List of works - Javier Corral

A novel mutation of antithrombin deficiency in six family siblings and the clinical combat

scientific article published on 16 July 2015

Evaluation of Novel Platelet Polymorphisms in Stroke. Dichotomic Effect of rs5443 in GNB3.

scientific article

Identification of a new potential mechanism responsible for severe bleeding in myeloma: immunoglobulins bind the heparin binding domain of antithrombin activating this endogenous anticoagulant

scientific article published on 16 June 2016

Genetic predisposition to fetal alcohol syndrome: association with congenital disorders of N-glycosylation.

scientific article published on 18 August 2017

Identification of Regulatory Mutations in SERPINC1 Affecting Vitamin D Response Elements Associated with Antithrombin Deficiency

scientific article

Antithrombin Katowice: exon 1 deletion in the SERPINC1 gene associated with type I antithrombin deficiency

scientific article published on 01 January 2015

A novel mutation in the antithrombin gene (insT 7429-30) causes superior mesenteric vein thrombosis

scientific article published on 12 July 2006

A simplified assay for the quantification of circulating activated protein C.

scientific article published in June 2016

Anticoagulant therapy in patients with congenital FXI deficiency

scientific article published on 20 October 2021

Hereditary thrombophilia: learnt lessons and pending duties

scientific article published on 01 May 2007

A KpnI RFLP at the human myeloperoxidase locus.

scientific article

Heparanase Activates Antithrombin through the Binding to Its Heparin Binding Site

scientific article

ALG12-CDG: An unusual patient without intellectual disability and facial dysmorphism, and with a novel variant

scientific article published on 12 June 2020

Antithrombin p.Thr147Ala: The First Founder Mutation in People of African Origin Responsible for Inherited Antithrombin Deficiency

scientific article published on 13 September 2020

Factor-V (Arg506 --> Gln) mutation in ischemic cerebrovascular disease.

scientific article published in May 1997

Correction: Recurrent mutations in a SERPINC1 hotspot associate with venous thrombosis without apparent antithrombin deficiency

scientific article

Transient desialylation in combination with a novel antithrombin deficiency causing a severe and recurrent thrombosis despite anticoagulation therapy

scientific article published on 17 March 2017

Inherited thrombophilic conditions

scientific article published on 01 April 2012

Archeogenetics of F11 p.Cys38Arg: a 5400-year-old mutation identified in different southwestern European countries

scientific article published on 01 May 2019

Recurrent mutations in a SERPINC1 hotspot associate with venous thrombosis without apparent antithrombin deficiency

scientific article published on 28 September 2017

Study of 18 functional hemostatic polymorphisms in mucocutaneous bleeding disorders

scientific article published on 09 June 2010

Fluctuations in coagulation activity among patients with atrial fibrillation who are stably anticoagulated.

scientific article published on March 2006

Genetic variants of the extra-large stimulatory Gs protein alpha-subunit and risk of thrombotic and haemorrhagic disorders.

scientific article

List of works by Javier Corral

A novel mutation of antithrombin deficiency in six family siblings and the clinical combat

Evaluation of Novel Platelet Polymorphisms in Stroke. Dichotomic Effect of rs5443 in GNB3.

Identification of a new potential mechanism responsible for severe bleeding in myeloma: immunoglobulins bind the heparin binding domain of antithrombin activating this endogenous anticoagulant

Genetic predisposition to fetal alcohol syndrome: association with congenital disorders of N-glycosylation.

Identification of Regulatory Mutations in SERPINC1 Affecting Vitamin D Response Elements Associated with Antithrombin Deficiency

Antithrombin Katowice: exon 1 deletion in the SERPINC1 gene associated with type I antithrombin deficiency

A novel mutation in the antithrombin gene (insT 7429-30) causes superior mesenteric vein thrombosis

A simplified assay for the quantification of circulating activated protein C.

Anticoagulant therapy in patients with congenital FXI deficiency

Hereditary thrombophilia: learnt lessons and pending duties

A KpnI RFLP at the human myeloperoxidase locus.

Heparanase Activates Antithrombin through the Binding to Its Heparin Binding Site

ALG12-CDG: An unusual patient without intellectual disability and facial dysmorphism, and with a novel variant

Antithrombin p.Thr147Ala: The First Founder Mutation in People of African Origin Responsible for Inherited Antithrombin Deficiency

Factor-V (Arg506 --> Gln) mutation in ischemic cerebrovascular disease.

Correction: Recurrent mutations in a SERPINC1 hotspot associate with venous thrombosis without apparent antithrombin deficiency

Transient desialylation in combination with a novel antithrombin deficiency causing a severe and recurrent thrombosis despite anticoagulation therapy

Inherited thrombophilic conditions

Archeogenetics of F11 p.Cys38Arg: a 5400-year-old mutation identified in different southwestern European countries

Recurrent mutations in a SERPINC1 hotspot associate with venous thrombosis without apparent antithrombin deficiency

Study of 18 functional hemostatic polymorphisms in mucocutaneous bleeding disorders

Fluctuations in coagulation activity among patients with atrial fibrillation who are stably anticoagulated.

Genetic variants of the extra-large stimulatory Gs protein alpha-subunit and risk of thrombotic and haemorrhagic disorders.