| Christian Counseling | |
|
142 S Lexington Ave Burlington NC 27215-5823 | |
| (336) 227-5476 | |
| Not Available |
| Full Name | Christian Counseling |
|---|---|
| Speciality | Community/behavioral Health |
| Location | 142 S Lexington Ave, Burlington, North Carolina |
| Authorized Official Name and Position | Robert Stogner (DIRECTOR) |
| Authorized Official Contact | 3362275476 |
| Accepts Medicare Insurance | This clinic does not participate in Medicare Program. |
| Mailing Address | Practice Location Address |
|---|---|
| Christian Counseling 142 S Lexington Ave Burlington NC 27215-5823 Ph: (336) 227-5476 | Christian Counseling 142 S Lexington Ave Burlington NC 27215-5823 Ph: (336) 227-5476 |
| NPI Number | 1013102730 |
|---|---|
| Provider Enumeration Date | 09/06/2007 |
| Last Update Date | 09/06/2007 |
| Identifier | Type | State | Issuer |
|---|---|---|---|
| 1013102730 | NPI | - | NPPES |
| Taxonomy | Type | License (State) | Status |
|---|---|---|---|
| 251S00000X | Community/behavioral Health | 6558 (North Carolina) | Primary |
News Archive
While conventional cigarette smoking is an established risk factor for osteoporosis and osteoporotic fracture, the effects of electronic cigarette (e-cigarette) use on bone health have not previously been studied.
On September 6(th), at Atlanta Motor Speedway, the No. 99 Aflac Ford Fusion will sport a colorful new look inspired by a 13-year-old patient at the Aflac Cancer Center. Aflac invited children at the Aflac Cancer Center and Blood Disorders Service to "Color Carl's Car" for the Labor Day weekend race.
A new study published in Circulation, a peer-reviewed journal of the American Heart Association and led by a cardiologist at the Peter Munk Cardiac Centre at Toronto General Hospital has found evidence that only one of the 21 genes normally associated with Brugada Syndrome, a serious genetic heart condition associated with the risk of sudden arrhythmic death, is a definitive cause of the condition.
Several diseases occur when mutations cause misfolding of proteins. These include "serpinopathies" which is a group of rare heritable diseases. They are caused by mutations of so-called "serpin" inhibitors of proteolytic enzymes involved in blood coagulation, tissue remodeling, and other important physiological functions.
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