NEUROFIBROMATOSIS

作品数:57被引量:64H指数:5
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相关领域:医药卫生更多>>
相关作者:龚树生陈广理陈沛孙建军郭红光更多>>
相关机构:华中科技大学中国人民解放军海军总医院首都医科大学上海交通大学医学院附属新华医院更多>>
相关期刊:《World Journal of Clinical Cases》《Journal of US-China Medical Science》《World Journal of Clinical Oncology》《国际耳鼻咽喉头颈外科杂志》更多>>
相关基金:国家自然科学基金国家重点基础研究发展计划国家高技术研究发展计划更多>>
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The 3rd Neurofibromatosis Forum of the 21st Shanghai international conference on plastic and aesthetic surgery was held in Shanghai
《Chinese Journal of Plastic and Reconstructive Surgery》2022年第3期144-145,共2页Beiyao Zhu Zhichao Wang 
Recently,the 11th Shanghai Plastic Surgery Forum and the 21st Shanghai International Plastic and Aesthetic Surgery Conference were successfully held in Shanghai.Among them,the Neurofibromatosis Forum was held on July ...
关键词:SURGERY FORUM attracting 
Case report of neurofibromatosis type 1 combined with primary ciliary dyskinesia被引量:2
《Frontiers of Medicine》2021年第6期933-937,共5页Chun Bian Xinyue Zhao Yaping Liu Minjiang Chen Shuying Zheng Xinlun Tian Kai-Feng Xu 
supported by the National Key Research and Development Program of China(No.2016YFC0901502);CAMS Innovation Fund for Medical Sciences(Nos.CIFMS-2018-I2M-1-003,CIFMS-2017-12M-2-001,CIFMS-2020-I2M-C&T-B-002,and CIFMS-2016-I2M-1-002).
Neurofibromatosis(NF)is a genetic disease in which the lungs are rarely involved.However,in NF cases with lung involvement,chest computed tomography may show bilateral basal reticulations,apical bullae,and cysts witho...
关键词:primary ciliary dyskinesia NEUROFIBROMATOSIS BRONCHIECTASIS transmission electron microscopy genetic sequencing 
Moyamoya Syndrome in Post-Transplant Children with Type 1 Neurofibromatosis and Congenital Nephrotic Syndrome
《Open Journal of Nephrology》2021年第4期459-466,共8页Reyner Loza Nathalie Rodriguez Angelica Ynguil Silvia Sotelo 
Background: Neurofibromatosis (NF) is a genetic disorder of the nervous system that affects the development and growth of neuronal tissues. It is characterized by the development of malignant and beni...
关键词:Kidney Transplantation Moyamoya Syndrome NEUROFIBROMATOSIS Congenital Nephrotic Syndrome 
Coexistent vestibular schwannoma and meningioma in a patient without neurofibromatosis:A case report and review of literature被引量:1
《World Journal of Clinical Cases》2021年第24期7251-7260,共10页Li-Yan Zhao Yi-Ning Jiang Yu-Bo Wang Yang Bai Ying Sun Yun-Qian Li 
BACKGROUND The simultaneous occurrence of schwannoma and meningioma in the absence of neurofibromatosis(NF)or a previous history of irradiation is exceedingly rare,as only 10 intracranial cases have been reported to d...
关键词:CONCURRENT Diagnosis MENINGIOMA NEUROFIBROMATOSIS SCHWANNOMA Case report 
Gene diagnosis of infantile neurofibromatosis type I:A case report
《World Journal of Clinical Cases》2020年第22期5678-5683,共6页Meng-Zhu Li Lin Yuan Zhi-Qiang Zhuo 
BACKGROUND Neurofibromatosis is an autosomal dominant genetic disorder with various manifestations.Systemic multiple neurofibromatosis is rare in infancy.The disease is difficult to identify in the early stage,and it ...
关键词:Genetic diagnosis Eurofibromatosis type I NEUROFIBROMATOSIS INFANT Case report Clinical manifestations 
Modified surgical treatment for a patient with neurofibromatosis scoliosis:A case report
《World Journal of Orthopedics》2020年第11期523-527,共5页Yan Shi Yun-He Li Zhi-Ping Guan Yong-Can Huang Bin-Sheng Yu 
The National Natural Science Foundation of China,No.U1613224;the Shenzhen Double Chain Project for Innovation and Development Industry,No.201806081018272960.
BACKGROUND The correction surgery for severely multidimensional spinal deformity in neurofibromatosis type I is very difficult and it is still a very big challenge for spine surgeons.CASE SUMMARY A 44-year-old woman p...
关键词:Neurofibromatosis type I Spinal thoracolumbar kyphosis Ponte osteotomy Satellite rods technique Case report 
Multiple neurofibromas plus fibrosarcoma with familial NF1 pathogenicity:A case report
《World Journal of Clinical Cases》2020年第7期1306-1310,共5页Yang Wang Xiao-Fan Lu Lu-Lu Chen Ying-Wei Zhang Bing Zhang 
BACKGROUND Neurofibromatosis(NF)is a genetic disease consisting of seven types,of which types 1 to 4 are caused by a dominant autosomal gene mutation;such disease sometimes arises in patients with NF type 1.However,it...
关键词:MULTIPLE NEUROFIBROMAS FIBROSARCOMA NEUROFIBROMATOSIS type 1 PATHOGENICITY Pseudochylothorax PLEURAL cavity Case report 
Isolated colonic neurofibroma in the setting of Lynch syndrome:A case report and review of literature被引量:1
《World Journal of Gastrointestinal Surgery》2020年第1期28-33,共6页Warren YL Sun Armaan Pandey Mark Lee Shawn Wasilenko Shahzeer Karmali 
BACKGROUND Gastrointestinal neurofibromas are commonly found in patients diagnosed with neurofibromatosis type 1.However,isolated gastrointestinal neurofibromas are a rare entity and only fourteen cases of isolated co...
关键词:Isolated gastrointestinal neurofibroma Colonic neurofibroma Gastrointestinal neurofibromatosis Lynch syndrome Case report 
KIT and platelet-derived growth factor receptor α wild-type gastrointestinal stromal tumor associated with neurofibromatosis type 1: Two case reports被引量:1
《World Journal of Clinical Cases》2019年第24期4398-4406,共9页You-Wei Kou Ying Zhang Ya-Ping Fu Zhe Wang 
Supported by National Natural Science Foundation of China,No.81601692;Program of Liaoning Province Department of Education,No.LK2016002
BACKGROUND Gastrointestinal stromal tumors(GISTs) associated with neurofibromatosis are uncommon compared to their gastrointestinal counterparts. Patients with neurofibromatosis type 1(NF-1) have an increased risk of ...
关键词:NEUROFIBROMATOSIS Gastrointestinal stromal KIT and platelet-derived growth factor receptorαwild type Molecular genetic studies Neurofibromatosis type 1 Case report 
Type Ⅰ neurofibromatosis with spindle cell sarcoma: A case report
《World Journal of Clinical Cases》2019年第19期3104-3110,共7页Yu Zhang Jiao-Jiao Chao Xiu-Feng Liu Shu-Kui Qin 
BACKGROUND Neurofibromatosis type Ⅰ(NF1) is the most frequent subtype of neurofibromatosis. Its related tumor-suppressor syndromes are characterized by a predisposition to multiple tumor types and other disorder pres...
关键词:NEUROFIBROMATOSIS TYPE  SPINDLE cell SARCOMA TARGETED therapy CRIZOTINIB Case report 
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