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  1. NTU Scholars
  2. Research Outputs

Browsing by Author 胡務亮


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Showing results 1 to 20 of 43  next >
Issue DateTitleAuthor(s)SourcescopusWOSFulltext/Archive link
1989Alkaptonuria in a Chinese Baby Case ReportWang, T. R.; 胡務亮; Hwu, Wuh-LiangJournal of Inherited Metabolic Disease
1994Case Report:Fucosidosis in a Chinese Girl胡務亮; Chuang, S. C.; Wang, W. C.; Wang, T. R.; Hwu, Wuh-Liang; Chuang, S. C.; Wang, T. R.Journal of Inherited Metabolic Disease
2011Citrin缺乏症在新生兒篩檢的基因突變研究王里勻; Wang, Li-Yun
1991A Clinical Observation in Achondroplasia胡務亮; Wang, T. R.; Hwu, Wuh-Liang; Wang, T. R.Journal of Acta Paediatrica Sinica
1991A Clinical Study in Intravenous Immunoglobulin Therapy for Childhood Idiopathic Chromobocytopenic PurpuraLin, D. T.; 胡務亮; Lin, K. H.; Lin, K. S.; Lin, D. T.; Hwu, Wuh-Liang; Lin, K. S.Journal of the Formosan Medical Association
1991COLOCALIZATION IN PERICENTRAL HEPATOCYTES IN ADULT MICE AND SIMILARITY IN DEVELOPMENTAL EXPRESSION PATTERN OF ORNITHINE AMINOTRANSFERASE AND GLUTAMINE SYNTHETASE IN mRNA顧泉; 胡務亮; KUO, FRANK C; HWU, WUH-LIANG; VALLE DPROCEEDINGS OF THE
1991Colocalization in Pericentral Hepatocytes in Adult Mice and Similarity in Developmental Expression Pattern of Ornithine Aminotransferase and Glutamine Synthetase mRNAKuo, F. C.; 胡務亮; Valle, D.; Darnell, J. E.; Hwu, Wuh-Liang; Valle, D.; Darnell, J. E.Proceedings of the National Academy of Sciences of the United States of America
1989Current Status of Detecting Fragible-X Syndrome Using Molecular Biology Techniques at the National Taiwan University HospitalWang, Tso-Ren; Hwu, Wuh-Liang; Wang, Tso-Ren; 胡務亮1992 San Diego Conference on Nucleic Acids:Genetic Recognition 
1995Cytogenetic Study of Mentally Retarded Children in TaipeiSheng, W. W.; Lai, Y. M.; 胡務亮; Wang, T. R.; Wuu, K. I.; Lai, Y. M.; Hwu, Wuh-Liang; Wang, T. R.; Wuu, K. I.Biomedical Science
1994The Diagnosis of I-Cell Disease胡務亮; Chuang, S. C.; Wang, W. C.; Wang, T. R.; Hwu, Wuh-Liang; Wang, W. C.; Wang, T. R.Journal of Acta Paediatrica Sinica
1994Diagnosis of I-Cell Disease胡務亮; 蔣書娟; 王文娟; 王作仁; HWU, WUH-LIANG; CHIANG, SHU-CHUAN; WANG, WEN-CHUAN; WANG, TSO-REN中華民國小兒科醫學會雜誌,v.35
1992DNA Fingerprinting in the Chinese with an Oligonucleotide Probe (GTG)林凱信; 陳榮隆; Wang, Tso-Renmin; Su, Ih-Jen; Lin, Kuo-Sin; 胡務亮; Su, Ih-Jen; Lin, Kuo-Sin; Hwu, Wuh-LiangJournal of the Formosan Medical Association
1993Fragile X Mental Retardation:A Combination of Cytogenetic and Molecular Approaches with More Stress on DNA AnalysisWang, T. R.; 胡務亮; Hou, J. W.; Chou, S. P.; Liu, C. H.; Hwu, Wuh-Liang; Hou, J. W.; Chou, S. P.Journal of Acta Paediatrica Sinica
1995Glucose-6-phosphate Gene G327 is a Common Mutation in Chinese Patients with Glycogen Storage Disease Type I胡務亮; Wang, W. C.; Cheng, J. R.; Chuang, S. C.; Tsai, L. P.; Wang, T. R.; Hwu, Wuh-Liang; Wang, W. C.; Chuang, S. C.; Tsai, L. P.; Wang, T. R.Human Molecular Genetics
2001GTP CYCLOHYDROLASE I 基因轉殖小鼠啟動子表現及表現型分析胡務亮
2002GTP Cyclohydrolase I 突變及Splicing之分子結構機轉(1/3)胡務亮
2003GTP Cyclohydrolase I 突變及Splicing之分子結構機轉(2/3)胡務亮
2004GTP Cyclohydrolase I 突變及Splicing之分子結構機轉(3/3)胡務亮Biochemical and Biophysical Research Communications (306),937–942 
1989Hereditary Progressive Dystonia with Marked Diurnal Fluctuation:Report of A Case王本榮; Shen, Y. Z.; 胡務亮; Wang, Pen-Jung; Shen, Y. Z.; Hwu, Wuh-LiangJournal of Acta Paediatrica Sinica
1989Hereditary Progrressive Dystonia with Marked Diurnal Fluctuation, Report of a Case胡務亮; Wang, P. J.; Shen, Y. Z.; Hwu, Wuh-Liang; Wang, P. J.Journal of Acta Paediatrica Sinica
Showing results 1 to 20 of 43  next >

臺大位居世界頂尖大學之列,為永久珍藏及向國際展現本校豐碩的研究成果及學術能量,圖書館整合機構典藏(NTUR)與學術庫(AH)不同功能平台,成為臺大學術典藏NTU scholars。期能整合研究能量、促進交流合作、保存學術產出、推廣研究成果。

To permanently archive and promote researcher profiles and scholarly works, Library integrates the services of “NTU Repository” with “Academic Hub” to form NTU Scholars.

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開放取用是從使用者角度提升資訊取用性的社會運動,應用在學術研究上是透過將研究著作公開供使用者自由取閱,以促進學術傳播及因應期刊訂購費用逐年攀升。同時可加速研究發展、提升研究影響力,NTU Scholars即為本校的開放取用典藏(OA Archive)平台。(點選深入了解OA)

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