Fabry Disease practice resource: Focused revision. Journal of Genetic Counseling. 2020; 29(5):715-717.
Tertiary Pediatric Academic Institution's Experience With Intraoperative Neuromonitoring for Nonspinal Surgery in Children With Mucopolysaccharidosis, Based on a Novel Evidence-Based Care Algorithm. Anesthesia and Analgesia. 2020; 130(6):1678-1684.
A single center’s experience with hematopoietic stem cell transplant in MPS IH from 2002-2015: A retrospective review of variables that may influence transplant outcome and complications. Molecular Genetics and Metabolism. 2016; 117(2):s120.
Support for siblings of children with lysosomal disorders. Molecular Genetics and Metabolism. 2015; 114(2):s22.
Enzyme replacement therapy for MPS I: When is the right time to stop? Molecular Genetics and Metabolism. 2013; 108(2):s24.
Home infusions: One center's experience with ERT and self-infusion in the home setting. Molecular Genetics and Metabolism. 2013; 108(2):s97.
A 4 Month Old With Hurler Syndrome and Mosaic Fragile X Syndrome: To Transplant Or Not To Transplant? Molecular Genetics and Metabolism. 2012; 105(2):s20-s21.
Developing Brain Imaging Markers of Treatment Response and Progression in Mucopolysaccharidosis Type II. Molecular Genetics and Metabolism. 2012; 105(2):s53-s54.
Lisa Berry, LGC, Cecilia M. Goueli, LGC9/20/2025