Results 81 to 90 of about 376,982 (341)
Abstract A 21‐month‐old, male poodle was referred for evaluation of acute lethargy, anorexia and hypovolaemic shock. Initial diagnostic work‐up revealed severe regenerative anaemia, thrombocytopenia and leukocytosis. Abdominal ultrasonography identified free fluid and a suspected mass, with haemoperitoneum confirmed via abdominocentesis.
Catherine Giraldo‐Pino
wiley +1 more source
Global Thrombosis Test - a possible monitoring system for the effects and safety of dabigatran [PDF]
© Otsui et al. 2015BACKGROUND: Dabigatran is an alternative to warfarin (WF) for the thromboprophylaxis of stroke in patients with non-valvular atrial fibrillation (NVAF). The advantage of dabigatran over WF is that monitoring is not required; however, a
Gorog, Diana A+8 more
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Partial thromboplastin time test with kaolin: Normal range and modifications for the diagnosis of haemophilia and Christmas disease [PDF]
Myrtle O. Matchett, G. I. C. Ingram
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Abstract Introduction This study aims to investigate patient factors affecting the rate of plasma volume target attained in hypertriglyceridemic pancreatitis (HTG‐AP) patients undergoing double filtration plasmapheresis (DFPP). Methods A retrospective analysis of 82 HTG‐AP‐interpreted patients from January 2019 to April 2024 compared target plasma ...
Hui Zhang, Chenqiang Zhu, Yunlong Wu
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Combined Factor VII and X Deficiency [PDF]
Factor VII deficiency and factor X deficiency and very rare disorders individually. Combined Factor VII and X is a rare congenital blood disorder with very few cases reported in the literature.
Arora, Sunita+2 more
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The Varied Sensitivity of Partial Thromboplastin and Prothrombin Time Reagents in the Demonstration of the Lupus‐Like Anticoagulant [PDF]
P.M. Mannucci+3 more
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Post‐Viral Acquired Idiopathic Purpura Fulminans Caused by Anti‐Protein S Antibodies
ABSTRACT Acquired Idiopathic purpura fulminans is a rare pathology caused by anti‐protein S antibodies. We have conducted a literature review focusing on the most recent developments in diagnosis and management. Diagnosis is based on the demonstration of typical necrotic purpura lesions on the legs. Treatment must be initiated without delay by infusion
Alexandre Theron+2 more
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Unsuitability of evacuated tubes for monitoring heparin therapy by activated partial thromboplastin time. [PDF]
A. du P. Heyns+3 more
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Anti‐PF4 disorders: Pathogenesis, diagnosis and treatment
Anti‐platelet factor 4 (PF4) disorders include heparin‐induced thrombocytopenia (HIT) and vaccine‐induced immune thrombocytopenia and thrombosis (VITT)/VITT‐like disorders. The formation of immunoglobulin G (IgG)/PF4 immune complexes facilitates uncontrolled activation of platelets, neutrophils and monocytes via IgG‐mediated Fcγ receptor binding.
Megan V. Preece+3 more
wiley +1 more source
Progeny, December 2011, Vol. 27, no. 4 [PDF]
This newsletter from The Department of Public Health about perinatal health care and ...
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