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[Neonatal epilepsy and inborn errors of metabolism].
Bahi-Buisson N, Mention K, Léger PL, Valayanopoulos V, Nabbout R, Kaminska A, Plouin P, Dulac O, de Lonlay P, Desguerre I. Bahi-Buisson N, et al. Among authors: mention k. Arch Pediatr. 2006 Mar;13(3):284-92. doi: 10.1016/j.arcped.2005.10.024. Epub 2005 Dec 15. Arch Pediatr. 2006. PMID: 16343871 Review. French.
What's new in metabolic and genetic hypoglycaemias: diagnosis and management.
Valayannopoulos V, Romano S, Mention K, Vassault A, Rabier D, Polak M, Robert JJ, de Keyzer Y, de Lonlay P. Valayannopoulos V, et al. Among authors: mention k. Eur J Pediatr. 2008 Mar;167(3):257-65. doi: 10.1007/s00431-007-0600-2. Epub 2007 Oct 3. Eur J Pediatr. 2008. PMID: 17912550 Review.
Spectrum of movement disorders associated with glutaric aciduria type 1: a study of 16 patients.
Gitiaux C, Roze E, Kinugawa K, Flamand-Rouvière C, Boddaert N, Apartis E, Valayannopoulos V, Touati G, Motte J, Devos D, Mention K, Dobbelaere D, Rodriguez D, Roubertie A, Chabrol B, Feillet F, Vidailhet M, Bahi-Buisson N. Gitiaux C, et al. Among authors: mention k. Mov Disord. 2008 Dec 15;23(16):2392-7. doi: 10.1002/mds.22313. Mov Disord. 2008. PMID: 18823014
Secondary creatine deficiency in ornithine delta-aminotransferase deficiency.
Valayannopoulos V, Boddaert N, Mention K, Touati G, Barbier V, Chabli A, Sedel F, Kaplan J, Dufier JL, Seidenwurm D, Rabier D, Saudubray JM, de Lonlay P. Valayannopoulos V, et al. Among authors: mention k. Mol Genet Metab. 2009 Jun;97(2):109-13. doi: 10.1016/j.ymgme.2008.12.010. Epub 2009 Mar 31. Mol Genet Metab. 2009. PMID: 19345633
Heterogeneity of follow-up procedures in French and Belgian patients with treated hereditary tyrosinemia type 1: results of a questionnaire and proposed guidelines.
Schiff M, Broue P, Chabrol B, De Laet C, Habes D, Mention K, Sarles J, Spraul A, Valayannopoulos V, Ogier de Baulny H; French-Belgian study group for HT-1. Schiff M, et al. Among authors: mention k. J Inherit Metab Dis. 2012 Sep;35(5):823-9. doi: 10.1007/s10545-011-9429-y. Epub 2011 Dec 14. J Inherit Metab Dis. 2012. PMID: 22167277
75 results