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Nature Reviews Neurology, ISSN 1759-4758, 2019, Volume 15, Issue 5, pp. 253 - 271
Organic acidurias (OADs) are inherited neurometabolic diseases largely caused by deficiencies in enzymes involved in amino acid degradation, which result in... 
IMPAIRS ENERGY-METABOLISM | GLUTARIC-ACIDURIA | PROTEIN OXIDATIVE DAMAGE | DEHYDROGENASE DEFICIENT MICE | METHYLMALONIC ACIDEMIA | BLOOD-BRAIN-BARRIER | CREATINE-KINASE ACTIVITY | CEREBRAL-CORTEX | CLINICAL NEUROLOGY | COA THIOLASE DEFICIENCY | INBORN-ERRORS
Journal Article
Journal of Bioenergetics and Biomembranes, ISSN 0145-479X, 2/2011, Volume 43, Issue 1, pp. 31 - 38
Journal Article
PLoS ONE, ISSN 1932-6203, 05/2013, Volume 8, Issue 5, p. e64372
Journal Article
Journal of Neurochemistry, ISSN 0022-3042, 04/2016, Volume 137, Issue 1, pp. 62 - 75
Journal Article
International journal of developmental neuroscience : the official journal of the International Society for Developmental Neuroscience, ISSN 0736-5748, 05/2019
Glutaric acidemia type I (GA I) is an inherited neurometabolic disease caused by deficient activity of the mitochondrial enzyme glutaryl-CoA dehydrogenase... 
Journal Article
Free Radical Biology and Medicine, ISSN 0891-5849, 07/2017, Volume 108, pp. S34 - S34
Journal Article
Free Radical Biology and Medicine, ISSN 0891-5849, 07/2017, Volume 108, p. S34
Non-ketotic hyperglycinemia (NKH) is an inborn error of metabolism caused by deficiency in the glycine (GLY) cleavage system and characterized by a high... 
Antioxidants | Phosphates | Enzymes | Evaluation | Physiological aspects | Superoxide | Glycine
Journal Article
Molecular Neurobiology, ISSN 0893-7648, 7/2018, Volume 55, Issue 7, pp. 5868 - 5878
Journal Article