Predicate |
Object |
assignee |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_2075c10c6897b7d9b1db8fc31e381d45 |
classificationCPCAdditional |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K9-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q2600-156 |
classificationCPCInventive |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K45-06 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P21-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61B5-1124 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61B5-4076 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K9-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q1-6883 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K31-10 |
classificationIPCInventive |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-10 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-6883 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K45-06 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61B5-11 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61B5-00 |
filingDate |
2019-06-26-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
inventor |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_81878e4f4003c51a5434621d5ce0d8f7 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8730d67403e75063d19c6b6fafb85f1c http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_47e13772d30692f8399bad72b9264164 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_161ddc0dbc4408a0662e9a1a8a3fdbe9 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_2a141c16a0ca10521121fa26689e0448 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6defdf2d33e129ca5f851cc3f16fbff0 |
publicationDate |
2021-05-12-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber |
KR-20210053877-A |
titleOfInvention |
How to treat mitochondrial dysfunction |
abstract |
The present invention relates to a method of treating or preventing mitochondrial dysfunction or mitochondrial disease in a subject, comprising administration of probucol or a pharmaceutically acceptable salt thereof. In addition, the present invention relates to a method of diagnosing a hereditary mitochondrial disease in a subject prior to and in combination with the treatment or prevention. In addition, the present invention relates to a method for evaluating and managing a subject suffering from mitochondrial dysfunction or mitochondrial disease using complex measurements. |
priorityDate |
2018-06-26-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
type |
http://data.epo.org/linked-data/def/patent/Publication |