http://rdf.ncbi.nlm.nih.gov/pubchem/patent/RU-2154823-C1

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_88b6445cd1d147b5a0c19551478764b2
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G01N33-49
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G01N33-48
filingDate 1999-01-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2000-08-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_79a92c3ab1352666e007eaaad71b01a1
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_0c48e62feab989efe2390c2c849ad6a8
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_83ca6324d9de094a765f2d75293dac0f
publicationDate 2000-08-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber RU-2154823-C1
titleOfInvention Method for predicting gestosis development in early pregnancy period
abstract FIELD: medicine. SUBSTANCE: method involves determining hemostasis constants in pregnant women at the first half of gestation period. Endotheliocyte system is studied by counting the number of circulating unbound endotheliocytes in pregnant woman blood. Willebrandt factor as hemostasis index is determined and diagnostic index P is calculated from formula: P = 0,018•K 1 +0,044•K 2 , where K 1 is the Willebrandt factor (%), and K 2 is the number of unbound endotheliocytes (x 10 x 4/l). The P value being greater than zero, gestosis development is predicted. The P value being less than zero, physiological pregnancy development is predicted. EFFECT: enhanced effectiveness in determining group of risk and making decision concerning etiopathogenic therapy to be applied.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/RU-2596798-C1
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/RU-2743851-C1
priorityDate 1999-01-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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