http://rdf.ncbi.nlm.nih.gov/pubchem/patent/RU-2361213-C2

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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G01N33-50
filingDate 2007-01-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2009-07-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5b0149a6ef10db3328086af54d881e30
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_29b4599573bfe095e4164676f74cc548
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_40c85556deba79b5663cc044e8d231fd
publicationDate 2009-07-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber RU-2361213-C2
titleOfInvention Retrospective (postnatal) express diagnostic technique for placental insufficiency to detect newborn group with high risk of pathology development in neonatal period
abstract FIELD: medicine. n SUBSTANCE: method refers to medicine and can be used in practical obstetrics and neonatology to detect within first postnatal hours the newborns with high risk of pathology development in neonatal period. Substance of retrospective (postnatal) express diagnostic technique of placental insufficiency consists in evaluation of histamine and catecholamine content in placental tissues of the puerperants with pregnancy combined with antiphospholipid syndrome (APL). If histamine content exceeds 150 c.u., while catecholamine is more than 12 c.u., chronic placental insufficiency is diagnosed. Application of the present technique allows within 2 hours after delivery making the authentic diagnosis of placental insufficiency and beginning the relevant timely treatment of the newborn with high risk of pathology development. n EFFECT: possibility within 2 hours after delivery to make the authentic diagnosis of placental insufficiency and beginning the relevant timely treatment of the newborn with high risk of pathology development. n 1 tbl, 4 ex
priorityDate 2007-01-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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