I. Tirado

发表

Rapid detection of the 46C --> T polymorphism in the factor XII gene, a novel genetic risk factor for thrombosis, by melting peak analysis using fluorescence hybridization probes.

J. Fontcuberta, J. Soria, I. Tirado, 2003, Genetic testing.

Risk of thrombosis associated with oral contraceptives of women from 97 families with inherited thrombophilia: high risk of thrombosis in carriers of the G20210A mutation of the prothrombin gene.

J. Fontcuberta, J. Souto, J. Soria, 2001, Haematologica.

Contribution of prothrombin 20210A allele and factor V Leiden mutation to thrombosis risk in thrombophilic families with other hemostatic deficiencies.

J. Fontcuberta, J. Souto, J. Soria, 2001, Haematologica.

Hemostatic Proteins and Their Association With Hematoma Growth in Patients With Acute Intracerebral Hemorrhage

R. Delgado-Mederos, J. Martí-Fàbregas, J. Fontcuberta, 2010, Stroke.

The c.1787G>T and c.1787G>A Mutations are not Found in the Prothrombin Gene in a Spanish Population

J. Fontcuberta, J. Souto, J. Mateo, 2017 .

Association after linkage analysis indicates that homozygosity for the 46C→T polymorphism in the F12 gene is a genetic risk factor for venous thrombosis

J. Fontcuberta, J. Souto, J. Soria, 2004, Thrombosis and Haemostasis.

Risk of Ischemic Stroke Associated With Functional Thrombin-Activatable Fibrinolysis Inhibitor Plasma Levels

J. Martí-Fàbregas, J. Fontcuberta, J. Souto, 2003, Stroke.

The ABO blood group genotype and factor VIII levels as independent risk factors for venous thromboembolism

J. Fontcuberta, J. Soria, J. Mateo, 2005, Thrombosis and Haemostasis.

Homozygosity of the T allele of the 46 C-->T polymorphism in the F12 gene is a risk factor for acute coronary artery disease in the Spanish population.

J. Fontcuberta, J. Soria, J. Mateo, 2004, Haematologica.

Platelet hyperaggregability and venous thrombosis risk: results from the RETROVE project.

J. Fontcuberta, J. Souto, J. Mateo, 2020, Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis.

VAMP8 and serotonin transporter levels are associated with venous thrombosis risk in a Spanish female population. Results from the RETROVE Project.

J. Fontcuberta, J. Souto, J. Mateo, 2019, Thrombosis research.

IgM anti-protein S antibodies as a risk factor for venous thrombosis

J. Fontcuberta, J. Mateo, A. Santamaría, 2008, Haematologica.

Incidence and clinical manifestations of activated protein C resistance and factor V Leiden in young patients with venous thromboembolic disease in Spain.

R. Cornudella, I. Tirado, G. Azaceta, 1998, Haematologica.

Low ADAMTS13 levels are associated with venous thrombosis risk in women.

J. Fontcuberta, J. Souto, J. Mateo, 2017, Thrombosis research.

Homozygosity of the T Allele of the 46 C→T Polymorphism in the F12 Gene Is a Risk Factor for Ischemic Stroke in the Spanish Population

J. Martí-Fàbregas, J. Fontcuberta, J. Souto, 2004, Stroke.

Linkage analysis demonstrates that the prothrombin G20210A mutation jointly influences plasma prothrombin levels and risk of thrombosis.

L. Almasy, J. Blangero, J. Fontcuberta, 2000, Blood.

Phosphorylation of gH2AX as a novel prognostic biomarker for laryngoesophageal dysfunction-free survival

A. Carnero, J. Pachón, D. Chinchón, 2016, Oncotarget.

Complexity of the genetic contribution of different thrombotic risk factors in a Spanish thrombophilic family

J. Fontcuberta, A. Santamaría, I. Tirado, 2005, Thrombosis and Haemostasis.

Protein S gene analysis reveals the presence of a cosegregating mutation in most pedigrees with type I but not type III PS deficiency

X. Estivill, M. Morell, J. Fontcuberta, 1999, Human mutation.

Double heterozygosity for Factor V Leiden and Factor V Cambridge mutations associated with low levels of activated protein C resistance in a Spanish thrombophilic family

J. Fontcuberta, J. Mateo, A. Santamaría, 2005, Thrombosis and Haemostasis.

Absence of linkage between type III protein S deficiency and the PROS1 and C4BP genes in families carrying the protein S Heerlen allele.

X. Estivill, D. Heine-Suñer, V. Volpini, 1997, Blood.

Detection of two new polymorphisms by PCR-SSCP analysis of the histidine-rich glycoprotein gene in three families with abnormal plasma HRG levels

S. Wakabayashi, J. Fontcuberta, T. Koide, 1997 .

Identification of a large deletion and three novel mutations in exon 13 of the factor V gene in a Spanish family with normal factor V coagulant and anticoagulant properties

L. Almasy, J. Blangero, J. Fontcuberta, 2002, Human Genetics.

Patients with venous thromboembolism have a lower APC response than controls. Should this be regarded as a continuous risk factor for venous thrombosis?

J. Fontcuberta, J. Souto, J. Mateo, 1999, Haematologica.

Antithrombin Cambridge II mutation as a risk factor to develop cerebral venous thrombosis

J. Fontcuberta, A. Santamaría, I. Tirado, 2008, Thrombosis and Haemostasis.

Endoscopic findings unrelated to portal hypertension in patients with liver cirrhosis undergoing a variceal screening programme

M. Rodríguez-Perálvarez, I. Tirado, Pilar Barrera Baena, 2022, Gastroenterología y Hepatología (English Edition).

Linkage analysis demonstrates that the prothrombin G20210A mutation jointly influences plasma prothrombin levels and risk of thrombosis

L. Almasy, J. Blangero, J. Fontcuberta, 2000 .