van Sprang FJ - Search Results

1

The cerebro-costo-mandibular syndrome: third report of familial occurrence.

Hennekam RC, Beemer FA, Huijbers WA, Hustinx PA, van Sprang FJ. Hennekam RC, et al. Among authors: van sprang fj. Clin Genet. 1985 Aug;28(2):118-21. doi: 10.1111/j.1399-0004.1985.tb00370.x. Clin Genet. 1985. PMID: 3899422

2

New defects of pyrimidine metabolism.

Wadman SK, Beemer FA, de Bree PK, Duran M, van Gennip AH, Ketting D, van Sprang FJ. Wadman SK, et al. Among authors: van gennip ah, van sprang fj. Adv Exp Med Biol. 1984;165 Pt A:109-14. doi: 10.1007/978-1-4684-4553-4_19. Adv Exp Med Biol. 1984. PMID: 6720361 No abstract available.

3

Adenylosuccinase deficiency: an inborn error of purine nucleotide synthesis.

Jaeken J, Wadman SK, Duran M, van Sprang FJ, Beemer FA, Holl RA, Theunissen PM, de Cock P, van den Bergh F, Vincent MF, et al. Jaeken J, et al. Among authors: van sprang fj. Eur J Pediatr. 1988 Nov;148(2):126-31. doi: 10.1007/BF00445919. Eur J Pediatr. 1988. PMID: 3234432

4

3-Methylglutaconic aciduria: a phenotype in which activity of 3-methylglutaconyl-coenzyme A hydratase is normal.

Gibson KM, Nyhan WL, Sweetman L, Narisawa K, Lehnert W, Divry P, Robinson BH, Roth KS, Beemer FA, van Sprang FJ, et al. Gibson KM, et al. Among authors: van sprang fj. Eur J Pediatr. 1988 Oct;148(1):76-82. doi: 10.1007/BF00441821. Eur J Pediatr. 1988. PMID: 3197737

5

Two sisters with isovaleric acidaemia, multiple attacks of ketoacidosis and normal development.

Duran M, van Sprang FJ, Drewes JG, Bruinvis L, Ketting D, Wadman SK. Duran M, et al. Among authors: van sprang fj. Eur J Pediatr. 1979 Jun 28;131(3):205-11. doi: 10.1007/BF00538944. Eur J Pediatr. 1979. PMID: 477679

6

A case of formiminoglutamic aciduria. Clinical and biochemical studies.

Duran M, Ketting D, de Bree PK, van Sprang FJ, Wadman SK, Penders TJ, Wilms RH. Duran M, et al. Among authors: van sprang fj. Eur J Pediatr. 1981 Jul;136(3):319-23. doi: 10.1007/BF00443002. Eur J Pediatr. 1981. PMID: 7262105

7

3-Hydroxydicarboxylic aciduria due to long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency associated with sudden neonatal death: protective effect of medium-chain triglyceride treatment.

Duran M, Wanders RJ, de Jager JP, Dorland L, Bruinvis L, Ketting D, Ijlst L, van Sprang FJ. Duran M, et al. Among authors: van sprang fj. Eur J Pediatr. 1991 Jan;150(3):190-5. doi: 10.1007/BF01963564. Eur J Pediatr. 1991. PMID: 2044590

8

Letter: Possible hazards of neomycin treatment in methylmalonic acidemia.

Duran M, Bakker HD, Wadman SK, van Sprang FJ. Duran M, et al. Among authors: van sprang fj. Pediatrics. 1974 May;53(5):765-6. Pediatrics. 1974. PMID: 4826734 No abstract available.

9

Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency: identification of a new inborn error of mitochondrial fatty acid beta-oxidation.

Wanders RJ, IJlst L, van Gennip AH, Jakobs C, de Jager JP, Dorland L, van Sprang FJ, Duran M. Wanders RJ, et al. Among authors: van sprang fj. J Inherit Metab Dis. 1990;13(3):311-4. doi: 10.1007/BF01799383. J Inherit Metab Dis. 1990. PMID: 2122092 No abstract available.

10

Rapid diagnosis of 3-hydroxy-3-methylglutaryl-coenzyme A lyase deficiency via enzyme activity measurements in leukocytes or platelets using a simple spectrophotometric method.

Wanders RJ, Zoeters PH, Schutgens RB, de Klerk JB, Duran M, Wadman SK, van Sprang FJ, Hemmes AM, Voorbrood BS. Wanders RJ, et al. Among authors: van sprang fj. Clin Chim Acta. 1990 Aug 31;189(3):327-34. doi: 10.1016/0009-8981(90)90314-i. Clin Chim Acta. 1990. PMID: 2225463

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