neurofibromatosis

1. The most staggering scene is, of course, that in which the alien picks up a young man with the facial condition neurofibromatosis, played by Adam Pearson.
   当然，影片中最惊人的一幕是外星人遇到一个涉世不深，外表因为多发性神经纤维瘤而丑陋的年轻男子，由亚当·皮尔森扮演。
2. 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
3. Objective: To study the MRI appearance of central nervous system in neurofibromatosis.
   目的：研究神经纤维瘤病的中枢神经系统MRI表现。
4. Objective To investigate the plastic surgery treating principle and methods of peripheral neurofibromatosis.
   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。
5. 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。
6. 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。
7. 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。
8. 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
9. 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。
10. Treatment of Spinal Deformities in Neurofibromatosis Type 1 with Segmental Pedicle Screw System in One-stage Posterior Procedure
    一期后路节段性椎弓根螺钉系统治疗神经纤维瘤性脊柱畸形
11. The team looks at a variety of additional diagnoses including various autoimmune diseases and neurofibromatosis.
    诊断小组也开始考虑其他病因，包括：各种自体免疫疾病和神经纤维瘤。
12. Methods: The long-term effects of16 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。
13. 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
14. Objective: To emphasize the diagnostic value of cranial MRI examination and enhanced scanning in neurofibromatosis type ⅱ.
    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。
15. 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。
16. 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。
17. 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。
18. Bilateral acoustic neuroma complicated with meningioma, especially with multiple meningioma in young patients, may be main accordance to diagnose neurofibromatosis.
    青年人患双侧听神经瘤并发脑膜瘤或视神经瘤，尤其多发性脑膜瘤可为诊断本病的重要依据。本文就本病诊断标准、颅脑影像的临床意义及鉴别诊断进行了讨论。
19. Novel mutation of neurofibromatosis type 1 in a patient with cerebral vasculopathy and fatal ischemic stroke
    1例脑血管病变和致命性缺血性卒中患者的1型神经纤维瘤病新突变
20. 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。
21. Neurofibromatosis of atypical presentation margin regularity between the typical and atypical medullary carcinomas.
    非典型与典型髓样癌间肿瘤边界的规则性有明显的差异。
22. Multiple myofibromas and an epidermal verrucous nevus in a child with neurofibromatosis type 1
    1例Ⅰ型多发性神经纤维瘤儿童的多发性肌纤维瘤和表皮疣状痣表现
23. Effect of p-AKT and PTEN on Neurofibromatosis ⅰ Pathogenesis
    p-AKT和PTEN在Ⅰ型神经纤维瘤病中的表达及意义
24. 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。
25. In this article 3 cases of neurofibromatosis with three generation familial inheritance are reported.
    本文通过3例具有3代家族关系发病史的神经纤维瘤病，进一步证明本病属常染色体显性遗传。
26. MRI study of neurofibromatosis type I
    神经纤维瘤病I型的MRI研究
27. Craniocerebral Imaging Analysis of Neurofibromatosis ( Analysis of 9 Cases)
    神经纤维瘤病的颅脑影像分析（附9例报告）
28. 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.
    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。
29. All of patients had no neurofibromatosis type 1 ( NF-1) and had impaired vision.
    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。

noun

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

   Synonym:    von Recklinghausen's disease