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標(biāo)題: Titlebook: Biology and Management of Unusual Plasma Cell Dyscrasias; Todd M. Zimmerman,Shaji K. Kumar Book 2017 Springer Science+Business Media New Y [打印本頁]

作者: 無法修復(fù)    時間: 2025-3-21 17:19
書目名稱Biology and Management of Unusual Plasma Cell Dyscrasias影響因子(影響力)




書目名稱Biology and Management of Unusual Plasma Cell Dyscrasias影響因子(影響力)學(xué)科排名




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書目名稱Biology and Management of Unusual Plasma Cell Dyscrasias網(wǎng)絡(luò)公開度學(xué)科排名




書目名稱Biology and Management of Unusual Plasma Cell Dyscrasias被引頻次




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書目名稱Biology and Management of Unusual Plasma Cell Dyscrasias讀者反饋學(xué)科排名





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Kommunale Selbstverwaltung im modernen Staatupon cooling. While the majority of the patients with a cryoglobulin are asymptomatic, unique clinical syndromes may occur often resulting in life-threatening complications. The Brouet classification uses the clonality of the cryoglobulin to define the subtype, and the clinical manifestations vary u
作者: ICLE    時間: 2025-3-23 10:20

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https://doi.org/10.1007/978-3-663-08632-1nal gammopathy of renal significance (MGRS) has been introduced to distinguish these patients from those with the benign monoclonal gammopathy of undetermined significance. Kidney diseases of MGRS can be classified according to the type of deposits in the kidney. The three major categories are organ
作者: 兩棲動物    時間: 2025-3-23 19:29

作者: BUST    時間: 2025-3-24 02:12
Book 2017globin deposition disease, and cryoglobulinemic syndromes, among others. The only book dedicated to this intriguing family of diseases,?.Biology and Management of Unusual Plasma Cell Dyscrasias.?will be a long-lasting reference for clinicians and scientists alike..
作者: ETHER    時間: 2025-3-24 03:39
Sabine Lorenz,Kai Wegrich,Hellmut Wollmannhave an excellent prognosis with local therapies; outcomes are less good, and therapies are less well established for the patients with multicentric CD with the exception of interleukin-6 and interleukin-6 receptor antibodies, which are useful in a subset of patients.
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https://doi.org/10.1007/978-3-663-08632-1ransplantation. This requires confirmation that a MGRS is responsible for the disease, which can only be done by a kidney biopsy. The treatment should optimally target the clone producing the MGRS rather than be based on renal histology.
作者: Fabric    時間: 2025-3-24 15:50
,Waldenstrom’s Macroglobulinemia,an be complex as many patients do not require treatment initially. When patients do require therapy, it is important to select therapies that do not limit future treatment options. To provide a simple risk-adapted approach to managing patients with Waldenstrom’s macroglobulinemia, a rational approach to this disease is presented.
作者: anaphylaxis    時間: 2025-3-24 19:04
Renal Disease Associated with Monoclonal Gammopathy,ransplantation. This requires confirmation that a MGRS is responsible for the disease, which can only be done by a kidney biopsy. The treatment should optimally target the clone producing the MGRS rather than be based on renal histology.
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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
作者: Definitive    時間: 2025-3-26 04:49
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
作者: 催眠    時間: 2025-3-26 17:27
Biology and Management of Unusual Plasma Cell Dyscrasias978-1-4419-6848-7
作者: 走調(diào)    時間: 2025-3-26 21:18
,Plasmacytoma—Current Approach to Diagnosis and Management,ogical symptoms from spinal cord compression. The role of adjuvant RT after complete surgical resection, adjuvant chemotherapy, or adjuvant bisphosphonates is not well defined and hence not recommended.
作者: 牲畜欄    時間: 2025-3-27 02:27
Immunoglobulin Deposition Diseases,drugs, 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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作者: 多節(jié)    時間: 2025-3-27 12:26
Idiopathic Systemic Capillary Leak Syndrome (Clarkson Disease),isorder, there remains a paucity of high-level evidence, particularly with regard to efficacy of the currently available therapies. This chapter outlines the diagnostic dilemmas and current approaches related to the management of idiopathic SCLS.
作者: insolence    時間: 2025-3-27 16:46
,Plasmacytoma—Current Approach to Diagnosis and Management,al plasma cells without evidence of bone marrow involvement or end-organ damage known as a solitary plasmacytoma (SP). SP of bone mostly occurs in axial skeleton, while it most often affects the head and neck region in case of extramedullary tumors. Their median age is 55?years and mostly present wi
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作者: 陶器    時間: 2025-3-28 06:09
Light Chain Amyloidosis,linical presentation. Prognosis of AL amyloidosis depends on organ, particularly cardiac, involvement. Treatment of AL amyloidosis includes chemotherapy using alkylators, novel therapies and autologous hematopoietic cell transplantation. Amyloid fibril-directed therapy is currently lacking. In this
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Circular Economy Best Practices in the Built Environmenthe unsustainable trends in current construction and demolition practices that extensively rely on new raw materials. It highlights the significant impact of the building sector on global resource consumption, energy utilization, and waste generation, with alarming statistics such as buildings accoun




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