Duran M - Search Results

1

Identification of methyl-branched chain dicarboxylic acids in amniotic fluid and urine in propionic and methylmalonic acidemia.

Jakobs C, Dorland L, Sweetman L, Duran M, Nyhan WL, Wadman SK. Jakobs C, et al. Among authors: duran m. Pediatr Res. 1984 Nov;18(11):1185-91. doi: 10.1203/00006450-198411000-00027. Pediatr Res. 1984. PMID: 6514446

2

D-glyceric acidemia: an inborn error associated with fructose metabolism.

Duran M, Beemer FA, Bruinvis L, Ketting D, Wadman SK. Duran M, et al. Pediatr Res. 1987 May;21(5):502-6. doi: 10.1203/00006450-198705000-00016. Pediatr Res. 1987. PMID: 3588091

3

Prenatal diagnosis of glutaric aciduria type II by direct chemical analysis of dicarboxylic acids in amniotic fluid.

Jakobs C, Sweetman L, Wadman SK, Duran M, Saudubray JM, Nyhan WL. Jakobs C, et al. Among authors: duran m. Eur J Pediatr. 1984 Jan;141(3):153-7. doi: 10.1007/BF00443213. Eur J Pediatr. 1984. PMID: 6698061

4

The identification of (E)-2-methylglutaconic acid, a new isoleucine metabolite, in the urine of patients with beta-ketothiolase deficiency, propionic acidaemia and methylmalonic acidaemia.

Duran M, Bruinvis L, Ketting D, Kamerling JP, Wadman SK, Schutgens RB. Duran M, et al. Biomed Mass Spectrom. 1982 Jan;9(1):1-5. doi: 10.1002/bms.1200090102. Biomed Mass Spectrom. 1982. PMID: 7059658

5

Magnetic resonance imaging and spectroscopy of the brain in propionic acidemia: clinical and biochemical considerations.

Bergman AJ, Van der Knaap MS, Smeitink JA, Duran M, Dorland L, Valk J, Poll-The BT. Bergman AJ, et al. Among authors: duran m. Pediatr Res. 1996 Sep;40(3):404-9. doi: 10.1203/00006450-199609000-00007. Pediatr Res. 1996. PMID: 8865276 Review.

6

[Methylmalonic acidemia. Diagnosis and treatment in various patients].

Bakker HD, Duran M, van Gennip AH, van Sprang FJ, Wadman SK. Bakker HD, et al. Among authors: duran m. Ned Tijdschr Geneeskd. 1978 May 20;122(20):707-12. Ned Tijdschr Geneeskd. 1978. PMID: 26029 Dutch. No abstract available.

7

Deranged isoleucine metabolism during ketotic attacks in patients with methylmalonic acidaemia.

Duran M, Bruinvis L, Ketting D, Wadman SK. Duran M, et al. J Inherit Metab Dis. 1978;1(3):105-7. doi: 10.1007/BF01805683. J Inherit Metab Dis. 1978. PMID: 116077

8

The variability of metabolite excretion in propionicacidaemia.

Duran M, Gompertz D, Bruinvis L, Ketting D, Wadman SK. Duran M, et al. Clin Chim Acta. 1978 Jan 2;82(1-2):93-9. doi: 10.1016/0009-8981(78)90030-x. Clin Chim Acta. 1978. PMID: 618687

9

Diagnosis of medium-chain acyl-CoA dehydrogenase deficiency in lymphocytes and liver by a gas chromatographic method: the effect of oral riboflavin supplementation.

Duran M, Cleutjens CB, Ketting D, Dorland L, de Klerk JB, van Sprang FJ, Berger R. Duran M, et al. Pediatr Res. 1992 Jan;31(1):39-42. doi: 10.1203/00006450-199201000-00007. Pediatr Res. 1992. PMID: 1594328

10

Direct identification of propionylcarnitine in propionic acidaemia: biochemical and clinical results of oral carnitine supplementation.

Duran M, Ketting D, Beckeringh TE, Leupold D, Wadman SK. Duran M, et al. J Inherit Metab Dis. 1986;9(2):202-7. doi: 10.1007/BF01799460. J Inherit Metab Dis. 1986. PMID: 3091925

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