANDRAPONTARA, ELENAMORPURGO, MARGHERITASARTORELLO, FRANCESCADAIDONE, VIVIANA + BRITISH JOURNAL OF HAEMATOLOGY - -
Identifying carriers of type 2N von Willebrand disease: procedures and significance. 2007 CASONATO, SANDRAPONTARA, ELENASARTORELLO, FRANCESCABERTOMORO, ANTONELLAGALLINARO, LISAPAGNAN, ANTONIO + CLINICAL AND APPLIED THROMBOSIS-HEMOSTASIS - -
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 - -
Multiple von Willebrand factor mutations in patients with recessive type 1 von Willebrand disease. 2007 CASONATO, SANDRAGALLINARO, LISAPONTARA, ELENASARTORELLO, FRANCESCADAIDONE, VIVIANAPAGNAN, ANTONIO + THROMBOSIS RESEARCH - -
Partial F8 gene duplication (Factor VIII Padua) associated with high factor VIII levels and familial thrombophilia 2020 Simioni, PaoloCagnin, StefanoSartorello, FrancescaSales, GabrielePagani, LucaBulato, CristianaGavasso, SabrinaChemello, FrancescoRadu, Claudia MariaTormene, DanielaSpiezia, LucaCampello, Elena + BLOOD - -
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 - -
Reduced von Willebrand factor survival in type Vicenza von Willebrand disease. 2002 CASONATO, SANDRAPONTARA, ELENASARTORELLO, FRANCESCAPADRINI, ROBERTOGIROLAMI, ANTONIO + BLOOD - -
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 - -
Thromboelastometry hypercoagulable profiles and portal vein thrombosis in cirrhotic patients with hepatocellular carcinoma 2017 ZANETTO, ALBERTOSENZOLO, MARCOVITALE, ALESSANDROCILLO, UMBERTORADU, CLAUDIA-MARIASARTORELLO, FRANCESCASPIEZIA, LUCACAMPELLO, ELENARODRIGUEZ CASTRO, KRYSSIA ISABELFERRARESE, ALBERTOFARINATI, FABIOBURRA, PATRIZIASIMIONI, PAOLO DIGESTIVE AND LIVER DISEASE - -