Søgeresultater - Niu, Dau‐Ming

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  1. 1
    AB001. Methylmalonic and propionic acidemias: comparative outcomes between liver transplantation versus non-liver transplantation groups

    AB001. Methylmalonic and propionic acidemias: comparative outcomes between liver transplantation versus non-liver transplantation groups af Chu, Tzu-Hung, Niu, Dau-Ming

    Udgivet 2017
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  2. 2
    AB017. The extended newborn screening by tandem mass in Taiwan—results from two national newborn screening centers: Taipei Institute of Pathology & Chinese Foundation of Health

    AB017. The extended newborn screening by tandem mass in Taiwan—results from two national newborn screening centers: Taipei Institute of Pathology & Chinese Foundation of Health af Niu, Dau-Ming, Chiang, Chuan-Chi, Ho, Hui-Chen

    Udgivet 2015
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  3. 3
    AB165. Extended follow-up of Taiwanese Chinese patients treated early for 6-pyruvoyl-tetrahydropterin synthase deficiency

    AB165. Extended follow-up of Taiwanese Chinese patients treated early for 6-pyruvoyl-tetrahydropterin synthase deficiency af Chu, Tzu-Hung, Yang, Chia-Feng, Niu, Dau-Ming

    Udgivet 2015
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  4. 4
    Genetic Analysis in a Taiwanese Cohort of 750 Index Patients with Clinically Diagnosed Familial Hypercholesterolemia

    Genetic Analysis in a Taiwanese Cohort of 750 Index Patients with Clinically Diagnosed Familial Hypercholesterolemia af Huang, Chin-Chou, Niu, Dau-Ming, Charng, Min-Ji

    Udgivet 2022
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  5. 5
    Three Novel Mutations in the PHEX Gene in Chinese Subjects with Hypophosphatemic Rickets Extends Genotypic Variability

    Three Novel Mutations in the PHEX Gene in Chinese Subjects with Hypophosphatemic Rickets Extends Genotypic Variability af Jap, Tjin-Shing, Chiu, Chih-Yang, Niu, Dau-Ming, Levine, Michael A.

    Udgivet 2011
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  6. 6
    AB066. Pseudohomozygous familial hypercholesterolemia has better outcome than homozygous familial hypercholesterolemia

    AB066. Pseudohomozygous familial hypercholesterolemia has better outcome than homozygous familial hypercholesterolemia af Yen, Chun-Yu, Chu, Tzu-Hung, Yang, Chia-Feng, Niu, Dau-Ming

    Udgivet 2015
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  7. 7
    Congenital hypopituitarism due to novel compound heterozygous POU1F1 gene mutation: A case report and review of the literature

    Congenital hypopituitarism due to novel compound heterozygous POU1F1 gene mutation: A case report and review of the literature af Chen, Wei-Yu, Niu, Dau-Ming, Chen, Li-Zhen, Yang, Chia-Feng

    Udgivet 2021
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  8. 8
    Fabry Disease and the Effectiveness of Enzyme Replacement Therapy (ERT) in Left Ventricular Hypertrophy (LVH) Improvement: A Review and Meta-Analysis

    Fabry Disease and the Effectiveness of Enzyme Replacement Therapy (ERT) in Left Ventricular Hypertrophy (LVH) Improvement: A Review and Meta-Analysis af Lee, Chung-Lin, Lin, Shuan-Pei, Niu, Dau-Ming, Lin, Hsiang-Yu

    Udgivet 2022
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  9. 9
    AB064. Autosomal recessive diseases caused by a rare mechanism: uniparental disomy

    AB064. Autosomal recessive diseases caused by a rare mechanism: uniparental disomy af Chen, Ya-Chi, Hsiel, Shu-Chen, Pai, Ju-Shan, Chu, Tzu-Hung, Niu, Dau-Ming

    Udgivet 2015
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  10. 10
    AB098. The mutation spectrum of the phenylalanine hydroxylase (PAH) gene in Taiwanese population

    AB098. The mutation spectrum of the phenylalanine hydroxylase (PAH) gene in Taiwanese population af Pai, Ju-Shan, Chen, Ya-Chi, Hsie, Shu-Chen, Yang, Chia-Feng, Niu, Dau-Ming

    Udgivet 2015
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  11. 11
    AB172. High-throughput and cost-effective newborn screening method for female with fabry disease by DNA mass spectrometry in Taiwan

    AB172. High-throughput and cost-effective newborn screening method for female with fabry disease by DNA mass spectrometry in Taiwan af Hsieh, Yu-Ping, Gao, He-Jin, Huang, Chun-Kai, Ho, Hui-Chen, Niu, Dau-Ming

