Physician
Allergy & Immunology
Dr. Arnold S. Kirshenbaum, MD
Arnold Kirshenbaum works in the field of Allergy & Immunology. He attended Georgetown University School of Medicine. Georgetown University School of Medicine has a rank of 49 in research and a 84 in primary care He received awards:"Top Doctors:Washington DC Area", "Top Doctors:Baltimore Area", "Top Doctors:Washington-Baltimore" and "Fellow (FAAAAI)". Arnold Kirshenbaum is a published physician as well. He has 38 publications published. The latest was: Inhibition of human mast cell growth and differentiation by interferon gamma-1b. Dr. Arnold S. Kirshenbaum accepts Medicare.
Publications
- Rictor Negatively Regulates High-Affinity Receptors for IgE-Induced Mast Cell Degranulation.
- Glycomic analysis of human mast cells, eosinophils and basophils.
- IgE-FcepsilonRI interactions determine HIV coreceptor usage and susceptibility to infection during ontogeny of mast cells.
- Human tissue mast cells are an inducible reservoir of persistent HIV infection.
- Growth of human mast cells from bone marrow and peripheral blood-derived CD34+ pluripotent progenitor cells.
- An immunohistochemical study of the bone marrow lesions of systemic mastocytosis: expression of stem cell factor by lesional mast cells.
- Growth of Human Mast Cells from Bone Marrow and Peripheral Blood-Derived CD34(+) Pluripotent Hematopoietic Cells.
- Human mast cells are capable of serotonin synthesis and release.
- Regulation of mast cell number and function.
- KIT D816V-associated systemic mastocytosis with eosinophilia and FIP1L1/PDGFRA-associated Chronic eosinophilic leukemia are distinct entities.
- Generation, isolation, and maintenance of human mast cells and mast cell lines derived from peripheral blood or cord blood.
- Regression of urticaria pigmentosa in adult patients with systemic mastocytosis: correlation with clinical patterns of disease.
- Expression of a functional high-affinity IgG receptor, Fc gamma RI, on human mast cells: Up-regulation by IFN-gamma.
- Analysis of the surface expression of c-kit and occurrence of the c-kit Asp816Val activating mutation in T cells, B cells, and myelomonocytic cells in patients with ma...
- Demonstration that human mast cells arise from a progenitor cell population that is CD34(+), c-kit(+), and expresses aminopeptidase N (CD13).
- Inhibition of human mast cell growth and differentiation by interferon gamma-1b.
- Activated T lymphocytes induce degranulation and cytokine production by human mast cells following cell-to-cell contact.
- Human mast cells produce the CD4+ T lymphocyte chemoattractant factor, IL-16.
- Treatment of three patients with systemic mastocytosis with interferon alpha-2b.
- Fibroblasts determine the fate of Fc epsilon RI+ cell populations in vitro by selectively supporting the viability of mast cells while internalizing and degrading baso...
- Congenital intrathoracic kidney: a 5-year radionuclide follow-up.
- Theophylline dosage.
- A formula for calculating the dosages of drugs in emergencies.
- Mastocytosis in infants and children: recognition of patterns of skin disease.
- Human macrophages cultured on agar but not agarose resemble mast cells.
- IL-3-dependent growth of basophil-like cells and mastlike cells from human bone marrow.
- A staphylococcal protein A rosetting assay for the demonstration of high affinity IgE receptors on rIL-3-dependent human basophil-like cells grown in mixed cell cultures.
- Characterization of basophil-like cells derived from nonhuman primate bone marrow.
- Early development of mast cells.
- Demonstration of the origin of human mast cells from CD34+ bone marrow progenitor cells.
- Sequential appearance of basophils and mast cells from human bone marrow in long-term suspension culture.
- Effect of IL-3 and stem cell factor on the appearance of human basophils and mast cells from CD34+ pluripotent progenitor cells.
- Induction of telomerase activity during development of human mast cells from peripheral blood CD34+ cells: comparisons with tumor mast-cell lines.
- Thrombopoietin alone or in the presence of stem cell factor supports the growth of KIT(CD117)low/ MPL(CD110)+ human mast cells from hematopoietic progenitor cells.
- Effects of tyrosine kinase inhibitor STI571 on human mast cells bearing wild-type or mutated c-kit.
- Characterization of novel stem cell factor responsive human mast cell lines LAD 1 and 2 established from a patient with mast cell sarcoma/leukemia; activation followin...
- Effect of lipopolysaccharide (LPS) and peptidoglycan (PGN) on human mast cell numbers, cytokine production, and protease composition.
Schools
Georgetown University School Of Medicine
Nrmc Affil Ucsf
National Institute Of Health
Procedures Preformed
- Allergy Shots
- Allergy Skin Testing
Conditions Treated
- Allergic Rhinitis
- Asthma
- Atopic Dermatitis (Eczema)
- Bronchitis
- View All
Doctors Specialties
- Pediatrics
- Allergy
- Immunology
Accepted Insurances
Awards
- Top Doctors:Washington DC Area
- Top Doctors:Baltimore Area
- Top Doctors:Washington-Baltimore
- Fellow (FAAAAI)
Education
-
Georgetown University School of Medicine
Hospital
-
Anne Arundel Medical Center
-
University of Maryland Baltimore Washington Medical Center
Drug Facts
| NPI NUMBER |
|
1831145903 |
| NPPES Provider LastName |
|
KIRSHENBAUM |
| NPPES Provider FirstName |
|
ARNOLD |
| NPPES Provider ZIPCode |
|
21061 |
| NPPES Provider State |
|
MD |
| Specialty Description |
|
Allergy/Immunology |
| Total Claim Count |
|
271.0 |
| Distinct Opioid Count |
|
0.0 |
| Opioid Claim Count |
|
0.0 |
| Percent Opioid Claims |
|
0.0 |
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Medicare Facts
| National Provider Identifier [NPI] |
1831145903 |
| Last Name Of The Provider |
KIRSHENBAUM |
| First Name Of The Provider |
ARNOLD |
| View All |
|
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