Zobrazeno 1 - 10
of 18
pro vyhledávání: '"XIAOXIN TONG"'
Publikováno v:
BMC Neurology, Vol 19, Iss 1, Pp 1-6 (2019)
Abstract Background Myofibrillar myopathies (MFMs) are a genetically heterogeneous group of muscle disorders. Mutations in the filamin C gene (FLNC) have previously been identified in patients with MFM. The phenotypes of FLNC-related MFM are heteroge
Externí odkaz:
https://doaj.org/article/08db1cd98cec43c3ba9984d3f6290b81
Publikováno v:
Magnetic Resonance Imaging. 39:89-97
Purpose To implement a fast (~ 15 min) MRI protocol for carotid plaque screening using 3D multi-contrast MRI sequences without contrast agent on a 3 Tesla MRI scanner. Materials and methods 7 healthy volunteers and 25 patients with clinically confirm
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0e928ed27240a8d9e005e3f0aaa01f9e
https://doi.org/10.1016/j.mri.2016.10.028
https://doi.org/10.1016/j.mri.2016.10.028
Autor:
Yuchi Li, Zhengyi Huang, Shuyun Liu, Jun Wu, Jun Hu, Xiaoxin Tong, Xin Cheng, Xiaonan Xu, Xuhui Chen, Zengxia Zhao, Yangyang Dai, Yongjun Tao, Yaoting Gui, Tingting Wang
Publikováno v:
Oncology Letters
Sturge-Weber syndrome (SWS) is a rare neurocutaneous disorder whose etiology remains unclear. To investigate the genetic contribution underlying this disease, the genetic variants of a 4-generation family with a history of SWS was analyzed in the pre
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::72906119a4e09fac1c54e856b649a569
http://europepmc.org/articles/PMC5403265
http://europepmc.org/articles/PMC5403265
Publikováno v:
BMC Neurology
BMC Neurology, Vol 19, Iss 1, Pp 1-6 (2019)
BMC Neurology, Vol 19, Iss 1, Pp 1-6 (2019)
Background: Myofibrillar myopathies (MFMs) are a genetically heterogeneous group of muscle disorders. Mutations in the filamin C gene (FLNC) have previously been identified in patients with MFM. The phenotypes of FLNC-related MFM are heterogeneous. C
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bb1498e4e96898db953b71e15613584d
http://europepmc.org/articles/PMC6697925
http://europepmc.org/articles/PMC6697925
Publikováno v:
Neuropathology. 36:485-489
Mutations in the gene encoding caveolin-3 (CAV3) can cause a broad spectrum of clinical phenotypes, including limb girdle muscular dystrophy, rippling muscle disease, distal myopathy (MD), idiopathic persistent elevation of serum creatine kinase and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0823686bf15ef7c48828070cfbc5ed13
https://doi.org/10.1111/neup.12297
https://doi.org/10.1111/neup.12297
Autor:
Jun Wu, Dan Liu, Ting Zhang, Da Zhou, Shuangshuang Cen, Xiaoxin Tong, Jiajia Bi, Li Yi, Lin Yang
Publikováno v:
Journal of Stroke and Cerebrovascular Diseases. 24:894-900
Background Several studies have demonstrated that variants on chromosome 9p21 confer susceptibility to ischemic stroke (IS) disease. But, the results of variants' roles in Chinese IS population are blank or inconsistent. Methods We performed a case
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3f3cd8e0dbc6cca35f447ae5ed22d4b9
https://doi.org/10.1016/j.jstrokecerebrovasdis.2014.12.020
https://doi.org/10.1016/j.jstrokecerebrovasdis.2014.12.020
Autor:
Zhigang Zhong, Kui Yuan, Xiaoxin Tong, Jun Hu, Zubiao Song, Guogao Zhang, Xiaobo Fang, Weixi Zhang
Publikováno v:
NeuroReport; 11/7/2018, Vol. 29 Issue 16, p1365-1372, 8p
Autor:
ZHENGYI HUANG, YUCHI LI, ZENGXIA ZHAO, JUN HU, XIAOXIN TONG, XUHUI CHEN, SHUYUN LIU, XIAONAN XU, YONGJUN TAO, TINGTING WANG, XIN CHENG, YANGYANG DAI, YAOTING GUI, JUN WU
Publikováno v:
Oncology Letters; Apr2017, Vol. 13 Issue 4, p2665-2669, 5p
Autor:
Dipti P. Rath, Zongcheng Jiang, Pierre-Marie Robitaille, Hui Zhu, Robert L. Hamlin, Xiaoxin Tong
Publikováno v:
Magnetic resonance in medicine. 38(6)
In this work, substrate selection was monitored in the left ventricle of the canine myocardium by following pyruvate and lactate oxidation under in vivo conditions at basal and elevated workloads. These studies were conducted in the open chest model
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e0f362adb89b0e940d969a341415d777
https://pubmed.ncbi.nlm.nih.gov/9402190
https://pubmed.ncbi.nlm.nih.gov/9402190
Autor:
Amir M. Abduljalil, Zongchen Jiang, Dipti P. Rath, Robert L. Hamlin, Hui Zhu, Charles M. Little, Huzeng Zhang, Xiaoxin Tong, Pierre-Marie Robitaille, Charles G. Brown
Publikováno v:
Circulation. 91(2)
Background Transmural analyses of the creatine phosphate (CP)/ATP ratio in various lamina of the canine myocardium have previously revealed significant variations in the CP/ATP ratio, with the subendocardial layer displaying a decreased ratio relativ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::be17401114ff7912b3c6fac9f6b7a6ad
https://pubmed.ncbi.nlm.nih.gov/7805252
https://pubmed.ncbi.nlm.nih.gov/7805252