Zobrazeno 1 - 10
of 194
pro vyhledávání: '"Kai–Feng Xu"'
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 19, Iss 1, Pp 1-6 (2024)
Abstract Patients with lymphangioleiomyomatosis (LAM) are considered high risk for most surgeries and require specific anesthetic considerations mainly because of the common spontaneous pneumothorax (PTX). To explore whether intraoperative mechanical
Externí odkaz:
https://doaj.org/article/5f29215d748e49db9702d39b9f2ec458
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 19, Iss 1, Pp 1-7 (2024)
Abstract Background Patients with relapsing polychondritis (RP) sometimes experience upper airway collapse or lower airway stenosis, and bronchoscopy may provide a valuable typical image to confirm the diagnosis. This study aimed to identify potentia
Externí odkaz:
https://doaj.org/article/6e9bda092dc54a36add22f367e82d9d2
Autor:
Chuanxin Duan, Wangji Zhou, Miaoyan Zhang, Chongsheng Cheng, Wenshuai Xu, Jinrong Dai, Shuzhen Meng, Keqi Chen, Yang Zhao, Song Liu, Shao-Ting Wang, Yanli Yang, Kai-Feng Xu, Xinlun Tian
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 18, Iss 1, Pp 1-8 (2023)
Abstract Background Autoimmune pulmonary alveolar proteinosis (aPAP) is a rare interstitial lung disease. COVID-19 is associated with worse prognosis in previous lung diseases patients. But the prognosis of aPAP patients after infection with COVID-19
Externí odkaz:
https://doaj.org/article/4f5aa18712f943bfa75523424edd226d
Autor:
Jiannan Huang, Wenshuai Xu, Peng Liu, Yaping Liu, Cheng Shen, Song Liu, Yani Wang, Jun Wang, Tengyue Zhang, Yudi He, Chongsheng Cheng, Luning Yang, Weihong Zhang, Xinlun Tian, Kai-Feng Xu
Publikováno v:
BMC Pulmonary Medicine, Vol 22, Iss 1, Pp 1-10 (2022)
Abstract Background Sporadic lymphangioleiomyomatosis (S-LAM) is a rare neoplasm with heterogeneous clinical features that is conventionally considered to be related to TSC2. This study serves to elucidate the mutation landscape and potential correla
Externí odkaz:
https://doaj.org/article/a02b1e2f9f1a433a809ff6ffe2290b34
Autor:
Chongsheng Cheng, Wenshuai Xu, Yani Wang, Tengyue Zhang, Luning Yang, Wangji Zhou, Danjing Hu, Yanli Yang, Xinlun Tian, Kai-Feng Xu
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 17, Iss 1, Pp 1-7 (2022)
Abstract Background Spontaneous pneumothorax has a high incidence and high rate of recurrence in patients with lymphangioleiomyomatosis (LAM). The risk factors for pneumothorax and the effects of sirolimus on pneumothorax in patients with LAM are unk
Externí odkaz:
https://doaj.org/article/a1d8f4aa47134731b76c59c1b25b631f
Autor:
Jiu-Wu Bai, Jian-nan Huang, Shen-yun Shi, Ai Ge, Hai-wen Lu, Xiao-li Sun, Shu-yi Gu, Shuo Liang, Ke-bin Cheng, Xin-lun Tian, Yong-long Xiao, Kai-feng Xu, Jin-Fu Xu
Publikováno v:
Frontiers in Medicine, Vol 10 (2023)
BackgroundThe high-resolution computed tomography (HRCT) score is an important component of the severity and prognosis score of pulmonary alveolar proteinosis (SPSP). However, the HRCT score in SPSP only considers the extent of opacity, which is insu
Externí odkaz:
https://doaj.org/article/c0bee96c55034868aa7c29416f4fa87e
Autor:
Jia Fu, Yanbo Liu, Yakun Zhao, Yuxiong Chen, Zhenge Chang, Kai-Feng Xu, Cheng Huang, Zhongjie Fan
Publikováno v:
Frontiers in Public Health, Vol 11 (2023)
PurposeAcute exacerbation of chronic obstructive pulmonary disease (AECOPD) has the adverse influence on quality of life and creates significant healthcare costs. However, there were sparse studies investigating the correlation between AECOPD hospita
Externí odkaz:
https://doaj.org/article/bd18278ce79b4036a1ecaab41d341d14
Autor:
Chen-Xi Zhang, Kai-Feng Xu, Qin Long, Xiao Zhang, Zhi-Kun Yang, Rong-Ping Dai, Zhi-Qiao Zhang
Publikováno v:
Frontiers in Cell and Developmental Biology, Vol 10 (2022)
Mammalian target of rapamycin (mTOR) inhibitors (sirolimus or everolimus) have been demonstrated effective in reducing the size of tuberous sclerosis complex (TSC)-associated retinal astrocytic hamartoma (RAH) in short term. To investigate the long-t
Externí odkaz:
https://doaj.org/article/674a2f526c8541999f815169b078a442
Autor:
Xinyue Zhao, Chun Bian, Keqiang Liu, Wenshuai Xu, Yaping Liu, Xinlun Tian, Jing Bai, Kai-Feng Xu, Xue Zhang
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 16, Iss 1, Pp 1-13 (2021)
Abstract Background Primary ciliary dyskinesia (PCD) is a rare, highly heterogeneous genetic disorder involving the impairment of motile cilia. With no single gold standard for PCD diagnosis and complicated multiorgan dysfunction, the diagnosis of PC
Externí odkaz:
https://doaj.org/article/9e17fc3d1e03415c99ce8fa7b7a70ce6
Autor:
Han Cui, Chongsheng Cheng, Wenshuai Xu, Xinlun Tian, Yanli Yang, Yani Wang, Jiannan Huang, Yudi He, Jun Wang, Ruie Feng, Weihong Zhang, Kai-Feng Xu
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 16, Iss 1, Pp 1-7 (2021)
Abstract Background The differential diagnosis of diffuse cystic lung disease (DCLD) is a clinical challenge. We wish to analyze the distribution of the etiology of DCLD based on data from a single lymphangioleiomyomatosis (LAM) clinic. Methods All D
Externí odkaz:
https://doaj.org/article/16b11e2484dd4cafb05eb1b2c581a73a