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FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|October 30, 2019
Glycocalyx breakdown is increased in African children with cerebral and uncomplicated falciparum malariaTsin W Yeo, Peggy A Bush, Youwei Chen, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|July 12, 2005
Evasion of immune responses to introduced human acid alpha-glucosidase by liver-restricted expression in glycogen storage disease type IILuis M Franco, Baodong Sun, Xiaoyi Yang, et al.
Molecular Genetics and Metabolism|August 21, 2021
MPS VI associated ocular phenotypes in an MPS VI murine model and the therapeutic effects of odiparcil treatmentEugeni Entchev, Sophie Antonelli, Virginie Mauro, et al.
JIMD Reports|January 14, 2026
Treatable Neonatal Molybdenum Cofactor Deficiency: Rapid Demise Despite Rapid Biochemical DiagnosisMolly M Crenshaw, Yasmeen Midgette, Shruthi Mohan, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 3, 2019
Liver fibrosis during clinical ascertainment of glycogen storage disease type III: a need for improved and systematic monitoringCarine A Halaby, Sarah P Young, Stephanie Austin, et al.
Journal of Inherited Metabolic Disease|March 31, 2022
Cerebrospinal fluid amino acids glycine, serine, and threonine in nonketotic hyperglycinemiaMichael A Swanson, Kristen Miller, Sarah P Young, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|August 20, 2009
Immunomodulatory gene therapy prevents antibody formation and lethal hypersensitivity reactions in murine pompe diseaseBaodong Sun, Michael D Kulis, Sarah P Young, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 27, 2025
Infantile-onset Pompe disease entering adulthood: Insights from 2 decades of enzyme replacement therapy experienceNeha Regmi, Daniel Kenney-Jung, Grace Stafford, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 28, 2012
The emerging phenotype of long-term survivors with infantile Pompe diseaseSean N Prater, Suhrad G Banugaria, Stephanie M DeArmey, et al.
Molecular Genetics and Metabolism Reports|November 25, 2021
A retrospective longitudinal study and comprehensive review of adult patients with glycogen storage disease type IIIGhada Hijazi, Anna Paschall, Sarah P Young, et al.
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