1. A new defect of peroxisomal function involving pristanic acid: a case report. Issue 3 (1st March 2002) Authors: McLean, B N; Allen, J; Ferdinandusse, S; Wanders, R J A Journal: Journal of neurology, neurosurgery and psychiatry Issue: Volume 72:Issue 3(2002) Page Start: 396 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. High tolerance for oral galactose in classical galactosaemia: dietary implications. Issue 11 (21st October 2004) Authors: Bosch, A M; Bakker, H D; de B Wenniger-Prick, L J M; Wanders, R J A; Wijburg, F A Journal: Archives of disease in childhood Issue: Volume 89:Issue 11(2004) Page Start: 1034 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Increased plasma malondialdehyde associated with cerebellar structural defects. Issue 3 (1st September 1997) Authors: Ramaekers, V Th; Bosman, B; Jansen, G A; Wanders, R J A Journal: Archives of disease in childhood Issue: Volume 77:Issue 3(1997) Page Start: 231 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Novel genotype of mevalonic aciduria with fatalities in premature siblings. Issue 1 (1st January 2004) Authors: Raupp, P; Varady, E; Duran, M; Wanders, R J A; Waterham, H R; Houten, S M Journal: Archives of disease in childhood Issue: Volume 89:Issue 1(2004) Page Start: F90 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Progression of abnormalities in adrenomyeloneuropathy and neurologically asymptomatic X-linked adrenoleukodystrophy despite treatment with "Lorenzo's oil". Issue 3 (1st September 1999) Authors: van Geel, B M; Assies, J; Haverkort, E B; Koelman, J H T M; Verbeeten, B; Wanders, R J A; Barth, P G Journal: Journal of neurology, neurosurgery and psychiatry Issue: Volume 67:Issue 3(1999) Page Start: 290 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Relapsing encephalopathy in a patient with α-methylacyl-CoA racemase deficiency. Issue 4 (21st November 2007) Authors: Thompson, S A; Calvin, J; Hogg, S; Ferdinandusse, S; Wanders, R J A; Barker, R A Journal: Journal of neurology, neurosurgery and psychiatry Issue: Volume 79:Issue 4(2008) Page Start: 448 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