Zobrazeno 1 - 10
of 32
pro vyhledávání: '"Chen Liang"'
Autor:
Wan Zi Chen, Chen Hua Wang, Yun Ting Kuo, Hsiu-Fen Lin, Wen-Chen Liang, Shigeaki Suzuki, Yuh-Jyh Jong, Ichizo Nishino
Publikováno v:
Kaohsiung Journal of Medical Sciences, Vol 36, Iss 8, Pp 649-655 (2020)
Immune‐mediated necrotizing myopathy (IMNM) has emerged as a new subgroup of idiopathic inflammatory myopathy in the past decade, associated with the presence of two autoantibodies against signal recognition particle and 3‐hydroxy‐3‐methylglu
Autor:
WU, Yue, LI, Zhen Jun, YU, Shi Cheng, CHEN, Liang, WANG, Ji Chun, QIN, Yu, SONG, Yu Dan, GAO, George F., DONG, Xiao Ping, WANG, Li Ping, ZHANG, Qun, HE, Guang Xue
Publikováno v:
Biomedical and Environmental Sciences
Objective We aimed to assess the features of notifiable infectious diseases found commonly in foreign nationals in China between 2004 and 2017 to improve public health policy and responses for infectious diseases. Methods We performed a descriptive s
Autor:
Cheng-Chang Lu, Wen-Chen Liang, Zi-Miao Liu, Shih-Hsiang Chou, Po-Chih Shen, Yin-Chun Tien, Yen-Mou Lu, Chia-Lung Shih, Yuh-Jyh Jong
Publikováno v:
Clinical Spine Surgery
Study Design: This was a single-center, retrospective study. Objective: The objective of this study was to assess the risk factors for deformity progression after scoliosis correction surgery in spinal muscular atrophy (SMA) patients. Summary of Back
Publikováno v:
Journal of the Chinese Medical Association. 82:161-165
Background The health-related quality of life (HRQoL) was affected in children and adolescents with scoliosis. However, there was lack of study to compare the HRQoL among patients with different types of scoliosis. We aimed to investigate whether the
Autor:
Kohei Hamanaka, Jianying Xi, Keisuke Ikemoto, Madoka Mori-Yoshimura, Yutaka Kawano, Tatsuya Fujii, Chongbo Zhao, Yukari Endo, Wan Zi Chen, Nobuyuki Murakami, Satomi Mitsuhashi, Yuh-Jyh Jong, Yurika Watanabe, Hirofumi Komaki, Wenhua Zhu, Ichizo Nishino, Atsuko Nishikawa, Yasushi Oya, Eri Takeshita, Akinori Uruha, Norihiro Suzuki, Shigeaki Suzuki, Wen-Chen Liang
Publikováno v:
Rheumatology (Oxford, England)
Objective. Antibodies against 3-hydroxy-3-methylglutaryl-coenzyme A reductase (HMGCR) have recently been associated with immune-mediated necrotizing myopathy, especially in patients with statin exposure. As the data are very limited concerning phenot
Autor:
Ichizo Nishino, Yuh-Jyh Jong, Po-Ching Chou, Yukiko K. Hayashi, Chia-Cheng Hung, Yi-Ning Su, Wen-Chen Liang, Tsu-Min Kan, Wan-Zi Chen
Publikováno v:
Journal of the Neurological Sciences. 362:304-308
Limb-girdle muscular dystrophy type 2D (LGMD2D), an autosomal-recessive inherited LGMD, is caused by the mutations in SGCA. SGCA encodes alpha-sarcoglycan (SG) that forms a heterotetramer with other SGs in the sarcolemma, and comprises part of the dy
Autor:
Chen Liang, Zhongjun Liu, Yunlong Ma, Lei Yong, Chenlong Yang, Bin Zhu, Hua Zhou, Peng Wang, Xiaoguang Liu, Xiao Liu
Publikováno v:
Cancer Science
Chordomas are rare bone tumors with a poor prognosis and no approved targeted therapy. Y-box binding protein-1 (YBX1) promotes tumor growth, invasion and drug resistance. However, the role of YBX1 in chordoma is unclear. In this study, we examined th
Publikováno v:
Anatolian Journal of Cardiology
This study aimed to assess the safety and feasibility of transcatheter device closure of atrial septal defects (ASDs) guided completely by transthoracic echocardiography (TTE).A total of 152 patients underwent transcatheter device closure of ASDs gui
Autor:
Chen Zhao Yang, Chen Liang-long, Chen Wan Hua, Chen Qiang, Fan Lin, Xiong Chang, Cao Hua, Ma Yuan Ji, Pan Wen Zhi, Ge Jun Bo
Publikováno v:
The Annals of Thoracic Surgery. 99:1664-1670
Transfemoral and perventricular device occlusions are performed for doubly committed subarterial ventricular septal defect (dcVSD) to reduce the invasiveness of the conventional surgical repair through a median sternotomy. Few comparative studies hav
Publikováno v:
Pediatrics and Neonatology, Vol 59, Iss 2, Pp 176-183 (2018)
Background: Duchenne muscular dystrophy (DMD) is the most common hereditary muscular dystrophy and caused by DMD gene mutation. In addition to progressive proximal muscle weakness, respiratory, orthopedic, and gastrointestinal complications are often