http://rdf.ncbi.nlm.nih.gov/pubchem/patent/RU-2009139873-A
Outgoing Links
| Predicate | Object |
|---|---|
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G01N33-50 |
| filingDate | 2009-10-28-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationDate | 2011-05-10-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | RU-2009139873-A |
| titleOfInvention | METHOD FOR DIAGNOSTIC OF A LASTING OPTION FOR THE COURSE OF JAUNDICE IN NEWBORNS AND CHILDREN OF THE FIRST YEAR OF LIFE |
| abstract | A method for diagnosing a protracted variant of the course of jaundice in newborns and children of the first year of life, which consists in conducting a standard examination: blood biochemistry with determination of the level of total bilirubin and its fractions, markers of cholestasis - alkaline phosphatase (ALP) and gamma glutamyl transferase (GGTP), alanine aminotransferase (ALT) and aspartate aminotransferase (ACT), blood sugar, protein and protein fractions, prothrombin, fibrinogen, characterized in that they decipher markers of TORCH infections and some genetic of malignancies: determine the level of ferritin, creatinine phosphokinase (CPK) and α-fetoprotein (α-FP): a high level of ferritin indicates a serious genetic disease - hereditary hemochromatosis; the KFK indicator within normal values allows to exclude hereditary progressive muscular dystrophies; α-FP makes it possible to exclude liver cancer. |
| isCitedBy | http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-115308422-A |
| priorityDate | 2009-10-28-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 119.