neurofibromatosis单词基本解析：

n.神经纤维瘤病

n.神经纤维瘤病；

neurofibromatosis变化用词：

neurofibromatosis英英释义：

Noun

1. autosomal dominant disease characterized by numerous neurofibromas and by spots on the skin and often by developmental abnormalities

名词 neurofibromatosis:

autosomal dominant disease characterized by numerous neurofibromas and by spots on the skin and often by developmental abnormalities

同义词：von Recklinghausen's disease

neurofibromatosis[ ,njuərəufi,brəumə'təusis ]n.autosomal dominant disease characterized by numerous neurofibromas and by spots on the skin and often by developmental abnormalities

同义词：von Recklinghausen's disease

neurofibromatosis中文词源：

neurofibromatosis用法和例句：

Neurofibromatosis is one of autosomal - dominant neurogenetic diseases with relatively low incidence.

神经纤维瘤病是一常染色体显性遗传性疾病,临床上较为少见.

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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.

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Neurofibromatosis is an autosomal dominant genetic disease, which also named as Von Recklinghausen disease before.

神经纤维瘤病, 以前又称vonRecknn沙ausen病,属常染色体显性遗传病.

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neurofibromatosis

A case of multiple cutaneous schwannomas;schwannomatosis or neurofibromatosis type 2?

1例多发性皮肤神经鞘瘤患者:神经鞘瘤病抑或2型神经纤维瘤?

Keywords Neurofibromatosis type 1;Neurofibromin;Neurofibroma;Malignant peripheral nerve sheath tumor（MPNST）;The optic pathway glioma;

1型神经纤维瘤病;神经纤维蛋白;神经纤维瘤;恶性周围神经鞘瘤;视通路胶质瘤;

gene for type 1 neurofibromatosis

1型神经纤维瘤病基因

Neurofibromatosis type 1 is a common autosomal dominant disorder with a high rate of penetrance.It is caused by the mutation of the tumor suppressor gene NF1, which encodes neurofibromin.

I型神经纤维瘤是一种常见的高外显率的常染色体显性遗传病，编码神经纤维蛋白的抑癌基因NF1的突变能导致I型神经纤维瘤。

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

[摘要] 目的 探讨周围型神经纤维瘤病患者的整形外科原则及。

neurofibromatosis type 1

Ⅰ型神经纤维瘤病

neurofibromatosis type2

Ⅱ型神经纤维瘤病

A deletion mutation with frameshift of neurofibromatosis type 2 gene was detected by DNA sequencing.

以DNA序列分析出，在第二型纤维细胞瘤基因上发生染色体缺失造成移码突变。

The authors conducted a study to evaluate the clinical characteristics and surgical outcomes in patients with spinal schwannomas and without neurofibromatosis (NF).

作者对存在脊髓神经鞘瘤、但无神经纤维瘤（NF）的患者进行研究，从而评估这此类患者的临床特点及手术治疗结果。

Keywords Auditory brainstem implant;Hearing loss;Acoustic neuroma;Neurofibromatosis type 2;

关键词听觉脑干电极植入;耳聋;听神经瘤;二型神经纤维瘤病;

Keywords Neurofibromatosis 2;Neurofibromatosis 1;Neurofibromatosis;Neuroma;acoustic;

关键词神经纤维瘤病;2型;1型;神经瘤;听;

The final diagnosis turned out to be mumps deafness in 3 patients, otic ototoxicity in 1, cryptococcal meningitis in 1 and neurofibromatosis in 1 patient.

其中三例为腮腺炎性耳聋，一例为耳滴济中毒症，一例为隐球菌性脑膜炎，一例为多发性神经纤维瘤症。

2. The final diagnosis turned out to be mumps deafness in 3 patients, otic ototoxicity in 1, cryptococcal meningitis in 1 and neurofibromatosis in 1 patient.

