Results 11 to 20 of about 49,507 (253)

Genetic and clinical characterization of two families with severe venous thromboembolism due to nonsense mutations in the SERPINC1 gene [PDF]

Thrombosis Journal
Antithrombin (AT) III is a key physiological anticoagulant, and its hereditary deficiency represents one of the most severe forms of inherited thrombophilia.
Xuqian Wei, Weibin Chen, Jian Zhang, Jianhua Mao   +3 more
doaj   +2 more sources

A COVID‐19 case report with low ACT(activated clotting time) and high serum D‐dimer level: Antithrombin III deficiency? [PDF]

Respirology Case Reports
The Coronavirus Disease 2019 (COVID‐19), caused by the virus named Severe Acute Respiratory Syndrome Coronavirus 2 (SARS‐CoV‐2), is a global public health problem in which atypical findings other than the usual fever and respiratory symptoms render early
Ayşe Şahin Tutak
doaj   +2 more sources

Successful treatment of a massive pulmonary embolism using rivaroxaban in a patient with antithrombin III deficiency. [PDF]

J Cardiol Cases, 2017
Yamaguchi J, Hara N, Yamaguchi T, Nagata Y, Nozato T, Miyamoto T.   +5 more
europepmc   +2 more sources

Proper diagnosis of antithrombin III deficiency. [PDF]

Anatol J Cardiol, 2017
Narlı Özdemir Z, Özcan M.
europepmc   +3 more sources

Case report: A case of new mutation in SERPINC1 leading to thrombotic microangiopathy

Frontiers in Genetics, 2023
Introduction: Hereditary antithrombin-III deficiency can significantly increase the risk for thrombosis, which is common in limb deep vein and pulmonary cases. However, thrombotic microangiopathy (TMA) caused by hereditary antithrombin deficiency is rare.
Bing Li, Xiaohui Zhang, Hailin Lv, Xiaoqing Yang, Yanxia Gao, Zhao Hu, Chengjun Ma   +6 more
doaj   +1 more source

Pulmonary Artery Endarterectomy with Deep Hypothermic Circulatory Arrest in a Patient with a Congenital Antithrombin III Deficiency [PDF]

Annals of Cardiac Anaesthesia
Sylvain Diop, Elie Fadel, Maria-Cristina Kassab, Thibaut Genty, Iolanda Ion   +4 more
doaj   +2 more sources

Management of antithrombin III deficiency in pregnancy: a representative case and a literature review

Акушерство, гинекология и репродукция, 2021
The work is aimed at discussing pregnancy management for the most thrombogenic genetic thrombophilia - antithrombin III (AT-III) deficiency. A detailed analysis of the literature and clinical case of pregnancy management in a patient with AT-III ...
S. V. Akinshina, P. K. Genina, V. O. Bitsadze, J. Kh. Khizroeva, V. I. Tsibizova, A. D. Makatsariya   +5 more
doaj   +1 more source

Elevated hemostasis markers after pneumonia increases one-year risk of all-cause and cardiovascular deaths [PDF]

, 2011
Background: Acceleration of chronic diseases, particularly cardiovascular disease, may increase long-term mortality after community-acquired pneumonia (CAP), but underlying mechanisms are unknown. Persistence of the prothrombotic state that occurs during
A. Murat Kaynar, AM Toschke, CN Serhan, CR Meier, DC Cowper, Derek C. Angus, EA Halm, EB Milbrandt, F Balkwill, FL Brancati, Florian Mayr, GD Lowe, Gina D'Angelo, GT Kinasewitz, GW Waterer, H Putter, I Koivula, J Bordon, J Kasal, J Kelly, JA Kellum, JL Hsu, JL Vincent, John A. Kellum, JU Hedlund, Kaikobad Irani, L Smeeth, Lisa Weissfeld, ME Charlson, MJ Fine, MJ Pencina, MM Doody, MM Levy, MM Samama, NM Sathiakumar, Patricia T. Bozza, PM Ridker, PR Woodhouse, S Yende, S Yende, Sachin Yende, SE Epstein, Tammy Young, TC Clayton, TT Keller, TT Keller, V Kaplan, VF Corrales-Medina, WA Knaus, WB Kannel   +49 more
core   +14 more sources

A Study of Prothrombotic Factors in Human Immunodeficiency Virus-Infected Patients

Indian Journal of Medical Specialities, 2021
Introduction: Human immunodeficiency virus (HIV) infection has been described as a hypercoagulable state. Some studies suggest that thrombotic events may be 2–10 times more prevalent in this group than in the general population.
Meena Lanjiwar, Pushpa Kumari, Jitendra Mohan Khunger, Narender Singh Negi   +3 more
doaj   +1 more source

Screening for inherited thrombophilias and prophylaxis of venous thromboembolism in pregnancy and puerperium [PDF]

Romanian Journal of Medical Practice, 2020
Thrombophilias are a group of coagulation disorders associated with a predisposition to thrombotic events. They could be inherited (genetic) or acquired. The most encountered inherited thrombophilias are factor V Leiden (FVL), prothrombin gene mutation (
Ana SCUTELNICU, Corina GICA, Radu BOTEZATU, Nicolae GICA, Anca Marina CIOBANU, Brindusa CIMPOCA, Gheorghe PELTECU, Anca Maria PANAITESCU   +7 more
doaj   +1 more source