amyloidosis的例句大全

The clinical analysis of 37 cases of Lichen amyloidosis was done.

对37例皮肤淀粉样变苔藓进行了临床分析。

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Conclusion: Most common clinical features are grain lesions, punctuate hemorrhage and xerostomia in early tongue amyloidosis.

结论：早期舌淀粉样变性病临床以灰白色颗粒、黏膜出血及口干最常见。

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Objective To investigate the clinicopathological manifestations of early renal amyloidosis ( AL) and its diagnostic criteria.

目的探讨光学显微镜尚未表现明显特点的早期肾淀粉样变（amyloidosis，AL）的临床病理特点及诊断方法。

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Objective To investigate the prevalence and risk factors of dialysis-related amyloidosis ( DRA).

目的了解长期血液透析（HD）患者透析相关性淀粉样变（DRA）的发病率和相关因素。

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Objective To evaluate the value of high resolution ultrasound diagnosing on the dialysis related amyloidosis ( DRA).

目的研究透析相关性淀粉样变（DRA）的声像图特点，评价超声技术对DRA的诊断价值。

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Objective To discussing the clinical manifestation, diagnosis and treatment of the dialysis-related amyloidosis ( DRA) in the long-term hemodialysis patients.

目的探讨长期血液透析患者透析相关淀粉样变（Dialysisrelatedamyloidosis，DRA）的临床及诊治方法。

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Two cases of familial amyloidosis were both neuropathic type.

家族性遗传性淀粉样变性病2例，均以神经系统受累症状为主。

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Hopefully, the availability of the technology that can make this happen will push the envelope and advance the state of the art in amyloidosis studies.

希望这项技术的出现能够推进淀粉样变性病研究的发展。

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Methods: Clinical characteristics, echocardiographic features of cardiac amyloidosis were studied and their chest X-rays, CT scans and serum biochemistry tests were analyzed. Results: ① All patients were more than 55 years.

方法对7例淀粉样变性心肌病患者行超声心动图、X线胸片、电子计算机断层摄影术（CT）及常规血生化检查，分析归纳其临床特点、超声表现及辅助检查结果。

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A case of primary hepatic amyloidosis with factor X deficiency

肝淀粉样变性合并凝血因子X缺乏1例

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Amyloidosis can go away if the CD disease is successfully treated.

如果CD病被成功的治疗后，淀粉样变性也会消失。

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Amyloidosis, a disease where abnormal proteins are deposited in tissues, can occur in CD.

淀粉样变性，异常蛋白在组织中积聚的一种疾病，可发生在CD。

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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缺乏的临床特征、发病机制及治疗方法。

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Conclusion: The mechanism of factor-X deficiency with primary amyloidosis was known as that the factor-X directly bind to amyloid fibrils and deposit in tissue.

结论：目前认为原发性系统性淀粉样变性并发凝血因子X缺乏的机制是淀粉样纤维与X因子特异性结合沉积在组织中形成的。

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PAS staining of vocal nodules rich in glycogen in epithelial tissues, showing amyloidosis myxoid degeneration.

PAS染色，声带小结组织上皮内糖原丰富，可见淀粉样变性粘液样变性。

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Objective Cardiac amyloidosis ( CAL) is a rare disease and we are not familiar with its clinical features.

目的心肌淀粉样变性（cardiac amyloidosis CAL）是临床上相对少见的疾病，对其临床特点认识不足。

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We report a case of pulmonary amyloidosis with multiple pulmonary nodules showing different uptake of18 F-fluorodeoxyglucose ( FDG) on PET.

我们报道报道一例肺多发结节的肺淀粉样变性病例，不同结节在PET上具有不同的摄取FDG表现。

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The Relativity Study between Clinical and TTR Gene Mutation of Familial Vitreous Amyloidosis

家族性玻璃体淀粉样变性的临床及TTR基因突变的相关性研究

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Objective To report a rare case of renal amyloidosis secondary to Castleman's disease, and to review literatures concerned.

目的报道1例罕见的Castleman病继发肾淀粉样变性，并进行相关文献复习。

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Histopathological Findings of Primary Cutaneous Lichenoid and Macular Amyloidosis

苔藓样型和斑状型原发性皮肤淀粉样变的病理改变

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