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"胡務亮"???jsp.browse.items-by-author.description???
Showing items 1-25 of 313 (13 Page(s) Totally)
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| 國立臺灣大學 |
2016 |
3-O-methyldopa levels in newborns: Result of newborn screening for aromatic L-amino-acid decarboxylase deficiency
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Chien, Yin-Hsiu; Chen, Pin-Wen; Lee, Ni-Chung; Hsieh, Wu-Shiun; Chiu, Pao-Chin; Hwu, Wuh-Liang; Tsai, Fuu-Jen; Lin, Shuan-Pei; Chu, Shao-Yin; Jong, Yuh-Jyh; Chao, Mei-Chyn; 胡務亮; 謝武勳; 李妮鍾; 簡穎秀 |
| 國立臺灣大學 |
2001 |
A Chinese Adult Onset Type Ii Citrullinaemia Patient with 851del4/1638ins 23 Mutations in the Slc25a13 Gene
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胡務亮; HWU, WUH-LIANG |
| 國立臺灣大學 |
1991 |
A Clinical Observation in Achondroplasia
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胡務亮; Wang, T. R.; Hwu, Wuh-Liang; Wang, T. R. |
| 國立臺灣大學 |
1991 |
A Clinical Study in Intravenous Immunoglobulin Therapy for Childhood Idiopathic Chromobocytopenic Purpura
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Lin, D. T.; 胡務亮; Lin, K. H.; Lin, K. S.; Lin, D. T.; Hwu, Wuh-Liang; Lin, K. H.; Lin, K. S. |
| 國立臺灣大學 |
2008 |
A Clinical Trial of Idursulease in Hunter Syndrome Patients 5 Years Old and Younger
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胡務亮; HWU, WUH-LIANG |
| 國立臺灣大學 |
2003 |
A Founder Mutation (R254x) of Slc22a5 (Octn2) in Chinese Primary Carnitine Deficiency Patients
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胡務亮; HWU, WUH-LIANG |
| 國立臺灣大學 |
2009 |
A Longitudinal Study of Taiwanese Sialidosis Type 1: An Insight into the Concept of Cherry-Red Spot Myoclonus Syndrome
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賴思佳; 翁意欣; 胡務亮; 陸清松; LAI, SZU-CHIA; WENG, YI-HSIN; HWU, WUH- LIANG; LU, CHIN-SONG |
| 國立臺灣大學 |
2014 |
A multicenter, open-label study evaluating safety and clinical outcomes in children (1.4-7.5 years) with Hunter syndrome receiving idursulfase enzyme replacement therapy
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Giugliani, Roberto; Hwu, Wuh-Liang; Tylki-Szymanska, Anna; Whiteman, David A. H.; Pano, Arian; 胡務亮 |
| 國立臺灣大學 |
2009 |
A Multicentre Retrospective Cohort Study of Miglustat in Patients with Niemann-Pick Disease Type C
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胡務亮; HWU, WUH-LIANG |
| 國立臺灣大學 |
2009 |
A Multicentre Retrospective Survey of Miglustat in Patients with Niemann- Pick Type C Disease
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胡務亮; HWU, WUH-LIANG |
| 國立臺灣大學 |
2012 |
A Novel 3670-Base Pair Mitochondrial DNA Deletion Resulting in Multi-systemic Manifestations in a Child
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Liu, Hsin-Ming; Tsai, Li-Ping; Chien, Yin-Hsiu; Wu, Jia-Feng; Weng, Wen-Chin; Peng, Shinn-Forng; Wu, En-Ting; Huang, Pei-Hsin; Lee, Wang-Tso; Tsai, I-Jun; Hwu, Wuh-Liang; Lee, Ni-Chung; 胡務亮; 彭信逢; 吳恩婷; 吳嘉峰; 蔡宜蓉; 李旺祚; 李妮鍾; 簡穎秀; 黃佩欣; 翁妏謹 |
| 臺大學術典藏 |
2018-09-10T09:16:21Z |
A novel 3670-base pair mitochondrial DNA deletion resulting in multi-systemic manifestations in a child
