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Unexplained familial benign methylmalonic aciduria.
Martens DH, Bakker JA, van der Meer SB, Spaapen LJ. Martens DH, et al. Among authors: spaapen lj. Eur J Pediatr. 2002 Apr;161(4):219-20. doi: 10.1007/s00431-002-0930-z. Eur J Pediatr. 2002. PMID: 12014390 No abstract available.
Metabolic investigation of a patient with Rett syndrome.
Vles JS, Spaapen LJ, Schrander-Stumpel C, van der Meer S. Vles JS, et al. Among authors: spaapen lj. Eur J Pediatr. 1989 Aug;148(8):786. doi: 10.1007/BF00443113. Eur J Pediatr. 1989. PMID: 2792136 No abstract available.
Untreated classical galactosemia patient with mild phenotype.
Panis B, Bakker JA, Sels JP, Spaapen LJ, van Loon LJ, Rubio-Gozalbo ME. Panis B, et al. Among authors: spaapen lj. Mol Genet Metab. 2006 Nov;89(3):277-9. doi: 10.1016/j.ymgme.2006.03.002. Epub 2006 Apr 18. Mol Genet Metab. 2006. PMID: 16621642
45 results