Duran M - Search Results

1

Plasma pipecolic acid is frequently elevated in non-peroxisomal disease.

Baas JC, van de Laar R, Dorland L, Duran M, Berger R, Poll-The BT, de Koning TJ. Baas JC, et al. Among authors: duran m. J Inherit Metab Dis. 2002 Dec;25(8):699-701. doi: 10.1023/a:1022889400302. J Inherit Metab Dis. 2002. PMID: 12705501

2

Cerebrospinal fluid organic acids in biotinidase deficiency.

Duran M, Baumgartner ER, Suormala TM, Bruinvis L, Dorland L, Smeitink JA, Poll-The BT. Duran M, et al. J Inherit Metab Dis. 1993;16(3):513-6. doi: 10.1007/BF00711668. J Inherit Metab Dis. 1993. PMID: 7609439 Clinical Trial. No abstract available.

3

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. J Inherit Metab Dis. 1993;16(1):155-6. doi: 10.1007/BF00711330. J Inherit Metab Dis. 1993. PMID: 8487495 No abstract available.

4

Inherited defects of purine and pyrimidine metabolism: laboratory methods for diagnosis.

Duran M, Dorland L, Meuleman EE, Allers P, Berger R. Duran M, et al. J Inherit Metab Dis. 1997 Jun;20(2):227-36. doi: 10.1023/a:1005360907238. J Inherit Metab Dis. 1997. PMID: 9211195 Review.

5

The effect of fasting, long-chain triglyceride load and carnitine load on plasma long-chain acylcarnitine levels in mitochondrial very long-chain acyl-CoA dehydrogenase deficiency.

Costa CG, Dorland L, de Almeida IT, Jakobs C, Duran M, Poll-The BT. Costa CG, et al. Among authors: duran m. J Inherit Metab Dis. 1998 Jun;21(4):391-9. doi: 10.1023/a:1005354624735. J Inherit Metab Dis. 1998. PMID: 9700596

6

Recurrent nonimmune hydrops fetalis associated with carbohydrate-deficient glycoprotein syndrome.

de Koning TJ, Toet M, Dorland L, de Vries LS, van den Berg IE, Duran M, Poll-The BT. de Koning TJ, et al. Among authors: duran m. J Inherit Metab Dis. 1998 Aug;21(6):681-2. doi: 10.1023/a:1005496920435. J Inherit Metab Dis. 1998. PMID: 9762608 No abstract available.

7

Muscle strength in children with medium-chain acyl-CoA dehydrogenase deficiency.

Custers JW, Poll-The BT, Duran M, de Klerk JB, Uiterwaal CS, Helders PJ. Custers JW, et al. Among authors: duran m. J Inherit Metab Dis. 1999 Apr;22(2):200-1. doi: 10.1023/a:1005491128746. J Inherit Metab Dis. 1999. PMID: 10234623 No abstract available.

8

Isolated and contiguous glycerol kinase gene disorders: a review.

Sjarif DR, Ploos van Amstel JK, Duran M, Beemer FA, Poll-The BT. Sjarif DR, et al. Among authors: duran m. J Inherit Metab Dis. 2000 Sep;23(6):529-47. doi: 10.1023/a:1005660826652. J Inherit Metab Dis. 2000. PMID: 11032329 Review.

9

Hyperketonaemia in glycerol kinase deficiency.

Sjarif DR, Dorland L, Sperl W, de Koning TJ, Beemer FA, Poll-The BT, Duran M. Sjarif DR, et al. Among authors: duran m. J Inherit Metab Dis. 2000 Nov;23(7):760-4. doi: 10.1023/a:1005680211483. J Inherit Metab Dis. 2000. PMID: 11117440 No abstract available.

10

Congenital microcephaly and seizures due to 3-phosphoglycerate dehydrogenase deficiency: outcome of treatment with amino acids.

De Koning TJ, Duran M, Van Maldergem L, Pineda M, Dorland L, Gooskens R, Jaeken J, Poll-The BT. De Koning TJ, et al. Among authors: duran m. J Inherit Metab Dis. 2002 May;25(2):119-25. doi: 10.1023/a:1015624726822. J Inherit Metab Dis. 2002. PMID: 12118526

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