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Pediatric Radiology|November 3, 1998
Chondrodysplasia punctata with multiple congenital anomalies: a new syndrome?G R Mortier, L M Messiaen, M Espeel, et al.
Kidney International|November 1, 1996
Hyperoxaluria with hyperglycoluria not due to alanine:glyoxylate aminotransferase defect: a novel type of primary hyperoxaluriaK J Van Acker, F J Eyskens, M F Espeel, et al.
European Journal of Pediatrics|December 1, 1996
Isolated dihydroxyacetonephosphate-acyl-transferase deficiency in rhizomelic chondrodysplasia punctata: clinical presentation, metabolic and histological findingsH Hebestreit, R J Wanders, R B Schutgens, et al.
Neuromuscular Disorders : NMD|January 1, 1992
Neonatal seizures and severe hypotonia in a male infant suffering from a defect in peroxisomal beta-oxidationL Van Maldergem, M Espeel, R J Wanders, et al.
Biological Trace Element Research|November 21, 2013
Use of laser microprobe mass analysis (LAMMA) for localizing multiple elements in soft and hard tissuesA H Verbueken, F L Van de Vyver, W J Visser, et al.
The Journal of Pediatrics|January 1, 1986
Pseudo-Zellweger syndrome: deficiencies in several peroxisomal oxidative activitiesS Goldfischer, J Collins, I Rapin, et al.
Neurology|November 18, 1998
Defective peroxisome biogenesis with a neuromuscular disorder resembling Werdnig-Hoffmann diseaseM R Baumgartner, N M Verhoeven, C Jakobs, et al.
Kidney International|April 1, 1984
Early effects of gentamicin, tobramycin, and amikacin on the human kidneyM E De Broe, G J Paulus, G A Verpooten, et al.
Clinical Nephrology|January 1, 1986
Cyclosporine nephrotoxicity: comparative cytochemical study of rat kidney and human allograft biopsiesG A Verpooten, I Wybo, V M Pattyn, et al.
The Journal of Pediatrics|October 1, 1994
A new type of peroxisomal disorder with variable expression in liver and fibroblastsH Mandel, M Espeel, F Roels, et al.
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