Search Results - "D. Ochs, Hans"
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Human Inborn Errors of Immunity: 2019 Update on the Classification from the International Union of Immunological Societies Expert Committee
Published in Journal of clinical immunology (2020)“…We report the updated classification of Inborn Errors of Immunity/Primary Immunodeficiencies, compiled by the International Union of Immunological Societies…”
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Human Inborn Errors of Immunity: 2019 Update of the IUIS Phenotypical Classification
Published in Journal of clinical immunology (2020)“…Since 2013, the International Union of Immunological Societies (IUIS) expert committee (EC) on Inborn Errors of Immunity (IEI) has published an updated…”
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Cancer in primary immunodeficiency diseases: Cancer incidence in the United States Immune Deficiency Network Registry
Published in Journal of allergy and clinical immunology (01-03-2018)“…Abstract Background We evaluated the overall and site-specific incidence of cancer in subjects with primary immunodeficiency diseases (PIDD) enrolled in the…”
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International Union of Immunological Societies: 2017 Primary Immunodeficiency Diseases Committee Report on Inborn Errors of Immunity
Published in Journal of clinical immunology (01-01-2018)“…Beginning in 1970, a committee was constituted under the auspices of the World Health Organization (WHO) to catalog primary immunodeficiencies. Twenty years…”
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The 2017 IUIS Phenotypic Classification for Primary Immunodeficiencies
Published in Journal of clinical immunology (01-01-2018)“…Since the 1990s, the International Union of Immunological Societies (IUIS) PID expert committee (EC), now called Inborn Errors of Immunity Committee, has…”
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Transcellular Diapedesis Is Initiated by Invasive Podosomes
Published in Immunity (Cambridge, Mass.) (01-06-2007)“…Diapedesis is critical for immune system function and inflammatory responses. This occurs by migration of blood leukocytes either directly through individual…”
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Primary Immunodeficiency Diseases: an Update on the Classification from the International Union of Immunological Societies Expert Committee for Primary Immunodeficiency 2015
Published in Journal of clinical immunology (01-11-2015)“…We report the updated classification of primary immunodeficiencies compiled by the Primary Immunodeficiency Expert Committee (PID EC) of the International…”
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Flow cytometry-based diagnosis of primary immunodeficiency diseases
Published in Allergology International (01-01-2018)“…Primary immunodeficiencies (PIDs) are a heterogeneous group of inherited diseases of the immune system. The definite diagnosis of PID is ascertained by genetic…”
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Clinical, Immunological, and Molecular Heterogeneity of 173 Patients With the Phenotype of Immune Dysregulation, Polyendocrinopathy, Enteropathy, X-Linked (IPEX) Syndrome
Published in Frontiers in immunology (01-11-2018)“…Immune Dysregulation, Polyendocrinopathy, Enteropathy, X-linked (IPEX) Syndrome is a rare recessive disorder caused by mutations in the gene. In addition,…”
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Immune dysregulation, polyendocrinopathy, enteropathy, X-linked: Forkhead box protein 3 mutations and lack of regulatory T cells
Published in Journal of allergy and clinical immunology (01-10-2007)“…The rare X-linked disorder immune dysregulation, polyendocrinopathy, enteropathy, X-linked (IPEX) and its murine counterpart scurfy have provided important new…”
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Primary immunodeficiency diseases: an update on the classification from the international union of immunological societies expert committee for primary immunodeficiency
Published in Frontiers in immunology (22-04-2014)“…We report the updated classification of primary immunodeficiencies (PIDs) compiled by the Expert Committee of the International Union of Immunological…”
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Activation-Induced Cytidine Deaminase Expression in Human B Cell Precursors Is Essential for Central B Cell Tolerance
Published in Immunity (Cambridge, Mass.) (17-11-2015)“…Activation-induced cytidine deaminase (AID), the enzyme-mediating class-switch recombination (CSR) and somatic hypermutation (SHM) of immunoglobulin genes, is…”
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The 2015 IUIS Phenotypic Classification for Primary Immunodeficiencies
Published in Journal of clinical immunology (01-11-2015)“…There are now nearly 300 single-gene inborn errors of immunity underlying phenotypes as diverse as infection, malignancy, allergy, auto-immunity, and…”
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From clinical observations and molecular dissection to novel therapeutic strategies for primary immunodeficiency disorders
Published in American journal of medical genetics. Part A (01-04-2018)“…The field of primary immunodeficiency diseases (PID) is rapidly expanding with more than 300 genetically defined disorders that have been clinically described…”
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Astrovirus encephalitis in boy with X-linked agammaglobulinemia
Published in Emerging infectious diseases (01-06-2010)“…Encephalitis is a major cause of death worldwide. Although >100 pathogens have been identified as causative agents, the pathogen is not determined for up to…”
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Primary immunodeficiency diseases: An update from the International Union of Immunological Societies Primary Immunodeficiency Diseases Classification Committee
Published in Journal of allergy and clinical immunology (01-10-2007)“…Primary immunodeficiency diseases (PIDs) are a genetically heterogeneous group of disorders that affect distinct components of the innate and adaptive immune…”
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Rubella persistence in epidermal keratinocytes and granuloma M2 macrophages in patients with primary immunodeficiencies
Published in Journal of allergy and clinical immunology (01-11-2016)“…[...]current data have clearly shown an association between defects in T-cell immunity, granulomas, and RV. A role for vaccine virus in Fuchs' uveitis is also…”
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Primary immunodeficiencies: 2009 update
Published in Journal of allergy and clinical immunology (01-12-2009)“…More than 50 years after Ogdeon Bruton's discovery of congenital agammaglobulinemia, human primary immunodeficiencies (PIDs) continue to unravel novel…”
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Autoimmunity and Inflammation in X-linked Agammaglobulinemia
Published in Journal of clinical immunology (01-08-2014)“…Purpose In the past, XLA was described as associated with several inflammatory conditions, but with adequate immune globulin treatment, these are presumed to…”
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Single-Cell Analysis of Normal and FOXP3-Mutant Human T Cells: FOXP3 Expression without Regulatory T Cell Development
Published in Proceedings of the National Academy of Sciences - PNAS (25-04-2006)“…Forkhead winged-helix transcription factor Foxp3 serves as the dedicated mediator of the genetic program governing CD25⁺CD4⁺ regulatory T…”
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