Rezultati - Chao, Mei‐Chyn

Monitoring Adherence Rate to Growth Hormone Therapy and Growth Outcomes in Taiwanese Children Using Easypod Connect: Observational Study od Su, Pen-Hua, Yang, Chen, Chao, Mei-Chyn, Chiang, Chung-Lin

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Growth Hormone Deficiency in a Case of Crouzon Syndrome with Hydrocephalus od Wen, Mei-Hong, Hsiao, Hui-Pin, Chao, Mei-Chyn, Tsai, Fuu-Jen

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Novel Vitamin D Receptor Mutations in Hereditary Vitamin D Resistant Rickets in Chinese od Lim, Lee-Moay, Zhao, Xuan, Chao, Mei-Chyn, Chang, Jer-Ming, Chang, Wei-Chiao, Kao, Hung-Ying, Hwang, Daw-Yang, Chen, Hung-Chun

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Low penetrance of retinoblastoma for p.V654L mutation of the RB1 gene od Hung, Chia-Cheng, Lin, Shin-Yu, Lee, Chien-Nan, Chen, Chih-Ping, Lin, Shuan-Pei, Chao, Mei-Chyn, Chiou, Shyh-Shin, Su, Yi-Ning

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Altered Pattern of Macrophage Polarization as a Biomarker for Severity of Childhood Asthma od Kuo, Chang-Hung, Tsai, Mei-Lan, Li, Chung-Hsiang, Hsiao, Hui-Pin, Chao, Mei-Chyn, Lee, Ming-Sheng, Lin, Yi-Ching, Hung, Chih-Hsing

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Intake of Phthalate-Tainted Foods Alters Thyroid Functions in Taiwanese Children od Wu, Ming-Tsang, Wu, Chia-Fang, Chen, Bai-Hsiun, Chen, Eric K., Chen, Yi-Ling, Shiea, Jentaie, Lee, Wei-Te, Chao, Mei-Chyn, Wu, Jiunn-Ren

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Fatty Acid Oxidation Disorders in a Chinese Population in Taiwan od Chien, Yin-Hsiu, Lee, Ni-Chung, Chao, Mei-Chyn, Chen, Li-Chu, Chen, Li-Hsin, Chien, Chun-Ching, Ho, Hui-Chen, Suen, Jeng-Hung, Hwu, Wuh-Liang

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CYP17A1 Intron Mutation Causing Cryptic Splicing in 17α-Hydroxylase Deficiency od Hwang, Daw-Yang, Hung, Chi-Chih, Riepe, Felix G., Auchus, Richard J., Kulle, Alexandra E., Holterhus, Paul-Martin, Chao, Mei-Chyn, Kuo, Mei-Chuan, Hwang, Shang-Jyh, Chen, Hung-Chun

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Novel B3GALTL mutations in classic Peters Plus syndrome and lack of mutations in a large cohort of patients with similar phenotypes od Weh, Eric, Reis, Linda M., Tyler, Rebecca C., Bick, David, Rhead, William J., Wallace, Stephanie, McGregor, Tracy L., Dills, Shelley K., Chao, Mei-Chyn, Murray, Jeffrey C., Semina, Elena V.

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CD40 Gene Polymorphisms Associated with Susceptibility and Coronary Artery Lesions of Kawasaki Disease in the Taiwanese Population od Kuo, Ho-Chang, Chao, Mei-Chyn, Hsu, Yu-Wen, Lin, Ying-Chi, Huang, Ying-Hsien, Yu, Hong-Ren, Hou, Ming-Feng, Liang, Chi-Di, Yang, Kuender D., Chang, Wei-Chiao, Wang, Chih-Lu

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Mutations in Pseudohypoparathyroidism 1a and Pseudopseudohypoparathyroidism in Ethnic Chinese od Wu, Yi-Lei, Hwang, Daw-Yang, Hsiao, Hui-Pin, Ting, Wei-Hsin, Huang, Chi-Yu, Tsai, Wen-Yu, Chen, Hung-Chun, Chao, Mei-Chyn, Lo, Fu-Sung, Tsai, Jeng-Daw, Yang, Stone, Shih, Shin-Lin, Lin, Shuan-Pei, Lin, Chiung-Ling, Lee, Yann-Jinn

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Survival and diagnostic age of 175 Taiwanese patients with mucopolysaccharidoses (1985–2019) od Lin, Hsiang-Yu, Lee, Chung-Lin, Chang, Chia-Ying, Chiu, Pao Chin, Chien, Yin-Hsiu, Niu, Dau-Ming, Tsai, Fuu-Jen, Hwu, Wuh-Liang, Lin, Shio Jean, Lin, Ju-Li, Chao, Mei-Chyn, Chang, Tung-Ming, Tsai, Wen-Hui, Wang, Tzu-Jou, Chuang, Chih-Kuang, Lin, Shuan-Pei

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Functional independence of Taiwanese patients with mucopolysaccharidoses od Lee, Chung‐Lin, Lin, Hsiang‐Yu, Chuang, Chih‐Kuang, Chiu, Huei‐Ching, Tu, Ru‐Yi, Huang, You‐Hsin, Hwu, Wuh‐Liang, Tsai, Fuu‐Jen, Chiu, Pao‐Chin, Niu, Dau‐Ming, Chen, Yann‐Jang, Chao, Mei‐Chyn, Chang, Tung‐Ming, Lin, Ju‐Li, Chang, Chia‐Ying, Kao, Yu‐Chia, Lin, Shuan‐Pei

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Epigenotype, Genotype, and Phenotype Analysis of Taiwanese Patients with Silver–Russell Syndrome od Lin, Hsiang-Yu, Lee, Chung-Lin, Fran, Sisca, Tu, Ru-Yi, Chang, Ya-Hui, Niu, Dau-Ming, Chang, Chia-Ying, Chiu, Pao-Chin, Chou, Yen-Yin, Hsiao, Hui-Pin, Tsai, Meng-Che, Chao, Mei-Chyn, Tsai, Li-Ping, Yang, Chia-Feng, Su, Pen-Hua, Pan, Yu-Wen, Lee, Chen-Hao, Chu, Tzu-Hung, Chuang, Chih-Kuang, Lin, Shuan-Pei

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