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Titlebook: Biology and Management of Unusual Plasma Cell Dyscrasias; Todd M. Zimmerman,Shaji K. Kumar Book 2017 Springer Science+Business Media New Y

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Sabine Lorenz,Kai Wegrich,Hellmut Wollmanndrugs, proteasome inhibitors, and with autologous stem cell transplantation. In this review, we address clinical presentation and outcomes with light-chain and heavy-chain monoclonal immunoglobulin deposition disease, Type I cryoglobulinemia, proliferative glomerulonephritis with monoclonal IgG depo
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Kommunale Selbstverwaltung im modernen Staatntrol. In Type I cryoglobulinemia, treatment of the underlying lymphoproliferative disorder remains the focus of the primary management, while with the mixed cryoglobulinemia, the management is dependent upon treating the infectious or non-infectious etiology. For patients with infectious mixed cryo
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Biology and Management of Unusual Plasma Cell Dyscrasias
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Biology and Management of Unusual Plasma Cell Dyscrasias978-1-4419-6848-7
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