公開日期 | 標題 | 作者 | 來源出版物 | scopus | WOS | 全文 |
---|---|---|---|---|---|---|
1996 | High frequency of two mutations in codon 778 in exon 8 of the ATP7B gene in Taiwanese families with Wilson disease | LEE-MING CHUANG ; HUEY-PEIR WU ; Jang M.-H.; Wang T.-R.; Sue W.-C.; Lin B.J.; Cox D.W.; TONG-YUAN TAI | Journal of Medical Genetics | 76 | 65 | |
1996 | Homocystinuria presenting as fatal common carotid artery occlusion | CHUN-YI LU ; Hou J.-W.; Wang P.-J.; Chiu H.-H.; Wang T.-R. | Pediatric Neurology | 14 | 15 | |
1998 | Human α-L-iduronidase (IDUA) gene: Apparent recombination in intron 2 by haplotype analysis in a Taiwanese population | Lee-Chen G.-J.; Wang T.-R.; WUH-LIANG HWU ; Day K.-R.; Wang C.-K. | Journal of the Formosan Medical Association | 2 | 2 | |
1999 | Hypercalcaemia in glycogen storage disease type Ia: A case with R83H and 341delG mutations | WUH-LIANG HWU ; Chiang S.-C.; Huang S.-F.; MEI-HWEI CHANG ; Wen W.-H.; Wang T.-R. | Journal of Inherited Metabolic Disease | 8 | 5 | |
2020 | Hyperpolarization of the subthalamic nucleus alleviates hyperkinetic movement disorders | CHUN-HWEI TAI ; MING-KAI PAN ; SHENG-HONG TSENG ; Wang T.-R.; Chung-Chin Kuo | Scientific Reports | 7 | 7 | |
1996 | Kleine-Levin syndrome in a boy with Prader-Willi syndrome | SUSAN SHUR-FEN GAU ; Soong W.-T.; HON-MAN LIU ; Hou J.-W.; WEN-YU TSAI ; YEN-NAN CHIU ; Yeh Y.-C.; Wang P.-J.; Wang T.-R. | Sleep | 27 | 18 | |
1997 | Microdeletion of chromosomal region 7q11.23 in Willias syndrome | Hou J.-W.; JOU-KOU WANG ; Wang T.-R. | Journal of the Formosan Medical Association | 4 | 3 | |
1999 | Molecular genetic study of Pompe disease in Chinese patients in Taiwan | TSANG-MING KO ; WUH-LIANG HWU ; Lin Y.-W.; LI-HUI TSENG ; HSIAO-LIN HWA ; Wang T.-R.; Chuang S.-M. | Human Mutation | 64 | ||
1998 | Mucopolysaccharidosis type II (Hunter's syndrome) in Taiwan | Su P.-H.; WUH-LIANG HWU ; Chiang S.-C.; Chiu P.-C.; Lin S.-J.; Shu S.-G.; Wang T.-R. | Journal of the Formosan Medical Association | 1 | 1 | |
1999 | Neonatal type of nonketotic hyperglycinemia | FRANK LEIGH LU ; Wang P.-J.; WUH-LIANG HWU ; Tsou Yau K.-I.; Wang T.-R. | Pediatric Neurology | 38 | 27 | |
1997 | Ornithine transcarbamylase deficiency | Yeh S.-J.; WUH-LIANG HWU ; Tsai W.-S.; Wu T.-J.; Tuchman M.; Wang T.-R. | Journal of the Formosan Medical Association | 2 | 3 | |
2004 | Phenylalanine hydroxylase deficiency: Intelligence of patients after early dietary treatment | YIN-HSIU CHIEN ; Chiang S.-C.; Huang A.; Lin J.-M.; YEN-NAN CHIU ; Chou S.-P.; Wang T.-R.; WUH-LIANG HWU | Acta Paediatrica Taiwanica | 4 | 0 | |
1998 | Recommendations for management of severe enterovirus infection in Taiwan | PING-ING LEE ; CHIN-YUN LEE ; Wang T.-R. | Acta Paediatrica Sinica | |||
2001 | Treatment and outcome of Taiwanese patients with 6-pyruvoyltetrahydropterin synthase gene mutations | YIN-HSIU CHIEN ; Chiang S.-C.; Huang A.; Lin J.-M.; YEN-NAN CHIU ; Chou S.-P.; Chu S.-Y.; Wang T.-R.; WUH-LIANG HWU | Journal of Inherited Metabolic Disease | 32 | 20 | |
1997 | Tricho-rhino-phalangeal syndrome type II associated with epiglottic aplasia and congenital nephrotic syndrome | FRANK LEIGH LU ; Hou J.-W.; Tsai W.-S.; Teng R.-J.; Yau K.-I.T.; Wang T.-R. | Journal of the Formosan Medical Association | 10 | 8 | |
1998 | Two common mutations 934C to G and 937C to G of fibroblast growth factor receptor 2 (FGFR2) gene in Chinese patients with apert syndrome | Tsai F.-J.; WUH-LIANG HWU ; Lin S.-P.; Chang J.-G.; Wang T.-R.; Tsai C.-H. | Human Mutation | 2 | 0 |