Results 191 to 200 of about 747,119 (356)

Genetic Polymorphisms Associated with Prothrombin Time and Activated Partial Thromboplastin Time in Chinese Healthy Population. [PDF]

open access: yesGenes (Basel), 2022
Zhang F   +11 more
europepmc   +1 more source

Activated Protein C Resistance Testing: An Update From Australasia/Asia‐Pacific

open access: yesInternational Journal of Laboratory Hematology, EarlyView.
ABSTRACT Introduction Activated protein C resistance (APCR) represents a risk factor for thrombosis and is usually due to factor V Leiden (FVL). Clinicians may order either test (i.e., APCR or FVL) to help assess ‘thrombophilia’ in patients who present with thrombosis. APCR testing is usually achieved using clot‐based assays, whereas FVL is assessed by
Emmanuel J. Favaloro   +8 more
wiley   +1 more source

Changes in Some Haemostatic Parameters Among Patients with Chronic Kidney Disease in Kano Metropolis

open access: yesSokoto Journal of Medical Laboratory Science, 2017
It has long been accepted that Chronic Kidney Disease (CKD) causes alterations in haemostatic parameters.  These changes have not been reported in our community.
Usman, M. D., *Garba, N., Danladi, S.B., Isah, S.Y., Audu, A., Dakata A.M., and Jelani, I.
doaj  

Measuring Direct Oral Anticoagulant (DOAC) Levels: Applications, Limitations, and Future Directions

open access: yesInternational Journal of Laboratory Hematology, EarlyView.
ABSTRACT Introduction There are important challenges with the measurement and interpretation of direct oral anticoagulant (DOAC) anticoagulant effect including a lack of therapeutic ranges, inaccuracy of routinely available coagulation assays, lack of established thresholds for clinically significant effect, and uncertainty about how to apply the ...
Siraj Mithoowani   +2 more
wiley   +1 more source

From Activated Partial Thromboplastin Time to Antifactor Xa and Back Again. [PDF]

open access: yesAm J Clin Pathol, 2022
May JE   +4 more
europepmc   +1 more source

Classification of Platelet‐Activating Anti‐Platelet Factor 4 Disorders

open access: yesInternational Journal of Laboratory Hematology, EarlyView.
ABSTRACT Introduction The prototypic anti‐platelet factor 4 (PF4) disorder—heparin‐induced thrombocytopenia and thrombosis (HITT)—features immunoglobulin G (IgG) class antibodies that activate platelets, monocytes, and neutrophils in a mainly heparin‐dependent fashion via Fcγ receptor‐dependent cellular activation.
Theodore E. Warkentin
wiley   +1 more source

Home - About - Disclaimer - Privacy