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Liu, Hsin-Ming;Tsai, Li-Ping;Chien, Yin-Hsiu;Wu, Jia-Feng;Weng, Wen-Chin;Peng, Shinn-Forng;Wu, En-Ting;Huang, Pei-Hsin;Lee, Wang-Tso;Tsai, I-Jun;Hwu, Wuh-Liang;Lee, Ni-Chung; Liu, H.-M. and Tsai, L.-P. and Chien, Y.-H. and Wu, J.-F. and Weng, W.-C. and Peng, S.-F. and Wu, E.-T. and Huang, P.-H. and Lee, W.-T. and Tsai, I.-J. and Hwu, W.-L. and Lee, N.-C.; 胡務亮 ;彭信逢 ;吳恩婷 ;吳嘉峰 ;蔡宜蓉 ;李旺祚 ;李妮鍾 ;簡穎秀 ;黃佩欣 ;翁妏謹; NI-CHUNG LEE; Liu, Hsin-Ming; WANG-TSO LEE; Tsai, Li-Ping; WEN-CHIN WENG; Chien, Yin-Hsiu; JIA-FENG WU; Wu, Jia-Feng; YIN-HSIU CHIEN; Weng, Wen-Chin; Peng, Shinn-Forng; I-JUNG TSAI; Wu, En-Ting; WUH-LIANG HWU; Huang, Pei-Hsin; PEI-HSIN HUANG; EN-TING WU; Lee, Wang-Tso; Tsai, I-Jun; Hwu, Wuh-Liang; Lee, Ni-Chung; �^�H�{ |
| 國立臺灣大學 |
2008 |
A Promoter Sequence Variant of Znf750 Is Linked with Familial Psoriasis
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楊奇凡; 胡務亮; 楊麗珍; 鍾文宏; 簡穎秀; 范盛娟; 廖楓; 陳垣崇; YANG, CHI-FAN; HWU, WUH-LIANG; YANG, LI- CHENG; CHUNG, WEN-HUNG; CHIEN, YIN-HSIU; FANN, CATHY SHENG-JIUAN; LIAO, FANG; CHEN, YUAN- TSONG |
| 國立臺灣大學 |
2006 |
A Retrospective, Multinational, Multicenter Study on the Natural History of Infantile-Onset Pompe Disease
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胡務亮; HWU, WUH-LIANG |
| 國立臺灣大學 |
2007 |
A Review of Treatment of Pompe Disease in Infants
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簡穎秀; 胡務亮; CHIEN, YIN-HSIU; HWU, WUH-LIANG |
| 國立臺灣大學 |
2004 |
A Step-Wise Diagnosis of Fragile X Syndrome in Taiwan
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黃淵德; 蔣書娟; 曾慶誠; 劉敬萱; 簡穎秀; 胡務亮; HUANG, YUAN-TE; CHIANG, SHU-CHUAN; TZENG, CHING-CHERNG; LIU, CHING-HSUAN; CHIEN, YIN-HSIU; HWU, WUH-LIANG |
| 國立臺灣大學 |
2008 |
Acute Metabolic Decompensation and Sudden Death in Barth Syndrome: Report of a Family and a Literature Review
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顏廷聿; 胡務亮; 簡穎秀; 吳美環; 林銘泰; 曹龍彥; 謝武勳; 李妮鍾; YEN, TING-YU; HWU, WUH-LIANG; CHIEN, YIN- HSIU; WU, MEI-HWAN; LIN, MING-TAI; TSAO, LON-YEN; HSIEH, WU-SHIUN; LEE, NI-CHUNG |
| 國立臺灣大學 |
2005 |
Adenoviral Interneuronal Transportation after Retrograde Gene Transfer in Mice
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蔡力凱; 蔡明勳; 徐松錕; 胡務亮; 李鴻; TSAI, LI-KAI; TSAI, MING-SHIUN; SHYUE, SONG-KUN; HWU, WUH-LIANG; LI, HUNG |
| 國立臺灣大學 |
2003 |
Adrenoleukodystrophy Initially Diagnosed as Idiopathic Addison's Disease in Two Patients: The Importance of Early Testing
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胡務亮; 簡穎秀; 梁昭鉉; 李旺祚; 王本榮; 蔡文友; HWU, WUH-LIANG; CHIEN, YIN-HSIU; LIANG, CHAO-HSUAN; LEE, WANG-TSO; WANG, PEN-JUNG; TSAI, WEN-YU |
| 國立臺灣大學 |
2016 |
Advances in newborn screening for Pompe disease and resulting clinical outcomes
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Chien, Yin-Hsiu; Hwu, Wuh-Liang; Lee, Ni-Chung; 胡務亮; 李妮鍾; 簡穎秀 |
| 國立臺灣大學 |
2008 |
Alglucosidase Alfa in Infants and Children with Advanced Pompe Disease
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胡務亮; HWU, WUH-LIANG |
| 國立臺灣大學 |
2008 |
Alglucosidase Alfa in Infants and Children with Pompe Disease
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胡務亮; HWU, WUH-LIANG |
| 國立臺灣大學 |
2008 |
Alglucosidase Alfa in Infants and Children with Pompe Disease
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胡務亮; HWU, WUH-LIANG |
| 國立臺灣大學 |
2008 |
Alglucosidase Alfa in Infants and Children with Pompe Disease
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胡務亮; HWU, WUH-LIANG |
| 國立臺灣大學 |
2008 |
Alglucosidase Alpha in Infants and Children with Pompe's Disease
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胡務亮; HWU, WUH-LIANG |
Showing items 1-25 of 313 (13 Page(s) Totally)
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