Hans D Ochs


Ontology type: schema:Person     


Person Info

NAME

Hans D

SURNAME

Ochs

Publications in SciGraph latest 50 shown

  • 2019-01 Rubella Virus-Associated Cutaneous Granulomatous Disease: a Unique Complication in Immune-Deficient Patients, Not Limited to DNA Repair Disorders in JOURNAL OF CLINICAL IMMUNOLOGY
  • 2018-02 Ralph Josiah Patrick Wedgwood (1924–2017) in JOURNAL OF CLINICAL IMMUNOLOGY
  • 2018-01 The 2017 IUIS Phenotypic Classification for Primary Immunodeficiencies in JOURNAL OF CLINICAL IMMUNOLOGY
  • 2018-01 International Union of Immunological Societies: 2017 Primary Immunodeficiency Diseases Committee Report on Inborn Errors of Immunity in JOURNAL OF CLINICAL IMMUNOLOGY
  • 2017-12 Soluble CD40L is associated with increased oxidative burst and neutrophil extracellular trap release in Behçet’s disease in ARTHRITIS RESEARCH & THERAPY
  • 2017-08 Efficacy and Safety of Human Intravenous Immunoglobulin 10% (Panzyga®) in Patients with Primary Immunodeficiency Diseases: a Two-Stage, Multicenter, Prospective, Open-Label Study in JOURNAL OF CLINICAL IMMUNOLOGY
  • 2017-04 Gastrointestinal Manifestations in X-linked Agammaglobulinemia in JOURNAL OF CLINICAL IMMUNOLOGY
  • 2016-08 Flebogamma® 5 % DIF Intravenous Immunoglobulin for Replacement Therapy in Children with Primary Immunodeficiency Diseases in JOURNAL OF CLINICAL IMMUNOLOGY
  • 2016-08 X-linked Hyper IgM Syndrome Presenting as Pulmonary Alveolar Proteinosis in JOURNAL OF CLINICAL IMMUNOLOGY
  • 2016-07 Health-Related Quality of Life and Health Resource Utilization in Patients with Primary Immunodeficiency Disease Prior to and Following 12 Months of Immunoglobulin G Treatment in JOURNAL OF CLINICAL IMMUNOLOGY
  • 2016-07 Hyper IgM Syndrome: a Report from the USIDNET Registry in JOURNAL OF CLINICAL IMMUNOLOGY
  • 2015-11 Primary Immunodeficiency Diseases: an Update on the Classification from the International Union of Immunological Societies Expert Committee for Primary Immunodeficiency 2015 in JOURNAL OF CLINICAL IMMUNOLOGY
  • 2015-11 The 2015 IUIS Phenotypic Classification for Primary Immunodeficiencies in JOURNAL OF CLINICAL IMMUNOLOGY
  • 2015-08 Subcutaneous Immunoglobulin Replacement Therapy with Hizentra® is Safe and Effective in Children Less Than 5 Years of Age in JOURNAL OF CLINICAL IMMUNOLOGY
  • 2015-02 DOCK8 Deficiency: Clinical and Immunological Phenotype and Treatment Options - a Review of 136 Patients in JOURNAL OF CLINICAL IMMUNOLOGY
  • 2015 Immunoglobulin Replacement Therapy: Past, Present, Future in AGAMMAGLOBULINEMIA
  • 2015-01 Hematopoietic Stem Cell Transplantation for X-Linked Thrombocytopenia With Mutations in the WAS gene in JOURNAL OF CLINICAL IMMUNOLOGY
  • 2014-08 Autoimmunity and Inflammation in X-linked Agammaglobulinemia in JOURNAL OF CLINICAL IMMUNOLOGY
  • 2014-02 First Report of the Hyper-IgM Syndrome Registry of the Latin American Society for Immunodeficiencies: Novel Mutations, Unique Infections, and Outcomes in JOURNAL OF CLINICAL IMMUNOLOGY
  • 2014-01 Ocular Involvement in Primary Immunodeficiency Diseases in JOURNAL OF CLINICAL IMMUNOLOGY
  • 2013-10 Combined De-Novo Mutation and Non-Random X-Chromosome Inactivation Causing Wiskott-Aldrich Syndrome in a Female with Thrombocytopenia in JOURNAL OF CLINICAL IMMUNOLOGY
  • 2013-08 A Phenotypic Approach for IUIS PID Classification and Diagnosis: Guidelines for Clinicians at the Bedside in JOURNAL OF CLINICAL IMMUNOLOGY
  • 2013-08 A Novel Gain-of-Function IKBA Mutation Underlies Ectodermal Dysplasia with Immunodeficiency and Polyendocrinopathy in JOURNAL OF CLINICAL IMMUNOLOGY
  • 2013-08 Prioritization of Evidence-Based Indications for Intravenous Immunoglobulin in JOURNAL OF CLINICAL IMMUNOLOGY
  • 2012-12 Home-Based Subcutaneous Immunoglobulin Versus Hospital-Based Intravenous Immunoglobulin in Treatment of Primary Antibody Deficiencies: Systematic Review and Meta Analysis in JOURNAL OF CLINICAL IMMUNOLOGY
