Zobrazeno 1 - 10
of 25
pro vyhledávání: '"Tung‐Ming Chang"'
Autor:
Sung-Tse Li, Nan-Chang Chiu, Kun-Long Hung, Che-Sheng Ho, Yung-Ting Kuo, Wen-Hsiang Wu, Chuan-Yu Wang, Huei-Shyong Wang, Kuang-Lin Lin, Po-Cheng Hung, Ying-Chao Chang, Pi-Lien Hung, Pi-Chuan Fan, Wang-Tso Lee, Rei-Cheng Yang, Fang-Jong Ko, Lung-Chang Lin, Po-Ching Chou, Jeng-Dau Tsai, Hui-Ju Chen, Kai-Ping Chang, Ting-Rong Hsu, Shyi-Jou Chen, Hueng-Chuen Fan, Hsu-Tung Lee, Ein-Yiao Shen, Huang-Tsung Kuo, Ming-Yuh Chang, Tung-Ming Chang, Geng-Chang Yeh
Publikováno v:
Pediatrics and Neonatology, Vol 61, Iss 6, Pp 606-612 (2020)
Background: Vagus nerve stimulation (VNS) is used as an add-on treatment for epilepsy. This study aimed to use Taiwanese nationwide registry data to analyze the therapeutic effects of VNS in children with refractory epilepsy (RE) and try to explore p
Autor:
Rong-Ching Wu, Chen-Sen Ouyang, Tung-Ming Chang, Sebastian Yu, Ching-Tai Chiang, Rei-Cheng Yang, Lung-Chang Lin
Publikováno v:
Clinical EEG and Neuroscience. 51:325-330
Attention-deficit hyperactivity disorder (ADHD) is a common childhood neuropsychiatric disorder. Differences in the presentations of ADHD between boys and girls have been well established. Three subtypes of ADHD exist. In addition to sex difference,
Autor:
Pi-Chuan Fan, Su-Ching Hu, Jao-Shwann Liang, Pi-Lien Hung, Ting-Rong Hsu, Inn-Chi Lee, Shyi-Jou Chen, Lee-Chin Wong, Tung-Ming Chang, Kuang-Lin Lin, Kun-Long Hung, Yi Fang Tu, Wang-Tso Lee, Hueng-Chuen Fan, Wei-Sheng Lin, I-Jun Chou, Chia-Hsuan Huang, I-Ching Chou, Che-Sheng Ho
Publikováno v:
Scientific Reports
Scientific Reports, Vol 11, Iss 1, Pp 1-9 (2021)
Scientific Reports, Vol 11, Iss 1, Pp 1-9 (2021)
Dravet syndrome (DS) is an uncommon epilepsy syndrome that may negatively affect the patients and their caregivers. However, reliable and valid measures of its impact on caregivers and the characteristics of patients with DS in Taiwan are lacking. Th
Autor:
Lee-Chin Wong, Kuang-Lin Lin, Pi-Lien Hung, Shyi-Jou Chen, Wang-Tso Lee, Jao-Shwann Liang, Che-Sheng Ho, Yi Fang Tu, I-Jun Chou, Tung-Ming Chang, Ting-Rong Hsu, Hueng-Chuen Fan, Kun-Long Hung, Chia-Hsuan Huang, Wei-Sheng Lin, I-Ching Chou, Inn-Chi Lee, Pi-Chuan Fan
Dravet syndrome (DS) is a rare and devastating epilepsy syndrome, and it can affect the patients and their caregivers. However, the lack of a reliable and valid measures of caregiver impact and the characteristic pattern in Taiwan. The purpose of thi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1aab6b5a2a85fc14bd70fb76a3960861
https://doi.org/10.21203/rs.3.rs-199977/v1
https://doi.org/10.21203/rs.3.rs-199977/v1
Autor:
Chih-Kuang Chuang, Ming-Ren Chen, Chung-Lieh Hung, Chung-Lin Lee, Shuan-Pei Lin, Shan-Miao Lin, Dau-Ming Niu, Tung-Ming Chang, Hsiang-Yu Lin
Publikováno v:
Diagnostics
Volume 11
Issue 1
Diagnostics, Vol 11, Iss 16, p 16 (2021)
Volume 11
Issue 1
Diagnostics, Vol 11, Iss 16, p 16 (2021)
