Hasil Pencarian - Wei-De Lin
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Current understanding of the genetics of tourette syndrome oleh Wei-De Lin, Fuu-Jen Tsai, I-Ching Chou
Diterbitkan 2022-04-01
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Heterogeneous neurodevelopmental disorders in children with Kawasaki disease: what is new today? oleh Chien-Heng Lin, Wei-De Lin, I-Ching Chou, Inn-Chi Lee, Syuan-Yu Hong
Diterbitkan 2019-11-01
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RUNX2 mutations in Taiwanese patients with cleidocranial dysplasia oleh Wei-De Lin, Shuan-Pei Lin, Chung-Hsing Wang, Yushin Tsai, Chih-Ping Chen, Fuu-Jen Tsai
Diterbitkan 2011-01-01
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Genome-wide association study identifies novel susceptible loci and evaluation of polygenic risk score for chronic obstructive pulmonary disease in a Taiwanese population oleh Wei-De Lin, Wen-Ling Liao, Wei-Cheng Chen, Ting-Yuan Liu, Yu-Chia Chen, Fuu-Jen Tsai
Diterbitkan 2024-06-01
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Effects of Acrylamide-Induced Vasorelaxation and Neuromuscular Blockage: A Rodent Study oleh Wei-De Lin, Chu-Chyn Ou, Shih-Hao Hsiao, Chih-Han Chang, Fuu-Jen Tsai, Jiunn-Wang Liao, Yng-Tay Chen
Diterbitkan 2021-05-01
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Epilepsy and Neurodevelopmental Outcomes in Children With Etiologically Diagnosed Central Nervous System Infections: A Retrospective Cohort Study oleh Chien-Heng Lin, Chien-Heng Lin, Wei-De Lin, I-Ching Chou, I-Ching Chou, Inn-Chi Lee, Inn-Chi Lee, Syuan-Yu Hong
Diterbitkan 2019-05-01
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Association Between Kawasaki Disease and Childhood Epilepsy: A Nationwide Cohort Study in Taiwan oleh Chien-Heng Lin, Chien-Heng Lin, Jung-Nien Lai, Jung-Nien Lai, Inn-Chi Lee, I-Ching Chou, I-Ching Chou, Wei-De Lin, Mei-Chen Lin, Mei-Chen Lin, Syuan-Yu Hong
Diterbitkan 2021-04-01
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GBA1 as a risk gene for osteoporosis in the specific populations and its role in the development of Gaucher disease oleh 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
Diterbitkan 2024-04-01
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