Results 11 to 20 of about 2,704,633 (236)
A Rare Cause of Acquired Factor X Deficiency in an 87-Year-Old Female [PDF]
Case Reports in Hematology, 2021 Factor X deficiency is a rare coagulopathy that can be inherited or acquired. Acquired factor X deficiency has been associated with plasma cell dyscrasias, amyloids, and use of vitamin K antagonists.
Ayrton Bangolo +6 more
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PB2326: SAFE AND EFFECTIVE PROPHYLAXIS WITH PLASMA-DERIVED FACTOR X CONCENTRATE IN AN ELDERLY PATIENT WITH HEREDITARY FACTOR X DEFICIENCY [PDF]
HemaSphere, 2022 H. Patel +3 more
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Çocuk Dergisi, 2023 Objective: Patients with a rare factor deficiency (RFD) may be asymptomatic or present with life-threatening bleeding. Studies have shown no direct relationship between factor activity level and bleeding severity, with difficulties being experienced in ...
Işık Odaman Al +3 more
doaj +1 more source
TH Open, 2020 SARS-CoV-2 infection (COVID-19) results in local and systemic activation of inflammation and coagulation. In this review article, we will discuss the potential role of coagulation factor Xa (FXa) in the pathophysiology of COVID-19. FXa, a serine protease,
Galit H. Frydman +3 more
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Temporal response of an injectable calcium phosphate material in a critical size defect
Journal of Orthopaedic Surgery and Research, 2021 Background Calcium phosphate-based bone graft substitutes are used to facilitate healing in bony defects caused by trauma or created during surgery.
Jacob T. Landeck +6 more
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Editorial: Resilience in the Space-Economy - in search of the X factor [PDF]
Eastern Journal of European Studies, 2021 The ‘X Factor’ is a British reality show – broadcasted all over the world – in which a heterogeneous set of contestants showcase their musical talent so as to obtain the winning bid from a jury.
Karima KOURTIT, Peter NIJKAMP
doaj +1 more source
Haematologica, 2008 Due to a homozygous Gly204Arg mutation in the factor X (FX) gene no detectable FX antigen was found in the plasma of a one-year old patient with severe bleeding diathesis.
Zsuzsanna Bereczky +7 more
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Journal of Blood Medicine, 2021 Tarinee Rungjirajittranon, Yingyong Chinthammitr, Chattree Hantaweepant Division of Hematology, Department of Medicine, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok, ThailandCorrespondence: Chattree HantaweepantClinical Lecturer of ...
Rungjirajittranon T +2 more
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Factor X deficiency: a comment on two recent case studies
The Journal of Haemophilia Practice, 2023 Hereditary factor X deficiency (HFXD) is a rare genetic bleeding disorder, affecting approximately 1 in 1,000,000 individuals globally, and resulting in abnormally low activity of clotting factor X (FX). Diagnosis may occur early in life, particularly in
Branchford Brian
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Farnesoid X receptor and fibroblast growth factor 15/19 as pharmacological targets
Liver Research, 2021 The farnesoid X receptor (FXR) is a nuclear receptor and transcriptional regulator activated by bile acids or synthetic FXR agonists. FXR is expressed highly in the liver and intestine where modulation of FXR critically regulates the expression of genes ...
Syeda Maliha, Grace L. Guo
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