Hepatitis c / febbre

Treatment of hepatitis C using hyperthermia

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FIELD OF THE INVENTION This invention relates to hyperthermic treatment of hepatitis C. BACKGROUND OF THE INVENTION Injected drug users are the largest group of people with hepatitis C infection. People who received a blood transfusion or kidney transplant before a diagnostic test became available

Treatment of hepatitis C using hyperthermia

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FIELD OF THE INVENTION This invention relates to hyperthermic treatment of hepatitis C. BACKGROUND OF THE INVENTION Injected drug users are the largest group of people with hepatitis C infection. People who received a blood transfusion or kidney transplant before a diagnostic test became available

Treatment of hepatitis C using hyperthermia

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FIELD OF THE INVENTION This invention relates to hyperthermic treatment of hepatitis C. BACKGROUND OF THE INVENTION Injected drug users are the largest group of people with hepatitis C infection. People who received a blood transfusion or kidney transplant before a diagnostic test became available

Use of endoperoxides for the treatment of infections caused by flaviviridae, including hepatitis C, bovine viral diarrhea and classical swine fever virus

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BACKGROUND OF THE INVENTION The invention relates generally to the use of sesquiterpene lactones in the treatment of infections caused by Flaviviridae and, more specifically, to the use of sesquiterpene lactone endoperoxides to treat hepatitis C infections, yellow fever, dengue fever, bovine viral

Inhibition and treatment of Hepatitis B virus and Flavivirus by Helioxanthin and its analogs

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FIELD OF THE INVENTION This invention relates to the anti-viral drugs such as Helioxanthin and its analogs compounds. These compounds may be used alone or in combination with other drugs for the treatment of the following: Hepatitis B virus (HBV), Hepatitis C virus (HCV), Yellow Fever, Dengue Virus,

Methods for real-time multiplex isothermal detection and identification of bacterial, viral, and protozoan nucleic acids

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SEQUENCE LISTING The sequence listing contained in the electronic file "2016-05-01 1464.8005_ST25.txt" created on May 2, 2016, comprising 60 KB is incorporated herein by reference". FIELD OF THE INVENTION This disclosure relates to rapid methods for real-time multiplex detection and identification

Use of a quinazoline compound in preparing a medicament against flaviviridae virus

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This application is the U.S. national phase of International Application No. PCT/CN2011/083357 filed 2 Dec. 2011 which designated the U.S. and claims priority to CN 201010581618.3 filed 9 Dec. 2010, the entire contents of each of which are hereby incorporated by reference. TECHNICAL FIELD The

Modified fluorinated nucleoside analogues

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FIELD OF THE INVENTION The present invention includes (2'R)-2'-deoxy-2'-fluoro-2'-C-methyl nucleosides having the natural .beta.-D configuration and methods for the treatment of Flaviviridae infections, especially hepatitis C virus (HCV). BACKGROUND OF THE INVENTION Hepatitis C virus (HCV) infection

Modified fluorinated nucleoside analogues

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FIELD OF THE INVENTION The present invention includes (2'R)-2'-deoxy-2'-fluoro-2'-C-methyl nucleosides having the natural .beta.-D configuration and methods for the treatment of Flaviviridae infections, especially hepatitis C virus (HCV). BACKGROUND OF THE INVENTION Hepatitis C virus (HCV) infection

Modified fluorinated nucleoside analogues

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FIELD OF THE INVENTION The present invention includes (2'R)-2'-deoxy-2'-fluoro-2'-C-methyl nucleosides having the natural .beta.-D configuration and methods for the treatment of Flaviviridae infections, especially hepatitis C virus (HCV). BACKGROUND OF THE INVENTION Hepatitis C virus (HCV) infection

2'-Ethynyl nucleoside derivatives for treatment of viral infections

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FIELD OF THE INVENTION This invention is directed to novel compounds which are useful in the treatment of viral infections. The invention is also directed to pharmaceutical compositions containing the compounds, processes for their preparation and uses of the compounds in various medicinal

2'-ethynyl nucleoside derivatives for treatment of viral infections

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FIELD OF THE INVENTION This invention is directed to novel compounds which are useful in the treatment of viral infections. The invention is also directed to pharmaceutical compositions containing the compounds, processes for their preparation and uses of the compounds in various medicinal

RNA virus vaccines and methods

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STATEMENT REGARDING FEDERALLY SPONSORED RESEARCH OR DEVELOPMENT Not Applicable. BACKGROUND The unstable nature of the RNA molecule enables RNA viruses to evolve far more rapidly than DNA viruses, frequently changing their surface structures. RNA viruses in general have very high mutation rates as

hepatitis c/febbre

Treatment of hepatitis C using hyperthermia

Treatment of hepatitis C using hyperthermia

Treatment of hepatitis C using hyperthermia

Use of endoperoxides for the treatment of infections caused by flaviviridae, including hepatitis C, bovine viral diarrhea and classical swine fever virus

Inhibition and treatment of Hepatitis B virus and Flavivirus by Helioxanthin and its analogs

Methods for real-time multiplex isothermal detection and identification of bacterial, viral, and protozoan nucleic acids

Use of a quinazoline compound in preparing a medicament against flaviviridae virus

Modified fluorinated nucleoside analogues

Modified fluorinated nucleoside analogues

Modified fluorinated nucleoside analogues

2'-Ethynyl nucleoside derivatives for treatment of viral infections

2'-ethynyl nucleoside derivatives for treatment of viral infections

RNA virus vaccines and methods

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