Zobrazeno 1 - 10
of 67
pro vyhledávání: '"Tung‐Ming Chang"'
Autor:
Sung-Ju Hsueh, Chin-Hsien Lin, Ni-Chung Lee, Tung-Ming Chang, Sung-Pin Fan, Wan-De Huang, Yea-Huey Lin, Li-Kai Tsai, Yin-Hsiu Chien, Ming-Jen Lee, Wuh-Liang Hwu, Hsueh Wen Hsueh, Chih-Chao Yang
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 19, Iss 1, Pp 1-7 (2024)
Abstract Background To investigate the peripheral nervous system involvement in S sialidosis with typical features of myoclonus, seizure, and giant waves in somatosensory evoked potentials suggesting hyperexcitability in the central nervous system. M
Externí odkaz:
https://doaj.org/article/0abe53ded10c4a81bffb009dfc2f1d65
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 18, Iss 1, Pp 1-7 (2023)
Abstract Background Tetrahydrobiopterin (BH4) deficiency caused by 6-pyruvoyl-tetrahydropterin synthase (PTPS) deficiency is a rare disorder that is one of the major causes of hyperphenylalaninemia in Taiwan. Methods In this study, we reviewed the cl
Externí odkaz:
https://doaj.org/article/d898d3715bb7457cb12fc0c21b3d1e54
Autor:
Tung-Ming Chang, Rong-Ching Wu, Rei-Cheng Yang, Ching-Tai Chiang, Yi-Hung Chiu, Chen-Sen Ouyang, Yun-Ming Wang, Ming-Hsu Wu, Guang-Chung Lin, Lung-Chang Lin
Publikováno v:
Pediatrics and Neonatology, Vol 64, Iss 1, Pp 46-52 (2023)
Background: Attention-deficit/hyperactivity disorder (ADHD) is the most common neuropsychiatric disorder in schoolchildren. ADHD diagnoses are generally made based on criteria from the Diagnostic and Statistical Manual of Mental Disorders, Fifth Edit
Externí odkaz:
https://doaj.org/article/d46807ed52f4430997dfce59ade8af6b
Publikováno v:
Biomedicines, Vol 12, Iss 1, p 144 (2024)
Attention-deficit/hyperactivity disorder (ADHD) is a prevalent neurodevelopmental disorder in children with unknown etiology. Impaired learning ability was commonly reported in ADHD patients and has been associated with dopamine uptake in the striatu
Externí odkaz:
https://doaj.org/article/368c463e060f46f099bf09e3be764871
Autor:
Chia-Hsuan Huang, Pi-Lien Hung, Pi-Chuan Fan, Kuang-Lin Lin, Ting-Rong Hsu, I-Jun Chou, Che-Sheng Ho, I-Ching Chou, Wei-Sheng Lin, Inn-Chi Lee, Hueng-Chuen Fan, Shyi-Jou Chen, Jao-Shwann Liang, Yi-Fang Tu, Tung-Ming Chang, Su-Ching Hu, Lee-Chin Wong, Kun-Long Hung, Wang-Tso Lee
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-9 (2021)
Abstract 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 la
Externí odkaz:
https://doaj.org/article/d12a8820811846fabf0c479b27cba1ec
Autor:
Hsiang-Yu Lin, Ming-Ren Chen, Chung-Lin Lee, Shan-Miao Lin, Chung-Lieh Hung, Dau-Ming Niu, Tung-Ming Chang, Chih-Kuang Chuang, Shuan-Pei Lin
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 16, Iss 1, Pp 1-14 (2021)
Abstract 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 evaluat
Externí odkaz:
https://doaj.org/article/c4c18a996dc746a387503e1600fc2db7
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
Externí odkaz:
https://doaj.org/article/a8e3c64635524192b328d564ed5f11f9
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
Externí odkaz:
https://doaj.org/article/434ea8fa49c448ca9cd153d58e7b7dbe
Autor:
Hsiang-Yu Lin, Chung-Lin Lee, Chia-Ying Chang, Pao Chin Chiu, Yin-Hsiu Chien, Dau-Ming Niu, Fuu-Jen Tsai, Wuh-Liang Hwu, Shio Jean Lin, Ju-Li Lin, Mei-Chyn Chao, Tung-Ming Chang, Wen-Hui Tsai, Tzu-Jou Wang, Chih-Kuang Chuang, Shuan-Pei Lin
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 15, Iss 1, Pp 1-11 (2020)
Abstract 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 e
Externí odkaz:
https://doaj.org/article/1a7cb82677974c78a14f127068c04131
Cardiac characteristics and natural progression in Taiwanese patients with mucopolysaccharidosis III
Autor:
Hsiang-Yu Lin, Ming-Ren Chen, Shan-Miao Lin, Chung-Lieh Hung, Dau-Ming Niu, Tung-Ming Chang, Chih-Kuang Chuang, Shuan-Pei Lin
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 14, Iss 1, Pp 1-10 (2019)
Abstract Background Mucopolysaccharidosis type III (MPS III), or Sanfilippo syndrome, is caused by a deficiency in one of the four enzymes involved in the lysosomal degradation of heparan sulfate. Cardiac abnormalities have been observed in patients
Externí odkaz:
https://doaj.org/article/c534731dc2994833a9759c5dce5b378f