vhl的例句大全

Methods: The hypermethylation was examined by methyl sensitive restrictive DNA endoenzyme analysis in 34 cases of angioreticuloma and the VHL gene mutations detected by PCR SSCP analysis.

方法：采用PCR SSCP法检测血管网织细胞瘤中VHL基因的突变率及甲基化，敏感限制性内切酶消化法检测血管网织细胞瘤中VHL基因的异常甲基化率。

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cns hemangioblastoma is one of the most common manifestations of vhl disease.

中枢神经系统血管母细胞瘤是VHL病最常见的表现。

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the vhl gene may be useful as a marker gene for the diagnosis of rcc and as a target gene for molecular therapy.

VHL基因可作为临床诊断指标，并可望成为肾透明细胞癌基因治疗的重要目的基因。

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Retinal hemangioblastomas may be the initial manifestation of VHL syndrome and can cause vision loss.

视网膜成血管瘤可能为VHL综合征首先发现的类型,通常表现为失明.

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Conclusion Imaging techniques still play an important role in the evaluation and management of VHL disease.

结论影像学检查在冯·希佩尔·林道病的诊治中仍起着极其重要的作用。

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The mutations of VHL gene were irrespective of the age and pathological grade and stage of patients.

结论：国人非遗传性肾透明细胞癌中存在VHL基因的突变，且与患者年龄，肿瘤分期、分级无相关性。

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Expression of VHL and HIF-1 α and its clinical significance in the lung cancer tissue

肺癌组织中VHL和HIF-1α表达及其临床意义

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The detection of mutations in VHL gene from a single cell in a patient with von Hippel-Lindau disease

单细胞水平检测von Hippel-Lindau病基因突变的实验研究

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Results Combining with the familial history, individual history, radiology and pathology, the diagnosis of VHL can be made.

结果结合家族史、个人史、影像学检查以及手术病理证实其诊断。

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Somatic mutations of VHL gene and HIF-1 α expression in primary renal clear cell carcinomas

肾透明细胞癌中VHL基因突变与缺氧诱导因子-1α表达的研究

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Objective To discuss imaging features of von Hippel-Lindau disease ( VHL disease).

目的探讨von Hippel-Lindau病（VHL病）的影像学特征。

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Results: The number of the cases of decannulation was 97, from 8 days to 1 year after operation, 11 cases without decannulatin ( VHL 6, HHL 2 and OHL 3).

结果术后拔管97例，拔管时间8d至1年，未拔管11例（垂直半喉6例，水平半喉2例，超半喉3例）。

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