Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Wan-Zi Chen"'
Autor:
Wen‐Chen Liang, Chen‐Hua Wang, Wan‐Zi Chen, Yun‐Ting Kuo, Hsiu‐Fen Lin, Shigeaki Suzuki, Ichizo Nishino, Yuh‐Jyh Jong
Publikováno v:
Kaohsiung Journal of Medical Sciences, Vol 36, Iss 8, Pp 649-655 (2020)
Abstract 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‐
Externí odkaz:
https://doaj.org/article/4d8891dc832f493f8c52a0f510e7ea95
Autor:
Wen-Chen Liang, Yuh-Jyh Jong, Chien-Hua Wang, Chen-Hua Wang, Xia Tian, Wan-Zi Chen, Tzu-Min Kan, Narihiro Minami, Ichizo Nishino, Lee-Jun C. Wong
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 15, Iss 1, Pp 1-10 (2020)
Abstract Background Limb-girdle muscular dystrophy (LGMD) is a genetically heterogeneous, hereditary disease characterized by limb-girdle weakness and histologically dystrophic changes. The prevalence of each subtype of LGMD varies among different et
Externí odkaz:
https://doaj.org/article/b9d1018908994e309627ccc9fcde0613
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
Externí odkaz:
https://doaj.org/article/b3164b26794b42f7971fbbc8b7e65a51
Autor:
Wen-Chen Liang, Xia Tian, Chung-Yee Yuo, Wan-Zi Chen, Tsu-Min Kan, Yi-Ning Su, Ichizo Nishino, Lee-Jun C Wong, Yuh-Jyh Jong
Publikováno v:
PLoS ONE, Vol 12, Iss 8, p e0183406 (2017)
[This corrects the article DOI: 10.1371/journal.pone.0170517.].
Externí odkaz:
https://doaj.org/article/aad47b1fdccf4f6e8ada95931a624ae6
Autor:
Wen-Chen Liang, Xia Tian, Chung-Yee Yuo, Wan-Zi Chen, Tsu-Min Kan, Yi-Ning Su, Ichizo Nishino, Lee-Jun C Wong, Yuh-Jyh Jong
Publikováno v:
PLoS ONE, Vol 12, Iss 2, p e0170517 (2017)
PURPOSE:Congenital muscular dystrophy (CMD) is a heterogeneous disease entity. The detailed clinical manifestation and causative gene for each subgroup of CMD are quite variable. This study aims to analyze the phenotypes and genotypes of Taiwanese pa
Externí odkaz:
https://doaj.org/article/b3d7bbadbb5b40678cb207ca54b72fb3
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5b0e6de9ed865b972759b53db8570df9
https://doi.org/10.1002/kjm2.12240
https://doi.org/10.1002/kjm2.12240
Autor:
Wan-Zi Chen, Yuh-Jyh Jong, Chien-Hua Wang, Ichizo Nishino, Tzu-Min Kan, Narihiro Minami, Xia Tian, Wen-Chen Liang, Chen-Hua Wang, Lee-Jun C. Wong
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 15, Iss 1, Pp 1-10 (2020)
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases
Background Limb-girdle muscular dystrophy (LGMD) is a genetically heterogeneous, hereditary disease characterized by limb-girdle weakness and histologically dystrophic changes. The prevalence of each subtype of LGMD varies among different ethnic popu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::88288db82c5c122768b157dbe8185785
http://link.springer.com/article/10.1186/s13023-020-01445-1
http://link.springer.com/article/10.1186/s13023-020-01445-1
Publikováno v:
Zhongguo shi yan xue ye xue za zhi. 28(5)
To investigate the clinical characteristics and prognosis of hematopathy patients with chromosome 3 abnormality.The clinical data of the 125 hematopathy patients with chromosome 3 abnormality in our hospital from January 2011 to June 2018 were retros
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::cd2abcf91cb10c74e01b4087ec92f1b2
https://pubmed.ncbi.nlm.nih.gov/33067937
https://pubmed.ncbi.nlm.nih.gov/33067937
Autor:
Liang, Wen-Chen, Jong, Yuh-Jyh, Chien-Hua Wang, Wang, Chen-Hua, Tian, Xia, Wan-Zi Chen, Tzu-Min Kan, Narihiro Minami, Ichizo Nishino, Lee-Jun C. Wong
Additional file 1.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0d2472e382a45e52e259ff2f4670147d
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cac73eef72f1e2d1521d360eda262fbd
https://doi.org/10.1093/rheumatology/kew386
https://doi.org/10.1093/rheumatology/kew386