Search Results - "Marlar, R A"
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1
Advantages, disadvantages and optimization of one‐stage and chromogenic factor activity assays in haemophilia A and B
Published in International journal of laboratory hematology (01-12-2018)“…Haemophilia A and B diagnosis and disease severity classification are determined on the basis of results from factor VIII (FVIII) and factor FIX (FIX) activity…”
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2
Laboratory testing issues for protein C, protein S, and antithrombin
Published in International journal of laboratory hematology (01-06-2014)“…Thrombophilia is a complex disease process, which clinically expresses as venous thrombosis. The presence of a genetic defect in one of the major contributing…”
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3
The effect of time and temperature variables on routine coagulation tests
Published in Blood coagulation & fibrinolysis (01-09-1998)“…This study evaluates the effects of time and temperature variables on routine coagulation assays [Prothrombin Time test and Activated Partial Thromboplastin…”
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4
Effect of 3.2% vs 3.8% sodium citrate concentration on routine coagulation testing
Published in American journal of clinical pathology (1997)“…The effects of 3.2% and 3.8% sodium citrate concentration on the results of routine coagulation assays (prothrombin time [PT] and activated partial…”
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5
Minimum specimen volume requirements for routine coagulation testing Dependence on citrate concentration
Published in American journal of clinical pathology (01-05-1998)“…We evaluated the effect of sample volume and citrate concentration on results of routine coagulation assays (prothrombin time [PT] and activated partial…”
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6
Coagulation and fibrinolytic profiles in patients with severe pulmonary hypertension
Published in Chest (01-09-1996)“…Although in situ thrombosis is a prominent finding in lung vessels from patients with primary and secondary pulmonary hypertension, to our knowledge, plasma…”
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7
Neonatal purpura fulminans due to homozygous protein C or protein S deficiencies
Published in Seminars in thrombosis and hemostasis (01-10-1990)“…Homozygous protein C deficiency or homozygous protein S deficiency are rare genetic diseases with catastrophic and fatal purpura fulminans-like or thrombotic…”
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8
Accurate testing for dysfunctional molecules: the potential for missing the diagnosis
Published in International journal of laboratory hematology (01-10-2011)Get full text
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9
The effect of instrumentation and laboratory site on the accuracy of the APTT-based heparin therapeutic range
Published in International journal of laboratory hematology (01-12-2012)“…Summary Background Monitoring of unfractionated heparin therapy by activated partial thromboplastin time using the ex vivo method for determining the heparin…”
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10
The First Mutation Identified in the Thrombomodulin Gene in a 45-Year-Old Man Presenting With Thromboembolic Disease
Published in Blood (15-01-1995)“…Thrombomodulin (TM) is the anticoagulant endothelial cell membrane-bound protein cofactor in the thrombin-medi-ated activation of protein C (PC). It has been…”
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11
Thrombomodulin gene variations and thromboembolic disease
Published in Thrombosis and haemostasis (01-07-1997)“…Thrombomodulin (TM) is the endothelial cell cofactor for protein C activation. Since deficiencies of other protein C system proteins are known to cause…”
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12
High-affinity RNA ligands to human α-thrombin
Published in Nucleic acids research (11-07-1994)“…Systematic Evolution of Ligands by Exponential enrichment (SELEX) was used to isolate from a population of 1013 RNA molecules two classes of high affinity RNAs…”
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13
Heparin levels to guide thromboembolism prophylaxis during pregnancy
Published in American journal of obstetrics and gynecology (01-12-1995)“…OBJECTIVE: Our purpose was to determine the dose of heparin required in pregnant women to achieve the same heparin levels as standard doses of 5000 units given…”
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14
Biosynthesis and Secretion of Factor VII, Protein C, Protein S, and the Protein C Inhibitor From a Human Hepatoma Cell Line
Published in Blood (01-01-1986)“…Using specific radioimmunoassays, 8 day cultures of Hep G2 cells were shown to contain in their supernatants 16, 74, and 828 ng/mL and in their cell lysates,…”
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15
Thrombomodulin gene defects in families with thromboembolic disease--a report on four families
Published in Thrombosis and haemostasis (01-03-1999)“…It has been suggested that an impaired thrombomodulin (TM) function could constitute an abnormality leading to thromboembolic disease (TED). The TM gene from…”
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16
Neonatal Purpura Fulminans: A Genetic Disorder Related to the Absence of Protein C in Blood
Published in Blood (01-01-1985)“…To confirm the pathogenesis and the genetic background of neonatal-onset purpura fulminans, two unrelated infants with this rare thrombotic syndrome and 47 of…”
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17
Human Endothelial Cells Synthesize Protein S
Published in Blood (01-04-1986)“…Human umbilical vein endothelial cells were analyzed for the presence of prothrombin, factor VII, protein C, and protein S in culture supernatants and cell…”
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18
Correlation of antiphospholipid antibodies and protein S deficiency with thrombosis in HIV-infected men
Published in Blood coagulation & fibrinolysis (01-08-1994)“…Antiphospholipid antibodies (aPL) and free protein S (PSF) deficiency have been associated with clinical thrombosis. Previous reports described a high…”
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19
Deficiency of protein C inhibitor in combined factor V/VIII deficiency disease
Published in The Journal of clinical investigation (01-11-1980)“…Activated protein C is an anticoagulant plasma protease enzyme that inactivates Factors V and VIII in plasma. Normal plasma contains a protein that inhibits…”
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20
Vitreoretinal findings similar to retinopathy of prematurity in infants with compound heterozygous protein S deficiency
Published in Ophthalmology (Rochester, Minn.) (01-08-1999)“…To present previously undescribed vitreoretinal findings similar to severe retinopathy of prematurity (ROP) in two siblings (daughter and son) with a…”
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