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European Journal of Pediatrics|October 1, 1995
Use of human somatotrophin in the treatment of a patient with methylmalonic aciduriaM D Bain, S S Nussey, M Jones, et al.Pediatric Research|December 1, 1991
Enzymologic studies on patients with methylmalonic aciduria: basis for a clinical trial of deoxyadenosylcobalamin in a hydroxocobalamin-unresponsive patientR A Chalmers, M D Bain, J Mistry, et al.Journal of Inherited Metabolic Disease|April 8, 2006
Diagnosis and management of trimethylaminuria (FMO3 deficiency) in childrenR A Chalmers, M D Bain, H Michelakakis, et al.European Journal of Pediatrics|June 1, 1990
Dietary treatment eliminates succinylacetone from the urine of a patient with tyrosinaemia type 1M D Bain, P Purkiss, M Jones, et al.British Journal of Haematology|July 11, 2000
In vitro and in vivo studies with human carrier erythrocytes loaded with polyethylene glycol-conjugated and native adenosine deaminaseB E Bax, M D Bain, L D Fairbanks, et al.Clinical Science (London, England : 1979)|January 27, 1999
Survival of human carrier erythrocytes in vivoB E Bax, M D Bain, P J Talbot, et al.Journal of Inherited Metabolic Disease|January 26, 2006
Methylmalonic aciduria: follow-up and enzymology on the original case after 36 yearsM D Bain, J Till, M G Jones, et al.Lancet (London, England)|May 14, 1988
Contribution of gut bacterial metabolism to human metabolic diseaseM D Bain, M Jones, S P Borriello, et al.Journal of Epidemiology and Community Health|July 9, 1999
Secondary analysis of economic data: a review of cost-benefit studies of neonatal screening for phenylketonuriaJ Lord, M J Thomason, P Littlejohns, et al.Journal of Public Health Medicine|October 30, 1998
A systematic review of evidence for the appropriateness of neonatal screening programmes for inborn errors of metabolismM J Thomason, J Lord, M D Bain, et al.Pageof 10