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Titlebook: Cellular Primary Immunodeficiencies; Mario Milco D‘Elios,Cosima Tatiana Baldari,Frances Book 2021 Springer Nature Switzerland AG 2021 T Ce

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发表于 2025-3-21 16:54:20 | 显示全部楼层 |阅读模式
书目名称Cellular Primary Immunodeficiencies
编辑Mario Milco D‘Elios,Cosima Tatiana Baldari,Frances
视频videohttp://file.papertrans.cn/224/223060/223060.mp4
概述Features updated management and all the latest genetic sof cellular primary immunodeficiencies.Offers in-depth description of the basis of cellular immune responses.Valued companion to immunologists,
丛书名称Rare Diseases of the Immune System
图书封面Titlebook: Cellular Primary Immunodeficiencies;  Mario Milco D‘Elios,Cosima Tatiana Baldari,Frances Book 2021 Springer Nature Switzerland AG 2021 T Ce
描述.This volume of the series .Rare Diseases of the Immune System. presents detailed state of the art knowledge on the cellular primary immunodeficiencies; it includes extensive coverage of both basic science discoveries and the latest clinical advances in the field. The book is structured in accordance with the most recent classification of PIDs and also covers updates on the T cell immunological synapse. Readers will find comprehensive, in-depth descriptions of novel cellular PID genes and related clinical applications, mucosal T cells, and the various clinical phenotypes of cellular PIDs.. Cellular Primary Immunodeficiencies . will be of high value for immunologists, pediatricians, rheumatologists, oncologists, internists, and infectious disease specialists and will also be informative for MD, Master and PhD students..
出版日期Book 2021
关键词T Cell; Antibodies; Immunodeficiency; Immune disease; Combined immuno deficiencies; innate immunity; cellu
版次1
doihttps://doi.org/10.1007/978-3-030-70107-9
isbn_softcover978-3-030-70109-3
isbn_ebook978-3-030-70107-9Series ISSN 2282-6505 Series E-ISSN 2283-6403
issn_series 2282-6505
copyrightSpringer Nature Switzerland AG 2021
The information of publication is updating

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发表于 2025-3-21 21:09:39 | 显示全部楼层
Primary Immunodeficiencies,Primary immunodeficiency diseases (PID) are a part of the growing field of inborn errors of immunity (IEI), sharing a raised susceptibility to infectious diseases and often associated to other features such as autoimmunity, autoinflammation, and lymphoproliferation and susceptibility to neoplastic disease and atopic diseases.
发表于 2025-3-22 03:28:46 | 显示全部楼层
Mario Milco D‘Elios,Cosima Tatiana Baldari,FrancesFeatures updated management and all the latest genetic sof cellular primary immunodeficiencies.Offers in-depth description of the basis of cellular immune responses.Valued companion to immunologists,
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https://doi.org/10.1007/978-3-540-49761-5pecific MHC-associated antigen, T lymphocytes assemble a highly organized intercellular junction, referred to as the immune synapse, on which T cell activation, proliferation, and differentiation crucially depend. Immune synapse assembly and function are impaired in a subgroup of human immunodeficie
发表于 2025-3-22 22:51:32 | 显示全部楼层
https://doi.org/10.1007/978-3-540-49761-5anical and chemical means, they prevent invasion by pathogens. The mucosal immune system consists of an innate and acquired system that interact with each other in a complex way. The mucosal immune system also has the delicate task of differentiating between pathogens and non-pathogens. The T and B
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Equipment, Instruments, and Materials,nogenic defects affecting phagocyte numbers and/or function have been described. A common hallmark of all congenital defects of phagocytes is an increased susceptibility to severe bacterial and fungal infections. Typical sites of infection are the skin, the oral mucosa and gingiva, lymph nodes, the
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