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Titlebook: Cytokine Storm Syndrome; Randy Q. Cron,Edward M. Behrens Book 20191st edition Springer Nature Switzerland AG 2019 Hemophagocytic lymphohis

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Elena G. Popkova,Bruno S. Sergilies on clinical and laboratory criteria; functional and genetic tests can help separate primary forms from secondary forms. Treatment with immunochemotherapy and hematopoietic stem cell transplantation has considerably improved survival in children with primary HLH, a formerly uniformly fatal disease.
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History of Hemophagocytic Lymphohistiocytosislies on clinical and laboratory criteria; functional and genetic tests can help separate primary forms from secondary forms. Treatment with immunochemotherapy and hematopoietic stem cell transplantation has considerably improved survival in children with primary HLH, a formerly uniformly fatal disease.
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Book 20191st editionanding this disorder is critical for all researchers and physicians to ensure timely and appropriate therapy. This textbook, the first of its kind, addresses all aspects of the disorder – from genetics, pathophysiology, and ongoing research,to clinical presentations, risk factors, and treatment..
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Transnational Threat in the ‘Globalized’ Erah neurologic symptoms, and tissue hemophagocytosis. Diagnostic strategies include an initial testing assessment to detect the above-described changes that support the clinical concern for HLH. Disease-specific testing, available only in few laboratories, includes levels of soluble CD25, NK cell func
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Constantin Schäfer,Martin Grossof proposed criteria in different patient populations evaluated prospectively. There is also the specific need to assess the diagnostic performance of criteria in patients with systemic JIA treated with biologics.
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