Congenital Antithrombin 3 Deficiency Latest Advances

Sustained Correction of Hereditary Antithrombin Deficiency in Mice by AAV8-Mediated Gene Delivery.

Journal: Arteriosclerosis, thrombosis, and vascular biology

Published: May 28, 2026

Facial Dysmorphism and Severe Vascular Phenotype in TRNT1 Deficiency with Concomitant Antithrombin III Deficiency.

Journal: Journal of clinical immunology

Published: May 10, 2026

Recurrent Coronary Restenosis in Takayasu Arteritis: A Stent-Sparing Strategy.

Journal: JACC. Case reports

Published: April 13, 2026

In a nutshell review of hereditary antithrombin deficiency in pregnancy.

Journal: British journal of haematology

Published: April 03, 2026

Cross-sectional imaging in an inferior vena cava agenesis associated with antiphospholipid syndrome, lower limb, and portomesenteric deep vein thrombosis and renal insufficiency in a young patient: A rare presentation.

Journal: Radiology case reports

Published: March 31, 2026

Clinical and genetic analysis of two families with combined defect in antithrombin and protein C genes

Journal: Zhonghua xue ye xue za zhi = Zhonghua xueyexue zazhi

Published: March 16, 2026

Inferior mesenteric vein thrombosis in an elderly woman with antiphospholipid syndrome: A case report and review of the literature.

Journal: Radiology case reports

Published: March 13, 2026

Hereditary Antithrombin Deficiency in Pediatric Patients: Pathophysiology, Clinical Features, Diagnosis, and Antithrombin Replacement Therapy.

Journal: Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis

Published: February 18, 2026

Congenital Protein C Deficiency Presenting as Neonatal Purpura Fulminans: A Report of Two Cases.

Journal: Cureus

Published: February 16, 2026

Novel SERPINC1 variants in hereditary antithrombin deficiency: first pathogenic deep-intronic variant, revealed by multiple genomic and transcriptomic approaches.

Journal: Journal of thrombosis and haemostasis : JTH

Published: January 20, 2026

Bridging laboratory assays, genetics, and clinical phenotypes in antithrombin deficiency: Rethinking the diagnostic paradigm.

Journal: Thrombosis research

Published: January 13, 2026

Severe Hemoperitoneum From a Ruptured Ovarian Cyst in a Patient with Antiphospholipid Syndrome and Antithrombin III Deficiency: A Case Report.

Journal: The American journal of case reports

Published: December 06, 2025

Congenital Antithrombin 3 Deficiency Latest Advances

Find the Latest Research About Congenital Antithrombin 3 Deficiency

Sustained Correction of Hereditary Antithrombin Deficiency in Mice by AAV8-Mediated Gene Delivery.

Sustained Correction of Hereditary Antithrombin Deficiency in Mice by AAV8-Mediated Gene Delivery.

Facial Dysmorphism and Severe Vascular Phenotype in TRNT1 Deficiency with Concomitant Antithrombin III Deficiency.

Facial Dysmorphism and Severe Vascular Phenotype in TRNT1 Deficiency with Concomitant Antithrombin III Deficiency.

Recurrent Coronary Restenosis in Takayasu Arteritis: A Stent-Sparing Strategy.

Recurrent Coronary Restenosis in Takayasu Arteritis: A Stent-Sparing Strategy.

In a nutshell review of hereditary antithrombin deficiency in pregnancy.

In a nutshell review of hereditary antithrombin deficiency in pregnancy.

Cross-sectional imaging in an inferior vena cava agenesis associated with antiphospholipid syndrome, lower limb, and portomesenteric deep vein thrombosis and renal insufficiency in a young patient: A rare presentation.

Cross-sectional imaging in an inferior vena cava agenesis associated with antiphospholipid syndrome, lower limb, and portomesenteric deep vein thrombosis and renal insufficiency in a young patient: A rare presentation.

Clinical and genetic analysis of two families with combined defect in antithrombin and protein C genes

Clinical and genetic analysis of two families with combined defect in antithrombin and protein C genes

Inferior mesenteric vein thrombosis in an elderly woman with antiphospholipid syndrome: A case report and review of the literature.

Inferior mesenteric vein thrombosis in an elderly woman with antiphospholipid syndrome: A case report and review of the literature.

Hereditary Antithrombin Deficiency in Pediatric Patients: Pathophysiology, Clinical Features, Diagnosis, and Antithrombin Replacement Therapy.

Hereditary Antithrombin Deficiency in Pediatric Patients: Pathophysiology, Clinical Features, Diagnosis, and Antithrombin Replacement Therapy.

Congenital Protein C Deficiency Presenting as Neonatal Purpura Fulminans: A Report of Two Cases.

Congenital Protein C Deficiency Presenting as Neonatal Purpura Fulminans: A Report of Two Cases.

Novel SERPINC1 variants in hereditary antithrombin deficiency: first pathogenic deep-intronic variant, revealed by multiple genomic and transcriptomic approaches.

Novel SERPINC1 variants in hereditary antithrombin deficiency: first pathogenic deep-intronic variant, revealed by multiple genomic and transcriptomic approaches.

Bridging laboratory assays, genetics, and clinical phenotypes in antithrombin deficiency: Rethinking the diagnostic paradigm.

Bridging laboratory assays, genetics, and clinical phenotypes in antithrombin deficiency: Rethinking the diagnostic paradigm.

Severe Hemoperitoneum From a Ruptured Ovarian Cyst in a Patient with Antiphospholipid Syndrome and Antithrombin III Deficiency: A Case Report.

Severe Hemoperitoneum From a Ruptured Ovarian Cyst in a Patient with Antiphospholipid Syndrome and Antithrombin III Deficiency: A Case Report.