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Journal Article
Pediatrics, ISSN 0031-4005, 05/2010, Volume 125, Issue 5, pp. e1249 - e1254
Journal Article
Lancet, The, ISSN 0140-6736, 2015, Volume 386, Issue 10007, pp. 1924 - 1925
Journal Article
Journal Article
European Journal of Paediatric Neurology, ISSN 1090-3798, 2012, Volume 17, Issue 1, pp. 1 - 6
Journal Article
Radiology Case Reports, ISSN 1930-0433, 06/2018, Volume 13, Issue 3, pp. 592 - 595
Molybdenum cofactor deficiency is an extremely rare and fatal metabolic disorder that should be considered in the differential diagnosis of hypoxic-ischemic encephalopathy... 
Spectroscopy | MRI | Molybdenum cofactor deficiency
Journal Article
Neuropediatrics, ISSN 0174-304X, 04/2019, Volume 50, Issue 2, pp. 126 - 129
Abstract Molybdenum cofactor deficiency (MoCD) is a rare autosomal recessive metabolic disease with severe neurological symptoms... 
Short Communication | molybdenum cofactor deficiency | status dystonicus | MOCS1 | persistent generalized muscle contraction | PEDIATRICS | CLINICAL NEUROLOGY
Journal Article
Coordination chemistry reviews, ISSN 0010-8545, 2011, Volume 255, Issue 9-10, pp. 1016 - 1038
Journal Article
Journal Article
European Journal of Paediatric Neurology, ISSN 1090-3798, 2017, Volume 21, pp. e124 - e124
...Objective: To evaluate molybdenum cofactor deficiency (MoCD) disease biomarkers in urine and plasma in patients with MoCD Type A treated with synthetic cyclic... 
Pediatrics | Neurology | Molybdenum
Journal Article
Molecular genetics and metabolism reports, ISSN 2214-4269, 2019, Volume 18, pp. 11 - 13
Newborns with cystic degeneration with or without intractable seizures should be investigated for inborn errors of metabolism, including molybdenum cofactor deficiency (MoCoD... 
Cystic | Inborn errors of metabolism | Molybdenum cofactor deficiency | Brain MRI | MUTATIONS | GENETICS & HEREDITY
Journal Article