神经纤维瘤病

方法回顾性分析了13例神经纤维瘤病的MRI表现，其中神经纤维瘤病1型（NF-1）8例，神经纤维瘤病2型（NF-2）5例。

Methods MRI findings of 13 cases with neurofibromatosis were analyzed retrospectively . Among them , 8 cases were neurofibromatosis-1 ( NF-1 ), 5 cases neurofibromatosis-2 ( NF-2 ) .

神经纤维瘤病II型与听觉脑干植入

Neurofibromatosis type 2 and Auditory Brainstem Implantation

神经纤维瘤病Ⅰ型累及脊柱脊髓的MR表现

MR Imaging of intramedullary and spinal canal tumors with neurofibromatosis type 1

神经纤维瘤病颅脑和脊柱CT、MRI表现

CT and MRI manifestations of neurofibromatosis in cranium and spinal column

神经纤维瘤病Ⅱ型的MRI表现及在临床诊断中的作用

MRI image of neurofibromatosis type 2 and its application in clinical diagnosis

II型神经纤维瘤病的MRI表现（附6例报道）

MRI diagnosis of neurofibromatosis type II ( report of 6 cases )

神经纤维瘤病的脑部CT评价

CT evaluation of intracranial neurofibromatosis

目的：研究神经纤维瘤病的中枢神经系统MRI表现。

Objective : To study the MRI appearance of central nervous system in neurofibromatosis .

神经纤维瘤病I型的MRI研究

MRI study of neurofibromatosis type I

神经纤维瘤病的MRI诊断

MRI diagnosis of neurofibromatosis

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。

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

目的：强调Ⅱ型神经纤维瘤病头部MRI的诊断和增强扫描价值。

Objective : To emphasize the diagnostic value of cranial MRI examination and enhanced scanning in neurofibromatosis type ⅱ .

结论：MRI是目前诊断神经纤维瘤病的最佳影像学检查方法，优于CT。

Conclusion : MRI can be considered as first choice of study in diagnosing of neurofibromatosis , it is superior to CT .

目的：认识神经纤维瘤病Ⅰ型的颅脑影像学表现，评价MRI和CT在诊断方面的价值。

Purpose : To understand cranial involvement of neurofibromatosis type I and to evaluate the value of CT and MRI in diagnostic aspect .

马尾神经鞘瘤16例MRI诊断分析40～49岁组发病率最高为28.78%，神经纤维瘤病患者并发神经鞘瘤占神经鞘瘤的1.66%。

Diagnostic Analysis of MRI in 16 Patients with Neurilemoma of Cauda Equina The incidence of neurofibromatosis in neurilemoma was 1.66 % .

目的认识神经纤维瘤病的颅脑及脊柱MRI表现，为临床进一步诊治提供客观依据。

Objective To understand MRI findings of neurofibromatosis in cranium and spinal column is helpful in providing reliable informations for further clinical management .

材料与方法：搜集我院行MR检查并经手术证实符合神经纤维瘤病诊断标准者3例，分析其头部MRI表现。

Materials and Methods : We collected 3 cases of neurofibromatosis type ⅱ proven by surgery and MR imaging system . The cranial MR appearences were reported .

p-AKT和PTEN在Ⅰ型神经纤维瘤病中的表达及意义

Effect of p-AKT and PTEN on Neurofibromatosis ⅰ Pathogenesis

目的探讨耳鼻咽部多发性神经纤维瘤病（neurofibromatosis，NF）的病理、临床表现及诊断和治疗。

Objective To investigate the growth characteristic , clinical manifestation , diagnosis and treatment of neurofibromatosis ( NF ) in otorhinolaryngology .

POEMS综合征和遗传性神经纤维瘤病I型（NFⅠ）是不同病因不同发病机制致病的两种疾病，但均可引起多系统损害，症状体征有交叉，二者合并病例很罕见。

POEMS syndrome and hereditary neurofibromatosis type I ( NF I ) are two different diseases with different causes and pathogenesis but both can cause multiple system lesions . The coexisting case was rare .

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。

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

伴上皮肿瘤内PTCH杂合子缺失的1型神经纤维瘤病患者的特征性临床表现

Distinctive clinical presentation of a NF-1 patient with loss of heterozygosity of PTCH in his epithelial tumors

24例患者均不伴有神经纤维瘤病1型（NF-1），临床表现均有视力下降。

All of patients had no neurofibromatosis type 1 ( NF-1 ) and had impaired vision .

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

神经纤维瘤病（NF1）是常见的常染色体显性遗传性疾病，国外报道，其发病率高达1：3000。这种疾病是由于NF1基因的突变而发生的。

Neurofibromatosis type 1 ( NF1 ) is a common , autosomal-dominant disorder caused by mutations in the NF1 tumor suppressor gene .

目的探讨17β-雌二醇（E2）和E2受体拮抗剂对Ⅰ型神经纤维瘤病（NF1）神经纤维瘤的形成和发展的影响。

Objective To explore the effects of 17 β - estradiol ( E_2 ) and E_2 receptor antagonist on the formation and development of neurofibromas in patients with neurofibromatosis type 1 ( NF1 ) .

目的：提高对神经纤维瘤病Ⅱ型（NF2）的病因、临床表现、诊断及治疗的认识。

Objective : To recognise the predisposing factors , clinical manifestations , diagnosis and treatment of neurofibromatosis type 2 ( NF2 ) .

多发性神经纤维瘤病&骨骼改变30例X线分析

Neurofibromatosis & A Radiologic Analysis of Bone Changes in 30 Cases

尼日利亚Ⅰ型神经纤维瘤病的临床病理学研究

Clinicopathological study of neurofibromatosis type 1 : An experience in Nigeria

神经纤维瘤病的颅脑影像分析（附9例报告）

Craniocerebral Imaging Analysis of Neurofibromatosis ( Analysis of 9 Cases )