Søgeresultater - Chao, Mei-Chyn

Monitoring Adherence Rate to Growth Hormone Therapy and Growth Outcomes in Taiwanese Children Using Easypod Connect: Observational Study af 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 af 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 af 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 af 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 af 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 af 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 af 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 af 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 af 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 af 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 af 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) af 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 af 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 af 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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