Related Experiment Videos
Nonsense mutation Arg197stop in a Dutch family with type 1 hereditary antithrombin (AT) deficiency causing
J J Michiels1, L van der Luit, H H van Vliet
1Department of Hematology, University Hospital Dijkzigt, Erasmus University Medical School Rotterdam, The Netherlands.
Thrombosis Research
|May 1, 1995
Abstract
No abstract available in PubMed .
Related Concept Videos
Articles linked to this work by shared authors, journal, and citation graph.
A comparative analysis of different automated von Willebrand factor glycoprotein Ib-binding activity assays in well typed von Willebrand disease patients.
Journal of thrombosis and haemostasis : JTH·2018
Influence of apixaban on commonly used coagulation assays: results from the Belgian national External Quality Assessment Scheme.
International journal of laboratory hematology·2017
Effects of Physical Exercise on Markers of Cellular Immunosenescence: A Systematic Review.
Calcified tissue international·2016
Detailed molecular characterization of a novel IDS exonic mutation associated with multiple pseudoexon activation.
Journal of molecular medicine (Berlin, Germany)·2016
Duplex ultrasound, clinical score, thrombotic risk, and D-dimer testing for evidence based diagnosis and management of deep vein thrombosis and alternative diagnoses in the primary care setting and outpatient ward.
International angiology : a journal of the International Union of Angiology·2014
[Rivaroxaban: Xarelto--recommendations for pharmacists].
Journal de pharmacie de Belgique·2013
Genetic and hemostatic characterization of PAI-1 deficiency and isolated hyperfibrinolysis: data from the RBiN study.
Research and practice in thrombosis and haemostasis·2026
A miniaturized chemiluminescent thrombin generation assay to assess the effect of APCC in persons with hemophilia A with inhibitors: an observational study.
Research and practice in thrombosis and haemostasis·2026
Artificial intelligence prediction of therapy response in newly diagnosed adult severe primary immune thrombocytopenia.
Research and practice in thrombosis and haemostasis·2026
Hematuria in children: causes and evaluation.
Childhood kidney diseases·2026
Atypical hemolytic uremic syndrome: pathophysiology, clinical presentation, and treatment strategies.
Childhood kidney diseases·2026
Refractory perirenal effusion in a pediatric patient with antithrombin III deficiency and KILT syndrome: a case report.
Childhood kidney diseases·2026