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neu·ro·fi·bro·ma·to·sis 英ˌnʊərəʊˌfaɪbrəʊməˈtəʊsɪs, ˌnjʊər-美ˌnʊroˌfaɪbroməˈtosɪs, ˌnjʊr-AHDn‹r'ō-fī'brō-mə-tōʹsĭs, ny‹r'- 高COCA⁹⁰³⁰¹BNC²³⁶²¹³⁺¹iWeb⁴³⁸⁷⁵Economist⁵³⁵⁸¹⁺¹
基本英英记法近义反义例句例句
神经纤维瘤病¹⁰⁰
Noun:
autosomal dominant disease characterized by numerous neurofibromas and by spots on the skin and often by developmental abnormalities词根记忆neuro-神经fibr-纤维-omat肿|瘤-osis病理状况⇒神经纤维瘤病近义词 von Recklinghausen's disease医 冯雷克林霍曾…
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ObjectiveTo study the diagnosis and therapy of hereditaryneurofibromatosis.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。 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。 blog.sina.com.cn
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。 cnki
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。 myoops
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。 lkong
Conclusion MRI can be considered as the first choice of study in diagnosing of neurofibromatosis.
结论 MRI是目前诊断神经纤维瘤病的最佳影像学检查方法。39kf
Materials and Methods:This study included12 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。 cnki
Methods The treatment of short bowel syndrome after retroperitoneal multiple neurofibromatosis operation was analyzed retrospectively in 2004a case.
方法总结我院2004年收治的一例多发性神经纤维瘤术后并发短肠综合征的治疗经过。 cnki
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。 chemyq
Miscellaneous group, which includes ectopic neurohypophysis, chronic stages of multiple sclerosis and neurofibromatosis type I.
其他，包括异位的神经垂体，多发性硬化的慢性阶段和神经纤维瘤病I型。 xctmr
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。 xctmr
Objective To detect the mutation on exons32,33 of Chinese the neurofibromatosis type1 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。 cnki
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。 dictall
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。 china-b
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。 cnki
Objective: To elucidate the molecular mechanism of neurofibromatosis type2NF2 with autosomal dominant inheritance disease in a Chinese kindred.
目的：探讨中国人常染色体显性遗传2型神经纤维瘤病的基因突变和分子诊断。 cnki
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。 chemyq
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。 chemyq
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。 adoop.cn
The result suggests the necessity of using CT for the patient with neurofibromatosis.
提示对神经纤维瘤病患者，进行颅脑CT 检查的必要性。 cnki
To explore the molecular pathogenesis of neurofibromas in the patients with neurofibromatosis type1 NF1.
探讨1型神经纤维瘤病 NF1患者神经纤维瘤发生、发展的分子病理机制。 dictall
X- ray findings of the changes of bones with neurofibromatosis in30 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。 cnki
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。 dictall |