公開日期 | 標題 | 作者 | 來源出版物 | scopus | WOS | 全文 |
---|---|---|---|---|---|---|
1994 | Cytogenetic study of mentally retarded children in Taipei | Wang-Wuu S.; Lai Y.-M.; WUH-LIANG HWU ; Wang T.-R.; Wuu K.-D. | Journal of Biomedical Science | 1 | 0 | |
1999 | Dopa-responsive dystonia induced by a recessive GTP cyclohydrolase I mutation | WUH-LIANG HWU ; Wang P.-J.; Hsiao K.-J.; Wang T.-R.; Chiou Y.-W.; Lee Y.-M. | Human Genetics | 35 | 28 | |
1997 | Duplication of proteolipid protein gene: A possible major cause of Pelizaeus-Merzbacher disease | Wang P.-J.; WUH-LIANG HWU ; WANG-TSO LEE ; Wang T.-R.; Shen Y.-Z. | Pediatric Neurology | 32 | 27 | |
1999 | Erratum: Molecular genetic study of Pompe disease in Chinese patients in Taiwan (Human Mutation (1999) 13 (380-384)) | TSANG-MING KO ; WUH-LIANG HWU ; Lin Y.-W.; LI-HUI TSENG ; HSIAO-LIN HWA ; Wang T.-R.; Chuang S.- M.; Hayashi K. | Human Mutation | 0 | ||
1991 | Esterase D and retinoblastoma gene loci are tightly linked to Wilson's disease in Chinese pedigrees from Taiwan | LEE-MING CHUANG ; TONG-YUAN TAI ; Wang T.-R.; Chang Y.-C.; Chen K.-H.; Lin R.-S.; Lin B.J. | Human Genetics | 11 | 11 | |
1992 | Familial nephrogenic diabetes insipidus: report of two families | Lee J.-S.; WEN-YU TSAI ; Tsai W.-S.; YONG-KWEI TSAU ; Chen C.-H.; Wang T.-R. | Journal of the Formosan Medical Association = Taiwan yi zhi | 0 | 0 | |
1996 | Fibroblast growth factor receptor 3 (FGFR3) gene G1138A mutation in Chinese patients with achondroplasia | Wang T.-R.; Wang W.-P.; WUH-LIANG HWU ; Lee M.-L. | Human Mutation | 6 | ||
1995 | Glucose-6-phosphatase gene G327A mutation is common in Chinese patients with glycogen storage disease type Ia | Hwu W.-L.; Chuang S.-C.; Tsai L.-P.; MEI-HWEI CHANG ; Chuang S.-M.; Wang T.-R. | Human Molecular Genetics | 4 | 0 | |
1995 | Glucose-6-phosphatase gene G327A mutation is common in Chinese patients with glycogen storage disease type la | WUH-LIANG HWU ; Chuang S.-C.; Tsai L.-P.; MEI-HWEI CHANG ; Chuang S.-M.; Wang T.-R. | Human Molecular Genetics | 26 | 29 | |
2000 | Glucose-6-phosphatase gene mutations in Taiwan Chinese patients with glycogen storage disease type Ia | Chiang S.-C.; Lee Y.-M.; MEI-HWEI CHANG ; Wang T.-R.; TSANG-MING KO ; WUH-LIANG HWU | Journal of Human Genetics | 12 | 9 | |
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 |