Primary Immunodeficiency Disorders

- A Historic and Scientific Perspective

Forfatter: info mangler
Bog
  • Format
  • Bog, hardback
  • Engelsk

Beskrivelse

Primary Immunodeficiency Disorders: A Historic and Scientific Perspective provides a complete historical context that is crucial for students and researchers concerned with primary immunodeficiency. When researchers have a poor understanding of the way we arrived where we are in research, they can miss important points about a disease, or miss out on how to approach new diseases. This historical knowledge of research can assist greatly by showing how it was done in the past, demonstrating the successes and failures, so that it can be done better in the future. This book provides an understanding of the process going from clinical problem to lab and back to the clinic, based on historical experiences. Its chapters proceed from the discovery of the T and B cell lineages through the first BMT for immunodeficiency disorder; lab investigation and gene therapy for PID; the discovery of the gene for AT and its function; understanding cytokine defects; and many other stops along the way.

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Detaljer
  • SprogEngelsk
  • Sidetal376
  • Udgivelsesdato29-08-2014
  • ISBN139780124071797
  • Forlag Academic Press Inc
  • FormatHardback
Størrelse og vægt
  • Vægt1070 g
  • coffee cup img
    10 cm
    book img
    19,1 cm
    23,4 cm

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    Africa Latin-america History Gene therapy Lentiviruses Immunodeficiency Bone Marrow Transplantation Autoimmunity Cellular immunity B cells Graft rejection Integrins Cerebellar ataxia Histocompatibility Leukocytosis Immunoglobulin Bone marrow transplant Cytotoxicity Innate immunity Humoral immunity Antibody Class switch recombination Allergy and atopy Common Variable Immune Deficiency ADA-Deficiency Immune deficiency Adverse reactions ATM Autosomal recessive agammaglobulinemia Gene transfer Agammaglobulinemia Graft-versus-Host-Disease (GvHD) Laboratory testing Dried blood spot 10 warning signs acquired G-CSF receptor mutations alexin animal (canine) models autosomal dominant and autosomal recessive hyper IgE-syndrome antibody deficiency branchial arch cellular pathology (Virchow) CGD Bursa of Fabricius Cohn fraction II cellular immunity/phagocytes (Metschnikoff) complement split products cold abscesses CD40 congenital neutropenia (CN) Chronic Granulomatous Disease bursectomy diagnostic immunology DOCK8 mutations bubble boy complement regulatory proteins complement testing DNA repair defect ELA-CN defective cytokine signaling Epstein-Barr virus-driven B-cell lymphoma enzyme replacement gammaglobulin cutaneous viral infections hemolytic complement defective bacterial killing hyperimmune immunoglobulin preparations hemophagocytic lymphohistiocytosis (HLH) isolation of microorganisms and proof of pathogenicity (Koch) IL-7Rα-deficiency IMIG discovery of WAS hypercytokinemia elevated serum IgE Kindlin 3 inducible co-stimulator etoposide Jeffrey Modell Foundation familial lymphohistiocytosis (FLH) Job syndrome Lectin pathway fucose G6PC3-CN HAX1-CN hematopoietic cell transplantation (HCT) hematopoietic stem cell transplantation (HSCT) G-CSF therapy Herpes Simplex Virus Encephalitis hypogammaglobulinemia immune globulin therapy Intravenous immunoglobulin (IVIG) leukocyte adhesion deficiency (LAD) immune defect Jeffrey Modell Centers Network IVIG leukemia and CN

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