  • 2012-06 DOCK8 functions as an adaptor that links TLR-MyD88 signaling to B cell activation in NATURE IMMUNOLOGY
  • 2012-04 Expanding the Clinical and Genetic Spectrum of Human CD40L Deficiency: The Occurrence of Paracoccidioidomycosis and Other Unusual Infections in Brazilian Patients in JOURNAL OF CLINICAL IMMUNOLOGY
  • 2012-02 Primary Immunodeficiency Diseases Associated with Neurologic Manifestations in JOURNAL OF CLINICAL IMMUNOLOGY
  • 2011-12 Monitoring serum IL-18 levels is useful for treatment of a patient with systemic juvenile idiopathic arthritis complicated by macrophage activation syndrome in PEDIATRIC RHEUMATOLOGY
  • 2011-08 Genetic analysis of contiguous X-chromosome deletion syndrome encompassing the BTK and TIMM8A genes in JOURNAL OF HUMAN GENETICS
  • 2010-03 Efficacy, Pharmacokinetics, Safety, and Tolerability of Flebogamma® 10% DIF, a High-Purity Human Intravenous Immunoglobulin, in Primary Immunodeficiency in JOURNAL OF CLINICAL IMMUNOLOGY
  • 2009-07 Mutations of the Wiskott–Aldrich Syndrome Protein affect protein expression and dictate the clinical phenotypes in IMMUNOLOGIC RESEARCH
  • 2008-11 Effect of Therapeutic Integrin (CD11a) Blockade with Efalizumab on Immune Responses to Model Antigens in Humans: Results of a Randomized, Single Blind Study in JOURNAL OF INVESTIGATIVE DERMATOLOGY
  • 2008-05 Primary Immune Deficiency Disorders Presenting as Autoimmune Diseases: IPEX and APECED in JOURNAL OF CLINICAL IMMUNOLOGY
  • 2007-11 Contiguous X-chromosome Deletion Syndrome Encompassing the BTK, TIMM8A, TAF7L, and DRP2 Genes in JOURNAL OF CLINICAL IMMUNOLOGY
  • 2007-10 Intensive postgrafting immune suppression combined with nonmyeloablative conditioning for transplantation of HLA-identical hematopoietic cell grafts: results of a pilot study for treatment of primary immunodeficiency disorders in BONE MARROW TRANSPLANTATION
  • 2007-07 IPEX, FOXP3 and regulatory T-cells: a model for autoimmunity in IMMUNOLOGIC RESEARCH
  • 2007 Immune Dysregulation, Polyendocrinopathy, Enteropathy, X-Linked Inheritance: Model for Autoaggression in IMMUNE-MEDIATED DISEASES
  • 2006-05 Safety and Efficacy of Self-Administered Subcutaneous Immunoglobulin in Patients with Primary Immunodeficiency Diseases in JOURNAL OF CLINICAL IMMUNOLOGY
  • 2006-01 Health-Related Quality of Life and Treatment Satisfaction in North American Patients with Primary Immunedeficiency Diseases Receiving Subcutaneous IgG Self-Infusions at Home in JOURNAL OF CLINICAL IMMUNOLOGY
  • 2005-07 Gains of glycosylation comprise an unexpectedly large group of pathogenic mutations in NATURE GENETICS
  • 2005-05 A new case of IPEX receiving bone marrow transplantation in BONE MARROW TRANSPLANTATION
  • 2005-01 Cognitive and motor deficits associated with HIV-2287 infection in infant pigtailed macaques: A nonhuman primate model of pediatric neuro-AIDS in JOURNAL OF NEUROVIROLOGY
  • 2004-10 The Hyper IgM Syndrome—An Evolving Story in PEDIATRIC RESEARCH
  • 2004-09 X-linked immunodeficiencies in CURRENT ALLERGY AND ASTHMA REPORTS
  • 2004-05 Octagam® 5%, an Intravenous IgG Product, Is Efficacious and Well Tolerated in Subjects with Primary Immunodeficiency Diseases in JOURNAL OF CLINICAL IMMUNOLOGY
  • 2003-10 Human uracil–DNA glycosylase deficiency associated with profoundly impaired immunoglobulin class-switch recombination in NATURE IMMUNOLOGY
  • 2003-04 Novel Artemis gene mutations of radiosensitive severe combined immunodeficiency in Japanese families in HUMAN GENETICS
  • 2002-07 Unimpaired Activation of c-Jun NH2-Terminal Kinase (JNK) 1 upon CD40 Stimulation in B Cells of Patients with X-Linked Agammaglobulinemia in JOURNAL OF CLINICAL IMMUNOLOGY
  • 2002-05 Immune reconstitution in ADA-SCID after PBL gene therapy and discontinuation of enzyme replacement in NATURE MEDICINE
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