http://rdf.ncbi.nlm.nih.gov/pubchem/patent/RU-2154479-C2

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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-56
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-44
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61M1-36
filingDate 1996-02-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2000-08-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c9ea158c95416f4473aaad0a0fe0609f
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_7bc29d315615151e87866e523ecf2095
publicationDate 2000-08-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber RU-2154479-C2
titleOfInvention Method of treatment of children with diphtheria polyneuropathy
abstract FIELD: medicine, pediatry. SUBSTANCE: method involves carrying out the complex therapy depending on time of appearance of neurological complication symptoms and their form. In early neuropathy (from 3-d to 15-th day of disease) in patients with subtoxic and chronic form of diphtheria 2-5 seances of hemosorption are carried out in break for 12-24 h and then pentoxyphyllin (4-10 mg/kg body mass per 24 h) and prednisolone (5 mg/kg body mass per 24 h for 5-7 days) are prescribed. In late generalized forms of disease appearing from 16-th to 60-th day in period of rise of symptoms plasmapheresis is carried out (2-3 seances in break for 24-36 h). In amyotrophic form in period of stabilization of paresis strychnine (dose is 1 ml in dilution 1:10000 per one year of life, 3 times per 24 h) and epaden (2 drops per one year of life, 3 times per a day in combination with vitamin E) are prescribed orally. EFFECT: decreased lethality, improved prognosis.
priorityDate 1996-02-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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