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Page 1
Correspondence.
Soler VJ, Mahieu L, Matonti F, Pagot-Mathis V. Soler VJ, et al. Among authors: mahieu l. Retina. 2015 Dec;35(12):e73-4. doi: 10.1097/IAE.0000000000000884. Retina. 2015. PMID: 26539797 No abstract available.
MRI features of demyelinating disease associated with anti-MOG antibodies in adults.
Denève M, Biotti D, Patsoura S, Ferrier M, Meluchova Z, Mahieu L, Heran F, Vignal C, Deschamps R, Gout O, Champfleur NM, Ayrignac X, Dallière CC, Labauge P, Dulau C, Tourdias T, Dumas H, Cognard C, Brassat D, Bonneville F. Denève M, et al. Among authors: mahieu l. J Neuroradiol. 2019 Sep;46(5):312-318. doi: 10.1016/j.neurad.2019.06.001. Epub 2019 Jun 20. J Neuroradiol. 2019. PMID: 31228536 Review.
Paediatric optic neuritis: factors leading to unfavourable outcome and relapses.
Averseng-Peaureaux D, Mizzi M, Colineaux H, Mahieu L, Pera MC, Brassat D, Chaix Y, Berard E, Deiva K, Cheuret E; Kidbiosep study group. Averseng-Peaureaux D, et al. Among authors: mahieu l. Br J Ophthalmol. 2018 Jun;102(6):808-813. doi: 10.1136/bjophthalmol-2016-309978. Epub 2017 Sep 13. Br J Ophthalmol. 2018. PMID: 28903961
A regulatory domain is required for Foxn4 activity during retinogenesis.
Lelièvre EC, Benayoun BA, Mahieu L, Roger JE, Sahel JA, Sennlaub F, Veitia RA, Goureau O, Guillonneau X. Lelièvre EC, et al. Among authors: mahieu l. J Mol Neurosci. 2012 Feb;46(2):315-23. doi: 10.1007/s12031-011-9585-4. Epub 2011 Jun 24. J Mol Neurosci. 2012. PMID: 21701787 Free PMC article.
FDXR Mutations Cause Sensorial Neuropathies and Expand the Spectrum of Mitochondrial Fe-S-Synthesis Diseases.
Paul A, Drecourt A, Petit F, Deguine DD, Vasnier C, Oufadem M, Masson C, Bonnet C, Masmoudi S, Mosnier I, Mahieu L, Bouccara D, Kaplan J, Challe G, Domange C, Mochel F, Sterkers O, Gerber S, Nitschke P, Bole-Feysot C, Jonard L, Gherbi S, Mercati O, Ben Aissa I, Lyonnet S, Rötig A, Delahodde A, Marlin S. Paul A, et al. Among authors: mahieu l. Am J Hum Genet. 2017 Oct 5;101(4):630-637. doi: 10.1016/j.ajhg.2017.09.007. Epub 2017 Sep 28. Am J Hum Genet. 2017. PMID: 28965846 Free PMC article.
14 results