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Endoneurial fibroblast-like cells.
Richard L, Topilko P, Magy L, Decouvelaere AV, Charnay P, Funalot B, Vallat JM. Richard L, et al. Among authors: funalot b. J Neuropathol Exp Neurol. 2012 Nov;71(11):938-47. doi: 10.1097/NEN.0b013e318270a941. J Neuropathol Exp Neurol. 2012. PMID: 23095846 Review.
[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.
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.
[Charcot-Marie-Tooth (CMT) disease: an update].
Vallat JM, Funalot B. Vallat JM, et al. Among authors: funalot b. Med Sci (Paris). 2010 Oct;26(10):842-7. doi: 10.1051/medsci/20102610842. Med Sci (Paris). 2010. PMID: 20929675 Free article. Review. French.
Homozygous deletion of an EGR2 enhancer in congenital amyelinating neuropathy.
Funalot B, Topilko P, Arroyo MA, Sefiani A, Hedley-Whyte ET, Yoldi ME, Richard L, Touraille E, Laurichesse M, Khalifa E, Chauzeix J, Ouedraogo A, Cros D, Magdelaine C, Sturtz FG, Urtizberea JA, Charnay P, Bragado FG, Vallat JM. Funalot B, et al. Ann Neurol. 2012 May;71(5):719-23. doi: 10.1002/ana.23527. Ann Neurol. 2012. PMID: 22522483
[Familial amyloidotic polyneuropathies].
Vallat JM, Funalot B, Faugeras F, Magy L. Vallat JM, et al. Among authors: funalot b. Bull Acad Natl Med. 2012 Oct;196(7):1321-9; discussion 1329-31. Bull Acad Natl Med. 2012. PMID: 23815017 Review. French.
The various Charcot-Marie-Tooth diseases.
Vallat JM, Mathis S, Funalot B. Vallat JM, et al. Among authors: funalot b. Curr Opin Neurol. 2013 Oct;26(5):473-80. doi: 10.1097/WCO.0b013e328364c04b. Curr Opin Neurol. 2013. PMID: 23945280 Review.
116 results