Objective to study the MRI features of neurofibromatosis.

目的探讨神经纤维瘤病的MRI影像特征。

Multiple meningiomas may also be associated with neurofibromatosis.

多发性的脊膜瘤可能也伴有神经纤维瘤病。

Objective to detect the mutation on exons 32, 33 of Chinese the neurofibromatosis type 1 (NF1) gene.

目的检测中国人神经纤维瘤病1型(nf1)基因32、33外显子突变。

X-ray findings of the changes of bones with neurofibromatosis in 30 cases are analysed and discussed.

本文对30例多发神经纤维瘤病骨骼改变的X线所见做了分析和讨论。

Huang Chuncai suffers from Neurofibromatosis, a rare genetic disorder that causes growth on nerve tissues.

黄春才所患的肿瘤是神经纤维瘤，属于一种罕见的遗传性疾病，肿瘤组织为快速生长的神经组织。

Materials and Methods: This study included 12 patients of neurofibromatosis, the MRI findings were analyzed.

材料与方法：收集12例神经纤维瘤病患者的临床资料并对其MRI表现进行分析。

Recent studies indicate that patients with type I neurofibromatosis usually have osteopenia or osteoporosis.

最近研究表明I型神经纤维瘤病患者常表现出不同程度的骨量减少或骨质疏松。

Objective to study the reconstructive and microsurgical treatment of facial neurofibroma and neurofibromatosis.

目的研究面部神经纤维瘤及面部巨大神经纤维瘤的整形和显微外科治疗。

Objective to explore the reason and treatment of short bowel syndrome after retroperitoneal multiple neurofibromatosis operation.

目的探讨腹膜后多发性神经纤维瘤术后致短肠综合征的原因和治疗。

Methods: The long-term effects of 16 cases of neurofibromatosis scoliosis treated by vascularized grafted rid were analyzed retrospectively.

方法：回顾性分析16例神经纤维瘤病性脊柱侧弯患者经过带血管蒂肋骨移植手术治疗后的随访资料。

Conclusion Plastic surgical treatment of peripheral neurofibromatosis can yield good results with complete excision and better reconstruction.

结论 四周型神经纤维瘤病采用整形外科方法切除及修复创面具有切除较彻底、修复塑形好的优点。

The National Neurofibromatosis Foundation of the U. S. addresses a set of genetic disorders which cause tumors to grow along various types of nerves.

美国国家神经纤维瘤化基金会：强调一组引起沿各种神经的肿瘤成长的基因疾病。

Methods: ct manifestations and clinical data of 15 cases with neurofibromatosis proved by clinic, surgery and pathology were analysed retrospectively.

方法：对15例经临床手术病理证实的神经纤维瘤病患者的临床资料与脑部ct资料进行了回顾性分析。

The exact pathogenesis of the deformity is still obscure, but most authors believe that macrodactyly is related to neurofibromatosis or lipomata degeneration.

确切发病原因尚不清楚，多认为与神经纤维瘤病或脂肪瘤退变有关。

Methods Retrospective analysis of the clinical date was carried out in 46 cases of peripheral neurofibromatosis admitted in our department from 1981 to 2005.

方法回顾性分析1981 ~ 2005年我科收治的46例周围型神经纤维瘤病的临床资料。

Results: Followed-up for 5 years, all the 16 patients with scoliosis caused by neurofibromatosis obtained satisfactory therapeutic efficacy by this technique.

结果：16例患者经本术式治疗后，经5年以上随访，均获得满意的治疗效果，全部病例平均6个月融合。

The show is presented by Simon Rimmer, Kate Quilton and actor Adam Pearson, who suffers from neurofibromatosis, which has left his face covered in dozens of non-cancerous tumours.

这档节目由西蒙里默、凯特丠尔顿和演员亚当皮尔逊主持。皮尔逊患有多发性神经纤维瘤，这导致他的脸部长有许多良性肿瘤。

Sphenoid wing dysplasia can occur as an isolated finding or in patients who have Neurofibromatosis type 1. Approximately 50% of cases are associated with neurofibromatosis type 1.

蝶骨翼发育不良可以是一个孤立性的发现，也可以见于神经纤维瘤病I型患者。

In the study conducted using a fruit fly, they found that negative feedback mediated by PI3K regulates the excitability of neurons, an issue in a number of ailments that include neurofibromatosis.

在用果蝇的实验中，研究人员发现由PI3K介导的负反馈可以调节神经的兴奋性，这个问题在包括神经纤维瘤等许多疾病中存在。

Objective To investigate the growth characteristic, clinical manifestations, diagnosis and treatment of neurofibromatosis type 1 (NF1) in oral and maxillofacial regions for the better curative effect.

目的探讨Ⅰ型神经纤维瘤病的临床表现、诊断、治疗，为临床积累经验，提高治疗效果。