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Expanding the phenotype of SCA19/22: Parkinsonism, cognitive impairment and epilepsy.
Huin V, Strubi-Vuillaume I, Dujardin K, Brion M, Delliaux M, Dellacherie D, Cuvellier JC, Cuisset JM, Riquet A, Moreau C, Defebvre L, Sablonnière B, Devos D. Huin V, et al. Among authors: dellacherie d. Parkinsonism Relat Disord. 2017 Dec;45:85-89. doi: 10.1016/j.parkreldis.2017.09.014. Epub 2017 Sep 19. Parkinsonism Relat Disord. 2017. PMID: 28947073 Free article.
Rhythm as an independent determinant of developmental dyslexia.
Bégel V, Dalla Bella S, Devignes Q, Vandenbergue M, Lemaître MP, Dellacherie D. Bégel V, et al. Among authors: dellacherie d. Dev Psychol. 2022 Feb;58(2):339-358. doi: 10.1037/dev0001293. Epub 2022 Jan 10. Dev Psychol. 2022. PMID: 35007111
Musical abilities in children with developmental cerebellar anomalies.
Guinamard A, Clément S, Goemaere S, Mary A, Riquet A, Dellacherie D. Guinamard A, et al. Among authors: dellacherie d. Front Syst Neurosci. 2022 Aug 18;16:886427. doi: 10.3389/fnsys.2022.886427. eCollection 2022. Front Syst Neurosci. 2022. PMID: 36061946 Free PMC article.
TMEM240 mutations cause spinocerebellar ataxia 21 with mental retardation and severe cognitive impairment.
Delplanque J, Devos D, Huin V, Genet A, Sand O, Moreau C, Goizet C, Charles P, Anheim M, Monin ML, Buée L, Destée A, Grolez G, Delmaire C, Dujardin K, Dellacherie D, Brice A, Stevanin G, Strubi-Vuillaume I, Dürr A, Sablonnière B. Delplanque J, et al. Among authors: dellacherie d. Brain. 2014 Oct;137(Pt 10):2657-63. doi: 10.1093/brain/awu202. Epub 2014 Jul 28. Brain. 2014. PMID: 25070513
19 results