Results 11 to 20 of about 2,765,640 (158)
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
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1. Dorothy M (Adcock) Funk, M.D.[⇑][1] 1. Esoterix Coagulation, 8490 Upland Drive, Ste.100, Englewood, CO 80112 2. Dennis Casciato, M.D. 1. David Geffen School of Medicine at UCLA, Los Angeles, CA 90095-1732 1. Address for Correspondence: Dorothy M (Adcock) Funk, M.D., Esoterix Coagulation, 8490 Upland Drive, Ste.100, Englewood, CO ...
Dorothy M, Funk, Dennis, Casciato
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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
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]
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
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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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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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Factor X deficiency: a comment on two recent case studies
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
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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Beyond the X Factor: Relevance of Sex Hormones in NAFLD Pathophysiology
Non-alcoholic fatty liver disease (NAFLD) is a major health issue worldwide, being frequently associated with obesity, unbalanced dietary regimens, and reduced physical activity. Despite their greater adiposity and reduced physical activity, women show a
Sara Della Torre
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