| Leopoldo M. Muniz, Md, Llc | |
|
101 Summerwood Way Aiken SC 29803-7701 | |
| (803) 642-3505 | |
| (803) 642-3918 |
| Full Name | Leopoldo M. Muniz, Md, Llc |
|---|---|
| Speciality | Family Medicine |
| Location | 101 Summerwood Way, Aiken, South Carolina |
| Authorized Official Name and Position | Leopoldo M Muniz (OWNER/PHYSICIAN) |
| Authorized Official Contact | 8036423505 |
| Accepts Medicare Insurance | This clinic does not participate in Medicare Program. |
| Mailing Address | Practice Location Address |
|---|---|
| Leopoldo M. Muniz, Md, Llc 101 Summerwood Way Aiken SC 29803-7701 Ph: (803) 642-3505 | Leopoldo M. Muniz, Md, Llc 101 Summerwood Way Aiken SC 29803-7701 Ph: (803) 642-3505 |
| NPI Number | 1043555774 |
|---|---|
| Provider Enumeration Date | 12/06/2012 |
| Last Update Date | 12/06/2012 |
| Identifier | Type | State | Issuer |
|---|---|---|---|
| 1043555774 | NPI | - | NPPES |
| 210007 | Medicaid | SC |
| Taxonomy | Type | License (State) | Status |
|---|---|---|---|
| 207Q00000X | Family Medicine | 21000 (South Carolina) | Primary |
News Archive
People who have biomarkers tied to inflammation in their blood in their 40s and 50s may have more brain shrinkage decades later than people without the biomarkers, according to a study published in the November 1, 2017, online issue of Neurology, the medical journal of the American Academy of Neurology. The brain cell loss was found especially in areas of the brain that are affected by Alzheimer's disease.
People with impaired mobility after a stroke soon may have a therapy that restores limb function long after the injury, if a supplemental protein works as well in humans as it does in paralyzed rats.
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The U.S. Food and Drug Administration today approved Libtayo (cemiplimab-rwlc) injection for intravenous use for the treatment of patients with metastatic cutaneous squamous cell carcinoma or locally advanced CSCC who are not candidates for curative surgery or curative radiation.
Lux Biosciences, Inc. today announced that the European Medicines Agency has accepted the filing of the company's Marketing Authorization Application (MAA) for the company's lead product, Luveniq™ (LX211; oral voclosporin) for the treatment of noninfectious uveitis involving the intermediate or posterior segments of the eye.
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