Zobrazeno 1 - 10
of 1 184
pro vyhledávání: '"Ni Chung"'
Publikováno v:
Journal of Orthopaedic Translation, Vol 15, Iss , Pp 81-90 (2018)
Summary: Background: Computed radiography (CR), digital radiography (DR) and biplanar radiography (EOS™ imaging system) are common imaging tools for radiographic evaluation of adolescent idiopathic scoliosis (AIS). The effect of imaging methods in
Externí odkaz:
https://doaj.org/article/059bd091723f42c29a8d2f1476623671
Publikováno v:
Taiwanese Journal of Obstetrics & Gynecology, Vol 63, Iss 5, Pp 771-776 (2024)
Objective: To present the ultrasound imaging and genetic diagnosis of a fetus with prenatal lethal form of Gaucher disease. Case report: A 37-year-old primiparous woman was pregnant at her 23 weeks of gestation and the prenatal fetal ultrasound revea
Externí odkaz:
https://doaj.org/article/843b99fd417a415daf64d3afa2e76e0f
Autor:
Pin‐Shiuan Chen, Ying‐Fa Chen, Jian‐Ying Chiu, Meng‐Chen Wu, Chun‐Hwei Tai, Yung‐Yee Chang, Min‐Yu Lan, Ni‐Chung Lee, Chin‐Hsien Lin
Publikováno v:
Annals of Clinical and Translational Neurology, Vol 11, Iss 6, Pp 1557-1566 (2024)
Abstract Objective IRF2BPL mutation has been associated with a rare neurodevelopmental disorder with abnormal movements, including dystonia. However, the role of IRF2BPL in dystonia remains elusive. We aimed to investigate IRF2BPL mutations in a Taiw
Externí odkaz:
https://doaj.org/article/850d1fcf49384b5eb997d8255da6a682
Autor:
Sung-Pin Fan, Ya-Fang Chen, Cheng-Hsuan Li, Yih-Chih Kuo, Ni-Chung Lee, Yin-Hsiu Chien, Wuh-Liang Hwu, Tai-Chung Tseng, Tung-Hung Su, Chien-Ting Hsu, Huey-Ling Chen, Chin-Hsien Lin, Yen-Hsuan Ni
Publikováno v:
NeuroImage, Vol 299, Iss , Pp 120829- (2024)
Background: Quantitative susceptibility mapping (QSM) is a post-processing technique that creates brain susceptibility maps reflecting metal burden through tissue magnetic susceptibility. We assessed topographic differences in magnetic susceptibility
Externí odkaz:
https://doaj.org/article/4dcb77ccfada4d6cb177102bd3205fc3
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
Autor:
Huang-Yi Li, Wei-An Chen, Hung-Yi Lin, Chi-Wei Tsai, Yu-Ting Chiu, Wen-Yi Yun, Ni-Chung Lee, Yin-Hsiu Chien, Wuh-Liang Hwu, Wei-Chieh Cheng
Publikováno v:
Communications Chemistry, Vol 7, Iss 1, Pp 1-9 (2024)
Abstract Isofagomine (IFG) and its analogues possess promising glycosidase inhibitory activities. However, a flexible synthetic strategy toward both C5a-functionalized IFGs remains to be explored. Here we show a practical synthesis of C5a-S and R ami
Externí odkaz:
https://doaj.org/article/c0dd006ba2b34bf5a153907505e3a8f8
Autor:
Chung-Hsing Wang, Yu‐Nan Huang, Wen-Ling Liao, Ai-Ru Hsieh, Wei-De Lin, Kai-Wen Liu, Wen-Li Lu, Chieh‐Chen Huang, Yin-Hsiu Chien, Ni-Chung Lee, Pen-Hua Su, Fuu-Jen Tsai
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 19, Iss 1, Pp 1-16 (2024)
Abstract Background Osteoporosis and its primary complication, fragility fractures, contribute to substantial global morbidity and mortality. Gaucher disease (GD) is caused by glucocerebrosidase (GBA1) deficiency, leading to skeletal complications. T
Externí odkaz:
https://doaj.org/article/0c1baf8b9b3b4b928fe4f713814a049b
Autor:
Chung‐Lin Lee, Yeun‐Wen Chang, Hsiang‐Yu Lin, Hung‐Chang Lee, Ting‐Chi Yeh, Li‐Ching Fang, Ni‐Chung Lee, Jeng‐Daw Tsai, Shuan‐Pei Lin
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 12, Iss 7, Pp n/a-n/a (2024)
Abstract Background We clinically and genetically evaluated a Taiwanese boy presenting with developmental delay, organomegaly, hypogammaglobulinemia and hypopigmentation without osteopetrosis. Whole‐exome sequencing revealed a de novo gain‐of‐f
Externí odkaz:
https://doaj.org/article/9d06fb6cc5c045609567437446f84d3c
Autor:
Lee, Ni-Chung, Hsu, Pei-Chun, Liu, Yu-Han, Wang, Hao-Chun, Chen, Tsu-I, Chien, Yin-Hsiu, Hwu, Wuh-Liang
Publikováno v:
In Neurobiology of Disease November 2024 202
Autor:
Fan, Sung-Pin, Chen, Ya-Fang, Li, Cheng-Hsuan, Kuo, Yih-Chih, Lee, Ni-Chung, Chien, Yin-Hsiu, Hwu, Wuh-Liang, Tseng, Tai-Chung, Su, Tung-Hung, Hsu, Chien-Ting, Chen, Huey-Ling, Lin, Chin-Hsien, Ni, Yen-Hsuan
Publikováno v:
In NeuroImage 1 October 2024 299