Keri Fredrickson

Variability of disease spectrum in children with liver phosphorylase kinase deficiency caused by mutations in the PHKG2 gene

Deeksha Bali, Jennifer Goldstein, Keri Fredrickson et al. · Molecular Genetics and Metabolism · 2013 · 56 citations

Mendelian Disorder, Hepatology, Genetic Disorder +10

Stbd1 is highly elevated in skeletal muscle of Pompe disease mice but suppression of its expression does not affect lysosomal glycogen accumulation

Haiqing Yi, Keri Fredrickson, S DAS et al. · Molecular Genetics and Metabolism · 2013 · 23 citations

Molecular Physiology, Disease Mechanism, Lysosomal Glycogen Accumulation +10

Clinical and Molecular Variability in Patients with PHKA2 Variants and Liver Phosphorylase b Kinase Deficiency

Deeksha Bali, Jennifer Goldstein, Keri Fredrickson et al. · JIMD Reports · 2017 · 18 citations · Full text

Alglucosidase alfa enzyme replacement therapy as a therapeutic approach for glycogen storage disease type III

Baodong Sun, Keri Fredrickson, Stephanie Austin et al. · Molecular Genetics and Metabolism · 2012 · 16 citations

Biochemistry, Enzyme Replacement Therapy, Medicine +5

Non-depleting anti-CD4 monoclonal antibody induces immune tolerance to ERT in a murine model of Pompe disease

Baodong Sun, Suhrad G. Banugaria, Sean N. Prater et al. · Molecular Genetics and Metabolism Reports · 2014 · 14 citations · Full text