Publicaciones en colaboración con investigadores/as de John Paul II Hospital (7)

2023

  1. Functional, biochemical, molecular and clinical characterization of antithrombin c.1157T>C (p.Ile386Thr), a recurrent Polish variant with a founder effect

    Haematologica

2022

  1. New SERPINC1 gene mutations in patients with antithrombin deficiency: Antithrombin Lodz I, II, III, and IV

    Polish Archives of Internal Medicine, Vol. 132, Núm. 1

2019

  1. A series of 10 Polish patients with thromboembolic events and antithrombin deficiency: Two new c.1154-1 G>C and c.1219-534 A>G SERPINC1 gene splicing mutations

    Blood Coagulation and Fibrinolysis, Vol. 30, Núm. 5, pp. 193-198

2018

  1. Identification of a New Mechanism of Antithrombin Deficiency Hardly Detected by Current Methods: Duplication of SERPINC1 Exon 6

    Thrombosis and Haemostasis

2017

  1. Defects of splicing in antithrombin deficiency

    Research and Practice in Thrombosis and Haemostasis, Vol. 1, Núm. 2, pp. 216-222

  2. High levels of latent antithrombin in plasma from patients with antithrombin deficiency

    Thrombosis and Haemostasis, Vol. 117, Núm. 5, pp. 880-888

2016

  1. Hypoglycosylation is a common finding in antithrombin deficiency in the absence of a SERPINC1 gene defect

    Journal of Thrombosis and Haemostasis, Vol. 14, Núm. 8, pp. 1549-1560