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Journal of Inherited Metabolic Disease|June 21, 2026
Gaucher Disease Treated With Lentiviral-Mediated Gene Therapy: First CaseMona Shafey, Nicole Prokopishyn, Aneal KhanThe Canadian Journal of Cardiology|January 1, 2019
Acute Decompensated Heart Failure After Initiation of Amiodarone in a Patient With Anderson-Fabry DiseaseNowell M Fine, Yinong Wang, Aneal KhanJournal of Child Neurology|July 29, 2008
Congenital muscle fiber-type disproportion in a patient with congenital central hypoventilation syndrome due to PHOX2B mutationsAneal Khan, Harvey B Sarnat, Renee SpaetgensMolecular Genetics and Metabolism Reports|June 9, 2020
Impact on bone microarchitecture and failure load in a patient with type I Gaucher disease who switched from Imiglucerase to EliglustatKaramjot Sidhu, Steven K Boyd, Aneal KhanEndocrinology, Diabetes & Metabolism Case Reports|July 29, 2019
Phosphate matters when investigating hypercalcemia: a mutation in SLC34A3 causing HHRHAndrew Tang, Laura Hinz, Aneal Khan, et al.Case Reports in Medicine|August 28, 2009
Side-alternating vibration training improves muscle performance in a patient with late-onset pompe diseaseAneal Khan, Barbara Ramage, Ion Robu, et al.Canadian Journal of Diabetes|August 6, 2014
Diabetes in pediatric patients with Kearns-Sayre syndrome: clinical presentation of 2 cases and a review of pathophysiologyJosephine Ho, Danièle Pacaud, Maja Rakic, et al.JPGN Reports|May 11, 2023
Secondary Ammonia Scavenge With Glycerol Phenylbutyrate Improves Hyperammonemia Following Portosystemic ShuntingSimone Kortbeek, Christy Gilkes, Aneal Khan, et al.JIMD Reports|March 4, 2015
Improvement in Bone Mineral Density and Architecture in a Patient with Gaucher Disease Using TeriparatideAneal Khan, David A Hanley, Colleen McNeil, et al.JIMD Reports|February 23, 2013
Cerebral edema in maple syrup urine disease despite newborn screening diagnosis and early initiation of treatmentKenneth A Myers, Melanie Reeves, Xing-Chang Wei, et al.Pageof 9