Dr Sara Ann Case, MD | |
62 Old Forge Hollow Rd, Bantam, CT 06750-1315 | |
(860) 567-8460 | |
(860) 567-8460 |
Full Name | Dr Sara Ann Case |
---|---|
Gender | Female |
Speciality | Surgery |
Location | 62 Old Forge Hollow Rd, Bantam, Connecticut |
Accepts Medicare Assignments | Does not participate in Medicare Program. She may not accept medicare assignment. |
Identifier | Type | State | Issuer |
---|---|---|---|
1003903956 | NPI | - | NPPES |
P00759522 | Other | CT | MEDICARE RAILROAD |
001271691 | Medicaid | CT | |
1003903956 | Other | NPI NUMBER | |
1003903956 | Medicaid | CT |
Taxonomy | Type | License (State) | Status |
---|---|---|---|
208600000X | Surgery | 027169 (Connecticut) | Primary |
Mailing Address | Practice Location Address |
---|---|
Dr Sara Ann Case, MD 62 Old Forge Hollow Rd, Bantam, CT 06750-1315 Ph: (860) 567-8460 | Dr Sara Ann Case, MD 62 Old Forge Hollow Rd, Bantam, CT 06750-1315 Ph: (860) 567-8460 |
News Archive
During embryo development, genes are dynamically, and very precisely, switched on and off to confer different properties to different cells and build a well-proportioned and healthy animal. Fgf8 is one of the key genes in this process, controlling in particular the growth of the limbs and the formation of the different regions of the brain. Researchers at EMBL have elucidated how Fgf8 in mammal embryos is, itself, controlled by a series of multiple, interdependent regulatory elements.
Adding a modified stroke drug to stem cells used to treat rats with spinal injury boosted the therapy and motor activity.
Fibrocartilage tissue in the knee is comprised of a more varied molecular structure than researchers previously appreciated, according to a new study by researchers from the Perelman School of Medicine at the University of Pennsylvania and the University of Delaware.
Non-small-cell lung cancer patients with very unusual epidermal growth factor receptor mutations may be more likely to be benefit from first-line chemotherapy than a tyrosine kinase inhibitor, research suggests.
The team of Dr. Robert Koenekoop which includes Dr. Irma Lopez from the Research Institute of the MUHC at the Montreal Children's Hospital played a crucial role in the international collaboration that led to the discovery of a new gene that causes Leber congenital amaurosis (LCA) and retinitis pigmentosa (RP), two devastating forms of childhood blindness.
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