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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G01N33-74
filingDate 2007-03-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2008-07-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_76ed52911c6ce8122f37aa81d274bc85
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publicationDate 2008-07-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber RU-2328747-C1
titleOfInvention Method of provided efficiency of non-adjuvant autohemochemotherapy for patients suffering from paget-type breast cancer
abstract FIELD: medicine; oncology. n SUBSTANCE: patient's blood is tested prior to and after radioimmunotherapy for contents of progesterone, estradiol, follicle- and lutein-stimulating hormones. Patients after treatment are diagnosed with increased progesterone amount from 1.50 to 4.7 nmole/l, reduced ratio of follicle-stimulating to lutein-stimulating hormones from 0.88 to 0.32 and reduced ratio of estradiol to progesterone from 208 to 117, and tumour regression is diagnosed with reduction of progesterone from 0.95-1.34 nmole/l to 0.41-0.83, increased ratio of follicle-stimulating to lutein-stimulating hormones from 0.83-3.81 to 2.07-4.41 and reduced ratio of estradiol to progesterone from 205.2-328.4 to 255.8-671.1. n EFFECT: method application allows detecting of autohemochemotherapy efficiency within postoperative period for patients suffering from Paget-type breast cancer, providing further therapy course correction. n 1 tbl, 2 ex
priorityDate 2007-03-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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