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Journal of Pediatric Ophthalmology and Strabismus|February 5, 2010
Clinical and histologic ocular findings in pompe diseaseTammy L Yanovitch, Suhrad G Banugaria, Alan D Proia, et al.
Molecular Genetics and Metabolism|January 12, 2010
Hypovitaminosis D in glycogen storage disease type ISuhrad G Banugaria, Stephanie L Austin, Anne Boney, et al.
Molecular Genetics and Metabolism|May 23, 2012
The impact of antibodies in late-onset Pompe disease: a case series and literature reviewTrusha T Patel, Suhrad G Banugaria, Laura E Case, et al.
Molecular Genetics and Metabolism|February 28, 2012
Persistence of high sustained antibodies to enzyme replacement therapy despite extensive immunomodulatory therapy in an infant with Pompe disease: need for agents to target antibody-secreting plasma cellsSuhrad G Banugaria, Trusha T Patel, Joanne Mackey, et al.
Orphanet Journal of Rare Diseases|June 22, 2013
Skeletal muscle pathology of infantile Pompe disease during long-term enzyme replacement therapySean N Prater, Trusha T Patel, Anne F Buckley, et al.
Molecular Genetics and Metabolism|September 6, 2011
Atypical immunologic response in a patient with CRIM-negative Pompe diseaseMary-Alice Abbott, Sean N Prater, Suhrad G Banugaria, et al.
Molecular Genetics and Metabolism|March 15, 2011
Enhanced efficacy of enzyme replacement therapy in Pompe disease through mannose-6-phosphate receptor expression in skeletal muscleDwight D Koeberl, Xiaoyan Luo, Baodong Sun, et al.
Dysphagia|September 19, 2009
Oropharyngeal dysphagia in infants and children with infantile Pompe diseaseHarrison N Jones, Carolyn W Muller, Min Lin, et al.
Molecular Genetics and Metabolism Reports|November 30, 2016
Non-depleting anti-CD4 monoclonal antibody induces immune tolerance to ERT in a murine model of Pompe diseaseBaodong Sun, Suhrad G Banugaria, Sean N Prater, et al.
Molecular Genetics and Metabolism|October 21, 2017
Neuroimaging findings in infantile Pompe patients treated with enzyme replacement therapyPaul T McIntosh, Lisa D Hobson-Webb, Zoheb B Kazi, et al.
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