GALLINARO, LISA

GALLINARO, LISA  

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Titolo Data di pubblicazione Autori Rivista Serie Titolo libro
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 - -
Diagnosis and follow-up of thrombotic thrombocytopenic purpura by means of von Willebrand factor collagen binding assay. 2006 CASONATO, SANDRAFABRIS, FABRIZIOPONTARA, ELENAGALLINARO, LISAGIROLAMI, ANTONIOPAGNAN, ANTONIO + CLINICAL AND APPLIED THROMBOSIS-HEMOSTASIS - -
Altered von Willebrand factor subunit proteolysis and multimer processing associated with the Cys236Phe mutation in the B2 domain 2007 CASONATO, SANDRAGALLINARO, LISASZTUKOWSKA, MARYTAPAGNAN, ANTONIO + THROMBOSIS AND HAEMOSTASIS - -
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 - -
Multiple von Willebrand factor mutations in patients with recessive type 1 von Willebrand disease. 2007 CASONATO, SANDRAGALLINARO, LISAPONTARA, ELENASARTORELLO, FRANCESCADAIDONE, VIVIANAPAGNAN, ANTONIO + THROMBOSIS RESEARCH - -
Identifying carriers of type 2N von Willebrand disease: procedures and significance. 2007 CASONATO, SANDRAPONTARA, ELENASARTORELLO, FRANCESCABERTOMORO, ANTONELLAGALLINARO, LISAPAGNAN, ANTONIO + CLINICAL AND APPLIED THROMBOSIS-HEMOSTASIS - -
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 - -
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 - -
Uneventful coronary artery bypass surgery without prophylatic replacement therapy in a patient with a novel heterozygous FVII gene deletion 2009 GALLINARO LCASONATO, SANDRAVIANELLO, FABRIZIOCELLA, GIUSEPPE + HAEMOPHILIA - -
Reduced survival of type 2B von Willebrand factor, irrespective of large multimer representation or thrombocytopenia. 2010 CASONATO, SANDRAGALLINARO, LISAPONTARA, ELENAPADRINI, ROBERTOBERTOMORO, ANTONELLADAIDONE, VIVIANAPAGNAN, ANTONIO + HAEMATOLOGICA - -
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 - -
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 - -
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 - -