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Archives of Disease in Childhood|May 1, 1997
Prolidase deficiency and systemic lupus erythematosusM Shrinath, J H Walter, M Haeney, et al.The Journal of Pediatrics|August 1, 1995
Magnetic resonance imaging in phenylketonuria: reversal of cerebral white matter changeM A Cleary, J H Walter, J E Wraith, et al.Journal of Inherited Metabolic Disease|February 5, 2009
Bloodspot acylcarnitine and amino acid analysis in cord blood samples: efficacy and reference data from a large cohort studyJ H Walter, A Patterson, J Till, et al.European Journal of Pediatrics|January 1, 1989
Chronic renal failure in methylmalonic acidaemiaJ H Walter, A Michalski, W M Wilson, et al.Journal of Inherited Metabolic Disease|July 26, 2006
Carnitine transporter defect: diagnosis in asymptomatic adult women following analysis of acylcarnitines in their newborn infantsS Vijay, A Patterson, S Olpin, et al.Veterinary Microbiology|June 1, 1992
Papillomavirus associated skin lesions in a cat seropositive for feline immunodeficiency virusH F Egberink, A Berrocal, H A Bax, et al.Lancet (London, England)|July 9, 1994
Magnetic resonance imaging of the brain in phenylketonuriaM A Cleary, J H Walter, J E Wraith, et al.Archives of Disease in Childhood|March 23, 1999
Generalised uridine diphosphate galactose-4-epimerase deficiencyJ H Walter, R E Roberts, G T Besley, et al.European Journal of Pediatrics|March 1, 1990
In vivo propionate oxidation as a prognostic indicator in disorders of propionate metabolismG N Thompson, J H Walter, J L Bresson, et al.European Journal of Pediatrics|October 12, 2013
Unsuccessful treatment of severe pyruvate carboxylase deficiency with triheptanoinC Breen, F J White, C A B Scott, et al.Pageof 8