公開日期 | 標題 | 作者 | 來源出版物 | scopus | WOS | 全文 |
2002 | Gene Analysis in Huntington's Disease | WUH-LIANG HWU ; Shu-Chuan Chiang | 台灣醫學 | | 0 | |
2008 | Gene symbol: GCDH. Disease: Glutaricacidaemia I. | Lin W.D.; WUH-LIANG HWU ; Wang C.H.; Chen C.P.; Tsai F.J. | Human genetics | 1 | 0 | |
2008 | Gene symbol: GLA. Disease: Fabry disease. | Lin W.D.; WUH-LIANG HWU ; Liu S.C.; Tsai F.J. | Human genetics | 1 | 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 | |
2004 | Gene symbol: WAS. Disease: Wiskott-Aldrich syndrome. | YIN-HSIU CHIEN ; WUH-LIANG HWU ; Ariga T. | Human genetics | 0 | 0 | |
2004 | Gene symbol: WAS. Disease: Wiskott-Aldrich syndrome. | YIN-HSIU CHIEN ; WUH-LIANG HWU ; Ariga T. | Human genetics | 1 | 0 | |
2024 | Gene therapy corrects the neurological deficits of mice with sialidosis | WUH-LIANG HWU ; Chang, Karine; Liu, Yu-Han; Wang, Hao-Chun; NI-CHUNG LEE ; YIN-HSIU CHIEN | Gene therapy | | | |
2012 | Gene therapy for aromatic L-amino acid decarboxylase deficiency | WUH-LIANG HWU ; Muramatsu S.-I.; SHENG-HONG TSENG ; KAI-YUAN TZEN ; NI-CHUNG LEE ; YIN-HSIU CHIEN ; Snyder R.O.; Byrne B.J.; CHUN-HWEI TAI ; RUEY-MEEI WU | Science Translational Medicine | 188 | 170 | |
2019 | Gene therapy improves brain white matter in aromatic l-amino acid decarboxylase deficiency | Tseng C.-H.; YIN-HSIU CHIEN ; NI-CHUNG LEE ; Hsu Y.-C.; STEVEN SHINN-FORNG PENG ; WEN-YIH TSENG ; WUH-LIANG HWU | Annals of Neurology | 20 | 18 | |
2021 | Gene therapy in the putamen for curing AADC deficiency and Parkinson's disease | WUH-LIANG HWU ; Kiening, Karl; Anselm, Irina; Compton, David R; Nakajima, Takeshi; Opladen, Thomas; Pearl, Phillip L; Roubertie, Agathe; Roujeau, Thomas; Muramatsu, Shin-Ichi | EMBO Molecular Medicine | 17 | 17 | |
2017 | Gene therapy with modified U1 small nuclear RNA | WUH-LIANG HWU ; Lee Y.-M.; NI-CHUNG LEE | Expert Review of Endocrinology and Metabolism | 3 | 0 | |
2008 | Genetic analysis of mucopolysaccharidosis type VI in Taiwanese patients | Lin W.-D.; Lin S.-P.; Wang C.-H.; WUH-LIANG HWU ; Chuang C.-K.; Lin S.-J.; Tsai Y.; Chen C.-P.; Tsai F.-J. | Clinica Chimica Acta | 24 | 21 | |
2017 | Genetic epidemiological study doesn't support GLA IVS4?+?919G?>?A variant is a significant mutation in Fabry disease | Chiang H.-L.; Wang N.H.-H.; Song I.-W.; Chang C.-P.; Wen M.-S.; YIN-HSIU CHIEN ; WUH-LIANG HWU ; Tsai F.-J.; Chen Y.-T.; Wu J.-Y. | Molecular Genetics and Metabolism | 8 | 7 | |
2010 | Genetic heterozygosity and pseudodeficiency in the Pompe disease newborn screening pilot program | Labrousse P.; YIN-HSIU CHIEN ; Pomponio R.J.; Keutzer J.; NI-CHUNG LEE ; Akmaev V.R.; Scholl T.; WUH-LIANG HWU | Molecular Genetics and Metabolism | 92 | 79 | |
2007 | The genetics of atopic dermatitis | YIN-HSIU CHIEN ; WUH-LIANG HWU ; BOR-LUEN CHIANG | Clinical Reviews in Allergy and Immunology | 29 | 25 | |
2012 | Genome-wide gene expression analysis implicates the immune response and lymphangiogenesis in the pathogenesis of fetal chylothorax | Yeang C.-H.; Ma G.-C.; JIN-CHUNG SHIH ; YU-SHIH YANG ; Chen C.-P.; Chang S.-P.; Wu S.-H.; Liu C.-S.; Kuo S.-J.; HUNG-CHIEH CHOU ; WUH-LIANG HWU ; Cameron A.D.; Ginsberg N.A.; Lin Y.-S.; Chen M. | PLoS ONE | 7 | 5 | |
2019 | Genotypic and phenotypic correlations of biotinidase deficiency in the Chinese population | Hsu R.-H.; YIN-HSIU CHIEN ; WUH-LIANG HWU ; Chang I.-F.; Ho H.-C.; Chou S.-P.; Huang T.-M.; NI-CHUNG LEE | Orphanet Journal of Rare Diseases | 16 | 14 | |
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 | |
2009 | Glycogen Storage Disease Type Ib: The First Case in Taiwan | Hsiao H.-J.; HSIU-HAO CHANG ; WUH-LIANG HWU ; Lam C.-W.; NI-CHUNG LEE ; YIN-HSIU CHIEN | Pediatrics and Neonatology | 4 | 3 | |