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Neurosurgical Focus|March 18, 2008
Central nervous system therapy for lysosomal storage disordersGregory M Enns, Stephen L HuhnJournal of Neurosurgery|May 10, 2008
Glutaric acidemia type I: a neurosurgical perspective. Report of two casesLewis C Hou, Anand Veeravagu, Andrew R Hsu, et al.Molecular 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 CowanMolecular Genetics and Metabolism|July 22, 2008
Cell-based therapies for metabolic liver diseaseGregory M Enns, Maria T MillanPageof 14