neurofibromatosis信息详情
n.神经纤维瘤病
X-ray findings of the changes of bones with neurofibromatosis in 30 cases are analysed and discussed.───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。
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。
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。
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。
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。
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。
Methods: The long-term effects of 16 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。
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。