| Grant D. Ringler, D.d.s., Pa | |
|
3008 Garden Grove Pkwy Hutchinson KS 67502-4216 | |
| (620) 669-0835 | |
| (620) 669-8740 |
| Full Name | Grant D. Ringler, D.d.s., Pa |
|---|---|
| Speciality | Dentist - General Practice |
| Location | 3008 Garden Grove Pkwy, Hutchinson, Kansas |
| Authorized Official Name and Position | Melanie Lynn Whitmore (PRACTICE ADMINISTRATOR) |
| Authorized Official Contact | 6206690835 |
| Accepts Medicare Insurance | This clinic does not participate in Medicare Program. |
| Mailing Address | Practice Location Address |
|---|---|
| Grant D. Ringler, D.d.s., Pa 3008 Garden Grove Pkwy Hutchinson KS 67502-4216 Ph: (620) 669-0835 | Grant D. Ringler, D.d.s., Pa 3008 Garden Grove Pkwy Hutchinson KS 67502-4216 Ph: (620) 669-0835 |
| NPI Number | 1245343904 |
|---|---|
| Provider Enumeration Date | 08/16/2006 |
| Last Update Date | 08/22/2020 |
| Identifier | Type | State | Issuer |
|---|---|---|---|
| 1245343904 | NPI | - | NPPES |
| Taxonomy | Type | License (State) | Status |
|---|---|---|---|
| 1223G0001X | Dentist - General Practice | 6475 (Kansas) | Primary |
News Archive
Amorfix Life Sciences, a company focused on treatments and diagnostics for brain wasting diseases, today announced it has achieved 100% specificity (no reproducible false positive results) upon testing 10,000 blood donations for variant Creutzfeldt-Jakob Disease ("vCJD"). with the EP-vCJD(TM) Blood Screening Assay at l'Etablissement Français du Sang de Pyrénées Méditerrannée ("EFS-PM") in Montpellier, France.
The World Health Organization, Stop TB Partnership, UNITAID and the Foundation for Innovative New Diagnostics on Monday announced a joint project to distribute a new diagnostic test for multi-drug resistant tuberculosis that can produce results in two days instead of the standard two or three months, the New York Times reports. Difficulty in identifying MDR-TB has been a "major obstacle" in controlling TB because many patients die or spread the disease while waiting for test results, the Times reports.
Cypher Genomics, Inc., the genome informatics company, announced today the identification of de novo KCNB1 missense mutations as a novel genetic cause of severe epileptic encephalopathy. Cypher's co-founder and Chief Scientific Officer Ali Torkamani, Ph.D. reviewed the data today at a platform presentation at the ASHG 2014 meeting being held October 18 to 22 in San Diego.
New hope for Duchenne muscular dystrophy (DMD) patients. A mouse genetic study in PLoS Medicine reports that targeting the P2RX7 gene, a purinoreceptor, may halt the progression of DMD.
› Verified 6 days ago
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