Assistant Professor of Pediatrics at the University of Washington
Pediatric Rheumatology
Dr. Troy Torgerson, MD
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Dr. Troy Torgerson practices Pediatric Rheumatology. He went to Vanderbilt University School of Medicine. Troy Torgerson is a published MD as well. He has 64 publications published. The latest was: Regulation of NF-kappa B, AP-1, NFAT, and STAT1 nuclear import in T lymphocytes by noninvasive delivery of peptide carrying the nuclear localization sequence of NF-kap...
Publications
- Hematopoietic Stem Cell Transplant for Immune Deficiency and Immune Dysregulation Disorders.
- Treosulfan-Based Conditioning and Hematopoietic Cell Transplantation for Nonmalignant Diseases: A Prospective Multicenter Trial.
- ICON: The Early Diagnosis of Congenital Immunodeficiencies.
- Intravenous injection of a foamy virus vector to correct canine SCID-X1.
- Early-Onset Stroke and Vasculopathy Associated with Mutations in ADA2.
- A Novel Gain-of-Function IKBA Mutation Underlies Ectodermal Dysplasia with Immunodeficiency and Polyendocrinopathy.
- Common variable immunodeficiency as the initial presentation of dyskeratosis congenita.
- Defective actin accumulation impairs human natural killer cell function in patients with dedicator of cytokinesis 8 deficiency.
- Clinical Ambiguities-Ongoing Questions.
- Overview of Routes of IgG Administration.
- Comparing Routes of IgG Administration for Primary Immunodeficiency Disorders.
- Vaccination with a UV irradiated genetically attenuated mutant of Staphylococcus aureus provides protection against subsequent systemic infection.
- Expanding the Clinical and Genetic Spectrum of Human CD40L Deficiency: The Occurrence of Paracoccidioidomycosis and Other Unusual Infections in Brazilian Patients.
- Dendritic cells from X-linked hyper-IgM patients present impaired responses to Candida albicans and Paracoccidioides brasiliensis.
- Heterozygous signal transducer and activator of transcription 3 mutations in hyper-IgE syndrome result in altered B-cell maturation.
- Genetic disorders with immune dysregulation.
- Outcomes and Duration of Pneumocystis jiroveci Pneumonia Therapy in Infants With Severe Combined Immunodeficiency.
- Long-term outcome and lineage-specific chimerism in 194 Wiskott-Aldrich Syndrome patients treated by hematopoietic cell transplantation between 1980-2009: an internati...
- Autoimmune Hepatitis Type 2 In A Child With IPEX Syndrome.
- Stable hematopoietic cell engraftment after low-intensity nonmyeloablative conditioning in patients with immune dysregulation, polyendocrinopathy, enteropathy, X-linke...
- A custom 148 gene-based resequencing chip and the SNP explorer software: new tools to study antibody deficiency.
- Diagnostic approach to the hyper-IgE syndromes: immunologic and clinical key findings to differentiate hyper-IgE syndromes from atopic dermatitis.
- Astrovirus encephalitis in boy with X-linked agammaglobulinemia.
- Autoantibodies in Scurfy mice and IPEX patients recognize keratin 14.
- Atypical presentation of IL-12 receptor beta1 deficiency with pneumococcal sepsis and disseminated nontuberculous mycobacterial infection in a 19-month-old girl born t...
- FOXP3 forkhead domain mutation and regulatory T cells in the IPEX syndrome.
- Comèl-Netherton syndrome defined as primary immunodeficiency.
- FOXP3 inhibits activation-induced NFAT2 expression in T cells thereby limiting effector cytokine expression.
- TH17 cells and regulatory T cells in primary immunodeficiency diseases.
- Immunologic reconstitution during PEG-ADA therapy in an unusual mosaic ADA deficient patient.
- Familial hemophagocytic lymphohistiocytosis in two brothers with X-linked agammaglobulinemia.
- Novel signal transducer and activator of transcription 3 (STAT3) mutations, reduced T(H)17 cell numbers, and variably defective STAT3 phosphorylation in hyper-IgE synd...
- Immune dysregulation in primary immunodeficiency disorders.
- Cutaneous noncaseating granulomas associated with Nijmegen breakage syndrome.
- Regulatory T cells in primary immunodeficiency diseases.
- STAT3 mutation in the original patient with Job's syndrome.
- Immune dysregulation, polyendocrinopathy, enteropathy, X-linked: forkhead box protein 3 mutations and lack of regulatory T cells.
- Severe food allergy as a variant of IPEX syndrome caused by a deletion in a noncoding region of the FOXP3 gene.
- A potential screening tool for IPEX syndrome.
- Immune dysregulation, polyendocrinopathy, enteropathy, X-linked inheritance: model for autoaggression.
- IPEX, FOXP3 and regulatory T-cells: a model for autoimmunity.
- Analysis of FOXP3 reveals multiple domains required for its function as a transcriptional repressor.
- Single-cell analysis of normal and FOXP3-mutant human T cells: FOXP3 expression without regulatory T cell development.
- Molecular analysis of a large cohort of patients with the hyper immunoglobulin M (IgM) syndrome.
- Immune dysregulation, polyendocrinopathy, enteropathy, and X-linked inheritance (IPEX), a syndrome of systemic autoimmunity caused by mutations of FOXP3, a critical re...
- Immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome: a model of immune dysregulation.
- NCI, NHLBI/PBMTC first international conference on late effects after pediatric hematopoietic cell transplantation: persistent immune deficiency in pediatric transplan...
- Successful use of the new immune-suppressor sirolimus in IPEX (immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome).
- Neuronal stress and injury in C57/BL mice after systemic kainic acid administration.
- Soft artificial ventricles for infants and adults, with or without a clamshell.
- Wiskott-Aldrich syndrome protein is required for regulatory T cell homeostasis.
- CD4+FOXP3+ regulatory T cells confer long-term regulation of factor VIII-specific immune responses in plasmid-mediated gene therapy-treated hemophilia mice.
- Primary immune deficiency disorders presenting as autoimmune diseases: IPEX and APECED.
- Intensive postgrafting immune suppression combined with nonmyeloablative conditioning for transplantation of HLA-identical hematopoietic cell grafts: results of a pilo...
- Regulation of NF-kappa B, AP-1, NFAT, and STAT1 nuclear import in T lymphocytes by noninvasive delivery of peptide carrying the nuclear localization sequence of NF-kap...
- Preparation of functionally active cell-permeable peptides by single-step ligation of two peptide modules.
- Inhibition of nuclear translocation of transcription factor NF-kappa B by a synthetic peptide containing a cell membrane-permeable motif and nuclear localization seque...
- FOXP3 acts as a rheostat of the immune response.
- Regulatory T cells in human autoimmune diseases.
- Subcutaneous immunoglobulin replacement therapy in the treatment of patients with primary immunodeficiency disease.
- Intraarticular corticosteroid injections of the temporomandibular joint in juvenile idiopathic Arthritis.
- The spectrum of autoantibodies in IPEX syndrome is broad and includes anti-mitochondrial autoantibodies.
- Effect of rituximab on human in vivo antibody immune responses.
Schools
Vanderbilt University School Of Medicine
University Of Wa School Of Med
Conditions Treated
- Arthritis
Doctors Specialties
- Pediatric Rheumatology
Accepted Insurances
Education
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University of Washington -
Vanderbilt University School of Medicine
Hospital
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Seattle Children's Hospital
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