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[Epilepsy in the child].
Milh M, Chabrol B. Milh M, et al. Among authors: chabrol b. Rev Prat. 2009 May 20;59(5):689-93. Rev Prat. 2009. PMID: 19552211 French. No abstract available.
[Epilepsy and mitochondrial diseases: retrospective study on 53 epileptic children].
Caietta E, Cano A, Halbert C, Hugonenq C, Mancini J, Milh M, Lépine A, Villeneuve N, Chaussenot A, Paquis-Flucklinger V, Chabrol B. Caietta E, et al. Among authors: chabrol b. Arch Pediatr. 2012 Aug;19(8):794-802. doi: 10.1016/j.arcped.2012.05.004. Epub 2012 Jul 11. Arch Pediatr. 2012. PMID: 22789745 French.
Heterogeneity of FHF1 related phenotype: Novel case with early onset severe attacks of apnea, partial mitochondrial respiratory chain complex II deficiency, neonatal onset seizures without neurodegeneration.
Villeneuve N, Abidi A, Cacciagli P, Mignon-Ravix C, Chabrol B, Villard L, Milh M. Villeneuve N, et al. Among authors: chabrol b. Eur J Paediatr Neurol. 2017 Sep;21(5):783-786. doi: 10.1016/j.ejpn.2017.04.001. Epub 2017 Apr 29. Eur J Paediatr Neurol. 2017. PMID: 28506426
336 results