Publications by authors named "Lisa Gallinaro"

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A common ancestor more than 10,000 years old for patients with R854Q-related type 2N von Willebrand's disease in Italy.
Alessandra Casonato, Viviana Daidone, Giovanni Barbon, Elena Pontara, Irene Di Pasquale, Lisa Gallinaro

Haematologica· January 2013

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An apparently silent nucleotide substitution (c.7056C>T) in the von Willebrand factor gene is responsible for type 1 von Willebrand disease.
Viviana Daidone, Lisa Gallinaro, Maria Grazia Cattini, Elena Pontara, Antonella Bertomoro

Haematologica· June 2011

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Reduced survival of type 2B von Willebrand factor, irrespective of large multimer representation or thrombocytopenia.
Alessandra Casonato, Lisa Gallinaro, Maria Grazia Cattini, Elena Pontara, Roberto Padrini

Haematologica· August 2010

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Type 1 von Willebrand disease due to reduced von Willebrand factor synthesis and/or survival: observations from a case series.
Alessandra Casonato, Lisa Gallinaro, Maria Grazia Cattini, Francesca Sartorello, Elena Pontara

Transl Res· April 2010

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Microsatellite (GT)(n) repeats and SNPs in the von Willebrand factor gene promoter do not influence circulating von Willebrand factor levels under normal conditions.
Viviana Daidone, Maria Grazia Cattini, Elena Pontara, Francesca Sartorello, Lisa Gallinaro

Thromb Haemost· February 2009

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A shorter von Willebrand factor survival in O blood group subjects explains how ABO determinants influence plasma von Willebrand factor.
Lisa Gallinaro, Maria Grazia Cattini, Maryta Sztukowska, Roberto Padrini, Francesca Sartorello

Blood· April 2008

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A novel von Willebrand factor mutation (I1372S) associated with type 2B-like von Willebrand disease: an elusive phenotype and a difficult diagnosis.
Alessandra Casonato, Francesca Sartorello, Elena Pontara, Lisa Gallinaro, Antonella Bertomoro

Thromb Haemost· December 2007

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Multiple von Willebrand factor mutations in patients with recessive type 1 von Willebrand disease.
Alessandra Casonato, Lisa Gallinaro, Elena Pontara, Letizia Bernardo, Francesca Sartorello

Thromb Res· September 2007

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Altered von Willebrand factor subunit proteolysis and multimer processing associated with the Cys2362Phe mutation in the B2 domain.
Alessandra Casonato, Luigi De Marco, Lisa Gallinaro, Maryta Sztukowska, Mario Mazzuccato

Thromb Haemost· April 2007

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Combined partial exon skipping and cryptic splice site activation as a new molecular mechanism for recessive type 1 von Willebrand disease.
Lisa Gallinaro, Francesca Sartorello, Elena Pontara, Maria Grazia Cattini, Antonella Bertomoro

Thromb Haemost· December 2006

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Identifying type Vicenza von Willebrand disease.
Alessandra Casonato, Elena Pontara, Francesca Sartorello, Maria Grazia Cattini, Lisa Gallinaro

J Lab Clin Med· February 2006

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Origins of mitochondrial thymidine triphosphate: dynamic relations to cytosolic pools.
Giovanna Pontarin, Lisa Gallinaro, Paola Ferraro, Peter Reichard, Vera Bianchi

Proc Natl Acad Sci U S A· October 2003

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Cytosolic and mitochondrial deoxyribonucleotidases: activity with substrate analogs, inhibitors and implications for therapy.
Cristina Mazzon, Chiara Rampazzo, Maria Chiara Scaini, Lisa Gallinaro, Anna Karlsson

Biochem Pharmacol· August 2003

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Human mitochondrial 5'-deoxyribonucleotidase. Overproduction in cultured cells and functional aspects.
Lisa Gallinaro, Katia Crovatto, Chiara Rampazzo, Giovanna Pontarin, Paola Ferraro

J Biol Chem· September 2002

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