神经纤维瘤病,neurofibromatosis
1)neurofibromatosis[英][,nju?r?ufai,br?um?'t?usis][美][,n?ro,fa?brom?'tos?s, ,nj?r-]神经纤维瘤病
1.Advances in diagnosis and treatment of Neurofibromatosis type 1;Ⅰ型神经纤维瘤病诊治进展
2.Type I neurofibromatosis with atrial septal defect: a case report;神经纤维瘤病I型并发房间隔缺损1例
3.MRI Appearance of Central Nervous System in Neurofibromatosis;神经纤维瘤病的中枢神经系统MRI表现
英文短句/例句

1.multiple neurofibromatosis多发性神经纤维瘤病
2.Nuerofibroma and Neurofibromatosis Development of Pathogenesis,Diagnosis and Treatment;神经纤维瘤与神经纤维瘤病发病机制、诊断与治疗进展
3.CT and MRI manifestations of neurofibromatosis in cranium and spinal column神经纤维瘤病颅脑和脊柱CT、MRI表现
4.The pathogenesis is discussed in detail.对神经纤维瘤病的发病机理做了较详细的讨论。
5.Clinicopathological study of neurofibromatosis type 1:An experience in Nigeria尼日利亚Ⅰ型神经纤维瘤病的临床病理学研究
6.Clinical Analysis of Neurofibromatosis Type 1 in Oral and Maxillofacial Regions;口腔颌面部Ⅰ型神经纤维瘤病临床病例分析
7.Manifestation of neurofibromatosis disease in Otolaryngology Head and Neck Surgery神经纤维瘤病在耳鼻咽喉—头颈外科中的表现
8.Clinical Analysis of 13 Patients with Neurofibromatosis and the Review of Literatures;13例神经纤维瘤病临床分析及文献复习
9.Neurofibromatosis Type 1 (NF1) Skeletal Lesion and Its Mechanism神经纤维瘤病(NF1)骨损害及其分子机理的研究
10.CT and MRI Diagnosis of Craniocerebral and Jugular Neurofibromatosis-type 1神经纤维瘤病Ⅰ型的头颈部CT和MRI表现
11.Neurofibromatosis type Ⅰ of the head and neck:clinical analysis of 23 cases头颈部Ⅰ型神经纤维瘤病23例临床分析
12.Study progress on neurofibromatosis type 1 in oral and maxillofacial region口腔颌面部Ⅰ型神经纤维瘤病研究进展
13.Clinical therapy of peripheral neurofibromatosis:9 cases report周围型神经纤维瘤病的临床治疗(附9例报告)
14.Surgical treatment of cervical kyphosis due to neurofibromatosis神经纤维瘤病性颈椎后凸畸形的外科治疗
15.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。
16.The Study on Mutation Detection on Exon 32、33 of NF1 Gene;神经纤维瘤病1型(NF1)基因32、33号外显子突变的研究*
17.Comparing Gene Profiles during the Malignant Transformation in Neurofibromatosis Type 1 Using Oligonucleotide Microarray;1型神经纤维瘤病恶变中基因表达谱差异的比较研究
18.Effect of PKB,PTEN and c-kit on neurofibromatosis type Ⅰ pathogenesisⅠ型神经纤维瘤病组织中蛋白激酶B、PTEN和c-kit蛋白的表达
相关短句/例句

neurofibromatosis type 1Ⅰ型神经纤维瘤病
1.Advances in diagnosis and treatment of Neurofibromatosis type 1;Ⅰ型神经纤维瘤病诊治进展
2.Objective To investigate the pathogenesis of neurofibromatosis type 1(NF1),and searching the experimental basis of discriminating the neurofibomas of NF1 and non-NF1.目的探讨Ⅰ型神经纤维瘤病(NF1)患者神经纤维瘤发生机制,为病理学诊断区分NF1及非NF1神经纤维瘤寻找初步实验依据。
3.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。
3)Neurofibromatosis type 2神经纤维瘤病Ⅱ型
1.Neurofibromatosis type 2;神经纤维瘤病Ⅱ型(附1例报告)
4)neurofibromatosis type 1神经纤维瘤病1型
5)neurofibromatosis typeⅠ/surgery神经纤维瘤病/外科学
6)Neurofibromin 1神经纤维瘤病Ⅰ型蛋白
延伸阅读

神经纤维瘤病神经纤维瘤病 又称"Von Recklingtmusen病"、"多发性神经纤维瘤"、"多发性神经纤维瘤综合征",是常染色体显性遗传的疾病。可侵犯皮肤、神经系统、骨骼,内分泌及其他脏器。临床表现为皮肤色素沉着,最常见于躯干和腋窝,尚可发生多发的皮肤纤维瘤和纤维软瘤,大小不一,质地较软,固定或有蒂。有些病例常伴有头颅、颈项、躯干或肢体相应部位皮肤和皮下组织的增生,可引起不对称性的局部肥大 (称神经瘤性橡皮病)。脑膜、椎管内也可发生,根据所在部位而出现局限的神经系统症状和癫痫发作,偏瘫,颅压增高等。尚无特效疗法,对引起症状的或生长迅速的肿瘤,应予手术摘除。