公開日期 | 標題 | 作者 | 來源出版物 | scopus | WOS | 全文 |
---|---|---|---|---|---|---|
2008 | Early detection of pompe disease by newborn screening is feasible: Results from the Taiwan screening program | YIN-HSIU CHIEN ; Chiang S.-C.; Zhang X.K.; Keutzer J.; NI-CHUNG LEE ; Huang A.-C.; CHUN-AN CHEN ; MEI-HWAN WU ; PEI-HSIN HUANG ; Tsai F.-J.; Chen Y.-T.; WUH-LIANG HWU | Pediatrics | 207 | 178 | |
2007 | Efficacy and safety of aripiprazole in the acute treatment of schizophrenia in Chinese patients with risperidone as an active control: A randomized trial | Chan H.-Y.; Lin W.-W.; Lin S.-K.; TZUNG-JENG HWANG ; Su T.-P.T.; Chiang S.-C.; HAI-GWO HWU | Journal of Clinical Psychiatry | 67 | 63 | |
2019 | An eight degree-of-freedom robotic endoscope holder | Chiang S.-C.; Huang Y.-C.; Shen K.; Yen J.-Y.; JIA-YUSH YEN | 2018 International Automatic Control Conference | |||
2011 | Elevation of urinary globotriaosylceramide (GL3) in infants with Fabry disease | YIN-HSIU CHIEN ; Olivova P.; Zhang X.K.; Chiang S.-C.; NI-CHUNG LEE ; Keutzer J.; WUH-LIANG HWU | Molecular Genetics and Metabolism | 10 | 9 | |
2018 | Enterobius vermicularis infection mimicking strongyloidiasis: A case report | Chou Y.-H.; Chiang S.-C.; Wei P.-F.; Chen S.-S.; KUAN-YIN LIN ; CHIEN-CHING HUNG | Journal of Microbiology, Immunology and Infection | 0 | 0 | |
2003 | Gene symbol: OTC: Disease: Ornithine carbamoyltransferase deficiency | WUH-LIANG HWU ; Huang Y.-T.; YIN-HSIU CHIEN ; Yeh H.-Y.; Lul F.; Chou S.-P.; Lin J.-M.; Chiang S.-C. | Human Genetics | 3 | 0 | |
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 | |
2006 | Heroin use among youths incarcerated for illicit drug use: Psychosocial environment, substance use history, psychiatric comorbidity, and route of administration | Chiang S.-C.; Chen S.-J.; Sun H.-J.; Chan H.-Y.; WEI J. CHEN | American Journal on Addictions | 22 | 22 | |
2011 | Human Pompe disease-induced pluripotent stem cells for pathogenesis modeling, drug testing and disease marker identification | HSIANG-PO HUANG ; Chen P.-H.; WUH-LIANG HWU ; Chuang C.-Y.; YIN-HSIU CHIEN ; Stone L.; CHUNG-LIANG CHIEN ; Li L.-T.; Chiang S.-C.; HSIN-FU CHEN ; HONG-NERNG HO ; Chen C.-H.; Kuo H.-C. | Human Molecular Genetics | 111 | 105 | |
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 | |
2022 | Improved diagnosis of citrin deficiency by newborn screening using a molecular second-tier test | HUI-AN CHEN ; Hsu R.-H.; Chen Y.-H.; Hsu L.-W.; Chiang S.-C.; NI-CHUNG LEE ; WUH-LIANG HWU ; Chiu P.-C.; YIN-HSIU CHIEN | Molecular Genetics and Metabolism | 8 | 5 | |
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 | |
2011 | Justifying the high prevalence of microalbuminuria for type 2 diabetic patients in Taiwan with conditional probability approach-a DEMAND II Study | Chiang S.-C.; Lee J.-K.; Chen C.-H.; LEE-MING CHUANG ; Tsan K.-W.; Sheu W.H.H.; Wu D.-A.; Wu T.-J.; Lin K.-C.; Juang J.-H.; CHIH-YUAN WANG ; Ho L.-T. | Journal of the Chinese Medical Association | 8 | 7 | |
2005 | KIF21A gene c.2860C>T mutation in congenital fibrosis of extraocular muscles type 1 and 3 | Lin L.-K.; YIN-HSIU CHIEN ; Wu J.-Y.; Wang A.-H.; Chiang S.-C.; WUH-LIANG HWU | Molecular Vision | 21 | 17 | |
2007 | Lack of mutations in spinocerebellar ataxia type 2 and 3 genes in a Taiwanese (Ethnic Chinese) cohort of familial and early-onset parkinsonism | CHIN-HSIEN LIN ; WUH-LIANG HWU ; Chiang S.-C.; CHUN-HWEI TAI ; RUEY-MEEI WU | American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics | 8 | 7 | |
2013 | Lyso-globotriaosylsphingosine (lyso-Gb3) levels in neonates and adults with the Fabry disease later-onset GLA IVS4+919G>A mutation | YIN-HSIU CHIEN ; Bodamer O.A.; Chiang S.-C.; Mascher H.; Hung C.; WUH-LIANG HWU | Journal of Inherited Metabolic Disease | 18 | 16 | |
2005 | Mapping of psoriasis to 17q terminus | WUH-LIANG HWU ; Yang C.-F.; Fann C.S.J.; Chen C.-L.; TSEN-FANG TSAI ; Chein Y.-H.; Chiang S.-C.; Chen C.-H.; Hung S.-I.; Wu J.-Y.; Chen Y.-T. | Journal of Medical Genetics | 45 | 39 | |
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 | |
2012 | A nation-wide analysis of venous thromboembolism in 497,180 cancer patients with the development and validation of a risk-stratification scoring system | Yu Y.-B.; Gau J.-P.; Liu C.-Y.; Yang M.-H.; Chiang S.-C.; Hsu H.-C.; Hong Y.-C.; Hsiao L.-T.; Liu J.-H.; Chiou T.-J.; Chen P.-M.; TZONG-SHYUAN LEE ; Chou L.-F.; Tzeng C.-H.; Chen T.-J. | Thrombosis and Haemostasis | 89 | 89 | |
2013 | Newborn screening for citrin deficiency and carnitine uptake defect using second-tier molecular tests | Wang L.-Y.; Chen N.-I.; Chen P.-W.; Chiang S.-C.; WUH-LIANG HWU ; NI-CHUNG LEE ; YIN-HSIU CHIEN | BMC Medical Genetics | 26 | 24 |