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Page 1
Psychiatric and cognitive phenotype of childhood myotonic dystrophy type 1.
Douniol M, Jacquette A, Cohen D, Bodeau N, Rachidi L, Angeard N, Cuisset JM, Vallée L, Eymard B, Plaza M, Héron D, Guilé JM. Douniol M, et al. Among authors: angeard n. Dev Med Child Neurol. 2012 Oct;54(10):905-11. doi: 10.1111/j.1469-8749.2012.04379.x. Epub 2012 Aug 3. Dev Med Child Neurol. 2012. PMID: 22861906 Free article. Review.
Analysis of Dp71 contribution in the severity of mental retardation through comparison of Duchenne and Becker patients differing by mutation consequences on Dp71 expression.
Daoud F, Angeard N, Demerre B, Martie I, Benyaou R, Leturcq F, Cossée M, Deburgrave N, Saillour Y, Tuffery S, Urtizberea A, Toutain A, Echenne B, Frischman M, Mayer M, Desguerre I, Estournet B, Réveillère C, Penisson-Besnier, Cuisset JM, Kaplan JC, Héron D, Rivier F, Chelly J. Daoud F, et al. Among authors: angeard n. Hum Mol Genet. 2009 Oct 15;18(20):3779-94. doi: 10.1093/hmg/ddp320. Epub 2009 Jul 14. Hum Mol Genet. 2009. PMID: 19602481
Unravelling the impact of frontal lobe impairment for social dysfunction in myotonic dystrophy type 1.
Morin A, Funkiewiez A, Routier A, Le Bouc R, Borderies N, Galanaud D, Levy R, Pessiglione M, Dubois B, Eymard B, Michon CC, Angeard N, Behin A, Laforet P, Stojkovic T, Azuar C. Morin A, et al. Among authors: angeard n. Brain Commun. 2022 May 17;4(3):fcac111. doi: 10.1093/braincomms/fcac111. eCollection 2022. Brain Commun. 2022. PMID: 35611304 Free PMC article.
17 results