Zobrazeno 1 - 10
of 71
pro vyhledávání: '"Chien Hua Wang"'
Autor:
Chien Hua Wang, 王健驊
97
In this study, based on a specific area related to the Taipei water management laws and regulations, combined with scientific, academic research is based on the completion of this study. Study between the views of different disciplines to car
In this study, based on a specific area related to the Taipei water management laws and regulations, combined with scientific, academic research is based on the completion of this study. Study between the views of different disciplines to car
Externí odkaz:
http://ndltd.ncl.edu.tw/handle/81197464090497048313
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
Autor:
Hui-Ju Tsai, Wen-Chen Liang, Chien-Hua Wang, Po-Ching Chou, Jong-Hau Hsu, Chia-Tsuan Huang, Yuh-Jyh Jong
Publikováno v:
Pediatrics and Neonatology, Vol 56, Iss 6, Pp 425-428 (2015)
Botulism is a severe neuroparalytic illness which is difficult to diagnose accurately, especially in children. We report a child with type A botulism intoxication, with very rapid progression to coma-like consciousness and respiratory failure. Carefu
Externí odkaz:
https://doaj.org/article/84e8f8f1d6514f7da3ad8a5c4dd3bc6f
Autor:
Guey-Ying Liao, Karine Bouyer, Anna Kamitakahara, Niaz Sahibzada, Chien-Hua Wang, Michael Rutlin, Richard B. Simerly, Baoji Xu
Publikováno v:
Molecular Metabolism, Vol 4, Iss 6, Pp 471-482 (2015)
Objective: Brain-derived neurotrophic factor (BDNF) is a potent regulator of neuronal development, and the Bdnf gene produces two populations of transcripts with either a short or long 3′ untranslated region (3′ UTR). Deficiencies in BDNF signali
Externí odkaz:
https://doaj.org/article/c6487db4ae374db7a9b8dc59a5a518f1
Publikováno v:
Pediatrics and Neonatology, Vol 56, Iss 1, Pp 62-65 (2015)
The autosomal recessive limb-girdle muscular dystrophy type 2A (LGMD2A) is caused by mutations in the calpain 3 (CAPN3) gene, and it is characterized by selective atrophy and weakness of proximal limb and girdle muscles. We report a 33-year-old woman
Externí odkaz:
https://doaj.org/article/4702c33d9d4a479bb09acdada3f39a65
Autor:
Hung-Yang, Lo, Chun-Wei, Huang, Chun-Chien, Chiu, Jui-Yuan, Chen, Fang-Chun, Shen, Che-Hung, Wang, Yen-Jung, Chen, Chien-Hua, Wang, Jan-Chi, Yang, Wen-Wei, Wu
Publikováno v:
Small (Weinheim an der Bergstrasse, Germany).
Recently, perovskite (PV) oxides with ABO
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ac6ed74dfde5825c9a6210f3f64bc595
https://pubmed.ncbi.nlm.nih.gov/36328712
https://pubmed.ncbi.nlm.nih.gov/36328712
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:
Pediatrics and Neonatology, Vol 53, Iss 6, Pp 374-377 (2012)
Dystrophinopathy is caused by mutations in the dystrophin gene at Xp21. Although manifesting carriers of dystrophinopathy have been documented in adults, symptomatic dystrophinopathy in female children is rare. We report on a 13-year-old girl with in
Externí odkaz:
https://doaj.org/article/ca9e39473d744c668ab91ceb01230725
Publikováno v:
Kaohsiung Journal of Medical Sciences, Vol 26, Iss 12, Pp 663-668 (2010)
Multiple organ infarctions are a very rare clinical event in children. We report a 3-month-old infant with sepsis and disseminated intravascular coagulation, who was diagnosed with cerebral ischemic stroke associated with middle cerebral artery steno
Externí odkaz:
https://doaj.org/article/9faaaa523d6c4806a16d4b39de561efc
Autor:
Kuan-Wei Huang, CHIEN-HUA WANG
Publikováno v:
2021 the 7th International Conference on Communication and Information Processing (ICCIP).
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::343d818f868323d5a931f2a77dd77d9d
https://doi.org/10.1145/3507971.3507978
https://doi.org/10.1145/3507971.3507978