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European Journal of Pediatrics|October 10, 2002
Glycogen storage disease type I: diagnosis and phenotype/genotype correlationDietrich Matern, Hans Hermann Seydewitz, Deeksha Bali, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 17, 2006
The use of acarbose inhibition in the measurement of acid alpha-glucosidase activity in blood lymphocytes for the diagnosis of Pompe diseaseRhona M Jack, Cindy Gordon, C R Scott, et al.Human Molecular Genetics|November 16, 2010
Glycogen-branching enzyme deficiency leads to abnormal cardiac development: novel insights into glycogen storage disease IVYi-Ching Lee, Chia-Jung Chang, Deeksha Bali, et al.Molecular Genetics and Metabolism|December 14, 2011
β2 Agonists enhance the efficacy of simultaneous enzyme replacement therapy in murine Pompe diseaseDwight D Koeberl, Songtao Li, Jian Dai, et al.Molecular Therapy. Methods & Clinical Development|July 12, 2019
Erratum: Assessment of toxicity and biodistribution of recombinant AAV8 vector-mediated immunomodulatory gene therapy in mice with Pompe diseaseGensheng Wang, Sarah P Young, Deeksha Bali, et al.Molecular Therapy. Methods & Clinical Development|May 28, 2015
Assessment of toxicity and biodistribution of recombinant AAV8 vector-mediated immunomodulatory gene therapy in mice with Pompe diseaseGensheng Wang, Sarah P Young, Deeksha Bali, et al.Molecular Therapy. Methods & Clinical Development|June 2, 2015
Corrigendum to "Assessment of toxicity and biodistribution of recombinant AAV8 vector-mediated immunomodulatory gene therapy in mice with Pompe disease"Gensheng Wang, Sarah P Young, Deeksha Bali, et al.Journal of Pediatric Hematology/Oncology|May 25, 2017
Wolman Disease: A Mimic of Infant LeukemiaKaduveettil G Gopakumar, Priyakumari Thankamony, Sheela Nampoothiri, et al.Journal of Hepatology|January 2, 2007
Glycogen storage disease type III-hepatocellular carcinoma a long-term complication?Erin Demo, Donald Frush, Marcia Gottfried, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 13, 2009
Long-term monitoring of patients with infantile-onset Pompe disease on enzyme replacement therapy using a urinary glucose tetrasaccharide biomarkerSarah P Young, Haoyue Zhang, Deyanira Corzo, et al.Pageof 6