Zobrazeno 1 - 10
of 49
pro vyhledávání: '"Quan-Fu Li"'
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 19, Iss 1, Pp 1-9 (2024)
Abstract Background Sialidosis type 1 (ST-1) is a rare autosomal recessive disorder caused by mutation in the NEU1 gene. However, limited reports on ST-1 patients in the Chinese mainland are available. Methods This study reported the genetic and clin
Externí odkaz:
https://doaj.org/article/77d2637d03f34ebca0c81b0edbb3ac14
Autor:
Zhen-Hao Li, Ting Xu, Ya-Juan Zhang, Jing-Hang Jiang, Yu-Ze Mi, Jia-Xuan Li, Jing Shen, Yi-Rui Fu, Bo-Ying Qin, Fan Lin, Dong-Jing Fu, Mei-Jin Yue, Shu-Mei Ma, Quan-Fu Li
Publikováno v:
Frontiers in Oncology, Vol 14 (2024)
ObjectivesIn this study, we compared the dynamic changes in body composition during XELOX/SOX chemotherapy in patients with gastric cancer. Furthermore, we investigated the potential impact of these changes on the occurrence of toxic side effects.Met
Externí odkaz:
https://doaj.org/article/1a5221a297204507a40b27e3bde625ed
Autor:
Ting Xu, Zhen-Hao Li, Ting Liu, Cai-Hong Jiang, Ya-Juan Zhang, Hui Li, Ying Jiang, Juan Zhao, Wen-Jing Guo, Jia-Yuan Guo, Lu Wang, Jia-Xuan Li, Jing Shen, Gao-Wa Jin, Ze-Wei Zhang, Quan-Fu Li
Publikováno v:
Frontiers in Pharmacology, Vol 13 (2022)
Objective: To review the research progress of reltionship between antitumor drugs and the dynamic changes of the skeletal muscles during treatment phase.Background: Sarcopenia is a common disease in patients with tumors, and it has been agreed that p
Externí odkaz:
https://doaj.org/article/868f4073b05b41a1a2ab1f352579a993
Publikováno v:
BMC Neurology, Vol 20, Iss 1, Pp 1-5 (2020)
Abstract Background Idiopathic hypereosinophilic syndrome (IHES) is associated with various organ system dysfunctions. Neurologic abnormalities have been previously noted in this syndrome. Cerebral infarction secondary to occlusion of large cerebral
Externí odkaz:
https://doaj.org/article/c44a727be97c4d2a9b818ae3a9ad2435
Publikováno v:
Frontiers in Neurology, Vol 13 (2022)
BackgroundParoxysmal kinesigenic dyskinesia (PKD) is characterized by recurrent episodes of movement-induced motor attacks. PKD patients may have concomitant epilepsy. Differentiation between the two disorders and effective control of both diseases r
Externí odkaz:
https://doaj.org/article/d0fe645937c04ecfaf83fde0596a0f7f
Publikováno v:
Asian Journal of Surgery, Vol 45, Iss 1, Pp 496-497 (2022)
Externí odkaz:
https://doaj.org/article/7482e1b7a3cd4708a8d461952df3c47a
Autor:
Quan-Fu Li, Yi Dong, Lu Yang, Juan-Juan Xie, Yin Ma, Yi-Chu Du, Hao-Ling Cheng, Wang Ni, Zhi-Ying Wu
Publikováno v:
Molecular Neurodegeneration, Vol 14, Iss 1, Pp 1-8 (2019)
Abstract Background Spinocerebellar ataxia type 3 (SCA3) is the most common subtype of autosomal dominantly inherited spinocerebellar ataxias (SCAs). No validated blood biomarker is available to assess either disease progression or therapeutic respon
Externí odkaz:
https://doaj.org/article/6a20af7848ef4960a82b9062773fde3a
Publikováno v:
Chinese Journal of Chemical Physics. 35:965-976
A novel electrochemical non-enzymatic glucose sensor based on three-dimensional Au/MXene nanocomposites was developed. MXenes were prepared using the mild etched method, and the porous foam of Au nanoparticles was combined with the MXene by means of
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 8, Iss 9, Pp n/a-n/a (2020)
Abstract Background Homozygous spinocerebellar ataxia type 3 (SCA3) patients, which have an expanded cytosine‐adenine‐guanine (CAG) repeat mutation in both alleles of ATXN3, are extremely rare. Clinical features and genetic characteristics of the
Externí odkaz:
https://doaj.org/article/2e66f5249a064951b58a887ed24aea4f
Publikováno v:
Chinese Journal of Chemical Physics. 35:570-577
In this study, the application of bovine serum albumin (BSA) as a carrier to glucose-sensitive materials for the detection of glucose was proposed. Au-CuO bimetallic nanoclusters (Au-CuO/BSA) were prepared using BSA as a template, the new sensing mat