Hasil Pencarian - Jeng-Daw Tsai

  • Menampilkan 1 - 18 hasil dari 18
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  1. 1
    Diagnosis of pediatric urinary tract infections

    Diagnosis of pediatric urinary tract infections oleh Jeng-Daw Tsai, Chun-Chen Lin, Stephan S. Yang

    Diterbitkan 2016-09-01
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  2. 2
    Superior mesenteric artery syndrome and nutcracker syndrome

    Superior mesenteric artery syndrome and nutcracker syndrome oleh Tzu-Hua Lin, Chun-Chen Lin, Jeng-Daw Tsai

    Diterbitkan 2020-06-01
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  3. 3
    Reappraisal of the effectiveness of 99mTc-dimercaptosuccinic acid scans for selective voiding cystourethrography in children with a first febrile urinary tract infection

    Reappraisal of the effectiveness of 99mTc-dimercaptosuccinic acid scans for selective voiding cystourethrography in children with a first febrile urinary tract infection oleh Bing-Fu Shih, Jeng-Daw Tsai, Chin-Ho Tsao, Fu-Yuan Huang

    Diterbitkan 2014-12-01
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  4. 4
    Pseudoureterocele

    Pseudoureterocele oleh Ming-Dar Lee, Chun-Chen Lin, Brian Pin-Hsuan Chang, Pei-Yi Lin, Jeng-Daw Tsai

    Diterbitkan 2018-02-01
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  5. 5
    Hemolytic Uremic Syndrome Caused by Enteroviral Infection

    Hemolytic Uremic Syndrome Caused by Enteroviral Infection oleh Ming-Dar Lee, Chin-Yuan Tzen, Chun-Chen Lin, Fu-Yuan Huang, Hsi-Che Liu, Jeng-Daw Tsai

    Diterbitkan 2013-06-01
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  6. 6
    Kidney Cysts in Children With Alport Syndrome: A Report of 3 Cases

    Kidney Cysts in Children With Alport Syndrome: A Report of 3 Cases oleh Yeun-Wen Chang, Daw-Yang Hwang, Tung-Ying Chen, Chun-Chen Lin, Min-Hua Tseng, Jeng-Daw Tsai

    Diterbitkan 2024-05-01
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  7. 7
    X-linked recessive Galloway-Mowat syndrome 2 caused by a specific LAGE3 variant

    X-linked recessive Galloway-Mowat syndrome 2 caused by a specific LAGE3 variant oleh Tsai-Ling Liu, Shuan-Pei Lin, Martin Zenker, Tung-Ying Chen, Jui-Hsing Chang, Chun-Chen Lin, Jeng-Daw Tsai

    Diterbitkan 2023-03-01
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  8. 8
    Phenotype, genotype, and clinical outcome of Taiwanese with congenital nephrotic syndrome

    Phenotype, genotype, and clinical outcome of Taiwanese with congenital nephrotic syndrome oleh Min-Hua Tseng, Shih-Hua Lin, Wen-Lang Fan, Ta-Wei Wu, Shuan-Pei Lin, Jhao-Jhuang Ding, I-Jung Tsai, Jeng-Daw Tsai

    Diterbitkan 2024-06-01
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  9. 9
    Allele-specific RT-PCR for the rapid detection of recurrent SLC12A3 mutations for Gitelman syndrome

    Allele-specific RT-PCR for the rapid detection of recurrent SLC12A3 mutations for Gitelman syndrome oleh Ming-Tso Yan, Sung-Sen Yang, Min-Hua Tseng, Chih-Jen Cheng, Jeng-Daw Tsai, Chih-Chien Sung, Yu-Juei Hsu, Shih-Hua Lin

    Diterbitkan 2021-08-01
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  10. 10
    Renal Calcification in Very Low Birth Weight Infants

    Renal Calcification in Very Low Birth Weight Infants oleh Hung-Yang Chang, Chyong-Hsin Hsu, Jeng-Daw Tsai, Sung-Tse Li, Han-Yang Hung, Hsin-An Kao, Jui-Hsing Chang, Hsueh-Yu Chung, Hsin-Kai Wang

    Diterbitkan 2011-06-01
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  11. 11
    Galloway-Mowat syndrome: Prenatal ultrasound and perinatal magnetic resonance imaging findings

