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European Journal of Pediatrics|January 1, 1991
Mitochondrial phosphoenolpyruvate carboxykinase deficiencyJ V Leonard, K Hyland, N Furukawa, et al.European Journal of Pediatrics|April 1, 1986
Mitochondrial phosphoenolpyruvate carboxykinase deficiencyP T Clayton, K Hyland, M Brand, et al.Neurology|October 1, 1992
Aromatic L-amino acid decarboxylase deficiency: clinical features, diagnosis, and treatment of a new inborn error of neurotransmitter amine synthesisK Hyland, R A Surtees, C Rodeck, et al.Gut|August 1, 1983
Wilson's disease and hepatocellular carcinoma: possible protective role of copperM L Wilkinson, B Portmann, R WilliamsAddictive Behaviors|June 24, 2023
Reasons for not drinking among young adults with simultaneous alcohol and cannabis use: A latent class analysis applied to daily diary dataM L Wilkinson, A N Linden-CarmichaelJournal of Inherited Metabolic Disease|January 1, 1992
3 beta-hydroxy-delta 5-C27-steroid dehydrogenase deficiency; effect of chenodeoxycholic acid therapy on liver histologyS P Horslen, A M Lawson, M Malone, et al.Pediatric Research|April 1, 1995
Familial giant cell hepatitis with low bile acid concentrations and increased urinary excretion of specific bile alcohols: a new inborn error of bile acid synthesis?P T Clayton, M Casteels, G Mieli-Vergani, et al.Clinica Chimica Acta; International Journal of Clinical Chemistry|December 15, 1986
Rapid diagnosis of Zellweger syndrome and infantile Refsum's disease by fast atom bombardment--mass spectrometry of urine bile saltsA M Lawson, M J Madigan, D Shortland, et al.American Journal of Medical Genetics|September 25, 1995
Increased first trimester nuchal translucency as a prenatal manifestation of Smith-Lemli-Opitz syndromeJ A Hyett, P T Clayton, G Moscoso, et al.European Journal of Pediatrics|April 1, 1986
Bronze baby syndrome, biliary hypoplasia, incomplete Beckwith-Wiedemann syndrome and partial trisomy 11J K Wales, V Walker, I E Moore, et al.Pageof 13