Reijngoud DJ - Search Results

1

End-stage liver disease as the only consequence of a mitochondrial respiratory chain deficiency: no contra-indication for liver transplantation.

Rake JP, van Spronsen FJ, Visser G, Ruitenbeek W, Schweizer JJ, Bijleveld CM, Peeters PM, de Jong KP, Slooff MJ, Reijngoud DJ, Niezen-Koning KE, Smit GP. Rake JP, et al. Among authors: reijngoud dj. Eur J Pediatr. 2000 Jul;159(7):523-6. doi: 10.1007/s004310051324. Eur J Pediatr. 2000. PMID: 10923228

2

Succinyl-CoA:acetoacetate transferase deficiency: identification of a new patient with a neonatal onset and review of the literature.

Niezen-Koning KE, Wanders RJ, Ruiter JP, Ijlst L, Visser G, Reitsma-Bierens WC, Heymans HS, Reijngoud DJ, Smit GP. Niezen-Koning KE, et al. Among authors: reijngoud dj. Eur J Pediatr. 1997 Nov;156(11):870-3. doi: 10.1007/s004310050733. Eur J Pediatr. 1997. PMID: 9392403 Review.

3

3-methylcrotonyl-CoA carboxylase deficiency in an infant with cardiomyopathy, in her brother with developmental delay and in their asymptomatic father.

Visser G, Suormala T, Smit GP, Reijngoud DJ, Bink-Boelkens MT, Niezen-Koning KE, Baumgartner ER. Visser G, et al. Among authors: reijngoud dj. Eur J Pediatr. 2000 Dec;159(12):901-4. doi: 10.1007/pl00008366. Eur J Pediatr. 2000. PMID: 11131348

4

The natural history of medium-chain acyl CoA dehydrogenase deficiency in the Netherlands: clinical presentation and outcome.

Derks TG, Reijngoud DJ, Waterham HR, Gerver WJ, van den Berg MP, Sauer PJ, Smit GP. Derks TG, et al. Among authors: reijngoud dj. J Pediatr. 2006 May;148(5):665-670. doi: 10.1016/j.jpeds.2005.12.028. J Pediatr. 2006. PMID: 16737882

5

Determination of medium chain acyl-CoA dehydrogenase activity in cultured skin fibroblasts using mass spectrometry.

Niezen-Koning KE, Chapman TE, Mulder IE, Smit GP, Reijngoud DJ, Berger R. Niezen-Koning KE, et al. Among authors: reijngoud dj. Clin Chim Acta. 1991 Jun 14;199(2):173-84. doi: 10.1016/0009-8981(91)90109-p. Clin Chim Acta. 1991. PMID: 1873916

6

Liver transplantation in tyrosinaemia type I: the Groningen experience.

Wijburg FA, Reitsma WC, Slooff MJ, van Spronsen FJ, Koetse HA, Reijngoud DJ, Smit GP, Berger R, Bijleveld CM. Wijburg FA, et al. Among authors: reijngoud dj. J Inherit Metab Dis. 1995;18(2):115-8. doi: 10.1007/BF00711743. J Inherit Metab Dis. 1995. PMID: 7564223 No abstract available.

7

Plasma phenylalanine and tyrosine responses to different nutritional conditions (fasting/postprandial) in patients with phenylketonuria: effect of sample timing.

van Spronsen FJ, van Rijn M, van Dijk T, Smit GP, Reijngoud DJ, Berger R, Heymans HS. van Spronsen FJ, et al. Among authors: reijngoud dj. Pediatrics. 1993 Oct;92(4):570-3. Pediatrics. 1993. PMID: 8414829

8

Phenylketonuria: plasma phenylalanine responses to different distributions of the daily phenylalanine allowance over the day.

van Spronsen FJ, van Dijk T, Smit GP, van Rijn M, Reijngoud DJ, Berger R, Heymans HS. van Spronsen FJ, et al. Among authors: reijngoud dj. Pediatrics. 1996 Jun;97(6 Pt 1):839-44. Pediatrics. 1996. PMID: 8657524 Clinical Trial.

9

[Deficiency of the fatty-acid oxidising enzyme medium-chain acyl-CoA dehydrogenase (MCAD) in an adult, detected during a neonatal screening programme].

Derks TG, Jakobs H, Gerding A, Niezen-Koning KE, Reijngoud DJ, Smit GP. Derks TG, et al. Among authors: reijngoud dj. Ned Tijdschr Geneeskd. 2004 Oct 30;148(44):2185-90. Ned Tijdschr Geneeskd. 2004. PMID: 15559414 Dutch.

10

Ventricular fibrillation without overt cardiomyopathy as first presentation of organic cation transporter 2-deficiency in adolescence.

Rijlaarsdam RS, van Spronsen FJ, Bink-Boelkens MT, Reijngoud DJ, Wanders RJ, Niezen-Koning KE, Van der Sluijs FH, Dorland B, Beaufort-Krol GC. Rijlaarsdam RS, et al. Among authors: reijngoud dj. Pacing Clin Electrophysiol. 2004 May;27(5):675-6. doi: 10.1111/j.1540-8159.2004.00507.x. Pacing Clin Electrophysiol. 2004. PMID: 15125729

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