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tension-type headache/headache
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Treatment of migraine, post-traumatic headache, tension-type headaches, atypical facial pain, cervical pain and muscle spasm
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BACKGROUND OF THE INVENTION
The present invention relates to a new method for the treatment of migraine, tension-type headaches, atypical facial pain, post-traumatic headache, cervical pain and muscle spasm.
In accordance with the invention, the method of treatment for these headaches, atypical
Method for treating tension type headaches or headaches associated with drugs or their withdrawal
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This invention relates to a new medical use for a certain indole derivative and pharmaceutical compositions containing it. In particular it relates to the use of 3-[2-(dimethylamino)-ethyl]-N-methyl-1H-indole-5-methanesulphonamide and physiologically acceptable salts and solvates thereof in treating
Intraoral topical anti-inflammatory treatment for relief of migraine, tension-type headache, post-traumatic headache, facial pain, and cervical-muscle spasm
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This invention relates to a method for treatment of migraine, tension-type headache, post-traumatic headache, facial pain and cervical-muscle spasm. More particularly the invention relates to a method of treatment which is non-invasive, non-toxic and non-sedating. The method of the invention
Intraoral topical anti-inflammatory treatment for relief of migraine, tension-type headache, post-traumatic headache facial pain, and cervical-muscle spasm
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This invention relates to a method for treatment of migraine, tension-type headache, post-traumatic headache, facial pain and cervical muscle spasm. More particularly the invention relates to a method of treatment which is non-invasive, non-toxic and non-sedating. The method of the invention
Benzoic acid and benzoic acid ester derivatives to treat headaches
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BACKGROUND OF THE PRESENT INVENTION
The present invention is novel compounds, which are derivatives of benzoic acid and benzoic acid esters--having antiinflammatory activity for the treatment of arthritis, asthma, Raynaud's disease, inflammatory bowel disorders, trigeminal or herpetic neuralgia,
Compositions, kits, and methods for inhibiting cerebral neurovascular disorders and muscular headaches
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FIELD OF THE INVENTION
This invention relates to compositions, kits, and methods for inhibiting muscular headaches and cerebral neurovascular disorders including, but not limited to, neurovascular headaches, migraines, cluster headaches, tinnitus, cerebrovascular spasm, ischemic disorders, and
Apparatus for administering composition for inhibiting cerebral neurovascular disorders and muscular headaches
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FIELD OF THE INVENTION
This invention relates to compositions, kits, methods, and apparatus for inhibiting muscular headaches and cerebral neurovascular disorders including, but not limited to, neurovascular headaches, migraines, cluster headaches, tinnitus, cerebrovascular spasm, ischemic
Substituted 4'-hydroxyphenylacetic acid derivatives having antiinflammatory and analgesic activity
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BACKGROUND OF THE INVENTION
The present invention is novel compounds, which are of 4'-hydroxyphenylacetic acid having antiinflammatory activity for the treatment of arthritis, asthma, Raynaud's disease, inflammatory bowel disorders, trigeminal or herpetic neuralgia, inflammatory eye disorders,
Intraoral semi-custom discluder device and method
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BACKGROUND OF THE INVENTION
This invention relates in general to the prevention of tension and common migraine headaches and temporomandibular syndrome and, more specifically, to an intraoral, semi-custom device for preventing those conditions.
Many people suffer from recurring tension, or muscle
Pharmaceutical composition for treatment of disease due to vascular constriction or vasodilation
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FIELD OF THE INVENTION
The present invention relates to a pharmaceutical composition for treatment and/or prevention of a disease due to constriction or vasodilation of blood vessels comprising EDG(Endothelial differentiation gene)-5 modulator which is useful as a drug, and relates to novel EDG-5
Vanilloid receptor ligands and their use in treatments
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BACKGROUND
The vanilloid receptor 1 (VR1) is the molecular target of capsaicin, the active ingredient in hot peppers. Julius et al. reported the molecular cloning of VR1 (Caterina et al., 1997). VR1 is a non-selective cation channel which is activated or sensitized by a series of different stimuli
Vanilloid receptor ligands and their use in treatments
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BACKGROUND
The vanilloid receptor 1 (VR1) is the molecular target of capsaicin, the active ingredient in hot peppers. Julius et al. reported the molecular cloning of VR1 (Caterina et al., 1997). VR1 is a non-selective cation channel which is activated or sensitized by a series of different stimuli
Vanilloid receptor ligands and their use in treatments
Only registered users can translate articles
Log In/Sign up
BACKGROUND
The vanilloid receptor 1 (VR1) is the molecular target of capsaicin, the active ingredient in hot peppers. Julius et al. reported the molecular cloning of VR1 (Caterina et al., 1997). VR1 is a non-selective cation channel which is activated or sensitized by a series of different stimuli
Vanilloid receptor ligands and their use in treatments
Only registered users can translate articles
Log In/Sign up
BACKGROUND
The vanilloid receptor 1 (VR1) is the molecular target of capsaicin, the active ingredient in hot peppers. Julius et al. reported the molecular cloning of VR1 (Caterina et al., 1997). VR1 is a non-selective cation channel which is activated or sensitized by a series of different stimuli
Vanilloid receptor ligands and their use in treatments
Only registered users can translate articles
Log In/Sign up
BACKGROUND
The vanilloid receptor 1 (VR1) is the molecular target of capsaicin, the active ingredient in hot peppers. Julius et al. reported the molecular cloning of VR1 (Caterina et al., 1997). VR1 is a non-selective cation channel which is activated or sensitized by a series of different stimuli
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