Torthaí cuardaigh - Hwang, Daw-Yang

The Role of Glucocorticoid Receptors in Podocytes and Nephrotic Syndrome de réir Zhao, Xuan, Hwang, Daw-Yang, Kao, Hung-Ying

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Deletion of the Noncoding GNAS Antisense Transcript Causes Pseudohypoparathyroidism Type Ib and Biparental Defects of GNAS Methylation in cis de réir Chillambhi, Smitha, Turan, Serap, Hwang, Daw-Yang, Chen, Hung-Chun, Jüppner, Harald, Bastepe, Murat

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Deletion of the Noncoding GNAS Antisense Transcript Causes Pseudohypoparathyroidism Type Ib and Biparental Defects of GNAS Methylation in cis de réir Chillambhi, Smitha, Turan, Serap, Hwang, Daw-Yang, Chen, Hung-Chun, Jüppner, Harald, Bastepe, Murat

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Novel Mutations Detection with Next-Generation Sequencing and Its Association with Clinical Outcome in Unilateral Primary Aldosteronism de réir Wu, Che-Hsiung, Peng, Kang-Yung, Hwang, Daw-Yang, Lin, Yen-Hung, Wu, Vin-Cent, Chueh, Jeff S.

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Atypical X-linked agammaglobulinaemia caused by a novel BTK mutation in a selective immunoglobulin M deficiency patient de réir Lim, Lee-Moay, Chang, Jer-Ming, Wang, I-Fang, Chang, Wei-Chiao, Hwang, Daw-Yang, Chen, Hung-Chun

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Novel Vitamin D Receptor Mutations in Hereditary Vitamin D Resistant Rickets in Chinese de réir 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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Genetic Polymorphisms of ORAI1 and Chronic Kidney Disease in Taiwanese Population de réir Hwang, Daw-Yang, Chien, Shu-Chen, Hsu, Yu-Wen, Kao, Chih-Chin, Cheng, Shih-Ying, Lu, Hui-Chen, Wu, Mai-Szu, Chang, Jer-Ming

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Whole-Exome Sequencing Reveals FAT4 Mutations in a Clinically Unrecognizable Patient with Syndromic CAKUT: A Case Report de réir van der Ven, Amelie T., Shril, Shirlee, Ityel, Hadas, Vivante, Asaf, Chen, Jing, Hwang, Daw-Yang, Laricchia, Kristen M., Lek, Monkol, Tasic, Velibor, Hildebrandt, Friedhelm

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Diabetic Retinopathy and Clinical Parameters Favoring the Presence of Diabetic Nephropathy could Predict Renal Outcome in Patients with Diabetic Kidney Disease de réir Hung, Chi-Chih, Lin, Hugo You-Hsien, Hwang, Daw-Yang, Kuo, I-Ching, Chiu, Yi-Wen, Lim, Lee-Moay, Hwang, Shang-Jyh, Chen, Hung-Chun

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Pyuria, urinary tract infection and renal outcome in patients with chronic kidney disease stage 3–5 de réir Kuo, I-Ching, Lee, Jia-Jung, Hwang, Daw-Yang, Lim, Lee-Moay, Lin, Hugo You-Hsien, Hwang, Shang-Jyh, Chen, Hung-Chun, Hung, Chi-Chih

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Molecular Genetic Characterization of Patients With Focal Epilepsy Using a Customized Targeted Resequencing Gene Panel de réir Tsai, Meng-Han, Chan, Chung-Kin, Chang, Ying-Chao, Lin, Chih-Hsiang, Liou, Chia-Wei, Chang, Wen-Neng, Ng, Ching-Ching, Lim, Kheng-Seang, Hwang, Daw-Yang

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Primary cardiac manifestation of autosomal dominant polycystic kidney disease revealed by patient induced pluripotent stem cell-derived cardiomyocytes de réir Lee, Jia-Jung, Cheng, Sin-Jhong, Huang, Ching-Ying, Chen, Chen-Yun, Feng, Li, Hwang, Daw-Yang, Kamp, Timothy J., Chen, Hung-Chun, Hsieh, Patrick C.H.

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Single-Cell Analysis of Different Stages of Oral Cancer Carcinogenesis in a Mouse Model de réir Huang, Ling-Yu, Hsieh, Yi-Ping, Wang, Yen-Yun, Hwang, Daw-Yang, Jiang, Shih Sheng, Huang, Wen-Tsung, Chiang, Wei-Fan, Liu, Ko-Jiunn, Huang, Tze-Ta

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Hyponatremia is Associated with Fluid Imbalance and Adverse Renal Outcome in Chronic Kidney Disease Patients Treated with Diuretics de réir Lim, Lee Moay, Tsai, Ni-Chin, Lin, Ming-Yen, Hwang, Daw-Yang, Lin, Hugo You-Hsien, Lee, Jia-Jung, Hwang, Shang-Jyh, Hung, Chi-Chih, Chen, Hung-Chun

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Mild Recessive Mutations in Six Fraser Syndrome–Related Genes Cause Isolated Congenital Anomalies of the Kidney and Urinary Tract de réir Kohl, Stefan, Hwang, Daw-Yang, Dworschak, Gabriel C., Hilger, Alina C., Saisawat, Pawaree, Vivante, Asaf, Stajic, Natasa, Bogdanovic, Radovan, Reutter, Heiko M., Kehinde, Elijah O., Tasic, Velibor, Hildebrandt, Friedhelm

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Both IgM and IgG Antibodies against Polyethylene Glycol Can Alter the Biological Activity of Methoxy Polyethylene Glycol-Epoetin Beta in Mice de réir Chang, Tien-Ching, Chen, Bing-Mae, Lin, Wen-Wei, Yu, Pei-Hua, Chiu, Yi-Wen, Chen, Yuan-Tsong, Wu, Jer-Yuarn, Cheng, Tian-Lu, Hwang, Daw-Yang, Roffler, Steve

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Whole-exome sequencing identified mutational profiles of urothelial carcinoma post kidney transplantation de réir Lim, Lee-Moay, Chung, Wen-Yu, Hwang, Daw-Yang, Yu, Chih-Chuan, Ke, Hung-Lung, Liang, Peir-In, Lin, Ting-Wei, Cheng, Siao Muk, Huang, A-Mei, Kuo, Hung-Tien

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The rs1014290 Polymorphism of the SLC2A9 Gene Is Associated with Type 2 Diabetes Mellitus in Han Chinese de réir Liu, Wan-Chun, Hung, Chi-Chih, Chen, Szu-Chia, Lin, Ming-Yen, Chen, Ling-I, Hwang, Daw-Yang, Chang, Jer-Ming, Tsai, Jer-Chia, Chen, Hung-Chun, Hwang, Shang-Jyh

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CYP17A1 Intron Mutation Causing Cryptic Splicing in 17α-Hydroxylase Deficiency de réir 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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Hypokalemia, Its Contributing Factors and Renal Outcomes in Patients with Chronic Kidney Disease de réir Wang, Hsiao-Han, Hung, Chi-Chih, Hwang, Daw-Yang, Kuo, Mei-Chuan, Chiu, Yi-Wen, Chang, Jer-Ming, Tsai, Jer-Chia, Hwang, Shang-Jyh, Seifter, Julian L., Chen, Hung-Chun

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