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Publisher Kare Publishing
Date 2017 May 4
PMID 28466834
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References
1.
Emmanuelle T, Husein B, Iqbal J, Macheta M, Isaacs P . Concomitant homozygosity for the prothrombin gene variant with mild deficiency of antithrombin III in a patient with multiple hepatic infarctions: a case report. J Med Case Rep. 2010; 4:122. PMC: 2868876. DOI: 10.1186/1752-1947-4-122. View

2.
Holm H, Kalvenes S, Abildgaard U . Changes in plasma antithrombin (heparin cofactor activity) during intravenous heparin therapy: observations in 198 patients with deep venous thrombosis. Scand J Haematol. 1985; 35(5):564-9. DOI: 10.1111/j.1600-0609.1985.tb02829.x. View

3.
Wiles K, Hastings L, Muthuppalaniappan V, Hanif M, Abeygunasekara S . Bilateral renal artery thrombosis in inherited thrombophilia: a rare cause of acute kidney injury. Int J Nephrol Renovasc Dis. 2014; 7:35-8. PMC: 3900314. DOI: 10.2147/IJNRD.S50948. View

4.
Hayiroglu M, Keskin M, Donmez C, Gunay M, Dayi S . Antithrombin III deficiency concomitant with atrial fibrillation causes thrombi in all chambers: 2D and 3D echocardiographic evaluation. Anatol J Cardiol. 2016; 16(12):E21-E22. PMC: 5324928. DOI: 10.14744/AnatolJCardiol.2016.7456. View

5.
Patnaik M, Moll S . Inherited antithrombin deficiency: a review. Haemophilia. 2009; 14(6):1229-39. DOI: 10.1111/j.1365-2516.2008.01830.x. View