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American Journal of Medical Genetics. Part A|August 19, 2004
Mild developmental delay in terminal chromosome 6p deletionKelly M Chen, Athena M Cherry, Jin S Hahn, et al.Pediatrics|August 3, 2004
Terminal 22q deletion syndrome: a newly recognized cause of speech and language disability in the autism spectrumMelanie A Manning, Suzanne B Cassidy, Carol Clericuzio, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 18, 2007
Array-based comparative genomic hybridization: clinical contexts for targeted and whole-genome designsSwaroop Aradhya, Athena M CherryMolecular Genetics and Metabolism|October 22, 2003
The contribution of mitochondria to common disordersGregory M EnnsSeminars in Pediatric Neurology|August 19, 2008
Neurologic damage and neurocognitive dysfunction in urea cycle disordersGregory M EnnsCurrent Opinion in Pediatrics|July 19, 2017
Pediatric mitochondrial diseases and the heartGregory M EnnsJournal of Child Neurology|July 3, 2014
Treatment of mitochondrial disorders: antioxidants and beyondGregory M EnnsMolecular Genetics and Metabolism|March 6, 2010
Nitrogen sparing therapy revisited 2009Gregory M EnnsAdolescent Medicine (Philadelphia, Pa.)|May 3, 2002
The adolescent with an inborn error of metabolism: medical issues and transition to adulthoodGregory M Enns, Wendy PackmanJournal of Clinical Medicine|May 4, 2017
Glutathione as a Redox Biomarker in Mitochondrial Disease-Implications for TherapyGregory M Enns, Tina M CowanPageof 21