Polymorphism of thrombin-activatable fibrinolysis inhibitor and risk of intracranial haemorrhage in factor XIII deficiency.

@article{Naderi2014PolymorphismOT,
  title={Polymorphism of thrombin-activatable fibrinolysis inhibitor and risk of intracranial haemorrhage in factor XIII deficiency.},
  author={Majid Naderi and A Dorgalaleh and S H Alizadeh and Zahra Kashani Khatib and Shadi Tabibian and Apolline Kaz{\'e}mi and Hussein Dargahi and Taregh Bamedi},
  journal={Haemophilia : the official journal of the World Federation of Hemophilia},
  year={2014},
  volume={20 1},
  pages={e89-92}
}
1 Maheshwari R, Kelley SP, Langkamer VG, Loveday E. Spontaneous recurrent haemarthrosis following unicompartmental knee arthroplasty and its successful treatment by coil embolisation. Knee 2004; 11: 413–5. 2 Karataglis D, Marlow D, Learmonth DJ. Atraumatic haemarthrosis following total knee replacement treated with selective embolisation. Acta Orthop Belg 2006; 72: 375–7. 3 Sandoval E, Ortega FJ, Garcia-Rayo MR, Resines C. Popliteal pseudoaneurysm after total knee arthroplasty secondary to… CONTINUE READING

Citations

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First cases of severe congenital factor XIII deficiency in Southwestern Afghanistan in the vicinity of southeast of Iran.

Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis • 2015

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