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Iodine status in pregnant women and their newborns: are our babies at risk of iodine deficiency?
Travers CA, Guttikonda K, Norton CA, Lewis PR, Mollart LJ, Wiley V, Wilcken B, Eastman CJ, Boyages SC. Travers CA, et al. Among authors: wilcken b. Med J Aust. 2006 Jun 19;184(12):617-20. Med J Aust. 2006. PMID: 16803441
Late-onset nonketotic hyperglycinemia with leukodystrophy and an unusual clinical course.
Chiong MA, Procopis P, Carpenter K, Wilcken B. Chiong MA, et al. Among authors: wilcken b. Pediatr Neurol. 2007 Oct;37(4):283-6. doi: 10.1016/j.pediatrneurol.2007.05.016. Pediatr Neurol. 2007. PMID: 17903674
AAV2/8-mediated correction of OTC deficiency is robust in adult but not neonatal Spf(ash) mice.
Cunningham SC, Spinoulas A, Carpenter KH, Wilcken B, Kuchel PW, Alexander IE. Cunningham SC, et al. Among authors: wilcken b. Mol Ther. 2009 Aug;17(8):1340-6. doi: 10.1038/mt.2009.88. Epub 2009 Apr 21. Mol Ther. 2009. PMID: 19384294 Free PMC article.
Problems in the management of urea cycle disorders.
Wilcken B. Wilcken B. Mol Genet Metab. 2004 Apr;81 Suppl 1:S86-91. doi: 10.1016/j.ymgme.2003.10.016. Mol Genet Metab. 2004. PMID: 15050980 Review.
Maternal phenylketonuria: a continuing problem.
Mowat DR, Hayden MC, Thompson SM, Wilcken B. Mowat DR, et al. Among authors: wilcken b. Med J Aust. 1999 Jun 21;170(12):592-5. Med J Aust. 1999. PMID: 10416429
Clumsiness, confusion, coma, and valproate.
Ellaway CJ, Bennetts B, Tuck RR, Wilcken B. Ellaway CJ, et al. Among authors: wilcken b. Lancet. 1999 Apr 24;353(9162):1408. doi: 10.1016/s0140-6736(99)01433-6. Lancet. 1999. PMID: 10227223 No abstract available.
Neonatal diagnosis of long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency and implications for newborn screening by tandem mass spectrometry.
Carpenter KH, Wilcken B. Carpenter KH, et al. Among authors: wilcken b. J Inherit Metab Dis. 1999 Oct;22(7):840-1. doi: 10.1023/a:1005566309942. J Inherit Metab Dis. 1999. PMID: 10518286 No abstract available.
Contiguous gene deletion syndrome in a female with ornithine transcarbamylase deficiency.
Balasubramaniam S, Rudduck C, Bennetts B, Peters G, Wilcken B, Ellaway C. Balasubramaniam S, et al. Among authors: wilcken b. Mol Genet Metab. 2010 Jan;99(1):34-41. doi: 10.1016/j.ymgme.2009.08.007. Mol Genet Metab. 2010. PMID: 19783189
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