Clinical and genetic characteristics of patients with fatty acid oxidation disorders identified by newborn screening-Reference-Cited by-同舟云学术

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Clinical and genetic characteristics of patients with fatty acid oxidation disorders identified by newborn screening

Published:2018-03-08 Issue:1 Volume:18 Page:
ISSN:1471-2431
Container-title:BMC Pediatrics
language:en
Short-container-title:BMC Pediatr

Author:

Kang Eungu,Kim Yoon-Myung,Kang Minji,Heo Sun-Hee,Kim Gu-Hwan,Choi In-Hee,Choi Jin-Ho,Yoo Han-Wook,Lee Beom Hee

Publisher

Springer Science and Business Media LLC

Subject

Pediatrics, Perinatology, and Child Health

Link

http://link.springer.com/content/pdf/10.1186/s12887-018-1069-z.pdf

Reference36 articles.

1. Houten SM, Wanders RJ. A general introduction to the biochemistry of mitochondrial fatty acid beta-oxidation. J Inherit Metab Dis. 2010;33(5):469–77.

2. Wanders RJ, Vreken P, den Boer ME, Wijburg FA, van Gennip AH, IJlst L. Disorders of mitochondrial fatty acyl-CoA beta-oxidation. J Inherit Metab Dis. 1999;22(4):442–87.

3. Rinaldo P, Matern D, Bennett MJ. Fatty acid oxidation disorders. Annu Rev Physiol. 2002;64:477–502.

4. Gregersen N, Andresen BS, Pedersen CB, Olsen RK, Corydon TJ, Bross P. Mitochondrial fatty acid oxidation defects--remaining challenges. J Inherit Metab Dis. 2008;31(5):643–57.

5. Lindner M, Hoffmann GF, Matern D. Newborn screening for disorders of fatty-acid oxidation: experience and recommendations from an expert meeting. J Inherit Metab Dis. 2010;33(5):521–6.

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