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European Journal of Pediatrics|February 1, 1992
Familial glucocorticoid deficiency with achalasia of the cardia associated with mixed neuropathy, long-tract degeneration and mild dementiaD B Grant, D B Dunger, I Smith, et al.Archives of Disease in Childhood|February 1, 1986
Neurological aspects of biopterin metabolismI Smith, R J Leeming, N P Cavanagh, et al.Journal of Neurochemistry|March 1, 1996
Neurochemical effects following peripheral administration of tetrahydropterin derivatives to the hph-1 mouseM P Brand, K Hyland, T Engle, et al.Plos Medicine|March 9, 2010
Where will the next generation of stroke treatments come from?D W Howells, G A DonnanJournal of Inherited Metabolic Disease|July 17, 1999
Neurochemistry and defects of biogenic amine neurotransmitter metabolismK HylandJournal of Inherited Metabolic Disease|January 1, 1993
Abnormalities of biogenic amine metabolismK HylandSeminars in Perinatology|May 20, 1999
Presentation, diagnosis, and treatment of the disorders of monoamine neurotransmitter metabolismK HylandJournal of Chromatography|September 13, 1985
Estimation of tetrahydro, dihydro and fully oxidised pterins by high-performance liquid chromatography using sequential electrochemical and fluorometric detectionK HylandJournal of Neurology, Neurosurgery, and Psychiatry|August 1, 1986
Subacute combined degeneration of the cord, dementia and parkinsonism due to an inborn error of folate metabolismP T Clayton, I Smith, B Harding, et al.Neurology|March 1, 1988
Demyelination and decreased S-adenosylmethionine in 5,10-methylenetetrahydrofolate reductase deficiencyK Hyland, I Smith, T Bottiglieri, et al.Pageof 190