其中三例为腮腺炎性耳聋，一例为耳滴济中毒症，一例为隐球菌性脑膜炎，一例为多发性神经纤维瘤症。收藏指正

For a patient presenting with neurofibromatosis and a submandibular mass, a neurofibroma of nerve origin should be considered in the differential diagnosis.

因此罹患神经纤维瘤病的患者，出现下颌腺肿瘤时，分布于此处的神经所长出的神经纤维瘤亦须纳入鑑别诊断。

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。

Neurofibromatosis type 1(NF1)is one of the most common neurogenetic diseases affecting adults and children.

型神经纤维瘤病(NF1)是一种常染色体显性遗传神经皮肤疾病,其临床表现多样、复杂,治疗困难。

Keywords Neurofibromatosis type 1;Therapy;Oral and maxillofacical region;

型神经纤维瘤病;治疗;口腔颌面部;

Keywords neurofibromatosis type 1;neurofibroma;neurofibromin;S100 protein;

型神经纤维瘤病;神经纤维瘤;神经纤维素;S100蛋白;

Research advances in molecular genetics of neurofibromatosis type

型神经纤维瘤病分子遗传学研究进展

Genes, Neurofibromatosis 1 ;Variation Genetics ;

基因, 神经纤维瘤病1型 ;

Keywords Gene;neurofibromatosis 2 Polymerase chain reaction Plasmids Transfection Gene expression;

基因;神经纤维瘤病2型;聚合酶链反应;质粒;转染;基因表达;

The neurofibromatosis type 2 (NF2) tumor suppressor is the only gene known to be frequently involved in early development of meningiomas.

多发性神经纤维瘤2型(NF2) 肿瘤抑制基因是已知唯一的经常出现在脑膜瘤早期发展过程中基因。

Multiple neurofibromatosis

多发性神经纤维瘤病

Clinical and molecular biology research of neurofibromatosis

多发神经纤维瘤病的临床和分子生物学研究

The Use of Dilator in Management of Giant Epicranium Neurofibroma and Neurofibromatosis

扩张器在头皮巨大神经纤维瘤外科治疗中的应用

A case of type I neurofibromatosis with atrial septal defect is reported.

报告1例神经纤维瘤病I型并发房间隔缺损。

Objective To study the diagnosis and therapy of hereditary neurofibromatosis.Methods Two families with multiple neurofibromatosis were analyzed.

摘要目的探讨多发性神经纤维瘤病的家族遗传性及诊断治疗的进展。

Objecive To study the best therapeutic and reconstructive method of giant epicrarium nenrofibroma and neurofibromatosis.

摘要目的探讨头皮大型神经纤维瘤的最佳治疗与整复方法。

Objective: To study the CT and MRI features of neurofibromatosis (NF), with their advantage and defect were compared.

摘要目的：探讨神经纤维瘤病的CT和MRI影像表现，并就二者的优劣进行比较。

disseminated neurofibromatosis

播散性神经纤维瘤病

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。

Wereport on a patient with enophthalmos caused by the greater sphenoid wing dyspiasia with simultaneous retinitis pigmentosa, but without stogmata or family history of neurofibromatosis.

本病例普未发现有第一型神经纤维瘤病的临床表徵或家族史，但发现有双眼视网膜色素变性。

One case report of extracranial vertebral aneurysm associated with neurofibromatosis

椎动脉颅外段动脉瘤合并神经纤维瘤一例报道

Objective:To investigate the clinical feature and therapeutic experience of peripheral neurofibromatosis.

目的:探讨周围型神经纤维瘤病的临床特点及治疗经验。

Objective: To study the edffct of mutation of neurofibromatosis 2(NF2) gene (exon 2) in schwannomas.

目的:研究神经鞘瘤中型多发神经纤维瘤病基因(NF2)外显子2的突变及其意义。

Objective: To evaluate the operative effect of neurofibromatosis scoliosis treated by vascularized grafted rid.

