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166 results

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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: cros d. Ann Neurol. 2012 May;71(5):719-23. doi: 10.1002/ana.23527. Ann Neurol. 2012. PMID: 22522483
IgG neuropathy: an immunoelectron microscopic study.
Vallat JM, Magy L, Sindou P, Magdelaine C, Cros D. Vallat JM, et al. Among authors: cros d. J Neuropathol Exp Neurol. 2005 May;64(5):386-90. doi: 10.1093/jnen/64.5.386. J Neuropathol Exp Neurol. 2005. PMID: 15892295
FOSMN syndrome: novel insight into disease pathophysiology.
Vucic S, Stein TD, Hedley-Whyte ET, Reddel SR, Tisch S, Kotschet K, Cros D, Kiernan MC. Vucic S, et al. Among authors: cros d. Neurology. 2012 Jul 3;79(1):73-9. doi: 10.1212/WNL.0b013e31825dce13. Epub 2012 Jun 20. Neurology. 2012. PMID: 22722633
Interferon beta-1a as an investigational treatment for CIDP.
Vallat JM, Hahn AF, Léger JM, Cros DP, Magy L, Tabaraud F, Bouche P, Preux PM. Vallat JM, et al. Among authors: cros dp. Neurology. 2003 Apr 1;60(8 Suppl 3):S23-8. doi: 10.1212/wnl.60.8_suppl_3.s23. Neurology. 2003. PMID: 12707419 Clinical Trial.
166 results