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Antithrombin heparin binding site deficiency: A challenging diagnosis of a not so benign thrombophilia.

artículo científico publicado en 2015

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

scientific article published on 13 September 2020

Belgian clinical guidance on anticoagulation management in hospitalised and ambulatory patients with COVID-19

scientific article published on 03 October 2020

Child-onset thrombotic thrombocytopenic purpura caused by p.R498C and p.G259PfsX133 mutations in ADAMTS13

scientific article published on 15 May 2018

Heterozygous FGA p.Asp473Ter (fibrinogen Nieuwegein) presenting as antepartum cerebral thrombosis.

artículo científico publicado en 2017

Homozygous antithrombin deficiency in adolescents presenting with lower extremity thrombosis and renal complications: two case reports from Turkey

artículo científico publicado en 2014

Identification of two de novo mutations responsible for type I antithrombin deficiency

scientific article published on 24 November 2011

Incidence and features of thrombosis in children with inherited antithrombin deficiency

artículo científico publicado en 2019

Recommendations for clinical laboratory testing for antithrombin deficiency; Communication from the SSC of the ISTH

artículo científico publicado en 2020

Routine haematology parameters in COVID-19 patients and clinical outcome: A Belgian single-centre study

scientific article published on 11 September 2020

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