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J Baruteau

Showing results (11-20 of 14) with videos related to

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Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|December 24, 2011
[Sjögren-Larsson syndrome: 2 case reports]C Galoin-Bertail, H Ogier de Baulny, R Wanders, et al.
Mitochondrion|July 11, 2014
Successful reversal of propionic acidaemia associated cardiomyopathy: evidence for low myocardial coenzyme Q10 status and secondary mitochondrial dysfunction as an underlying pathophysiological mechanismJ Baruteau, I Hargreaves, S Krywawych, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|January 17, 2012
[Medium-chain acyl-CoA-dehydrogenase (MCAD) deficiency: French consensus for neonatal screening, diagnosis, and management]F Feillet, H Ogier, D Cheillan, et al.
Molecular Genetics and Metabolism|October 12, 2013
Dietary management of urea cycle disorders: European practiceS Adam, M F Almeida, M Assoun, et al.
Pageof 2

Showing results (11-20 of 14) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 14 results.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|December 24, 2011
[Sjögren-Larsson syndrome: 2 case reports]C Galoin-Bertail, H Ogier de Baulny, R Wanders, et al.
Mitochondrion|July 11, 2014
Successful reversal of propionic acidaemia associated cardiomyopathy: evidence for low myocardial coenzyme Q10 status and secondary mitochondrial dysfunction as an underlying pathophysiological mechanismJ Baruteau, I Hargreaves, S Krywawych, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|January 17, 2012
[Medium-chain acyl-CoA-dehydrogenase (MCAD) deficiency: French consensus for neonatal screening, diagnosis, and management]F Feillet, H Ogier, D Cheillan, et al.
Molecular Genetics and Metabolism|October 12, 2013
Dietary management of urea cycle disorders: European practiceS Adam, M F Almeida, M Assoun, et al.
Pageof 2