目的:评价采用带血管蒂肋骨转位治疗神经纤维瘤病性脊柱侧弯的远期疗效。

ObjectiveTo study the diagnosis and therapy of hereditary neurofibromatosis.

目的探讨多发性神经纤维瘤病的家族遗传性及诊断治疗的进展。

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

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。

Keywords neurofibroma;plexiform;neurofibromatosis type 1;pathology;clinical;

神经纤维瘤;丛状;神经纤维瘤病1型;病理学;临床;

neurofibromatosis gene

神经纤维瘤基因

Brain morphometry, T2-weighted hyperintensities, and IQ in children with neurofibromatosis type 1

神经纤维瘤病1型患儿的脑形态测量学、T2加权高信号及IQ研究

neurofibromatosis 2

神经纤维瘤病2型

Keywords Neurofibromatosis;central;Neuro fibromatosis type 2;MRI;

神经纤维瘤病;中枢型;神经纤维瘤病2型;磁共振成像;

Keywords Neurofibromatosis;Oral and maxillofacial region;Surgery;Laser therapy;

神经纤维瘤病;颌面部;手术;激光治疗;

Neurofibromatosis type 2

神经纤维瘤病Ⅱ型

MR imaging of neurofibromatosis in CNS

神经纤维瘤病中枢神经系统的MRI表现

Surgical management of scoliosis in neurofibromatosis

神经纤维瘤病性脊柱侧凸的治疗

Neurofibromatosis is one of autosomal-dominant neurogenetic diseases with relatively low incidence.

神经纤维瘤病是一常染色体显性遗传性疾病，临床上较为少见。

MRI Appearance of Central Nervous System in Neurofibromatosis

神经纤维瘤病的中枢神经系统MRI表现

Magnetic resonance diagnosis of neurofibromatosis

神经纤维瘤病的磁共振诊断

Neurofibromatosis dystrophic scoliosis: imaging feature and its clinical significance

神经纤维瘤病致营养不良性脊柱侧凸的影像学特征和临床意义

neurofibromatosis protein

神经纤维瘤病蛋白

Neurofibromatosis is an autosomal dominant genetic disease, which also named as Von Recklinghausen disease before.

神经纤维瘤病，以前又称von Recknn沙ausen病，属常染色体显性遗传病。

neurofibromatosis type I/surgery

神经纤维瘤病／外科学

neurofibromatosis syndrome

神经纤维瘤综合征

neurofibromatosis of mediastinum

纵隔神经纤维瘤病

ResultsThere were 1 case of intestinal neurofibroma, 1 case of mesenteric neurofibromatosis and 2 cases ofposterior peritonecem neurilemmoma.

结果1例肠系膜多发性神经纤维瘤,1例为小肠巨大神经纤维瘤,1例后腹膜多发性神经鞘瘤,1例后腹膜单发性神经鞘瘤。

Results In 7 cases of neurofibromatosis,the findings of CT and MRI displayed 3 cases of bilateral vestibular schwannoma,2 of which were combined with optical nerve glioma;

结果影像学表现为颅骨和椎管异常2例,椎体后缘呈明显的切凹改变,CT和MRI均可见硬脊膜囊扩大,部分延伸至椎旁神经根处;双侧听神经瘤3例,2例合并视神经胶质瘤;

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

结论 周围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。

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

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。

Conclusions: Enophthalmos with dysplasia of sphenoid greater wing is a rare condition, which is usually accociated with type I neurofibromatosis.

结论：蝶骨大翼缺损是一种罕见的疾病，可能导致眼球内陷或外凸，它常与第一型神经纤维瘤病相关。

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。

A Case of Huge Neurofibromatosis on Face

颜面部巨大神经纤维瘤病一例

neurofibromatosis of bone

骨神经纤维瘤病

ObjectiveTo study the diagnosis and therapy of hereditary neurofibromatosis.
目的探讨多发性神经纤维瘤病的家族遗传性及诊断治疗的进展。

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