Autoimmune manifestations in common variable immunodeficiency. - Wikidata - wikimedia - TriplyDB

Autoimmune manifestations in common variable immunodeficiency.

Autoimmune manifestations in common variable immunodeficiency.

http://www.wikidata.org/entity/Q33378880

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The transmembrane activator TACI triggers immunoglobulin class switching by activating B cells through the adaptor MyD88 Seronegative Celiac Disease and Immunoglobulin Deficiency: Where to Look in the Submerged Iceberg?Update in understanding common variable immunodeficiency disorders (CVIDs) and the management of patients with these conditions Autoimmunity in common variable immunodeficiency: epidemiology, pathophysiology and management.The spectrum of disease manifestations in patients with common variable immunodeficiency disorders and partial antibody deficiency in a university hospital.Common variable immunodeficiency unmasked by treatment of immune thrombocytopenic purpura with Rituximab Granulomatous disease in common variable immunodeficiency.Autoimmunity in primary immune deficiency: taking lessons from our patients.Common variable immunodeficiency complicated with hemolytic uremic syndrome Autoimmune cytopenias in common variable immunodeficiency.Common variable immunodeficiency, immune thrombocytopenia, rituximab and splenectomy: important considerations.CD81 gene defect in humans disrupts CD19 complex formation and leads to antibody deficiency.Use of combination chemotherapy for treatment of granulomatous and lymphocytic interstitial lung disease (GLILD) in patients with common variable immunodeficiency (CVID).Pathogenesis, diagnosis, and management of primary antibody deficiencies and infections.Disturbed homeostasis and multiple signaling defects in the peripheral blood B-cell compartment of patients with severe chronic sarcoidosis Proteomic analysis of sera from common variable immunodeficiency patients undergoing replacement intravenous immunoglobulin therapy.Intestinal Amyloidosis in Common Variable Immunodeficiency and Rheumatoid Arthritis.Regulatory T cell dysfunction in subjects with common variable immunodeficiency complicated by autoimmune disease.Primary immunodeficiencies of the B lymphocyte Intravenous immunoglobulins in immunodeficiencies: more than mere replacement therapy.Modern management of primary B-cell immunodeficiencies.B-lymphocyte lineage cells and the respiratory system.Autoimmunity in immunodeficiency.A review on guidelines for management and treatment of common variable immunodeficiency.Primary immunodeficiencies: a decade of shifting paradigms, the current status and the emergence of cutting-edge therapies and diagnostics.Evaluation of the T helper 17 cell specific genes and the innate lymphoid cells counts in the peripheral blood of patients with the common variable immunodeficiency.Autoimmunity in Primary Antibody Deficiencies.Common Variable Immunodeficiency and Liver Involvement.Myeloid glycosylation defects lead to a spontaneous common variable immunodeficiency-like condition with associated hemolytic anemia and antilymphocyte autoimmunity.CD4+CD25+Foxp3+ T regulatory cells, Th1 (CCR5, IL-2, IFN-γ) and Th2 (CCR4, IL-4, Il-13) type chemokine receptors and intracellular cytokines in children with common variable immunodeficiency.Intravenous Immunoglobulin Monotherapy for Granulomatous Lymphocytic Interstitial Lung Disease in Common Variable Immunodeficiency.Long-term remission after allogeneic hematopoietic stem cell transplantation in LPS-responsive beige-like anchor (LRBA) deficiency Defects of B-cell terminal differentiation in patients with type-1 Kabuki syndrome.An update on treatment strategies for common variable immunodeficiency.Perigranuloma localization and abnormal maturation of B cells: emerging key players in sarcoidosis?Guidelines on the management of drug-induced immune and secondary autoimmune, haemolytic anaemia.Evaluation of infectious and non-infectious complications in patients with primary immunodeficiency.Granulomatous-lymphocytic interstitial lung disease as the first manifestation of common variable immunodeficiency.Hypogammaglobulinemia Observed One Year after Rituximab Treatment for Idiopathic Thrombocytopenic Purpura.Common Variable Immunodeficiency

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P2860

Autoimmune manifestations in common variable immunodeficiency.

http://www.wikidata.org/entity/Q33378880

description

2008 nî lūn-bûn

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2008 թուականի Մարտին հրատարակուած գիտական յօդուած

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2008 թվականի մարտին հրատարակված գիտական հոդված

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2008年の論文

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2008年学术文章

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2008年学术文章

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2008年学术文章

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2008年学术文章

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2008年学术文章

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2008年學術文章

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Autoimmune manifestations in common variable immunodeficiency.

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Autoimmune manifestations in common variable immunodeficiency.

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Autoimmune manifestations in common variable immunodeficiency.

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Autoimmune manifestations in common variable immunodeficiency.

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Autoimmune manifestations in common variable immunodeficiency.

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Autoimmune manifestations in common variable immunodeficiency.

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Journal of Clinical Immunology

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Autoimmune manifestations in common variable immunodeficiency.

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C Cunningham-Rundles

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TACI is mutant in common variable immunodeficiency and IgA deficiency

CD40 ligand expression is defective in a subset of patients with common variable immunodeficiency.

Autoimmune thrombocytopenic purpura and common variable immunodeficiency: analysis of 21 cases and review of the literature.

Treatment and outcome of autoimmune hematologic disease in common variable immunodeficiency (CVID).

Partial response to anti-CD20 monoclonal antibody treatment of severe immune thrombocytopenic purpura in a patient with common variable immunodeficiency.

Inflammatory and autoimmune complications of common variable immune deficiency.

Treatment with rituximab in benign and malignant hematologic disorders in children.

Immune thrombocytopenic purpura in adults.

Transmembrane activator and calcium-modulating cyclophilin ligand interactor mutations in common variable immunodeficiency: clinical and immunologic outcomes in heterozygotes.

Sarcoidosis and common variable immunodeficiency. Report of 8 cases and review of the literature.

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s10875-008-9182-7

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28 Suppl 1

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2008-03-06T00:00:00Z

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