Zobrazeno 1 - 10
of 25
pro vyhledávání: '"Aping Sun"'
Autor:
Chen Zhao, Xiaolu Liu, Jingchao Wang, Yan Zhang, Yingshuang Zhang, Yan Ma, Aping Sun, Hongsong Song, Liping Wang, Yuanjin Zhang, Xiaoxuan Liu, Wenqing Yuan, Shixian Gu, Dongsheng Fan, Shan Ye
Publikováno v:
Medical Education Online, Vol 29, Iss 1 (2024)
Undergraduate medical education in China has shifted from educator-centered learning to self-directed learning (SDL) over the past few decades. Careful design of public engagement activities can enable SDL and empower medical students to pioneer publ
Externí odkaz:
https://doaj.org/article/b77a6162a66e4fa4814671738ac7bb2c
Autor:
Xiangyi Liu, Yingshuang Zhang, Shuo Zhang, Aping Sun, Danfeng Zheng, Dongsheng Fan, Xiaoxuan Liu
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 17, Iss 1, Pp 1-7 (2022)
Abstract Background GNE myopathy is a rare distal myopathy caused by mutations of the GNE gene. A few cases of GNE myopathy accompanied by neurogenic features of electrophysiology mimicking hereditary motor neuropathy were reported recently. We confi
Externí odkaz:
https://doaj.org/article/3e196ff2e5994388b52ace658b2b69d1
Publikováno v:
Frontiers in Neurology, Vol 12 (2021)
Introduction: Charcot–Marie–Tooth disease type 2A (CMT2A) is a group of clinically and genetically heterogeneous disorders, which is mostly caused by mutations of the mitofusin2 (MFN2) gene. As the genotype–phenotype characteristics of CMT2A we
Externí odkaz:
https://doaj.org/article/8ece77e9a3ff4e26ba5716aa17e98d1e
Publikováno v:
Frontiers in Neurology, Vol 11 (2020)
Charcot-Marie-Tooth (CMT) disease is a clinically and genetically heterogeneous group of inherited neuropathies. The GJB1 gene is the pathogenic gene of CMTX1. In this study, we screened a cohort of 465 unrelated Chinese CMT patients from years 2007
Externí odkaz:
https://doaj.org/article/715de12c28634988bf913abf6665dc90
Autor:
Xiangyi Liu, Yingshuang Zhang, Shuo Zhang, Aping Sun, Danfeng Zheng, Dongsheng Fan, Xiaoxuan Liu
Publikováno v:
Orphanet journal of rare diseases. 17(1)
Background GNE myopathy is a rare distal myopathy caused by mutations of the GNE gene. A few cases of GNE myopathy accompanied by neurogenic features of electrophysiology mimicking hereditary motor neuropathy were reported recently. We confirmed this
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d373b8a1da0a25624c9a1e7854a55563
https://pubmed.ncbi.nlm.nih.gov/35590323
https://pubmed.ncbi.nlm.nih.gov/35590323
Publikováno v:
Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology. 41(5)
Obstructive sleep apnea (OSA) is a common sleep disorder in Parkinson’s disease (PD). However, the relationship between OSA and PD is still inconsistent. Our study was aimed to evaluate the relationship between PD and OSA. Studies on OSA and PD wer
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::94f7b71cedfe08c37cfa7d29ff424438
https://pubmed.ncbi.nlm.nih.gov/31897944
https://pubmed.ncbi.nlm.nih.gov/31897944
Publikováno v:
European journal of neurologyReferences. 27(7)
BACKGROUND AND PURPOSE Distal hereditary motor neuropathies (dHMNs) are a clinically and genetically heterogeneous group of disorders. The purpose of this study was to identify the genetic distribution of dHMNs in a large cohort of Chinese patients a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2680bccbdf9e9c504d145734e942f24d
https://pubmed.ncbi.nlm.nih.gov/32298515
https://pubmed.ncbi.nlm.nih.gov/32298515
Publikováno v:
Neural Regeneration Research, Vol 10, Iss 1, Pp 112-118 (2015)
Neural Regeneration Research
Neural Regeneration Research
Multiple mononeuropathy is an unusual form of peripheral neuropathy involving two or more nerve trunks. It is a syndrome with many different causes. We reviewed the clinical, electrophysiological and nerve biopsy findings of 14 patients who suffered
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3819a9ad64e6872186584dec8378121b
http://www.nrronline.org/article.asp?issn=1673-5374
http://www.nrronline.org/article.asp?issn=1673-5374
Autor:
Aping, Sun, Yingshuang, Zhang, Xiangyi, Liu, Lu, Chen, Qingli, Sun, Shuo, Zhang, Dongsheng, Fan
Publikováno v:
Zhonghua yi xue za zhi. 96(11)
To investigate the clinical characteristics, electrophysiological findings and treatment response of Lewis-Sumner syndrome (LSS).Data of nine patients with LSS, who were diagnosed and treated from May 2008 to August 2014 in Department of Neurology, P
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::bb5d51317924d78fcebdd6ad91679c09
https://pubmed.ncbi.nlm.nih.gov/27045647
https://pubmed.ncbi.nlm.nih.gov/27045647
Autor:
Zhao, Chen1 (AUTHOR), Liu, Xiaolu1 (AUTHOR), Wang, Jingchao2 (AUTHOR), Zhang, Yan1 (AUTHOR), Zhang, Yingshuang1 (AUTHOR), Ma, Yan1 (AUTHOR), Sun, Aping1 (AUTHOR), Song, Hongsong1 (AUTHOR), Wang, Liping1 (AUTHOR), Zhang, Yuanjin1 (AUTHOR), Liu, Xiaoxuan1 (AUTHOR), Yuan, Wenqing3 (AUTHOR), Gu, Shixian3 (AUTHOR), Fan, Dongsheng1 (AUTHOR), Ye, Shan1 (AUTHOR) yeshanbysy@163.com
Publikováno v:
Medical Education Online. 2024, Vol. 29 Issue 1, p1-7. 7p.