Mr Chandrakant I Udani, MD | |
5548 Asbury Ave., Ocean City, NJ 08226-1236 | |
(609) 399-1519 | |
(609) 398-4712 |
Full Name | Mr Chandrakant I Udani |
---|---|
Gender | Male |
Speciality | General Practice |
Location | 5548 Asbury Ave., Ocean City, New Jersey |
Accepts Medicare Assignments | Medicare enrolled and may accept medicare through third-party reassignment. May prescribe medicare part D drugs. |
Identifier | Type | State | Issuer |
---|---|---|---|
1518974229 | NPI | - | NPPES |
1490303 | Medicaid | NJ |
Taxonomy | Type | License (State) | Status |
---|---|---|---|
208D00000X | General Practice | 25MA03731800 (New Jersey) | Primary |
Mailing Address | Practice Location Address |
---|---|
Mr Chandrakant I Udani, MD 5548 Asbury Ave., Ocean City, NJ 08226 Ph: (609) 399-1519 | Mr Chandrakant I Udani, MD 5548 Asbury Ave., Ocean City, NJ 08226-1236 Ph: (609) 399-1519 |
News Archive
According to a study published in Nature Biotechnology, the sVNT is capable of detecting the functional neutralizing antibodies (NAbs) that can block the binding of the coronavirus spike protein to the angiotensin-converting enzyme 2 (ACE2) host receptor, which mimics the virus-host interaction.
A team of UTSA researchers has discovered that economic implications because of COVID-19 can have a devastating ripple effect on children.
Colon cancer is more likely to be lethal in children and young adults than middle-aged adults. In a single-institution study, researchers at The University of Texas MD Anderson Cancer Center, Houston, Tex., found that differences in mortality rates persist regardless of whether pediatric, adolescent, and young adult patients (aged 24 and younger) were born with a predisposition for colon abnormalities or disease and for the first time conclude that young people are more likely to have metastases outside the colon, into the abdominal cavity, when they are diagnosed.
Supernus Pharmaceuticals, Inc. today announced that its Phase IIa U.S. clinical trial of SPN-812 in adults for the treatment of attention deficit hyperactivity disorder (ADHD) met the primary endpoints of safety and tolerability, and showed statistically significant median reduction versus placebo in both investigator-rated and patient-rated ADHD symptom scores.
Vertex Pharmaceuticals Incorporated announced today that the U.S. Food and Drug Administration (FDA) has accepted the New Drug Application (NDA) for telaprevir and granted the company's request for six-month Priority Review. Telaprevir is Vertex's lead medicine in development for people with genotype 1 chronic hepatitis C.
› Verified 2 days ago
Ms. Kathleen Patricia Denesha, RN General Practice Medicare: Not Enrolled in Medicare Practice Location: 500 E 6th St, Ocean City, NJ 08226 Phone: 609-399-1862 Fax: 609-339-9157 |