    Galloway-Mowat syndrome: Prenatal ultrasound and perinatal magnetic resonance imaging findings oleh Chih-Ping Chen, Shuan-Pei Lin, Yu-Peng Liu, Jeng-Daw Tsai, Chen-Yu Chen, Shin-Lin Shih, Fuu-Jen Tsai, Pei-Chen Wu, Wayseen Wang

    Diterbitkan 2011-06-01
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  12. 12
    Multisystem disorder associated with a pathogenic variant in CLCN7 in the absence of osteopetrosis

    Multisystem disorder associated with a pathogenic variant in CLCN7 in the absence of osteopetrosis oleh Chung‐Lin Lee, Yeun‐Wen Chang, Hsiang‐Yu Lin, Hung‐Chang Lee, Ting‐Chi Yeh, Li‐Ching Fang, Ni‐Chung Lee, Jeng‐Daw Tsai, Shuan‐Pei Lin

    Diterbitkan 2024-07-01
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  13. 13
    Atypical hemolytic uremic syndrome: Consensus of diagnosis and treatment in Taiwan

    Atypical hemolytic uremic syndrome: Consensus of diagnosis and treatment in Taiwan oleh Min-Hua Tseng, Shih-Hua Lin, Jeng-Daw Tsai, Mai-Szu Wu, I-Jung Tsai, Yeu-Chin Chen, Min-Chih Chang, Wen-Chien Chou, Yee-Hsuan Chiou, Chiu-Ching Huang

    Diterbitkan 2023-05-01
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  14. 14
    Detection of recurrent transmission of 17q12 microdeletion by array comparative genomic hybridization in a fetus with prenatally diagnosed hydronephrosis, hydroureter, and multicystic kidney, and variable clinical spectrum in the family

    Detection of recurrent transmission of 17q12 microdeletion by array comparative genomic hybridization in a fetus with prenatally diagnosed hydronephrosis, hydroureter, and multicys... oleh Chih-Ping Chen, Shuenn-Dyh Chang, Tzu-Hao Wang, Liang-Kai Wang, Jeng-Daw Tsai, Yu-Peng Liu, Schu-Rern Chern, Peih-Shan Wu, Jun-Wei Su, Yu-Ting Chen, Wayseen Wang

    Diterbitkan 2013-12-01
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  15. 15
    Management of nocturnal enuresis in Taiwan: Consensus statements of the Taiwan enuresis expert committeeStatement 1.1Statement 1.2Statement 1.3Statement 1.4Statement 2.1Statement 2.2Statement 3.1Statement 3.2Statement 3.3Statement 3.4Statement 3.5Statement 3.6

    Management of nocturnal enuresis in Taiwan: Consensus statements of the Taiwan enuresis expert committeeStatement 1.1Statement 1.2Statement 1.3Statement 1.4Statement 2.1Statement 2... oleh Ta-Min Wang, Stephen Shei-Dei Yang, Jeng-Daw Tsai, Mei-Ching Yu, Yee-Hsuan Chiou, Kuo-Liang Chen, Hong-Lin Cheng, Jesun Lin, Hsiao-Wen Chen, Hann-Chorng Kuo, Shyh-Chyan Chen

    Diterbitkan 2019-06-01
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  16. 16
    Galloway-Mowat syndrome in Taiwan: OSGEP mutation and unique clinical phenotype

    Galloway-Mowat syndrome in Taiwan: OSGEP mutation and unique clinical phenotype oleh Pei-Yi Lin, Min-Hua Tseng, Martin Zenker, Jia Rao, Friedhelm Hildebrandt, Shih-Hua Lin, Chun-Chen Lin, Jui-Hsing Chang, Chyong-Hsin Hsu, Ming-Dar Lee, Shuan-Pei Lin, Jeng-Daw Tsai

    Diterbitkan 2018-12-01
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  17. 17
    Factors associated with diabetic nephropathy in children, adolescents, and adults with type 1 diabetes

    Factors associated with diabetic nephropathy in children, adolescents, and adults with type 1 diabetes oleh Chi-Yu Huang, Wei-Hsin Ting, Fu-Sung Lo, Jeng-Daw Tsai, Fang-Ju Sun, Chon-In Chan, Ya-Ting Chiang, Chao-Hsu Lin, Bi-Wen Cheng, Yi-Lei Wu, Chen-Mei Hung, Yann-Jinn Lee

    Diterbitkan 2017-12-01
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  18. 18
    Mutations in pseudohypoparathyroidism 1a and pseudopseudohypoparathyroidism in ethnic Chinese.

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

    Diterbitkan 2014-01-01
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