Disease: Congenital antithrombin 3 deficiency
- A pilot study on the impact of congenital thrombophilia in COVID-19
- Acquired SERPINC1/antithrombin deficiency during oral contraceptive consumption: a case report
- Analysis of AlphaFold and molecular dynamics structure predictions of mutations in serpins
- Bleeding Disorders
- Bleeding Disorders
- Cardiac Arrest Due to Pulmonary Embolism After Posterior Spinal Fusion in a Patient With Acute Paraplegia Caused by a Metastatic Spinal Tumor Associated With Congenital Antithrombin III Deficiency
- High penetrance of inferior vena cava system atresia in severe thrombophilia caused by homozygous antithrombin Budapest 3 variant: Description of a new syndrome
- Impact of SERPINC1 mutation on thrombotic phenotype in children with congenital antithrombin deficiency-first analysis of the International Society on Thrombosis and Haemostasis pediatric antithrombin deficiency database and biorepository
- Long-range and real-time PCR identification of a large SERPINC1 deletion in a patient with antithrombin deficiency
- Managing venous thrombosis in a pediatric patient with short bowel and congenital nephrotic syndromes: a case report emphasizing rivaroxaban level monitoring
- Molecular and clinical characterization of transient antithrombin deficiency: A new concept in congenital thrombophilia
- Normalizing Anti-Thrombin III for heparin management during routine cardiopulmonary bypass for congenital cardiothoracic surgery: A single institution practice review
- PMM2-CDG
- Prevalence, Genetic Background, and Clinical Phenotype of Congenital Thrombophilia in Chronic Thromboembolic Pulmonary Hypertension
- Prevention of venous thromboembolism in pregnant women with congenital antithrombin deficiency: a retrospective study of a candidate protocol
- The Vascular Endothelium and Coagulation: Homeostasis, Disease, and Treatment, with a Focus on the Von Willebrand Factor and Factors VIII and V
- Thromboelastography
- Thromboelastography
- Two SERPINC1 variants affecting N-glycosylation of Asn224 cause severe thrombophilia not detected by functional assays
- Unique clinical presentations and follow-up outcomes from experience with congenital disorders of glycosylation: PMM2-PGM1-DPAGT1-MPI-POMT2-B3GALNT2-DPM1-SRD5A3-CDG
- Usefulness and Limitations of Multiple Ligation-Dependent Probe Amplification in Antithrombin Deficiency