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Molecular Genetics and Metabolism|September 28, 2011
Nutrition in phenylketonuriaA MacDonald, J C Rocha, M van Rijn, et al.Pediatric Neurology|May 18, 1999
Necrotizing encephalopathy and macrocephaly with mitochondrial complex I deficiencyF Feillet, B Mousson, Y Grignon, et al.Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|December 11, 2013
[L-2-hydroxyglutaric aciduria: report on two cases]S Wagner, C Vianey-Saban, G-S Salomons, et al.Pediatric Pulmonology|February 25, 1998
Respiratory oscillation mechanics in infants with bronchiolitis during mechanical ventilationR Gauthier, C Beyaert, F Feillet, et al.Revue Neurologique|January 1, 1987
[Lesions of the basal ganglia in mumps. Clinical and neuroradiological development in a case]B P Leheup, F Feillet, J Roland, et al.Journal of Chromatography. B, Biomedical Sciences and Applications|April 1, 2000
Analysis of riboflavin and riboflavin cofactor levels in plasma by high-performance liquid chromatographyC D Capo-chichi, J L Guéant, F Feillet, et al.Molecular Genetics and Metabolism|September 21, 2013
Undiagnosed phenylketonuria in parents of phenylketonuric patients, is it worthwhile to be checked?A Wiedemann, B Leheup, S-F Battaglia-Hsu, et al.The Journal of Pediatrics|May 10, 2000
Resting energy expenditure in disorders of propionate metabolismF Feillet, O A Bodamer, M A Dixon, et al.Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|February 6, 2004
[Mitochondrial cytopathy: an unusual infantile cause of total villous atrophy]C Bonnemains, J Berthelot, B Mousson de Camaret, et al.The American Journal of Clinical Nutrition|October 1, 1993
Lipoprotein metabolism in marasmic children of northern MauritaniaF Feillet, H J Parra, K Kamian, et al.Pageof 7