Physician
Family Medicine
Dr. Michael H. Albert, MD
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Michael Albert works in the field of Family Medicine. He went to University of Mississippi School of Medicine. Michael Albert is also a published physician. He has 33 publication published. The most recent publication is: A Novel Gain-of-Function IKBA Mutation Underlies Ectodermal Dysplasia with Immunodeficiency and Polyendocrinopathy. He accepts Medicare payments and is listed with Medicare.gov.
Publications
- A Novel Gain-of-Function IKBA Mutation Underlies Ectodermal Dysplasia with Immunodeficiency and Polyendocrinopathy.
- Defective actin accumulation impairs human natural killer cell function in patients with dedicator of cytokinesis 8 deficiency.
- Preemptive immunotherapy in childhood acute myeloid leukemia for patients showing evidence of mixed chimerism after allogeneic stem cell transplantation.
- Sorafenib and cisplatin/doxorubicin (PLADO) in pediatric hepatocellular carcinoma.
- Long-term outcome and lineage-specific chimerism in 194 Wiskott-Aldrich Syndrome patients treated by hematopoietic cell transplantation between 1980-2009: an internati...
- (123)I-MIBG scintigraphy/SPECT versus (18)F-FDG PET in paediatric neuroblastoma.
- Clinical spectrum, pathophysiology and treatment of the Wiskott-Aldrich syndrome.
- Reduced methotrexate clearance and renal impairment in a boy with osteosarcoma and earlier undetected autosomal dominant polycystic kidney disease (ADPKD).
- X-linked thrombocytopenia (XLT) due to WAS mutations: clinical characteristics, long-term outcome, and treatment options.
- Therapeutic strategy in p47-phox deficient chronic granulomatous disease presenting as inflammatory bowel disease.
- The most frequent DCLRE1C (ARTEMIS) mutations are based on homologous recombination events.
- ORAI1 deficiency and lack of store-operated Ca2+ entry cause immunodeficiency, myopathy, and ectodermal dysplasia.
- Ethylenecarbodiimide-coupled allogeneic antigen presenting cells induce human CD4+ regulatory T cells.
- Incidence, predisposing factors, and outcome of engraftment syndrome in pediatric allogeneic stem cell transplant recipients.
- Tracking cell proliferation using the far red fluorescent dye SNARF-1.
- Intravenous immunoglobulins contain naturally occurring antibodies that mimic antineutrophil cytoplasmic antibodies and activate neutrophils in a TNFalpha-dependent an...
- Patients with adenosine deaminase deficiency surviving after hematopoietic stem cell transplantation are at high risk of CNS complications.
- The genotype of the original Wiskott phenotype.
- Alloantigen affinity and CD4 help determine severity of graft-versus-host disease mediated by CD8 donor T cells.
- Prevention of lethal acute GVHD with an agonistic CD28 antibody and rapamycin.
- CD28 ligation induces transplantation tolerance by IFN-gamma-dependent depletion of T cells that recognize alloantigens.
- T-cell-depleted peripheral blood stem cell transplantation for alpha-mannosidosis.
- Stable nonviral gene transfer into primary human T cells.
- Successful SCT for Nijmegen breakage syndrome.
- Successful long-term correction of autosomal recessive hyper-IgE syndrome due to DOCK8 deficiency by hematopoietic stem cell transplantation.
- Intracellular T-cell cytokine levels are age-dependent in healthy children and adults.
- Parenteral nutrition is not superior to replacement fluid therapy for the supportive treatment of chemotherapy induced oral mucositis in children.
- Antigen-dependent suppression of alloresponses by Foxp3-induced regulatory T cells in transplantation.
- Cytokine profile in PFAPA syndrome suggests continuous inflammation and reduced anti-inflammatory response.
- T regulatory cells as an immunotherapy for transplantation.
- "Hair-on-end" skull induced by long-term G-CSF treatment in severe congenital neutropenia.
- Oral graft vs. host disease in children--treatment with topical tacrolimus ointment.
Schools
University Of Mississippi School Of Medicine
University Miss Med Center
Doctors Specialties
- Geriatric Medicine
- Family Medicine
Accepted Insurances
Education
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University of Mississippi Medical Center -
University of Mississippi School of Medicine
Drug Facts
| NPI NUMBER | 1679562094 | |
| NPPES Provider LastName | ALBERT | |
| NPPES Provider FirstName | MICHAEL | |
| NPPES Provider ZIPCode | 392084042 | |
| NPPES Provider State | MS | |
| Specialty Description | Family Practice | |
| Total Claim Count | 44881.0 | |
| Distinct Opioid Count | 10.0 | |
| Opioid Claim Count | 1886.0 | |
| Percent Opioid Claims | 4.2 |
Helpful Reviews
Medicare Facts
| National Provider Identifier [NPI] | 1679562094 |
| Last Name Of The Provider | ALBERT |
| First Name Of The Provider | MICHAEL |
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