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Molecular characterization of 3-phosphoglycerate dehydrogenase deficiency--a neurometabolic disorder associated with reduced L-serine biosynthesis.
Klomp LW, de Koning TJ, Malingré HE, van Beurden EA, Brink M, Opdam FL, Duran M, Jaeken J, Pineda M, Van Maldergem L, Poll-The BT, van den Berg IE, Berger R. Klomp LW, et al. Among authors: berger r. Am J Hum Genet. 2000 Dec;67(6):1389-99. doi: 10.1086/316886. Epub 2000 Oct 27. Am J Hum Genet. 2000. PMID: 11055895 Free PMC article.
D-serine in the developing human central nervous system.
Fuchs SA, Dorland L, de Sain-van der Velden MG, Hendriks M, Klomp LW, Berger R, de Koning TJ. Fuchs SA, et al. Among authors: berger r. Ann Neurol. 2006 Oct;60(4):476-80. doi: 10.1002/ana.20977. Ann Neurol. 2006. PMID: 17068790
Prenatal diagnosis of type I hereditary tyrosinaemia.
Ploos van Amstel JK, Jansen RP, Verjaal M, van den Berg IE, Berger R. Ploos van Amstel JK, et al. Among authors: berger r. Lancet. 1994 Jul 30;344(8918):336. doi: 10.1016/s0140-6736(94)91375-7. Lancet. 1994. PMID: 7914281 No abstract available.
Neurotransmitters in 3-phosphoglycerate dehydrogenase deficiency.
de Koning TJ, Duran M, Dorland L, Jakobs C, Wevers RA, Berger R, Poll-The BT. de Koning TJ, et al. Among authors: berger r. Eur J Pediatr. 2000 Dec;159(12):939-40. doi: 10.1007/pl00008379. Eur J Pediatr. 2000. PMID: 11131361 No abstract available.
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