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231 results
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Rare diseases and the assessment of intervention: what sorts of clinical trials can we use?
Wilcken B. Wilcken B. J Inherit Metab Dis. 2001 Apr;24(2):291-8. doi: 10.1023/a:1010387522195. J Inherit Metab Dis. 2001. PMID: 11405347 Review.
3-Methylcrotonyl-CoA carboxylase deficiency: to screen or not to screen?
Wilcken B. Wilcken B. J Inherit Metab Dis. 2016 Mar;39(2):171-2. doi: 10.1007/s10545-015-9906-9. Epub 2015 Dec 11. J Inherit Metab Dis. 2016. PMID: 26660660 No abstract available.
Expanded newborn screening in New South Wales: missed cases.
Estrella J, Wilcken B, Carpenter K, Bhattacharya K, Tchan M, Wiley V. Estrella J, et al. Among authors: wilcken b. J Inherit Metab Dis. 2014 Nov;37(6):881-7. doi: 10.1007/s10545-014-9727-2. Epub 2014 Jun 27. J Inherit Metab Dis. 2014. PMID: 24970580
Clinical practice and the development of evidence.
Wilcken B. Wilcken B. J Inherit Metab Dis. 2012 Jan;35(1):3-4. doi: 10.1007/s10545-011-9380-y. J Inherit Metab Dis. 2012. PMID: 21863278 No abstract available.
Newborn screening: how are we travelling, and where should we be going?
Wilcken B. Wilcken B. J Inherit Metab Dis. 2011 Jun;34(3):569-74. doi: 10.1007/s10545-011-9326-4. Epub 2011 Apr 16. J Inherit Metab Dis. 2011. PMID: 21499716 Review.
Diagnosis and management of glutaric aciduria type I--revised recommendations.
Kölker S, Christensen E, Leonard JV, Greenberg CR, Boneh A, Burlina AB, Burlina AP, Dixon M, Duran M, García Cazorla A, Goodman SI, Koeller DM, Kyllerman M, Mühlhausen C, Müller E, Okun JG, Wilcken B, Hoffmann GF, Burgard P. Kölker S, et al. Among authors: wilcken b. J Inherit Metab Dis. 2011 Jun;34(3):677-94. doi: 10.1007/s10545-011-9289-5. Epub 2011 Mar 23. J Inherit Metab Dis. 2011. PMID: 21431622 Free PMC article. Review.
Fatty acid oxidation disorders: outcome and long-term prognosis.
Wilcken B. Wilcken B. J Inherit Metab Dis. 2010 Oct;33(5):501-6. doi: 10.1007/s10545-009-9001-1. Epub 2010 Jan 5. J Inherit Metab Dis. 2010. PMID: 20049534 Review.
Newborn screening for cystic fibrosis: techniques and strategies.
Wilcken B. Wilcken B. J Inherit Metab Dis. 2007 Aug;30(4):537-43. doi: 10.1007/s10545-007-0584-0. Epub 2007 May 12. J Inherit Metab Dis. 2007. PMID: 17505915
Asymmetric dimethylarginine in homocystinuria due to cystathionine beta-synthase deficiency: relevance of renal function.
Wilcken DE, Wang J, Sim AS, Green K, Wilcken B. Wilcken DE, et al. Among authors: wilcken b. J Inherit Metab Dis. 2006 Feb;29(1):30-7. doi: 10.1007/s10545-006-0208-0. J Inherit Metab Dis. 2006. PMID: 16601865
Mini-symposium: newborn screening for inborn errors of metabolism--clinical effectiveness.
Wilcken B. Wilcken B. J Inherit Metab Dis. 2006 Apr-Jun;29(2-3):366-9. doi: 10.1007/s10545-005-0254-z. J Inherit Metab Dis. 2006. PMID: 16763903
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