Wadman SK - Search Results

1

3-hydroxy-3-methylglutaryl coenzyme A lyase deficiency: postnatal management following prenatal diagnosis by analysis of maternal urine.

Duran M, Schutgens RB, Ketel A, Heymans H, Bertssen MW, Ketting D, Wadman SK. Duran M, et al. Among authors: wadman sk. J Pediatr. 1979 Dec;95(6):1004-7. doi: 10.1016/s0022-3476(79)80297-8. J Pediatr. 1979. PMID: 91680 No abstract available.

2

Lethal hypoglycemia in a child with a deficiency of 3-hydroxy-3-methylglutarylcoenzyme A lyase.

Schutgens RB, Heymans H, Ketel A, Veder HA, Duran M, Ketting D, Wadman SK. Schutgens RB, et al. Among authors: wadman sk. J Pediatr. 1979 Jan;94(1):89-91. doi: 10.1016/s0022-3476(79)80364-9. J Pediatr. 1979. PMID: 758433 No abstract available.

3

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: wadman sk. Eur J Pediatr. 1979 Jun 28;131(3):205-11. doi: 10.1007/BF00538944. Eur J Pediatr. 1979. PMID: 477679

4

Organic acid excretion in a patient with 3-hydroxy-3-methylglutaryl-CoA lyase deficiency: facts and artefacts.

Duran M, Ketting D, Wadman SK, Jakobs C, Schutgens RB, Veder HA. Duran M, et al. Among authors: wadman sk. Clin Chim Acta. 1978 Dec 1;90(2):187-93. doi: 10.1016/0009-8981(78)90521-1. Clin Chim Acta. 1978. PMID: 719902

5

Propionyl-CoA carboxylase deficiency with overflow of metabolites of isoleucine catabolism at all levels.

Przyrembel H, Bremer HJ, Duran M, Bruinvis L, Ketting D, Wadman SK, Baumgartner R, Irle U, Bachmann C. Przyrembel H, et al. Among authors: wadman sk. Eur J Pediatr. 1979 Jan 18;130(1):1-14. doi: 10.1007/BF00441893. Eur J Pediatr. 1979. PMID: 759179

6

3-methyl-3-butenoic acid: an artefact in the urinary metabolic pattern of patients with 3-hydroxy-3-methylglutaryl-CoA lyase deficiency.

Jakobs C, Bojasch M, Duran M, Ketting D, Wadman SK, Leupold D. Jakobs C, et al. Among authors: wadman sk. Clin Chim Acta. 1980 Sep 8;106(1):85-9. doi: 10.1016/0009-8981(80)90377-0. Clin Chim Acta. 1980. PMID: 6157502 No abstract available.

7

Clinical and biochemical observations on a child with a deficiency of 3-hydroxy-3-methylglutaryl coenzyme A lyase.

Ketel A, Ket JL, Schutgens RB, Duran M, Wadman SK. Ketel A, et al. Among authors: wadman sk. J Inherit Metab Dis. 1980;3(3):89-90. doi: 10.1007/BF02312535. J Inherit Metab Dis. 1980. PMID: 6158624 No abstract available.

8

Inherited 3-methylglutaconic aciduria in two brothers--another defect of leucine metabolism.

Duran M, Beemer FA, Tibosch AS, Bruinvis L, Ketting D, Wadman SK. Duran M, et al. Among authors: wadman sk. J Pediatr. 1982 Oct;101(4):551-4. doi: 10.1016/s0022-3476(82)80698-7. J Pediatr. 1982. PMID: 6181239

9

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: wadman sk. Eur J Pediatr. 1981 Jul;136(3):319-23. doi: 10.1007/BF00443002. Eur J Pediatr. 1981. PMID: 7262105

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: wadman sk. 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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