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Molecular Neurobiology|September 13, 2017
A Neuron-Specific Gene Therapy Relieves Motor Deficits in Pompe Disease MiceNi-Chung Lee, Wuh-Liang Hwu, Shin-Ichi Muramatsu, et al.
JAMA|August 12, 2004
Feasibility of eliminating ocular Chlamydia trachomatis with repeat mass antibiotic treatmentsMuluken Melese, Jaya Devi Chidambaram, Wondu Alemayehu, et al.
Science Translational Medicine|May 18, 2012
Gene therapy for aromatic L-amino acid decarboxylase deficiencyWuh-Liang Hwu, Shin-ichi Muramatsu, Sheng-Hong Tseng, et al.
Archiv Der Pharmazie|September 30, 2011
Synthesis, telomerase evaluation and anti-proliferative studies on various series of diaminoanthraquinone-linked aminoacyl residue derivativesFong-Chun Huang, Kuo-Feng Huang, Ruey-Hui Chen, et al.
European Journal of Medicinal Chemistry|September 21, 2013
Structure-based design, synthesis and biological evaluation of novel anthra[1,2-d]imidazole-6,11-dione homologues as potential antitumor agentsTsung-Chih Chen, Dah-Shyong Yu, Kuo-Feng Huang, et al.
The Journal of Pediatrics|December 4, 2014
Long-term prognosis of patients with infantile-onset Pompe disease diagnosed by newborn screening and treated since birthYin-Hsiu Chien, Ni-Chung Lee, Chun-An Chen, et al.
Orphanet Journal of Rare Diseases|February 5, 2020
Newborn screening for Morquio disease and other lysosomal storage diseases: results from the 8-plex assay for 70,000 newbornsYin-Hsiu Chien, Ni-Chung Lee, Pin-Wen Chen, et al.
Clinical Neurology and Neurosurgery|October 20, 2020
Clinical characteristics of ataxia-telangiectasia presenting dystonia as a main manifestationMinkyeong Kim, Ah Reum Kim, Jongkyu Park, et al.
Molecular Pharmaceutics|October 18, 2025
Altered Abundance of Barrier-Related Proteins in Brain Microvascular Endothelial Cells of the GL261 Mouse Model of GlioblastomaLiam M Koehn, Diana Cao, Joel R Steele, et al.
Medicine|May 9, 2020
Comprehensive analysis of mutations of renal cell carcinoma in an autosomal dominant polycystic kidney disease patientKwang Eon Shim, Chung Lee, Jin Up Kim, et al.
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