Subject
Genetics (clinical),Genetics
Reference11 articles.
1. Chalmers, R. A., Lawson, A. M., Whitelaw, A. and Purkiss, P. Twin siblings with a Reye's-like syndrome associated with an abnormal organic aciduria, hypoglycemia, diarrhea, vomiting with close similarities to Jamaican vomiting sickness.Pediatr. Res. 14 (1980) 1097–1103
2. Gregersen, N. Studies on the effects of saturated and unsaturated short-chain monocarboxylic acids on the energy metabolism of rat liver mitochondria.Pediatr. Res. 13 (1979) 1227–1230
3. Gregersen, N., Rosleff, F., Kølvraa, S., Hobolth, N., Rasmussen, K. and Lauritzen, R. Non-ketotic C6-C10-dicarboxylic aciduria: Biochemical investigations of two cases.Clin. Chim. Acta 102 (1980a) 179–189
4. Gregersen, N., Kølvraa, S., Rasmussen, K., Christensen, E., Brandt, N. J., Ebbesen, F. and Hansen, F. A. Biochemical studies in a patient with defects in the metabolism of acyl-CoA and sarcosine: Another case of glutaric aciduria type II.J. Inher. Metab. Dis. 3 (1980b) 67–72
5. Gregersen, N., Wintzensen, H., Kølvraa, S., Christensen, E., Christensen, M. F., Brandt, N. J. and Rasmussen, K. Riboflavin treatment of a patient with β-oxidation defect.Proceedings from 2nd Clinical Research Centre symposium on ‘Advances in the treatment of inborn errors of metabolism’, London 1981
Cited by
30 articles.
订阅此论文施引文献
订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献