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Pediatric Transplantation|August 13, 2009
Long-term outcome following pediatric liver transplantation for metabolic disordersTerrell Stevenson, Maria T Millan, Karen Wayman, et al.Plos One|June 19, 2014
Degree of glutathione deficiency and redox imbalance depend on subtype of mitochondrial disease and clinical statusGregory M Enns, Tereza Moore, Anthony Le, et al.Pediatric Neurosurgery|June 5, 2003
Cortical ependymoma. A case report and reviewNorman L Lehman, Michelle A Jorden, Stephen L Huhn, et al.The European Journal of Neuroscience|January 27, 2012
Transplantation of human central nervous system stem cells - neuroprotection in retinal degenerationTrevor J McGill, Benjamin Cottam, Bin Lu, et al.Pediatric Transplantation|January 26, 2013
Liver transplantation for urea cycle disorders in pediatric patients: a single-center experienceIrene K Kim, Anna-Kaisa Niemi, Casey Krueger, et al.Genes|July 27, 2024
Newborn Screening for X-Linked Adrenoleukodystrophy (X-ALD): Biochemical, Molecular, and Clinical Characteristics of Other Genetic ConditionsCarlos F Mares Beltran, Christina G Tise, Rebekah Barrick, et al.Journal of Inherited Metabolic Disease|February 6, 2026
Clinical Characteristics of Arginase 1 Deficiency: Natural History Insights From International Clinical TrialsMattias Rudebeck, Nancy Braverman, Richard Chang, et al.Translational Vision Science & Technology|July 7, 2021
The Present and Future of Mitochondrial-Based Therapeutics for Eye DiseaseMarco H Ji, Alexander Kreymerman, Kinsley Belle, et al.Plos One|December 2, 2011
A novel mutation in the HSD17B10 gene of a 10-year-old boy with refractory epilepsy, choreoathetosis and learning disabilityLaurie H Seaver, Xue-Ying He, Keith Abe, et al.Journal of Inherited Metabolic Disease|July 27, 2025
Long-Term Efficacy and Tolerability of Pegzilarginase in Arginase 1 Deficiency: Results of Two International Multicentre Open-Label Extension StudiesMarkey McNutt, Frank Rutsch, Rossana Sanchez Russo, et al.Pageof 14