http://rdf.ncbi.nlm.nih.gov/pubchem/patent/RU-2464576-C1

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_d78d7b5f1eae1d6c5aaf3a2efd8db15b
http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_390ef3f822fbc49a3c0bc2c21e5d1a71
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G01N33-74
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G01N33-574
filingDate 2011-06-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2012-10-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a0d38b0aba5a8aba913cac8565b1655f
publicationDate 2012-10-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber RU-2464576-C1
titleOfInvention Method of determining clinical effectiveness in cervical cancer
abstract FIELD: medicine. n SUBSTANCE: one week after the termination of polychemotherapy, daily urine is examined for the amount of cortisol and cortisone, while blood is examined for adrenocorticotropic hormone. It is followed by calculating the relation of total cortisol and cortisone to adrenocorticotropic hormone. If the derived value is 0.74 and higher, high responsiveness to chemopreparations is stated. n EFFECT: use of the method enables selecting the most adequate complex of anticancer chemopreparations for each patient, performing a surgical intervention in more conservative extent. n 1 ex
priorityDate 2011-06-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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