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Inherited peripheral neuropathies due to mitochondrial disorders.
Cassereau J, Codron P, Funalot B. Cassereau J, et al. Among authors: funalot b. Rev Neurol (Paris). 2014 May;170(5):366-74. doi: 10.1016/j.neurol.2013.11.005. Epub 2014 Apr 24. Rev Neurol (Paris). 2014. PMID: 24768438 Review.
Metabo-lipidomics of Fibroblasts and Mitochondrial-Endoplasmic Reticulum Extracts from ALS Patients Shows Alterations in Purine, Pyrimidine, Energetic, and Phospholipid Metabolisms.
Veyrat-Durebex C, Bris C, Codron P, Bocca C, Chupin S, Corcia P, Vourc'h P, Hergesheimer R, Cassereau J, Funalot B, Andres CR, Lenaers G, Couratier P, Reynier P, Blasco H. Veyrat-Durebex C, et al. Among authors: funalot b. Mol Neurobiol. 2019 Aug;56(8):5780-5791. doi: 10.1007/s12035-019-1484-7. Epub 2019 Jan 24. Mol Neurobiol. 2019. PMID: 30680691
[Hereditary peripheral neuropathies].
Vallat JM, Tazir M, Calvo J, Funalot B. Vallat JM, et al. Among authors: funalot b. Presse Med. 2009 Sep;38(9):1325-34. doi: 10.1016/j.lpm.2009.01.014. Epub 2009 Mar 26. Presse Med. 2009. PMID: 19327944 Review. French.
Genotype-phenotype correlations in Charcot-Marie-Tooth disease type 2 caused by mitofusin 2 mutations.
Calvo J, Funalot B, Ouvrier RA, Lazaro L, Toutain A, De Mas P, Bouche P, Gilbert-Dussardier B, Arne-Bes MC, Carrière JP, Journel H, Minot-Myhie MC, Guillou C, Ghorab K, Magy L, Sturtz F, Vallat JM, Magdelaine C. Calvo J, et al. Among authors: funalot b. Arch Neurol. 2009 Dec;66(12):1511-6. doi: 10.1001/archneurol.2009.284. Arch Neurol. 2009. PMID: 20008656
Nerve biopsy: requirements for diagnosis and clinical value.
Vallat JM, Funalot B, Magy L. Vallat JM, et al. Among authors: funalot b. Acta Neuropathol. 2011 Mar;121(3):313-26. doi: 10.1007/s00401-011-0804-4. Epub 2011 Feb 4. Acta Neuropathol. 2011. PMID: 21293868 Review.
115 results