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臺灣學術機構典藏系統 (Taiwan Academic Institutional Repository, TAIR)
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"胡務亮"???jsp.browse.items-by-author.description???

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Showing items 261-285 of 313  (13 Page(s) Totally)
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Institution Date Title Author
國立臺灣大學 2001 A Chinese Adult Onset Type Ii Citrullinaemia Patient with 851del4/1638ins 23 Mutations in the Slc25a13 Gene 胡務亮; HWU, WUH-LIANG
國立臺灣大學 2001 Cloning of Dimethylglycine Dehydrogenase and a New Human Inborn Error of Metabolism, Dimethylglycine Dehydrogenase Deficiency 胡務亮; HWU, WUH-LIANG
國立臺灣大學 2001 Mri in a Case of Adult-Onset Citrullinemia 廖漢文; 胡務亮; LIU, HON-MAN; HWU, WUH-LIANG
國立臺灣大學 2001 Treatment and Outcome of Taiwanese Patients with 6- Pyruvoyltetrahydropterin Synthase Gene Mutations 簡穎秀; 王作仁; 胡務亮; CHIEN, YIN-HSIU; WANG, TSO-REN; HWU, WUH-LIANG
國立臺灣大學 2000 GTP CYCLOHYDROLASE I 缺乏症基因轉殖小鼠之遺傳及生化分析 胡務亮
國立臺灣大學 2000 Dopa-Responsive Dystonia Is Induced by a Dominant-Negative Mechanism 胡務亮; HWU, WUH-LIANG
國立臺灣大學 2000 Congenital Contractural Arachnodactyly (Beals Syndrome) 胡務亮; HWU, WUH-LIANG
國立臺灣大學 2000 Carnitine Transporter Defect Presenting with Hyperammonemia, Report of One Case 胡務亮; HWU, WUH-LIANG
國立臺灣大學 2000 Identification and Characterization of-3c-G Acceptor Splice Site Mutation in Human Alpha-L-Iduronidase Associated with Mucopolysaccharidosis Type Ih/S 王作仁; 胡務亮; WANG, TSO-REN; HWU, WUH-LIANG
國立臺灣大學 1999 GTP-CYCLOHYDROLASE I 缺乏症轉殖小鼠之建立 胡務亮
國立臺灣大學 1999 早老症粒線體基因突變之研究 胡務亮
國立臺灣大學 1999 Molecular Diagnosis of Apert Syndrome in Chinese Patients 胡務亮; HWU, WUH-LIANG
國立臺灣大學 1999 Dopa-Responsive Dystonia Induced by a Recessive Gtp Cyclohydrolase I 胡務亮; HWU, WUH-LIANG
國立臺灣大學 1999 Millington Ds (1999) 3-Hydroxy-3-Methylglutaric Aciduria Presenting with Reye Like Syndrome: Report of One Case 胡務亮; HWU, WUH-LIANG
國立臺灣大學 1999 Hypercalcaemia in Glycogen Storage Disease Type Ia : A Case with R83h and 341delg Mutations 胡務亮; 張美惠; HWU, WUH-LIANG; CHANG, MEI-HWEI
國立臺灣大學 1999 Allele Distribution at the Fmr1 Locus in the General Chinese Population 王作仁; 胡務亮; WANG, TSO-REN; HWU, WUH-LIANG
國立臺灣大學 1999 Niemann-Pick Disease Type C (a Cellular Cholesterol Lipidosis) Treated by Bone Marrow Transplantation 徐玉山; 胡務亮; 盧孟佑; 陳榮隆; 林東燦; 彭信逢; 林凱信; HSU, Y-S; HWU, WUH-LIANG; LU, MENG-YAO; CHEN, RONG-LONG; LIN, DONG-TSAMN; PENG, SHINN-FORNG; LIN, KAI-HSIN
國立臺灣大學 1999 Homozygous 341delg/101x of Gulcose-6-Phosphatase(G6pt) Gene Causes Glycogen Storage Disease Type Ia (Von Gierke Disease) in a Chinese Patient 柯滄銘; 胡務亮; KO, TSANG-MING; HWU, WUH-LIANG
國立臺灣大學 1999 Molecular Genetic Study of Pompe Disease in Chinese Patients in Taiwan 柯滄銘; 胡務亮; 林玉婉; 曾麗慧; 華筱玲; 王作仁; 莊壽洺; KO, TSANG-MING; HWU, WUH-LIANG; LIN, YU-WAN; TSENG, LI-HUI; HWA, HSIAO-LIN; WANG, TSO-REN; CHUANG, SOU-MING
國立臺灣大學 1999 Neonatal type of nonketotic hyperglycinemia 呂立; 王本榮; 胡務亮; 鄒國英; 王作仁; LU, FRANK L; WANG, PEN-JUNG; HWU, WUH-LIANG; YAU KOU-INN, TSOU; WANG, TSO-REN
國立臺灣大學 1998 以抗體阻斷纖維芽細胞生長激素受體活化之研究 胡務亮
國立臺灣大學 1998 Mucopolysaccharidosis Type Ii (Hunter's Syndrome) in Taiwan 胡務亮; HWU, WUH-LIANG
國立臺灣大學 1998 Linkage Disequilibrium and Linkage Analysis of the Glucose-6-Phosphatase Gene 胡務亮; HWU, WUH-LIANG
國立臺灣大學 1998 The Controversy Regaring Criteria for Early Myoclonic Encephalopathy 王本榮; 胡務亮; 楊千立; 鄒國英; 沈友仁; 李旺祚; WANG, PEN-JUNG; HWU, WUH-LIANG; YOUNG, CHAINLLIE; YAU, KOU-INN, TSOU; SHEN, YU-ZEN; LEE, WANG-TSO
國立臺灣大學 1998 Human Alpha-L-Iduronidase (Idua) Gene: Apparent Recombination in Intron 2 by Haplotype Analysis in a Taiwanese Population 胡務亮; HWU, WUH-LIANG

Showing items 261-285 of 313  (13 Page(s) Totally)
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