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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_10c465602e603e6d011c47e60a36781c
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G01N33-53
filingDate 2010-03-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2011-07-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e58c140b642a82b2bf79173088bb08f4
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_4e60d14ba6066c43dc8147c174d8f9d7
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publicationDate 2011-07-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber RU-2425381-C1
titleOfInvention Method of evaluating immunosuppressive response rate in children with chronic glomerulonephritis
abstract FIELD: medicine. ^ SUBSTANCE: invention describes a method of evaluating an immunosuppressive response rate in children with chronic glomerulonephritis characterised by determining the peripheral blood cell kinetics by flow DNA-cytometry; evaluating a cell fraction in a proliferation phases not less than 0.74% enables to consider the immunosuppressive therapy to be prescribed, and observing a decreased cell level in proliferation phases in 2-3 weeks after the beginning of administration at least in 2 times, the therapy is considered to be effective; the absence of positive dynamics requires dosage change or preparation replacement. ^ EFFECT: higher accuracy and reduced number of research injures, derived clinical laboratory criteria of immunosuppressive prescription and prediction of a therapeutic effect. ^ 4 dwg, 1 tbl, 3 ex
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/RU-2609794-C1
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priorityDate 2010-03-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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