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Page 1
Prenatal diagnosis of Hunter syndrome using fetal plasma.
Lissens W, Van Lierde M, Decaluwe J, Foulon W, Evrard P, Van Hoof F, Freund M, Liebaers I. Lissens W, et al. Among authors: van lierde m, van hoof f. Prenat Diagn. 1988 Jan;8(1):59-62. doi: 10.1002/pd.1970080108. Prenat Diagn. 1988. PMID: 3125535
Bile acids in peroxisomal disorders.
Van Eldere JR, Parmentier GG, Eyssen HJ, Wanders RJ, Schutgens RB, Vamecq J, Van Hoof F, Poll-The BT, Saudubray JM. Van Eldere JR, et al. Among authors: van hoof f. Eur J Clin Invest. 1987 Oct;17(5):386-90. doi: 10.1111/j.1365-2362.1987.tb01131.x. Eur J Clin Invest. 1987. PMID: 2446876
Altered acyl-CoA metabolism in riboflavin deficiency.
Veitch K, Draye JP, Vamecq J, Causey AG, Bartlett K, Sherratt HS, Van Hoof F. Veitch K, et al. Among authors: van hoof f. Biochim Biophys Acta. 1989 Dec 18;1006(3):335-43. doi: 10.1016/0005-2760(89)90021-0. Biochim Biophys Acta. 1989. PMID: 2574596
Mitochondrial and peroxisomal metabolism of glutaryl-CoA.
Vamecq J, de Hoffmann E, Van Hoof F. Vamecq J, et al. Among authors: van hoof f. Eur J Biochem. 1985 Feb 1;146(3):663-9. doi: 10.1111/j.1432-1033.1985.tb08702.x. Eur J Biochem. 1985. PMID: 3971969 Free article.
111 results