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Molecular Therapy : the Journal of the American Society of Gene Therapy|September 22, 2006
Enhanced efficacy of an AAV vector encoding chimeric, highly secreted acid alpha-glucosidase in glycogen storage disease type IIBaodong Sun, Haoyue Zhang, Daniel K Benjamin, et al.
Molecular Therapy. Methods & Clinical Development|January 8, 2020
Comparisons of Infant and Adult Mice Reveal Age Effects for Liver Depot Gene Therapy in Pompe DiseaseSang-Oh Han, Songtao Li, Angela McCall, et al.
Molecular Genetics and Metabolism|December 5, 2025
Focused ultrasound delivery of enzyme replacement therapy to the brain of Gaa-/- Pompe disease micePaige Nowlin, Yongzhi Zhang, Amanda Chrisholm, et al.
Molecular Genetics and Metabolism|May 19, 2020
A comprehensive testing algorithm for the diagnosis of Fabry disease in males and femalesAshlee R Stiles, Haoyue Zhang, Jian Dai, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 17, 2006
Comparison of maltose and acarbose as inhibitors of maltase-glucoamylase activity in assaying acid alpha-glucosidase activity in dried blood spots for the diagnosis of infantile Pompe diseaseHaoyue Zhang, Helmut Kallwass, Sarah P Young, et al.
Molecular Genetics and Metabolism|September 27, 2025
Quantitative muscle ultrasound as a window into disease progression in infantile-onset Pompe diseaseNeelam Makhijani, Myriam Boueri, Bijan Abar, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|May 23, 2020
Comparison of dermatan sulfate and heparan sulfate concentrations in serum, cerebrospinal fluid and urine in patients with mucopolysaccharidosis type I receiving intravenous and intrathecal enzyme replacement therapyHaoyue Zhang, Patricia I Dickson, Ashlee R Stiles, et al.
Annals of Epidemiology|October 16, 2012
Systemic oxidative stress, as measured by urinary allantoin and F(2)-isoprostanes, is not increased in Down syndromeAdviye A Tolun, Peter M Scarbrough, Haoyue Zhang, et al.
Basic Research in Cardiology|July 11, 2024
The attenuated hepatic clearance of propionate increases cardiac oxidative stress in propionic acidemiaYou Wang, Suhong Zhu, Wentao He, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 7, 2020
Higher dosing of alglucosidase alfa improves outcomes in children with Pompe disease: a clinical study and review of the literatureAleena A Khan, Laura E Case, Mrudu Herbert, et al.
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