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Clinical and biochemical spectrum of D-bifunctional protein deficiency.
Ferdinandusse S, Denis S, Mooyer PA, Dekker C, Duran M, Soorani-Lunsing RJ, Boltshauser E, Macaya A, Gärtner J, Majoie CB, Barth PG, Wanders RJ, Poll-The BT. Ferdinandusse S, et al. Among authors: denis s. Ann Neurol. 2006 Jan;59(1):92-104. doi: 10.1002/ana.20702. Ann Neurol. 2006. PMID: 16278854
Molecular analysis of disorders of peroxisomal beta-oxidation.
Wanders RJ, van Roermund CW, Denis S, Schutgens RB, Ijlst L, Tager JM. Wanders RJ, et al. Among authors: denis s. Prog Clin Biol Res. 1992;375:507-19. Prog Clin Biol Res. 1992. PMID: 1438395 Review. No abstract available.
Phytanoyl-CoA hydroxylase is present in human liver, located in peroxisomes, and deficient in Zellweger syndrome: direct, unequivocal evidence for the new, revised pathway of phytanic acid alpha-oxidation in humans.
Jansen GA, Mihalik SJ, Watkins PA, Moser HW, Jakobs C, Denis S, Wanders RJ. Jansen GA, et al. Among authors: denis s. Biochem Biophys Res Commun. 1996 Dec 4;229(1):205-10. doi: 10.1006/bbrc.1996.1781. Biochem Biophys Res Commun. 1996. PMID: 8954107 Free article.
Metabolic aspects of peroxisomal disorders.
Wanders RJ, Jansen G, van Roermund CW, Denis S, Schutgens RB, Jakobs BS. Wanders RJ, et al. Among authors: denis s. Ann N Y Acad Sci. 1996 Dec 27;804:450-60. doi: 10.1111/j.1749-6632.1996.tb18636.x. Ann N Y Acad Sci. 1996. PMID: 8993564
Complementation analysis of fibroblasts from peroxisomal fatty acid oxidation deficient patients shows high frequency of bifunctional enzyme deficiency plus intragenic complementation: unequivocal evidence for differential defects in the same enzyme protein.
van Grunsven EG, van Roermund CW, Denis S, Wanders RJ. van Grunsven EG, et al. Among authors: denis s. Biochem Biophys Res Commun. 1997 Jun 9;235(1):176-9. doi: 10.1006/bbrc.1997.6755. Biochem Biophys Res Commun. 1997. PMID: 9196058
220 results