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Showing items 11-25 of 25  (1 Page(s) Totally)
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Institution Date Title Author
國立成功大學 2023-02 Whole-Exome Sequencing Identified Rare Genetic Variants Associated with Undervirilized Genitalia in Taiwanese Pediatric Patients Tsai;Meng-Che;Weng;Yun-Han;Lin;Yu-Fang;Wang;Yi-Chieh;Yu;Hui-Wen;Chou;Yen-Yin;Chen;Peng-Chieh
國立成功大學 2023-01 Active-fluidics versus gravity-fluidics in lens extraction: A systematic review and meta-analysis of randomized controlled trials Su;Yu-Chen;Lee;Yen-Yin;Su;Yu-Chi
國立成功大學 2022-05 Postnatal Serum Total Thyroxine Level Associated with Short- and Long-Term Anthropometric Outcomes in Very Preterm Infants Chen;Yen-Ju;Chu;Wei-Ying;Pan;Yu-Wen;Wang;Chen-Yueh;Chou;Yen-Yin;Lin;Chyi-Her;Tsuda;Kennosuke;Iwata;Osuke;Yu;Wen-Hao;Lin;Yung-Chieh
國立成功大學 2022-05 Whole exome sequencing identifies a novel FRAS1 mutation and aids in vitro fertilization with preimplantation genetic diagnosis in Fraser syndrome Ou;Tsung-Ying;Tsai;Meng-Che;Kuo;Pao-Lin;Lee;Ni-Chung;Chou;Yen-Yin
國立成功大學 2022-04-8 Genetic Diagnosis of Rubinstein-Taybi Syndrome With Multiplex Ligation-Dependent Probe Amplification (MLPA) and Whole-Exome Sequencing (WES): Case Series With a Novel CREBBP Variant Lee;Yu-Rong;Lin;Yu-Chen;Chang;Yi-Han;Huang;Hsin-Yu;Hong;Yi-Kai;Aala;Wilson, Jr F.;Tu;Wei-Ting;Tsai;Meng-Che;Chou;Yen-Yin;Hsu;Chao-Kai
國立成功大學 2022-01-11 PAX2 Mutation-Related Renal Hypodysplasia: Review of the Literature and Three Case Reports Chang;Yu-Ming;Chen;Chih-Chia;Lee;Ni-Chung;Sung;Junne-Ming;Chou;Yen-Yin;Chiou;Yuan-Yow
國立成功大學 2021-09 Is Non-Stimulated C-Peptide at Diagnosis a Good Predictive Value for Insulin Use at Two Years after Diagnosis in Pediatric Diabetic Patients? Chou;Wei-Chih;Chou;Yen-Yin;Pan;Yu-Wen;Tsai;Meng-Che
國立成功大學 2021-07-28 New Structural and Single Nucleotide Mutations in Type I and Type II Collagens in Taiwanese Children With Type I and Type II Collagenopathies Tsai;Meng-Che;Chou;Yen-Yin;Li;Chia-Yi;Wang;Yi-Chieh;Yu;Hui-Wen;Chen;Chia-Hsiang;Chen;Peng-Chieh
國立成功大學 2021-07 Precocious puberty as a consequence of anti-NMDA receptor encephalitis in children Wu;Po-Ming;Teng;Chao-Ku;Chou;Yen-Yin;Tu;Yi-Fang
國立成功大學 2021-04 Postnatal Serum Total Thyroxine of Very Preterm Infants and Long-Term Neurodevelopmental Outcome Lin;Yung-Chieh;Wang;Chen-Yueh;Pan;Yu-Wen;Chen;Yen-Ju;Yu;Wen-Hao;Chou;Yen-Yin;Huang;Chi-Hsien;Chu;Wei-Ying;Lin;Chyi-Her;Iwata;Osuke
國立成功大學 2020-06 A synchrotron X-ray imaging strategy to map large animal brains Chin;An-Lun;Yang;Shun-Min;Chen;Hsiang-Hsin;Li;Min-Tsang;Lee;Tsung-Tse;Chen;Ying-Jie;Lee;Ting-Kuo;Petibois;Cyril;Cai;Xiaoqing;Low;Chian-Ming;Tan;Kuan, Francis Chee;Teo;Alvin;Tok;Soon, Eng;Ong;Edwin, B. L.;Lin;Yen-Yin;Lin;I-Jin;Tseng;Yi-Chi;Chen;Nan-Yow;Shih;Chi-Tin;Lim;Jae-Hong;Lim;Jun;Je;Jung-Ho;Kohmura;Yoshiki;Ishikawa;Tetsuya;Margaritondo;Giorgio;Chiang;Ann-Shyn;Hwu;Yeukuang
國立成功大學 2020-06 Segmental isodisomy in Prader-Willi syndrome patients: The experience of a single diagnostic center Pan;Yu-Wen;Chang;Chia-Wei;Jong;Yiin-Jeng;Chou;Yen-Yin;Kuo;Pao-Lin
國立成功大學 2019-12 The relationship between nonalcoholic fatty liver disease and pediatric congenital hypothyroidism patients Pan;Yu-Wen;Tsai;Meng-Che;Yang;Yao-Jong;Chen;Ming-Yin;Chen;Shou-Yen;Chou;Yen-Yin
國立成功大學 2018-04-18 Rare Compound Heterozygous Frameshift Mutations in &ITALMS1&IT Gene Identified Through Exome Sequencing in a Taiwanese Patient With Alstrom Syndrome Tsai;Meng-Che;Yu;Hui-Wen;Liu;Tsunglin;Chou;Yen-Yin;Chiou;Yuan-Yow;Chen;Peng-Chieh
國立成功大學 2018-02-3 Metabolic correlates of health-related quality of life among overweight and obese adolescents Lee;Chih-Ting;Lin;Chung-Ying;Strong;Carol;Lin;Yu-Fang;Chou;Yen-Yin;Tsai;Meng-Che

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