| Claudia Ahumada, Lcsw, Pllc | |
|
2556 31st St Ste 302 Astoria NY 11102 | |
| (917) 960-1713 | |
| (718) 606-9190 |
| Full Name | Claudia Ahumada, Lcsw, Pllc |
|---|---|
| Speciality | Social Worker - Clinical |
| Location | 2556 31st St Ste 302, Astoria, New York |
| Authorized Official Name and Position | Claudia Isabel Ahumada (CEO) |
| Authorized Official Contact | 9179601713 |
| Accepts Medicare Insurance | This clinic does not participate in Medicare Program. |
| Mailing Address | Practice Location Address |
|---|---|
| Claudia Ahumada, Lcsw, Pllc 2414 21st St Apt 5 Astoria NY 11102-3417 Ph: (917) 960-1713 | Claudia Ahumada, Lcsw, Pllc 2556 31st St Ste 302 Astoria NY 11102 Ph: (917) 960-1713 |
| NPI Number | 1134626740 |
|---|---|
| Provider Enumeration Date | 04/10/2018 |
| Last Update Date | 05/29/2018 |
| Identifier | Type | State | Issuer |
|---|---|---|---|
| 1134626740 | NPI | - | NPPES |
| 085510-1 | Other | NY | NYS LICENSE |
| 085510-1 | Other | NY | LICENSE |
| Taxonomy | Type | License (State) | Status |
|---|---|---|---|
| 1041C0700X | Social Worker - Clinical | 085510-1 (New York) | Primary |
News Archive
Open Monoclonal Technology, Inc. (OMT) today announced an antibody discovery collaboration with Merck KGaA. OMT and Merck KGaA have entered into a collaboration whereby OMT will use its OmniRats to generate antibodies against several targets selected by Merck KGaA.
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.
New research, available as a preprint on the bioRxiv* server, has focused on the role played by T cell immunity, particularly CD8+ cytotoxic T cells, on preventing lethal infection with SARS-CoV-2 in mice infused with peptide-loaded antigen-presenting dendritic cells (DCs).
A new international study of children with a severe form of acute lymphoblastic leukemia(ALL) shows that certain chromosome losses can signal an especially poor response to therapy, but that other chromosome abnormalities have no effect on treatment survival.
By using a modern genome-wide knockout approach to single out coronavirus host factors in human cells, researchers from Rega Institute in Belgium discovered a potential new target that might be exploited for developing drugs against the ongoing coronavirus disease (COVID-19) pandemic, but also future outbreaks of highly pathogenic coronaviruses
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