神经纤维

The only way of preventing neurofibromatosis is by pre-pregnancy genetic counselling for couples where there is a family history of the problem.

唯一的办法防止神经纤维瘤病是由孕前遗传咨询的夫妇有一个家庭的历史问题。

Abstract］ Objective To investigate the plastic surgery treating principle and methods of peripheral neurofibromatosis.

e#［摘要］目的探讨周围型神经纤维瘤病患者的整形外科治疗原则及方法。

Objective:To investigate the characteristics of the intellectual disability of neurofibromatosis type 1 (NF1) and it's relative factors.

目的：研究1型神经纤维瘤病（neurofibromatosistype1，NF1）智力损害的特征及其影响因素。

Objective: To retrospectively investigate the surgical treatment and its clinical efficacy of cervical kyphotic deformity due to neurofibromatosis.

目的：探讨神经纤维瘤病性颈椎后凸畸形的外科治疗方法及其疗效。

Neurofibromatosis should be suspected when such a tumor is found in children.

当儿童出现脑膜瘤时，需要怀疑神经纤维瘤的可能。

Objective To investigate the effect of the neurofibromatosisⅡ(NF2) gene on cell cycle and proliferation in rat schwannoma cell line.

目的 观察Ⅱ型神经纤维瘤（neurofibromatosisⅡ，NF2）基因对细胞增殖和细胞周期的影响。

About 5% of acoustic neuromas are caused by a rare, inherited condition called neurofibromatosis.

约5 ％的听神经瘤是因一种罕见的遗传性神经纤维瘤病的所谓条件。

Type I neurofibromatosis (NF1, or von Recklinghausens disease) occurs equally in men and women at a rate of one in every 2,500 people.

I型神经纤维瘤病（ nf1 ，或冯recklinghausen 病）发生同样在男性和女性的比率之一，在每2500人。

Objective A retrospective study of surgical treatment of 45 patients with scoliosis caused by neurofibromatosis in order to analyse the rehtionship between the curve types and clinical results.

目的 回顾性研究45例神经纤维瘤病性脊柱侧凸患者的外科治疗结果，分析侧凸分类与手术效果的关系。

Neurofibromatosis is a genetic disorder the problem is a faulty gene on one chromosome.

神经纤维瘤病是一种遗传性疾病问题是一个错误的基因对1号染色体。

The split between the two groups can hardly be papered over.

这两个团体间的分歧难以掩饰。

This approach not only encourages a greater number of responses, but minimizes the likelihood of stale groupthink.

这种做法不仅鼓励了更多的反应，而且减少跟风的可能性。