Yukari T Jain D.d.s, Inc. | |
860 E Remington Dr Suite D Sunnyvale CA 94087-2995 | |
(408) 481-0555 | |
(408) 481-0551 |
Full Name | Yukari T Jain D.d.s, Inc. |
---|---|
Speciality | Dentist |
Location | 860 E Remington Dr, Sunnyvale, California |
Authorized Official Name and Position | Hemant Sawhney (BUSINESS MANAGER) |
Authorized Official Contact | 4084810555 |
Accepts Medicare Insurance | This clinic does not participate in Medicare Program. |
Mailing Address | Practice Location Address |
---|---|
Yukari T Jain D.d.s, Inc. 860 E Remington Dr Suite D Sunnyvale CA 94087-2995 Ph: (408) 481-0555 | Yukari T Jain D.d.s, Inc. 860 E Remington Dr Suite D Sunnyvale CA 94087-2995 Ph: (408) 481-0555 |
NPI Number | 1003084740 |
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Provider Enumeration Date | 02/15/2008 |
Last Update Date | 02/15/2008 |
Identifier | Type | State | Issuer |
---|---|---|---|
1003084740 | NPI | - | NPPES |
Taxonomy | Type | License (State) | Status |
---|---|---|---|
122300000X | Dentist | (* (Not Available)) | Primary |
News Archive
Viventia Biotech has announced results of in vitro cytotoxicity and in vivo pharmacokinetic studies conducted to evaluate the potential for combining its phase III anti-cancer antibody therapeutic, Proxinium, with first-line standard of care therapy for squamous cell carcinoma of the head & neck (SCCHN).
In a study published this week in Nature Neuroscience, Bess Frost, PhD, and co-authors, identify abnormal expression of genes, resulting from DNA relaxation, that can be detected in the brain and blood of Alzheimer's patients.
Physicians and policy-makers know that drugs are frequently prescribed to treat certain diseases despite a lack of FDA approval - a practice known as off-label prescribing.
REGENT is a multicenter, randomized trial for comparison of intracoronary infusion of bone marrow-derived unselected mononuclear cells (MNC) and selected CD34+CXCR4+ cells in 200 patients with acute myocardial infarction and reduced LVEF ¡Ü 40%.
The Senate overwhelmingly passed significant prescription drug safety reforms to give the Food and Drug Administration more power to deal with unsafe medicines on the market, moving the issue of drug safety to the House, where a strong bill has been introduced but has yet to be considered.
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