• Treating primary systemic amyloidosis.

    原发性系统性淀粉样变治疗

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  • Objective To improve the recognition of the primary systemic amyloidosis.

    目的提高原发性淀粉样变认识

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  • Objective: To study and analyse clinically 21 cases of primary systemic amyloidosis.

    目的临床研究分析原发性系统性淀粉样变21

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  • Objective: To explore the clinical characteristics and pathogenesis of primary systemic amyloidosis.

    前言:目的:探讨原发性系统性淀粉样变病临床特点发病机制

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  • Ask your doctor whether these treatments are appropriate for you. For primary systemic amyloidosis, some of these include.

    请询问医生这些治疗手段是否适合

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  • Objective: to investigate the clinical feature, pathogenesis, and therapy of Primary systemic amyloidosis with acquired factor-X deficiency.

    目的探讨原发性系统性淀粉样变性并发凝血因子x缺乏临床特征发病机制治疗方法。

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  • Primary amyloidosis is a systemic disorder characterized by the clonal production and tissue deposition of immunoglobulin light chain (LC) proteins.

    原发性淀粉样变一种系统性疾病特点为免疫球蛋白LC蛋白克隆产生分布于各组织

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  • Primary amyloidosis is a systemic disorder characterized by the clonal production and tissue deposition of immunoglobulin light chain (LC) proteins.

    原发性淀粉样变一种系统性疾病特点为免疫球蛋白LC蛋白克隆产生分布于各组织

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