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Selective screening for amino acid disorders.
Duran M, Dorland L, de Bree PK, Berger R. Duran M, et al. Among authors: berger r. Eur J Pediatr. 1994;153(7 Suppl 1):S33-7. doi: 10.1007/BF02138775. Eur J Pediatr. 1994. PMID: 7957384
Formiminoglutamic/hydantoinpropionic aciduria in two siblings.
Duran M, Dorland L, Meuleman EE, Renardel de Lavalette PA, Poll-The BT, Berger R. Duran M, et al. Among authors: berger r. J Inherit Metab Dis. 1993;16(1):155-6. doi: 10.1007/BF00711330. J Inherit Metab Dis. 1993. PMID: 8487495 No abstract available.
Equine biochemical multiple acyl-CoA dehydrogenase deficiency (MADD) as a cause of rhabdomyolysis.
Westermann CM, de Sain-van der Velden MG, van der Kolk JH, Berger R, Wijnberg ID, Koeman JP, Wanders RJ, Lenstra JA, Testerink N, Vaandrager AB, Vianey-Saban C, Acquaviva-Bourdain C, Dorland L. Westermann CM, et al. Among authors: berger r. Mol Genet Metab. 2007 Aug;91(4):362-9. doi: 10.1016/j.ymgme.2007.04.010. Epub 2007 May 30. Mol Genet Metab. 2007. PMID: 17540595
Acquired multiple Acyl-CoA dehydrogenase deficiency in 10 horses with atypical myopathy.
Westermann CM, Dorland L, Votion DM, de Sain-van der Velden MG, Wijnberg ID, Wanders RJ, Spliet WG, Testerink N, Berger R, Ruiter JP, van der Kolk JH. Westermann CM, et al. Among authors: berger r. Neuromuscul Disord. 2008 May;18(5):355-64. doi: 10.1016/j.nmd.2008.02.007. Epub 2008 Apr 11. Neuromuscul Disord. 2008. PMID: 18406615
Dihydropyrimidinuria: a new inborn error of pyrimidine metabolism.
Duran M, Rovers P, de Bree PK, Schreuder CH, Beukenhorst H, Dorland L, Berger R. Duran M, et al. Among authors: berger r. J Inherit Metab Dis. 1991;14(3):367-70. doi: 10.1007/BF01811705. J Inherit Metab Dis. 1991. PMID: 1770794 No abstract available.
4,099 results