Results 21 to 30 of about 8,876 (241)
Vitamin K-dependent and other rare coagulation factor deficiencies: a single-center experience [PDF]
Italian Journal of PediatricsBackground Rare coagulation factor deficiency (RFD) is characterized by a deficiency of factor (F) I, FII, FV, FVII, FX, FXI, FXII, FXIII, or a combined deficiency of FV + FVIII or vitamin K-dependent factors and accounts for approximately 5% of all ...
Özlem Terzi, Sadık Sami Hatipoğlu
doaj +2 more sources
A comparison of the effects of factor XII deficiency and prekallikrein deficiency on thrombus formation [PDF]
Thrombosis Research, 2016 Keith Mccrae +2 more
exaly +2 more sources
Donor-to-recipient transmission of factor XII deficiency by orthotopic liver transplantation [PDF]
Baylor University Medical Center Proceedings, 2019 Hussien Elsiesy, Mohamed Abdelfattah
exaly +2 more sources
Aortic valve replacement and ventricular septal defect repair in factor XII deficiency: An anesthetic challenge [PDF]
Saudi Journal of Anaesthesia, 2019 Swapnil Verma +3 more
doaj +2 more sources
Journal of Neuroanaesthesiology and Critical Care, 2020 Factor XII deficiency is a rare disorder that can complicate the perioperative management of a patient. Factor XII plays an important role in the activation of intrinsic pathway of coagulation; the deficiency, therefore, results in prolongation of ...
Mouleeswaran Sundaram +2 more
doaj +1 more source
Factor XI Deficiency Alters the Cytokine Response and Activation of Contact Proteases during Polymicrobial Sepsis in Mice. [PDF]
PLoS ONE, 2016 Sepsis, a systemic inflammatory response to infection, is often accompanied by abnormalities of blood coagulation. Prior work with a mouse model of sepsis induced by cecal ligation and puncture (CLP) suggested that the protease factor XIa contributed to ...
Charles E Bane +10 more
doaj +1 more source
Advances in Oral and Maxillofacial Surgery, 2021 A 21-year-old man with mandibular prognathism was referred to Tokyo Medical University Hospital. The patient was diagnosed as having skeletal prognathism.
Hayato Hamada +4 more
doaj +1 more source
RGUHS Journal of Medical Sciences, 2017 Acase of Factor XII deficiency which was incidentally recognized in a child who presented with purpuric lesions is reported ...
Baldua V +5 more
openaire +1 more source
The complex role of kininogens in hereditary angioedema
Frontiers in Allergy, 2022 Human high molecular weight kininogen (HK) is the substrate from which bradykinin is released as a result of activation of the plasma “contact” system, a cascade that includes the intrinsic coagulation pathway, and a fibrinolytic pathway leading to the ...
Allen P. Kaplan +2 more
doaj +1 more source
Mechanisms involved in hereditary angioedema with normal C1-inhibitor activity
Frontiers in Physiology, 2023 Patients with the inherited disorder hereditary angioedema (HAE) suffer from episodes of soft tissue swelling due to excessive bradykinin production.
Aleksandr Shamanaev +9 more
doaj +1 more source