Showing results (1-10 of 37) with videos related to
Sort By:
Pageof 4
Journal of Inherited Metabolic Disease|January 1, 1986
Glycerol-3-phosphate excretion in fructose-1,6-diphosphatase deficiencyS Krywawych, G Katz, A M Lawson, et al.American Journal of Medical Genetics|January 1, 1987
DOOR syndrome (deafness, onycho-osteodystrophy, and mental retardation): elevated plasma and urinary 2-oxoglutarate in three unrelated patientsM A Patton, S Krywawych, R M Winter, et al.Journal of Inherited Metabolic Disease|January 1, 1981
The adult presenting idiopathic Fanconi syndromeD P Brenton, D A Isenberg, D C Cusworth, et al.Clinica Chimica Acta; International Journal of Clinical Chemistry|February 1, 1979
Thin-layer chromatography of non-volatile organic acids in clinical chemistryS KrywawychJournal of Inherited Metabolic Disease|June 23, 2000
The adult and adolescent clinic for inborn errors of metabolismD P BrentonEuropean Journal of Pediatrics|October 24, 2000
Adult care in phenylketonuria and hyperphenylalaninaemia: the relevance of neurological abnormalitiesD P Brenton, J PietzEuropean Journal of Pediatrics|July 1, 1996
Maternal phenylketonuria. A study from the United KingdomD P Brenton, M LilburnAnnals of the Rheumatic Diseases|April 1, 1982
Engelmann's disease of bone--a systemic disorder?A J Crisp, D P BrentonBritish Journal of Hospital Medicine|August 1, 1984
Fluid and electrolyte disorders. MagnesiumD P Brenton, T E GordonPageof 4