| Beth Schorr-lesnick | |
|
984 N Broadway Yonkers NY 10701-1318 | |
| (914) 966-9787 | |
| (914) 966-9793 |
| Full Name | Beth Schorr-lesnick |
|---|---|
| Speciality | Internal Medicine |
| Location | 984 N Broadway, Yonkers, New York |
| Authorized Official Name and Position | Beth Schorr-lesnick (OWNER) |
| Authorized Official Contact | 9149669787 |
| Accepts Medicare Insurance | This clinic does not participate in Medicare Program. |
| Mailing Address | Practice Location Address |
|---|---|
| Beth Schorr-lesnick 984 N Broadway Yonkers NY 10701-1318 Ph: (914) 966-9787 | Beth Schorr-lesnick 984 N Broadway Yonkers NY 10701-1318 Ph: (914) 966-9787 |
| NPI Number | 1124193602 |
|---|---|
| Provider Enumeration Date | 11/21/2006 |
| Last Update Date | 08/31/2007 |
| Identifier | Type | State | Issuer |
|---|---|---|---|
| 1124193602 | NPI | - | NPPES |
| Taxonomy | Type | License (State) | Status |
|---|---|---|---|
| 207R00000X | Internal Medicine | 166893 (New York) | Primary |
News Archive
Ampligen, the first drug ever seeking approval to treat chronic fatigue syndrome/myalgic encephalomyelitis (CFS/ME), recently hit another roadblock with the U.S. Food and Drug Administration (FDA).
The latest data from the Centers for Disease Control's (CDC) National Health Statistics Reports shows continued use of the nation's emergency rooms for conditions that could be treated in an urgent care setting.
FibroGen, Inc., today announced that new data from a phase 2a study of patients with stage 3-4 Chronic Kidney Disease and anemia will be presented demonstrating that its first-in-class, investigational oral anemia therapy FG-4592 works differently than erythropoiesis stimulating agents (ESAs) to increase hemoglobin.
Drug delivery company pSivida Corp. today announced it has entered into an evaluation agreement with Hospital for Special Surgery (HSS), a world leader in orthopedics, rheumatology and rehabilitation, to investigate pSivida's drug delivery technologies in orthopedics.
Inhibitex, Inc. today announced its financial results for the first quarter ended March 31, 2010. The Company also announced that it has initiated a Phase I single ascending dose trial of INX-189, its lead HCV nucleotide polymerase inhibitor, in healthy volunteers under an Investigational New Drug application with the U.S. Food and Drug Administration.
› Verified 2 days ago
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