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Journal of Inherited Metabolic Disease|January 1, 1985
Comparative column chromatographic estimations of phenylalanine in plasma, whole blood, native and paper-dried capillary blood of healthy children and adults, and patients with hyperphenylalaninaemiaK Becker, J Harenz, N Kalle, et al.Journal of Inherited Metabolic Disease|January 1, 1985
An evaluation of protein requirements in methylmalonic acidaemiaD Ney, C Bay, J M Saudubray, et al.Journal of Inherited Metabolic Disease|January 1, 1985
Evaluation of cofactor responsivenessJ V Leonard, P DaishJournal of Inherited Metabolic Disease|January 1, 1985
Clinical role of pteridine therapy in tetrahydrobiopterin deficiencyI Smith, K Hyland, B KendallJournal of Inherited Metabolic Disease|January 1, 1985
Biotinidase deficiency: a novel vitamin recycling defectB Wolf, R E Grier, J R Secor McVoy, et al.Journal of Inherited Metabolic Disease|January 1, 1985
Riboflavin-responsive defects of beta-oxidationN GregersenJournal of Inherited Metabolic Disease|January 1, 1985
Recent advances in the mechanism of pyridoxine-responsive disordersB FowlerJournal of Inherited Metabolic Disease|August 1, 1997
Treatment products and approaches for phenylketonuria: improved palatability and flexibility demonstrate safety, efficacy and acceptance in US clinical trialsA P Prince, M P McMurray, N R BuistJournal of Inherited Metabolic Disease|August 1, 1997
Mitochondrial abnormalities of liver in two children with citrullinaemiaS A Zamora, A Pinto, R B Scott, et al.Journal of Inherited Metabolic Disease|August 1, 1997
Identification of 'private' mutations in patients with ornithine transcarbamylase deficiencyM Tuchman, H Morizono, B S Rajagopal, et al.Pageof 429