http://rdf.ncbi.nlm.nih.gov/pubchem/patent/SU-1603303-A1

Outgoing Links

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_06e2cd3d95a5bf6f59693ed40cc4042b
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K39-395
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G01N33-53
filingDate 1988-02-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1990-10-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_fcaedb05554b50d6419411b47e2a242b
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_4896671139b8de3cc9c67aa5c09c5763
publicationDate 1990-10-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber SU-1603303-A1
titleOfInvention Method of assessing activity of systematic sclerodermia
abstract The invention relates to the field of medicine and can be used in pediatrics to determine the activity of systemic scleroderma in children. The goal is to improve the accuracy of the method and reduce the time of the study. After the diagnosis of systemic scleroderma in the patient's serum has been established, the level of total immunoglobulin E is determined using a radio pulse sorbent test on paper disks. After 3 h, the content of JG E on the gamma counter is determined, and with its content 316, 72 kI, i.e. an increase of 1-2 standard deviations from the geometric age norm according to the Kjellman table (23.66 kI) determines the active area of the SDS, and if it is kept within the norm, the reactive phase of the SDS is determined. The accuracy of the method increases by 40.3% and reduces the time of diagnosis.
priorityDate 1988-02-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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Total number of triples: 20.