Background: Cardiovascular abnormalities have been observed in patients with mucopolysaccharidosis (MPS) of any type, with the most documented abnormalities being valvular regurgitation and stenosis and cardiac hypertrophy. Only a few studies have fo
Publikováno v:
Journal of the Formosan Medical Association, Vol 120, Iss 1, Pp 744-754 (2021)
Background: KCNQ2-associated epilepsy is most common in neonatal genetic epilepsy. A prompt diagnosis to initialize early treatment is important. Methods: We studied the electroencephalographic (EEG) changes including automated EEGs and conventional
Autor:
Hsiang-Yu Lin, Shan Miao Lin, Dau Ming Niu, Chung Lin Lee, Tung Ming Chang, Chih-Kuang Chuang, Ming-Ren Chen, Shuan-Pei Lin, Chung-Lieh Hung
Publikováno v:
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases, Vol 16, Iss 1, Pp 1-14 (2021)
Orphanet Journal of Rare Diseases, Vol 16, Iss 1, Pp 1-14 (2021)
Background Cardiac abnormalities have been observed in patients with mucopolysaccharidosis type II (MPS II). The aim of this study was to investigate the cardiac features and natural progression of Taiwanese patients with MPS II, and evaluate the imp
Autor:
Yin-Hsiu Chien, Wen-Hui Tsai, Shio Jean Lin, Ju-Li Lin, Dau-Ming Niu, Chih-Kuang Chuang, Chung-Lin Lee, Wuh-Liang Hwu, Tzu-Jou Wang, Pao Chin Chiu, Fuu Jen Tsai, Shuan-Pei Lin, Hsiang-Yu Lin, Tung-Ming Chang, Mei-Chyn Chao, Chia-Ying Chang
Publikováno v:
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases, Vol 15, Iss 1, Pp 1-11 (2020)
Orphanet Journal of Rare Diseases, Vol 15, Iss 1, Pp 1-11 (2020)
Background Mucopolysaccharidoses (MPSs) are a group of inherited metabolic diseases, which are characterized by the accumulation of glycosaminoglycans, and eventually lead to the progressive damage of various tissues and organs. Methods An epidemiolo
Autor:
Tung-Ming Chang, Shan-Miao Lin, Ming-Ren Chen, Chung-Lin Lee, Shuan-Pei Lin, Chih-Kuang Chuang, Chung-Lieh Hung, Hsiang-Yu Lin, Charles Jia-Yin Hou, Dau-Ming Niu, Kuo-Tzu Sung
Publikováno v:
Diagnostics, Vol 10, Iss 2, p 62 (2020)
Diagnostics
Volume 10
Issue 2
Diagnostics
Volume 10
Issue 2
Background: Mucopolysaccharidoses (MPSs) are a group of rare inherited metabolic disorders that can damage various organs, including the heart. Cardiac abnormalities have been observed in patients with all MPS types, with the most documented abnormal
Autor:
Wuh-Liang Hwu, Pao Chin Chiu, Chung Lin Lee, Ju Li Lin, Fuu Jen Tsai, Shio Jean Lin, Tung Ming Chang, Hsiang-Yu Lin, Chih-Kuang Chuang, Dau Ming Niu, Shuan-Pei Lin
Publikováno v:
Diagnostics, Vol 9, Iss 4, p 148 (2019)
Diagnostics
Volume 9
Issue 4
Diagnostics
Volume 9
Issue 4
Background: Children with mucopolysaccharidosis (MPS) generally appear unaffected at birth but may develop multiple clinical manifestations including profound growth impairment as they grow older. Each type of MPS has a variable age at onset and vari