Dr Matt E Brunson, MD | |
2411 Royal Ln, Pelham, AL 35124-2622 | |
(205) 908-8770 | |
(205) 733-9269 |
Full Name | Dr Matt E Brunson |
---|---|
Gender | Male |
Speciality | General Practice |
Location | 2411 Royal Ln, Pelham, Alabama |
Accepts Medicare Assignments | Does not participate in Medicare Program. He may not accept medicare assignment. |
Identifier | Type | State | Issuer |
---|---|---|---|
1053640763 | NPI | - | NPPES |
Taxonomy | Type | License (State) | Status |
---|---|---|---|
208D00000X | General Practice | 11237 (Alabama) | Primary |
Mailing Address | Practice Location Address |
---|---|
Dr Matt E Brunson, MD 2411 Royal Ln, Pelham, AL 35124-2622 Ph: (205) 908-8770 | Dr Matt E Brunson, MD 2411 Royal Ln, Pelham, AL 35124-2622 Ph: (205) 908-8770 |
News Archive
Removing the PKCI/HINT1 gene from mice has an anti-depressant-like and anxiolytic-like effect. Researchers writing in the open access journal BMC Neuroscience applied a battery of behavioral tests to the PKCI/HINT1 knockout animals, concluding that the deleted gene may have an important role in mood regulation.
Over the last two years, Voices for Healthy Kids, a joint initiative of the Robert Wood Johnson Foundation and the American Heart Association, has directly supported more than 50 coalitions, in 20 cities and states, working to help all young people grow up at a healthy weight.
Carcinogenicity and regulation of caramel colorings by Michael Jacobson, (Executive Director, Center for Science in the Public Interest, USA), an article due to be published in the International Journal of Occupational and Environmental Health, states that Coca-Cola sold in California now contains little of the cancer-causing chemical 4-methylimidizole (4-MI).
Watson Pharmaceuticals, Inc. today announced an exclusive, worldwide licensing agreement with Itero Biopharmaceuticals, Inc., a venture-backed specialty biopharmaceutical company, to develop and commercialize Itero's Recombinant Follicle Stimulating Hormone. The product is currently in preclinical development as a biosimilar molecule for the treatment of female infertility.
The U.S. Food and Drug Administration announced today that it has posted on its Web site its first quarterly report that lists certain drugs that are being evaluated for potential safety issues. The drugs have been identified based on a review of reports in FDA's Adverse Event Reporting System (AERS).
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