Mark Robert Bellucci, DC | |
155 Hazard Ave, Enfield, CT 06082-4580 | |
(860) 763-4848 | |
(860) 763-4850 |
Full Name | Mark Robert Bellucci |
---|---|
Gender | Male |
Speciality | Chiropractic |
Experience | 36 Years |
Location | 155 Hazard Ave, Enfield, Connecticut |
Accepts Medicare Assignments | Yes. He accepts the Medicare-approved amount; you will not be billed for any more than the Medicare deductible and coinsurance. |
Identifier | Type | State | Issuer |
---|---|---|---|
1790700979 | NPI | - | NPPES |
Taxonomy | Type | License (State) | Status |
---|---|---|---|
111N00000X | Chiropractor | 000701 (Connecticut) | Primary |
Mailing Address | Practice Location Address |
---|---|
Mark Robert Bellucci, DC 155 Hazard Ave, Enfield, CT 06082-4580 Ph: (860) 763-4848 | Mark Robert Bellucci, DC 155 Hazard Ave, Enfield, CT 06082-4580 Ph: (860) 763-4848 |
News Archive
"Global health projections leave little doubt that chronic diseases are rapidly overtaking infectious diseases, such as malaria, AIDS and tuberculosis (TB), as the world's biggest killers - a shift emphasized by a recent World Health Organization (WHO) report on global health risks," Reuters writes in a story analyzing the future of drug pricing in the developing world. Longer life-spans in developing countries "and changing patterns of food, alcohol and tobacco consumption are creating a 'double burden' for poor nations, piling chronic diseases on top of infectious diseases," the news service writes.
Palatin Technologies, Inc. today announced that a second phase I clinical trial of AZD2820, a subcutaneously-administered peptide melanocortin receptor partial agonist under development for the treatment of obesity, has commenced.
Researchers from the John Theurer Cancer Center at Hackensack University Medical Center played an important role in a study that led to the Food & Drug Administration's (FDA) recent fast tracking of ipilimumab, a promising treatment for metastatic melanoma. The FDA based its decision largely on the results of a pivotal study published in the New England Journal of Medicine on August 19, 2010 – the same day the agency accepted Bristol-Myers Squibb's application for the drug's approval and granted the application priority review status.
Cumberland Pharmaceuticals Inc. announced today that its Phase III study on intravenous ibuprofen as a post-operative analgesic was published in Volume 31, Number 9 of the peer-reviewed journal Clinical Therapeutics, distributed in October. The study concludes that patients emerging from orthopedic and abdominal surgeries required less narcotic and experienced less pain with 800 mg of intravenous ibuprofen every six hours compared to morphine alone.
Demand for real-time continuous data, including personal health information, early warning scores, and alerting when a patient's condition is deteriorating, is driving the market for complete monitoring systems in hospital and home care settings globally.
› Verified 1 days ago
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