Funalot B - Search Results

1

Krox20 inactivation in the PNS leads to CNS/PNS boundary transgression by central glia.

Coulpier F, Decker L, Funalot B, Vallat JM, Garcia-Bragado F, Charnay P, Topilko P. Coulpier F, et al. Among authors: funalot b. Rev Neurol (Paris). 2011 Jan;167(1):51-6. doi: 10.1016/j.neurol.2010.07.043. Epub 2010 Dec 28. Rev Neurol (Paris). 2011. PMID: 21193208

2

CNS/PNS boundary transgression by central glia in the absence of Schwann cells or Krox20/Egr2 function.

Coulpier F, Decker L, Funalot B, Vallat JM, Garcia-Bragado F, Charnay P, Topilko P. Coulpier F, et al. Among authors: funalot b. J Neurosci. 2010 Apr 28;30(17):5958-67. doi: 10.1523/JNEUROSCI.0017-10.2010. J Neurosci. 2010. PMID: 20427655 Free PMC article.

3

[Krox20 inactivation in the PNS leads to CNS/PNS boundary transgression by central glia].

Charnay P, Coulpier F, Decker L, Funalot B, Vallat JM, Garcia-Bragado F, Topilko P. Charnay P, et al. Among authors: funalot b. Bull Acad Natl Med. 2010 Apr-May;194(4-5):743-4. Bull Acad Natl Med. 2010. PMID: 21568047 French.

4

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

5

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.

6

Motor neuronopathy in Chediak-Higashi syndrome.

Mathis S, Cintas P, de Saint-Basile G, Magy L, Funalot B, Vallat JM. Mathis S, et al. Among authors: funalot b. J Neurol Sci. 2014 Sep 15;344(1-2):203-7. doi: 10.1016/j.jns.2014.06.026. Epub 2014 Jun 21. J Neurol Sci. 2014. PMID: 25043664

7

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.

8

[Peripheral neuropathies due to mitochondrial disorders].

Funalot B. Funalot B. Rev Neurol (Paris). 2009 Dec;165(12):1118-21. doi: 10.1016/j.neurol.2009.10.001. Rev Neurol (Paris). 2009. PMID: 19942242 French.

9

[Exogenous risk factors in sporadic ALS: a review of the literature].

Gil J, Funalot B, Torny F, Lacoste M, Couratier P. Gil J, et al. Among authors: funalot b. Rev Neurol (Paris). 2007 Nov;163(11):1021-30. doi: 10.1016/s0035-3787(07)74174-7. Rev Neurol (Paris). 2007. PMID: 18033040 Review. French.

10

INF2 mutations in Charcot-Marie-Tooth disease with glomerulopathy.

Boyer O, Nevo F, Plaisier E, Funalot B, Gribouval O, Benoit G, Huynh Cong E, Arrondel C, Tête MJ, Montjean R, Richard L, Karras A, Pouteil-Noble C, Balafrej L, Bonnardeaux A, Canaud G, Charasse C, Dantal J, Deschenes G, Deteix P, Dubourg O, Petiot P, Pouthier D, Leguern E, Guiochon-Mantel A, Broutin I, Gubler MC, Saunier S, Ronco P, Vallat JM, Alonso MA, Antignac C, Mollet G. Boyer O, et al. Among authors: funalot b. N Engl J Med. 2011 Dec 22;365(25):2377-88. doi: 10.1056/NEJMoa1109122. N Engl J Med. 2011. PMID: 22187985 Free article.

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