J C Souto|J Fontcuberta - JoVE Visualize

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Digestive Diseases and Sciences|September 1, 1995

Prothrombotic state and signs of endothelial lesion in plasma of patients with inflammatory bowel diseaseJ C Souto, E Martínez, M Roca, et al.

Annals of Hematology|November 28, 2002

Enhanced risk of thrombotic disease in patients with acquired vitamin B12 and/or folate deficiency: role of hyperhomocysteinemiaA F Remacha, J C Souto, E Rámila, et al.

Haematologica|July 16, 1999

Homozygotes for prothrombin gene 20210 A allele in a thrombophilic family without clinical manifestations of venous thromboembolismJ C Souto, J Mateo, J M Soria, et al.

Human Mutation|August 14, 1999

Protein S gene analysis reveals the presence of a cosegregating mutation in most pedigrees with type I but not type III PS deficiencyY Espinosa-Parrilla, M Morell, J C Souto, et al.

Human Mutation|May 2, 2000

Optimization of a simple and rapid single-strand conformation analysis for detection of mutations in the PROS1 gene: identification of seven novel mutations and three novel, apparently neutral, variantsY Espinosa-Parrilla, M Morell, M Borrell, et al.

Thrombosis and Haemostasis|February 24, 2001

Genetic regulation of plasma levels of vitamin K-dependent proteins involved in hematostatis: results from the GAIT Project. Genetic Analysis of Idiopathic ThrombophiliaJ C Souto, L Almasy, J Blangero, et al.

Haematologica|April 11, 2000

Platelet function during cardiopulmonary bypass not changed by two different doses of aprotininA Santamaría, J Mateo, E Muñíz-Díaz, et al.

Thrombosis and Haemostasis|October 6, 1998

The prothrombin 20210A allele is the most prevalent genetic risk factor for venous thromboembolism in the Spanish populationJ C Souto, I Coll, D Llobet, et al.

Haematologica|September 5, 2001

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 geneA Santamaría, J Mateo, A Oliver, et al.

Circulation|April 4, 2000

Genetic determinants of hemostasis phenotypes in Spanish familiesJ C Souto, L Almasy, M Borrell, et al.

Pageof 13

Showing results (11-20 of 130) with videos related to

Sort By:

Pageof 13

Digestive Diseases and Sciences|September 1, 1995

Prothrombotic state and signs of endothelial lesion in plasma of patients with inflammatory bowel diseaseJ C Souto, E Martínez, M Roca, et al.

Annals of Hematology|November 28, 2002

Enhanced risk of thrombotic disease in patients with acquired vitamin B12 and/or folate deficiency: role of hyperhomocysteinemiaA F Remacha, J C Souto, E Rámila, et al.

Haematologica|July 16, 1999

Homozygotes for prothrombin gene 20210 A allele in a thrombophilic family without clinical manifestations of venous thromboembolismJ C Souto, J Mateo, J M Soria, et al.

Human Mutation|August 14, 1999

Protein S gene analysis reveals the presence of a cosegregating mutation in most pedigrees with type I but not type III PS deficiencyY Espinosa-Parrilla, M Morell, J C Souto, et al.

Human Mutation|May 2, 2000

Optimization of a simple and rapid single-strand conformation analysis for detection of mutations in the PROS1 gene: identification of seven novel mutations and three novel, apparently neutral, variantsY Espinosa-Parrilla, M Morell, M Borrell, et al.

Thrombosis and Haemostasis|February 24, 2001

Genetic regulation of plasma levels of vitamin K-dependent proteins involved in hematostatis: results from the GAIT Project. Genetic Analysis of Idiopathic ThrombophiliaJ C Souto, L Almasy, J Blangero, et al.

Haematologica|April 11, 2000

Platelet function during cardiopulmonary bypass not changed by two different doses of aprotininA Santamaría, J Mateo, E Muñíz-Díaz, et al.

Thrombosis and Haemostasis|October 6, 1998

The prothrombin 20210A allele is the most prevalent genetic risk factor for venous thromboembolism in the Spanish populationJ C Souto, I Coll, D Llobet, et al.

Haematologica|September 5, 2001

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 geneA Santamaría, J Mateo, A Oliver, et al.

Circulation|April 4, 2000

Genetic determinants of hemostasis phenotypes in Spanish familiesJ C Souto, L Almasy, M Borrell, et al.

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