| Dr David L Killen, DC | |
|
521 Ontario Ave, Bogalusa, LA 70427-2612 | |
| (985) 735-1112 | |
| (985) 735-1386 |
| Full Name | Dr David L Killen |
|---|---|
| Gender | Male |
| Speciality | Chiropractor |
| Location | 521 Ontario Ave, Bogalusa, Louisiana |
| Accepts Medicare Assignments | Does not participate in Medicare Program. He may not accept medicare assignment. |
| Identifier | Type | State | Issuer |
|---|---|---|---|
| 1992884936 | NPI | - | NPPES |
| 2127390 | Medicaid | LA |
| Taxonomy | Type | License (State) | Status |
|---|---|---|---|
| 111N00000X | Chiropractor | 1416 (Louisiana) | Primary |
| Mailing Address | Practice Location Address |
|---|---|
| Dr David L Killen, DC 521 Ontario Ave, Bogalusa, LA 70427-2612 Ph: (985) 735-1112 | Dr David L Killen, DC 521 Ontario Ave, Bogalusa, LA 70427-2612 Ph: (985) 735-1112 |
News Archive
Amylin Pharmaceuticals, Inc. and Takeda Pharmaceutical Company Limited today announced that they are discontinuing development of pramlintide/metreleptin, an investigational combination therapy for the treatment of obesity that comprises pramlintide, an analog of the natural hormone amylin, and metreleptin, an analog of the natural hormone leptin.
The results of a large community-based study have shown that the probability of major depressive disorder in children and adolescents with high, low, or normal body mass index differs according to gender.
Taro Pharmaceutical Industries Ltd. announced that the U.S. Patent and Trademark Office has issued United States Patent No. 7,683,071 covering T2007. The patent, entitled "Composition and method for improved bioavailability and enhanced brain delivery of 5,5-diphenyl barbituric acid," is for one of a class of non-sedating barbiturate compounds currently in development by the Company.
Ethnic minorities may have particular problems with alcohol use, yet may not be seeking help, warns a senior psychiatrist in this week's British Medical Journal.
Researchers in a recent paper published as a preprint on the preprint medRxiv, study the clinical factors, the laboratory assays to streamline plasma donor selection, and the durability of nAb responses in adults.
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