I. Coll

发表

Genetic susceptibility to thrombosis and its relationship to physiological risk factors: the GAIT study. Genetic Analysis of Idiopathic Thrombophilia.

L. Almasy, L. Almasy, J. Blangero, 2000, American journal of human genetics.

The Prothrombin 20210A Allele Is the Most Prevalent Genetic Risk Factor for Venous Thromboembolism in the Spanish Population

J. Fontcuberta, J. Souto, J. Mateo, 1998, Thrombosis and Haemostasis.

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.

The prothrombin 20210A allele influences clinical manifestations of hemophilia A in patients with intron 22 inversion and without inhibitors.

M. Baiget, E. Tizzano, J. Fontcuberta, 2002, Haematologica.

Two cases of dysfibrinogenemia characterized by abnormal FPB release: fibrinogen Madrid I & II.

M. Borrell, I. Coll, N. González, 1987, Thrombosis research.

Fibrinogen Barcelona II: a new case of A alpha 16 Arg----His substitution.

J. Fontcuberta, M. Borrell, I. Coll, 1990, Haemostasis.

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.

A Quantitative Trait Locus Influencing Free Plasma Protein S Levels on Human Chromosome 1q: Results From the Genetic Analysis of Idiopathic Thrombophilia (GAIT) Project

L. Almasy, J. Blangero, M. Lathrop, 2003, Arteriosclerosis, Thrombosis and Vascular Biology.

Homozygotes for prothrombin gene 20210 A allele in a thrombophilic family without clinical manifestations of venous thromboembolism.

J. Fontcuberta, J. Souto, J. Soria, 1999, Haematologica.

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.

Homozygotes for prothrombin gene 20210 A allele in a thrombophilic family without clinical manifestations of venous thromboembolism.

J. Souto, M. Borrell, I. Coll, 1999, Haematologica.