Lista de obras - Marta Spreafico - Dominio Público Uruguay

A cluster of human immunodeficiency virus Type 1 recombinant form escaping detection by commercial genomic amplification assays.

artículo científico publicado en 2010

Bacterial contamination in platelet concentrates

scientific article published on 01 April 2014

Combined Factor V and Factor VIII Deficiency.

artículo científico publicado en 2009

Congenital hypofibrinogenemia: characterization of two missense mutations affecting fibrinogen assembly and secretion

artículo científico publicado en 2008

Dosing anticoagulant therapy with coumarin drugs: is genotyping clinically useful? No.

artículo científico publicado en 2008

Evaluation of assay methods to measure plasma ADAMTS13 activity in thrombotic microangiopathies

artículo científico publicado en 2010

Evidence of distinct tumour-propagating cell populations with different properties in primary human hepatocellular carcinoma

artículo científico publicado en 2011

Genetic diagnosis of haemophilia and other inherited bleeding disorders.

artículo científico publicado en 2006

Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants

artículo científico publicado en 2009

High serum levels of HDV RNA are predictors of cirrhosis and liver cancer in patients with chronic hepatitis delta

artículo científico publicado en 2014

Influence of 9p21.3 Genetic Variants on Clinical and Angiographic Outcomes in Early-Onset Myocardial Infarction

Lack of Siglec-7 expression identifies a dysfunctional natural killer cell subset associated with liver inflammation and fibrosis in chronic HCV infection.

artículo científico publicado en 2015

Meta-Analysis of Multiple Sclerosis Microarray Data Reveals Dysregulation in RNA Splicing Regulatory Genes.

artículo científico publicado en 2015

Molecular characterization of three novel splicing mutations causing factor V deficiency and analysis of the F5 gene splicing pattern.

artículo científico publicado en 2008

Mutations in the MCFD2 gene and a novel mutation in the LMAN1 gene in Indian families with combined deficiency of factor V and VIII.

artículo científico publicado en 2005

Mutations in the MCFD2 gene are predominant among patients with hereditary combined FV and FVIII deficiency (F5F8D) in India

scientific journal article

One size doesn't fit all: Should we reconsider the introduction of cold-stored platelets in blood bank inventories?

artículo científico publicado en 2017

Plasmodium genome in blood donors at risk for malaria after several years of residence in Italy

artículo científico publicado en 2014

Poor efficacy of nucleic acid testing in identifying occult HBV infection and consequences for safety of blood supply in Italy.

artículo científico publicado en 2015

Rare bleeding disorders

artículo científico publicado en 2008

The association of factor V Leiden with myocardial infarction is replicated in 1880 patients with premature disease

artículo científico publicado en 2010

Warfarin and acenocoumarol dose requirements according to CYP2C9 genotyping in North-Italian patients.

artículo científico publicado en 2003

Lista de obras de Marta Spreafico

A cluster of human immunodeficiency virus Type 1 recombinant form escaping detection by commercial genomic amplification assays.

Bacterial contamination in platelet concentrates

Combined Factor V and Factor VIII Deficiency.

Congenital hypofibrinogenemia: characterization of two missense mutations affecting fibrinogen assembly and secretion

Dosing anticoagulant therapy with coumarin drugs: is genotyping clinically useful? No.

Evaluation of assay methods to measure plasma ADAMTS13 activity in thrombotic microangiopathies

Evidence of distinct tumour-propagating cell populations with different properties in primary human hepatocellular carcinoma

Genetic diagnosis of haemophilia and other inherited bleeding disorders.

Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants

High serum levels of HDV RNA are predictors of cirrhosis and liver cancer in patients with chronic hepatitis delta

Influence of 9p21.3 Genetic Variants on Clinical and Angiographic Outcomes in Early-Onset Myocardial Infarction

Lack of Siglec-7 expression identifies a dysfunctional natural killer cell subset associated with liver inflammation and fibrosis in chronic HCV infection.

Meta-Analysis of Multiple Sclerosis Microarray Data Reveals Dysregulation in RNA Splicing Regulatory Genes.

Molecular characterization of three novel splicing mutations causing factor V deficiency and analysis of the F5 gene splicing pattern.

Mutations in the MCFD2 gene and a novel mutation in the LMAN1 gene in Indian families with combined deficiency of factor V and VIII.

Mutations in the MCFD2 gene are predominant among patients with hereditary combined FV and FVIII deficiency (F5F8D) in India

One size doesn't fit all: Should we reconsider the introduction of cold-stored platelets in blood bank inventories?

Plasmodium genome in blood donors at risk for malaria after several years of residence in Italy

Poor efficacy of nucleic acid testing in identifying occult HBV infection and consequences for safety of blood supply in Italy.

Rare bleeding disorders

The association of factor V Leiden with myocardial infarction is replicated in 1880 patients with premature disease

Warfarin and acenocoumarol dose requirements according to CYP2C9 genotyping in North-Italian patients.