http://rdf.ncbi.nlm.nih.gov/pubchem/patent/RU-2227301-C2

Outgoing Links

Predicate Object
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G01N33-86
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G01N33-68
filingDate 2002-06-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2004-04-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_9382a64793ea7d214fa1fb1de24d065a
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_779a136c3f9e638de9c7b2299016d437
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_2e59d85051ed410cad3e811818cb16b9
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_483060076e200861909d4d2e7bad1f69
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publicationDate 2004-04-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber RU-2227301-C2
titleOfInvention Method for defining early period criteria for detecting hypercoagulation sings in treating acute leucosis patients
abstract FIELD: medicine. SUBSTANCE: method involves determining soluble fibrin monomer complexes, D-dimers in blood and fibrinogen, prothrombin index, ethanol test fibrinogen-fibrin degradation products, plasminogen values, Hagemann-dependent euglobulin lysis time and blood platelets number. Fibrinogen level being 4,21±0,2 g/l, prothrombin index being 91,9±1,3% as high, soluble fibrin monomer complexes in orthophenantrolin one being 188,0±13,9 mcg/l and ethanol test fibrinogenfibrin degradation products level being equal to 1-2 conditional units, D-dimers being higher than 500 mg/ml, plasminogen being available in the amount of 123,0±8,9%, Hagemann- dependent euglobulin lysis time being equal to 27±4,2 min and blood platelets number in blood being equal to 128±19,7•10 9 /l, pre-DIC stage is to be diagnosed. EFFECT: high accuracy of diagnosis. 3 tbl
priorityDate 2002-06-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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