Ketonuria and medium-chain acyl-CoA dehydrogenase deficiency-Reference-Cited by-同舟云学术

Ketonuria and medium-chain acyl-CoA dehydrogenase deficiency

Published:1995 Issue:1 Volume:18 Page:98-99
ISSN:0141-8955
Container-title:Journal of Inherited Metabolic Disease
language:en
Short-container-title:J Inherit Metab Dis

Author:

Patel J. S.,Leonard J. V.

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

http://www.springerlink.com/index/pdf/10.1007/BF00711392

Reference3 articles.

1. Edwards MA, Gray RGF, Rayner PWH, Green A, Pollitt RJ, Coates PM (1986) Two siblings with medium chain acyl CoA dehydrogenase deficiency.24th Annual Meeting of the Society for the Study of Inborn Errors of Metabolism 1986, Amersfoort, The Netherlands, Poster 68.

2. Fletcher JM, Pitt JJ, Thompson GN (1993) Fasting MCAD patients can make ketones.31st Annual Meeting of the Society for the Study of Inborn Errors of Metabolism 1993, Manchester, UK, Poster 57.

3. Heales SJR, Thompson GN, Massoud AF, Rahman S, Halliday D, Leonard JV (1994) Production and disposal of medium-chain fatty acids in children with medium-chain acyl-CoA dehydrogenase deficiency.J Inher Metab Dis 16: 74?80.

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