公開日期 | 標題 | 作者 | 來源出版物 | scopus | WOS | 全文 |
---|---|---|---|---|---|---|
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 | |
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 | ||
2015 | Elevated postvoid residual urine volume predicting recurrence of urinary tract infections in toilet-trained children | SHANG-JEN CHANG ; Tsai L.-P.; Hsu C.-K.; Yang S.S. | Pediatric Nephrology | 24 | 22 | |
2018 | Functional independence of Taiwanese children with Prader–Willi syndrome | Lee C.-L.; Lin H.-Y.; Tsai L.-P.; Chiu H.-C.; Tu R.-Y.; Huang Y.-H.; YIN-HSIU CHIEN ; NI-CHUNG LEE ; Niu D.-M.; Chao M.-C.; Tsai F.-J.; Chou Y.-Y.; Chuang C.-K.; Lin S.-P. | American Journal of Medical Genetics, Part A | 1 | 2 | |
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 | |
2021 | High prevalence of lower urinary tract dysfunction in patients with Prader–Willi syndrome | Chao T.-C.; Yang S.S.D.; SHANG-JEN CHANG ; Tsai L.-P. | Neurourology and Urodynamics | 1 | 1 | |
2015 | Incidence of severe combined immunodeficiency through newborn screening in a Chinese population | YIN-HSIU CHIEN ; Chiang S.-C.; Chang K.-L.; HSIN-HUI YU ; Lee W.-I.; Tsai L.-P.; Hsu L.-W.; Hu M.-H.; WUH-LIANG HWU | Journal of the Formosan Medical Association | 56 | 37 | |
2009 | Incidence of the Mucopolysaccharidoses in Taiwan, 1984-2004 | Lin H.-Y.; Lin S.-P.; Chuang C.-K.; Niu D.-M.; Chen M.-R.; Tsai F.-J.; Chao M.-C.; Chiu P.-C.; Lin S.-J.; Tsai L.-P.; WUH-LIANG HWU ; Lin J.-L. | American Journal of Medical Genetics, Part A | 155 | 139 | |
2012 | A novel 3670-base pair mitochondrial DNA deletion resulting in multi-systemic manifestations in a child | Liu H.-M.; Tsai L.-P.; YIN-HSIU CHIEN ; JIA-FENG WU ; WEN-CHIN WENG ; STEVEN SHINN-FORNG PENG ; EN-TING WU ; PEI-HSIN HUANG ; WANG-TSO LEE ; I-JUNG TSAI ; WUH-LIANG HWU ; NI-CHUNG LEE | Pediatrics and Neonatology | 10 | 9 | |
2005 | Prevalence of the FMR1 mutation in Taiwan assessed by large-scale screening of newborn boys and analysis of DXS548-FRAXAC1 haplotype | Tzeng C.-C.; Tsai L.-P.; WUH-LIANG HWU ; Lin S.-J.; Chao M.-C.; Jong Y.-J.; Chu S.-Y.; Chao W.-C.; Lu C.-L. | American Journal of Medical Genetics | 56 | 51 |