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New practical definitions for the diagnosis of autosomal recessive spastic ataxia of Charlevoix-Saguenay.
Pilliod J, Moutton S, Lavie J, Maurat E, Hubert C, Bellance N, Anheim M, Forlani S, Mochel F, N'Guyen K, Thauvin-Robinet C, Verny C, Milea D, Lesca G, Koenig M, Rodriguez D, Houcinat N, Van-Gils J, Durand CM, Guichet A, Barth M, Bonneau D, Convers P, Maillart E, Guyant-Marechal L, Hannequin D, Fromager G, Afenjar A, Chantot-Bastaraud S, Valence S, Charles P, Berquin P, Rooryck C, Bouron J, Brice A, Lacombe D, Rossignol R, Stevanin G, Benard G, Burglen L, Durr A, Goizet C, Coupry I. Pilliod J, et al. Among authors: milea d. Ann Neurol. 2015 Dec;78(6):871-86. doi: 10.1002/ana.24509. Epub 2015 Nov 14. Ann Neurol. 2015. PMID: 26288984
Reversible optic neuropathy with OPA1 exon 5b mutation.
Cornille K, Milea D, Amati-Bonneau P, Procaccio V, Zazoun L, Guillet V, El Achouri G, Delettre C, Gueguen N, Loiseau D, Muller A, Ferré M, Chevrollier A, Wallace DC, Bonneau D, Hamel C, Reynier P, Lenaers G. Cornille K, et al. Among authors: milea d. Ann Neurol. 2008 May;63(5):667-71. doi: 10.1002/ana.21376. Ann Neurol. 2008. PMID: 18360822 Free article.
Hereditary optic neuropathies share a common mitochondrial coupling defect.
Chevrollier A, Guillet V, Loiseau D, Gueguen N, de Crescenzo MA, Verny C, Ferre M, Dollfus H, Odent S, Milea D, Goizet C, Amati-Bonneau P, Procaccio V, Bonneau D, Reynier P. Chevrollier A, et al. Among authors: milea d. Ann Neurol. 2008 Jun;63(6):794-8. doi: 10.1002/ana.21385. Ann Neurol. 2008. PMID: 18496845 Free article.
OPA1-associated disorders: phenotypes and pathophysiology.
Amati-Bonneau P, Milea D, Bonneau D, Chevrollier A, Ferré M, Guillet V, Gueguen N, Loiseau D, de Crescenzo MA, Verny C, Procaccio V, Lenaers G, Reynier P. Amati-Bonneau P, et al. Among authors: milea d. Int J Biochem Cell Biol. 2009 Oct;41(10):1855-65. doi: 10.1016/j.biocel.2009.04.012. Epub 2009 Apr 21. Int J Biochem Cell Biol. 2009. PMID: 19389487 Free article. Review.
Genetically determined optic neuropathies.
Milea D, Amati-Bonneau P, Reynier P, Bonneau D. Milea D, et al. Curr Opin Neurol. 2010 Feb;23(1):24-8. doi: 10.1097/WCO.0b013e3283347b27. Curr Opin Neurol. 2010. PMID: 19915464 Free article. Review.
Never too old to harbour a young man's disease?
Giraudet S, Lamirel C, Amati-Bonneau P, Reynier P, Bonneau D, Miléa D, Cochereau I. Giraudet S, et al. Among authors: milea d. Br J Ophthalmol. 2011 Jun;95(6):887, 896-7. doi: 10.1136/bjo.2009.161539. Br J Ophthalmol. 2011. PMID: 20675733 No abstract available.
[Hereditary optic neuropathies].
Milea D, Verny C. Milea D, et al. Rev Neurol (Paris). 2012 Oct;168(10):706-9. doi: 10.1016/j.neurol.2012.08.005. Epub 2012 Sep 16. Rev Neurol (Paris). 2012. PMID: 22989781 Review. French.
Maculopathy and spinocerebellar ataxia type 1: a new association?
Lebranchu P, Le Meur G, Magot A, David A, Verny C, Weber M, Milea D. Lebranchu P, et al. Among authors: milea d. J Neuroophthalmol. 2013 Sep;33(3):225-31. doi: 10.1097/WNO.0b013e31828d4add. J Neuroophthalmol. 2013. PMID: 23584155
Mitochondrial dysfunction affecting visual pathways.
Leruez S, Amati-Bonneau P, Verny C, Reynier P, Procaccio V, Bonneau D, Milea D. Leruez S, et al. Among authors: milea d. Rev Neurol (Paris). 2014 May;170(5):344-54. doi: 10.1016/j.neurol.2014.03.009. Epub 2014 May 3. Rev Neurol (Paris). 2014. PMID: 24798923 Review.
292 results