Prevalence of factor V Leiden (G1619A) and prothrombin gene (G20210A) mutation in Egyptian children with sickle cell disease

2012 ◽  
Vol 22 (4) ◽  
pp. 697-702
Author(s):  
Mona Salah El-Din Hamdy ◽  
Heba Mahmoud Gouda ◽  
Iman Abdel-Mohsen Shaheen ◽  
Mervat M. Khorshied ◽  
Rania Hosny Tomerak
1996 ◽  
Vol 75 (05) ◽  
pp. 859-860
Author(s):  
M A Laffan ◽  
T Vulliamy ◽  
E Schmitz ◽  
D Swisky

2015 ◽  
Vol 32 (1-2) ◽  
pp. 93-104 ◽  
Author(s):  
Amany A. Osman ◽  
Amal Abd El Hamed ◽  
Abeer A. Saad

2016 ◽  
Vol 68 (1) ◽  
pp. 73
Author(s):  
Sanjay Pandey ◽  
Rahasya Mani Mishra ◽  
Sweta Pandey ◽  
Renu Saxena

<p>Vascular complications are an important and perplexing aspect of the clinical spectrum of sickle cell anemia. Patients with sickle cell disease show activation of the blood coagulation, fibrinolytic systems, increased platelet activity and consumption of coagulation inhibitors during vaso‑occlusive crises.</p>


Author(s):  
Fernanda L. Andrade ◽  
Joyce M. Annichino-Bizzacchi ◽  
Sara T. O. Saad ◽  
Fernando F. Costa ◽  
Valder R. Arruda

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