    Udgivet 2015
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  12. 12
    Assessment of bone mineral density by dual energy x-ray absorptiometry in patients with mucopolysaccharidoses

    Assessment of bone mineral density by dual energy x-ray absorptiometry in patients with mucopolysaccharidoses af Lin, Hsiang-Yu, Shih, Shou-Chuan, Chuang, Chih-Kuang, Chen, Ming-Ren, Niu, Dau-Ming, Lin, Shuan-Pei

    Udgivet 2013
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  13. 13
    AB173. Heterozygous carriers of classical homocystinuria tend to have higher fasting serum homocysteine concentrations than non-carriers in a folate deficiency area where has inordinately high homocystinuria prevalence

    AB173. Heterozygous carriers of classical homocystinuria tend to have higher fasting serum homocysteine concentrations than non-carriers in a folate deficiency area where has inord... af Lin, Yu-Ting, Lu, Yung-Hsiu, Chen, Ya-Chi, Pai, Ju-Shan, Hsu, Ting-Rong, Niu, Dau-Ming

    Udgivet 2015
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  14. 14
    AB171. RNA alternative splicing modulator can effectively increase lymphoblast enzyme activity in patients with cardiac fabry disease caused by IVS4+919G >A mutation

    AB171. RNA alternative splicing modulator can effectively increase lymphoblast enzyme activity in patients with cardiac fabry disease caused by IVS4+919G >A mutation af Lu, Yung-Hsiu, Li, Cheng-Fang, Huang, Chun-Kai, Lin, Yu-Ting, Hsu, Ting-Rong, Niu, Dau-Ming

    Udgivet 2015
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  15. 15
    AB150. Mutation spectrum of the fibrillin-1 (FBN1) gene in Taiwanese patients with Marfan syndrome

    AB150. Mutation spectrum of the fibrillin-1 (FBN1) gene in Taiwanese patients with Marfan syndrome af Hsieh, Shu-Chen, Lu, Yung-Hsiu, Chen, Ya-Chi, Pai, Ju-Shan, Hsieh, Yu-Ping, Niu, Dau-Ming

    Udgivet 2015
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  16. 16
    AB018. Revisited later-onset cardiac type Fabry disease—cardiac damages progressed in silence—experiences from an extremely high prevalent area, Taiwan

    AB018. Revisited later-onset cardiac type Fabry disease—cardiac damages progressed in silence—experiences from an extremely high prevalent area, Taiwan af Niu, Dau-Ming, Hsu, Ting-Rong, Yang, Chia-Feng, Chu, Tzu-Hung, Chiang, Chuan-Chi, Ho, Hui-Chen

    Udgivet 2015
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  17. 17
    AB067. Glucose tetrasaccharide (Glc4) level in urine sample as a biomarker for Pompe patients

    AB067. Glucose tetrasaccharide (Glc4) level in urine sample as a biomarker for Pompe patients af Huang, Chun-Kai, Liao, Hsuan-Chieh, Hsieh, Yu-Ping, Chen, Ya-Chi, Yang, Chia-Feng, Niu, Dau-Ming

    Udgivet 2015
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  18. 18
    Modulation the alternative splicing of GLA (IVS4+919G>A) in Fabry disease

    Modulation the alternative splicing of GLA (IVS4+919G>A) in Fabry disease af Chang, Wen-Hsin, Niu, Dau-Ming, Lu, Chi-Yu, Lin, Shyr-Yi, Liu, Ta-Chih, Chang, Jan-Gowth

    Udgivet 2017
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  19. 19
    AB028. Very early treatment for infantile-onset Pompe disease contributes to better outcomes: 10-year experience in one institute

    AB028. Very early treatment for infantile-onset Pompe disease contributes to better outcomes: 10-year experience in one institute af Yang, Chia-Feng, Chu, Tzu-Hung, Huang, Ling-Yi, Liao, Hsuan-Chieh, Soong, Wen-Jue, Niu, Dau-Ming

    Udgivet 2017
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  20. 20
    AB029. Rare condition of hepatic Gaucheroma in a type I Gaucher patient with enzyme replacement therapy

    AB029. Rare condition of hepatic Gaucheroma in a type I Gaucher patient with enzyme replacement therapy af Tseng, Szu Yin, Yang, Chia Feng, Hung, Chu Tzu, Chiang, Chuan-Chi, Ho, Hui-Chen, Niu, Dau-Ming

    Udgivet 2017
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