Variability in the clinical management of fatty acid oxidation disorders: results of a survey of Canadian metabolic physicians-Reference-Cited by-同舟云学术

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Variability in the clinical management of fatty acid oxidation disorders: results of a survey of Canadian metabolic physicians

Published:2011-06-01 Issue:1 Volume:35 Page:115-123
ISSN:0141-8955
Container-title:Journal of Inherited Metabolic Disease
language:en
Short-container-title:J Inherit Metab Dis

Author:

Potter Beth K.,Little Julian,Chakraborty Pranesh,Kronick Jonathan B.,Evans Jessica,Frei Julia,Sutherland Sarah C.,Wilson Kumanan,Wilson Brenda J.

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

http://www.springerlink.com/index/pdf/10.1007/s10545-011-9352-2

Reference25 articles.

1. Arnold GL, VanHove J, Freedenberg D et al. (2009) A Delphi clinical practice protocol for the management of very long chain acyl-CoA dehydrogenase deficiency. Mol Genet Metab 96:85–90

2. Arnold GL, Saavedra-Matiz CA, Galvin-Parton PA et al. (2010) Lack of genotype-phenotype correlations and outcome in MCAD deficiency diagnosed by newborn screening in New York State. Mol Genet Metab 99:263–268

3. Clancy C, Collins FS (2010) Patient-centred outcomes research institute: the intersection of science and health care. Sci Transl Med 2:37cm18

4. Dillman DA (2007) Mail and Internet Surveys. The Tailored Design Method. 2nd ed, 2007 update. New York: Wiley, Inc

5. Djouadi F, Aubey F, Schlemmer D et al. (2005) Bezafibrate increases very-long-chain acyl-CoA dehydrogenase protein and mRNA expression in deficient fibroblasts and is a potential therapy for fatty acid oxidation disorders. Hum Mol Genet 14:2695–2703

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