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Showing items 261-285 of 326  (14 Page(s) Totally)
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Institution Date Title Author
國立臺灣大學 2003 A Founder Mutation (R254x) of Slc22a5 (Octn2) in Chinese Primary Carnitine Deficiency Patients 胡務亮; HWU, WUH-LIANG
國立臺灣大學 2003 Debate in Newborn Screening for Metabolic Disorders in Taiwan--a Voluntary Screening? Mandatory Screening? Or Both? 胡務亮; HWU, WUH-LIANG
國立臺灣大學 2003 Adrenoleukodystrophy Initially Diagnosed as Idiopathic Addison's Disease in Two Patients: The Importance of Early Testing 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 2003 Living-Related Liver Transplantation for Methylmalonic Acidemia: Report of One Case. 許瑞育; 簡穎秀; 朱紹盈; 呂立; 陳慧玲; 何明志; 李伯皇; 胡務亮; HSUI, JUI-YU; CHIEN, YIN-HSIU; CHU, SHAO-YIN; LU, FRANK L; CHEN, HUEY-LING; HO, MING-CHIH; LEE, PO-HUANG; HWU, WUH-LIANG
國立臺灣大學 2003 Phenotype and Genotype Analyses of Ornithine Transcarbamylase Deficiency in Taiwanese 黃淵德; 簡穎秀; 葉慧英; 林秀娟; 呂立; 周西平; 林京美; 蔣書娟; 胡務亮; HUANG, YUAN-TE; CHIEN, YIN-HSIU; YEH, HUI-YING; LIN, SHIO-JEAN; LU, FRANK L; CHOU, SHI-PING; LIN, JING-MEEI; CHIANG, SHU-CHUAN; HWU, WUH-LIANG
國立臺灣大學 2003 Pamidronate Treatment of Severe Osteogenesis Imperfecta in a Newborn Infant 簡穎秀; 朱紹盈; 許嘉琪; 胡務亮; CHIEN, YIN-HSIU; CHU, SHAO-YIN; HSU, CHIA-CHI; HWU, WUH-LIANG
國立臺灣大學 2003 Common Variable Immunodeficiency with Hypoglycemia, Kikuchi Lymphadenitis , and Hemiparesis in Two Siblings 簡穎秀; 胡務亮; 江伯倫; CHIEN, YIN-HSIU; HWU, WUH-LIANG; CHIANG, BOR-LUEN
國立臺灣大學 2002 Mucopolysaccharidosis Type I in Taiwan 胡務亮; HWU, WUH-LIANG
國立臺灣大學 2002 Neonatal Screening for Congenital Adrenal Hyperplasia in Taiwan: A Pilot Study 朱紹盈; 蔡文友; 陳麗新; 魏明麗; 簡穎秀; 胡務亮; CHU, SHAO-YIN; TSAI, WEN-YU; CHEN, LI- HSIN; WEI, MING-LEE; CHIEN, YIN-HSIU; HWU, WUH-LIANG
國立臺灣大學 2002 Spontaneous Chylothorax in a Case of Cardio-Facio-Cutaneous Syndrome 詹珮君; 邱顯清; 胡務亮; CHAN, PEI-CHUN; CHIU, HSIEN-CHING; HWU, WUH-LIANG
國立臺灣大學 2002 Clinical, 18f-Dopa Pet, and Genetic Analysis of an Ethnic Chinese Kindred with Early-Onset Parkinsonism and Parkin Gene Mutations 吳瑞美; 胡務亮; WU, RUEY-MEEI; HWU, WUH-LIANG
國立臺灣大學 2002 Enzyme Replacement Therapy with Imiglucerase in Taiwanese Patients with Type I Gaucher Disease 許嘉琪; 簡穎秀; 賴明陽; 胡務亮; HSU, CHIA-CHI; CHIEN, YIN-HSIU; LAI, MING-YANG; HWU, WUH-LIANG
國立臺灣大學 2002 Cockayne Syndrome in a Family 簡穎秀; 周弘傑; 胡務亮; CHIEN, YIN-HSIU; CHOU, HUNG-CHIEH; HWU, WUH-LIANG
國立臺灣大學 2002 Screening of Mitochondrial DNA Mutation in Subjects with Non-Syndromic Familial Hearing Impairment in Taiwan 簡穎秀; 胡務亮; CHIEN, YIN-HSIU; HWU, WUH-LIANG
國立臺灣大學 2002 An Infant with Heart Murmur and Dysmorphic Face 簡穎秀; 郭保麟; 胡務亮; CHIEN, YIN-HSIU; KUO, PAO-LIN; HWU, WUH-LIANG
國立臺灣大學 2002 Cranial Mr Spectroscopy of Tetrahydrobiopterin Deficiency 簡穎秀; 彭信逢; 胡務亮; CHIEN, YIN-HSIU; PENG, SHINN-FORNG; HWU, WUH-LIANG
國立臺灣大學 2002 Digeorge Sequence with Hypogammaglobulinemia: A Case Report 簡穎秀; 楊曜旭; 朱紹盈; 胡務亮; 江伯倫; CHIEN, YIN-HSIU; YANG, YAO-HSU; CHU, SHAO-YIN; HWU, WUH-LIANG; CHIANG, BOR-LUEN
國立臺灣大學 2001 Epileptic Seizures and Electroencephalographic Evolution in Genetic Leukodystrophies 王本榮; 胡務亮; 沈友仁; WANG, PEN-JUNG; HWU, WUH-LIANG; SHEN, YU- ZEN
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 Cloning of Dimethylglycine Dehydrogenase and a New Human Inborn Error of Metabolism, Dimethylglycine Dehydrogenase Deficiency Binzak, Barbara A.; Wevers, Ron A.; Moolenaar, Sytske H.; Lee, Yu-May; Hwu, Wuh-Liang; Poggi-Bach, Jo; Engelke, Udo F.H.; Hoard, Heidi M.; Vockley, Joseph G.; Vockley, Jerry
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 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

Showing items 261-285 of 326  (14 Page(s) Totally)
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