| Issue Date | Title | Author(s) | Source | scopus | WOS | Fulltext/Archive link |
|---|---|---|---|---|---|---|
| 1999 | 3-hydroxy-3-methylglutaric aciduria presenting with Reye like syndrome: Report of one case | Lee C.; Tsai F.-J.; Wu J.-Y.; Peng C.-T.; Tsai C.-H.; WUH-LIANG HWU ; Wang T.-R.; Millington D.S. | Acta Paediatrica Taiwanica | 3 | 0 | |
| 1989 | Alkaptonuria in a Chinese baby | Wang T.-R.; WUH-LIANG HWU | Journal of Inherited Metabolic Disease | 1 | 1 | |
| 1999 | Allele distribution at the FMR1 locus in the general Chinese population | Chiang S.-C.; Lee Y.-M.; Wang T.-R.; WUH-LIANG HWU | Clinical Genetics | 19 | 14 | |
| 1996 | Arylsulfatase A pseudodeficiency in Chinese | WUH-LIANG HWU ; Tsai L.-P.; Wang W.-C.; Chuang S.-C.; Wang P.-J.; Wang T.-R. | Human Genetics | 6 | 4 | |
| 2020 | Author Correction: Hyperpolarization of the subthalamic nucleus alleviates hyperkinetic movement disorders (Scientific Reports, (2020), 10, 1, (8278), 10.1038/s41598-020-65211-w) | CHUN-HWEI TAI ; MING-KAI PAN ; SHENG-HONG TSENG ; Wang T.-R.; Chung-Chin Kuo | Scientific Reports | 0 | 0 | |
| 2000 | Carnitine transport defect presenting with hyperammonemia: Report of one case | WUH-LIANG HWU ; Chiang S.-C.; MEI-HWEI CHANG ; Wang T.-R. | Acta Paediatrica Taiwanica | 8 | 0 | |
| 1997 | CATCH 22: Deletion of locus 22Q11 in velocardiofacial syndrome, digeorge anomaly, and nonsyndromic conotruncal defects | Hou J.-W.; JOU-KOU WANG ; WEN-YU TSAI ; Chou C.-C.; Wang T.-R. | Journal of the Formosan Medical Association | 14 | 12 | |
| 2000 | Congenital contractural arachnodactyly (Beals syndrome) | Su P.-H.; Hou J.-W.; WUH-LIANG HWU ; MEI-HWAN WU ; JOU-KOU WANG ; Wang T.-R. | Acta Paediatrica Taiwanica | 13 | 0 | |
| 1995 | Corrigendum: Glucose-6-phosphatase gene G327A mutation is common in Chinese patients with glycogen storage disease type Ia (Human Molecular Genetics (1995) 4 (1095-1096)) | WUH-LIANG HWU ; Chuang S.-C.; Tsai L.-P.; MEI-HWEI CHANG ; Chang S.-M.; Wang T.-R. | Human Molecular Genetics | 1 | ||
| 2002 | Cranial MR spectroscopy of tetrahydrobiopterin deficiency | YIN-HSIU CHIEN ; STEVEN SHINN-FORNG PENG ; Wang T.-R.; WUH-LIANG HWU | American Journal of Neuroradiology | 10 | 8 | |
| 1996 | Cytochrome C oxidase deficiency in fibroblasts of a patient with mitochondrial encephalomyopathy | WANG-TSO LEE ; Wang P.-J.; Young C.; Wang T.-R.; Shen Y.-Z. | Journal of the Formosan Medical Association | 8 | 8 | |
| 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 | 31 | 27 | |
| 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 | 30 | 26 | |
| 1999 | Erratum: Molecular genetic study of Pompe disease in Chinese patients in Taiwan (Human Mutation (1999) 13 (380-384)) | Ko T.-M.; 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 ; Tai T.-Y.; Wang T.-R.; Chang Y.-C.; Chen K.-H.; Lin R.-S.; Lin B.J. | Human Genetics | 10 | 10 | |
| 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 | |||
| 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 |
