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[MRI morphometry, an insight into brain function].
Curie A, Guibaud L, Des Portes V. Curie A, et al. Arch Pediatr. 2006 Jun;13(6):674-7. doi: 10.1016/j.arcped.2006.03.099. Epub 2006 May 12. Arch Pediatr. 2006. PMID: 16697610 French. No abstract available.
Epigenetic modification of the FMR1 gene in fragile X syndrome is associated with differential response to the mGluR5 antagonist AFQ056.
Jacquemont S, Curie A, des Portes V, Torrioli MG, Berry-Kravis E, Hagerman RJ, Ramos FJ, Cornish K, He Y, Paulding C, Neri G, Chen F, Hadjikhani N, Martinet D, Meyer J, Beckmann JS, Delange K, Brun A, Bussy G, Gasparini F, Hilse T, Floesser A, Branson J, Bilbe G, Johns D, Gomez-Mancilla B. Jacquemont S, et al. Among authors: curie a. Sci Transl Med. 2011 Jan 5;3(64):64ra1. doi: 10.1126/scitranslmed.3001708. Sci Transl Med. 2011. PMID: 21209411 Clinical Trial.
Implicit procedural learning in fragile X and Down syndrome.
Bussy G, Charrin E, Brun A, Curie A, des Portes V. Bussy G, et al. Among authors: curie a. J Intellect Disabil Res. 2011 May;55(5):521-8. doi: 10.1111/j.1365-2788.2011.01410.x. Epub 2011 Mar 15. J Intellect Disabil Res. 2011. PMID: 21418366
Syntax at hand: common syntactic structures for actions and language.
Roy AC, Curie A, Nazir T, Paulignan Y, des Portes V, Fourneret P, Deprez V. Roy AC, et al. Among authors: curie a. PLoS One. 2013 Aug 22;8(8):e72677. doi: 10.1371/journal.pone.0072677. eCollection 2013. PLoS One. 2013. PMID: 23991140 Free PMC article.
40 results