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Page 1
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. Among authors: magdelaine c. Ann Neurol. 2012 May;71(5):719-23. doi: 10.1002/ana.23527. Ann Neurol. 2012. PMID: 22522483
Autosomal-recessive Charcot-Marie-Tooth diseases.
Vallat JM, Tazir M, Magdelaine C, Sturtz F, Grid D. Vallat JM, et al. Among authors: magdelaine c. J Neuropathol Exp Neurol. 2005 May;64(5):363-70. doi: 10.1093/jnen/64.5.363. J Neuropathol Exp Neurol. 2005. PMID: 15892292 Review.
IgG neuropathy: an immunoelectron microscopic study.
Vallat JM, Magy L, Sindou P, Magdelaine C, Cros D. Vallat JM, et al. Among authors: magdelaine c. J Neuropathol Exp Neurol. 2005 May;64(5):386-90. doi: 10.1093/jnen/64.5.386. J Neuropathol Exp Neurol. 2005. PMID: 15892295
[Autosomal recessive forms of Charcot-Marie-Tooth disease].
Vallat JM, Grid D, Magdelaine C, Sturtz F, Levy N, Tazir M. Vallat JM, et al. Among authors: magdelaine c. Bull Acad Natl Med. 2005 Jan;189(1):55-68; discussion 68-9. Bull Acad Natl Med. 2005. PMID: 16119880 Review. French.
A highly specific microarray method for point mutation detection.
Baaj Y, Magdelaine C, Ubertelli V, Valat C, Talini L, Soussaline F, Khomyakova E, Funalot B, Vallat JM, Sturtz FG. Baaj Y, et al. Among authors: magdelaine c. Biotechniques. 2008 Jan;44(1):119-26. doi: 10.2144/000112630. Biotechniques. 2008. PMID: 18254389 Free article.
53 results