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Page 1
Congenital Mirror Movements.
Méneret A, Trouillard O, Dunoyer M, Depienne C, Roze E. Méneret A, et al. Among authors: dunoyer m. 2015 Mar 12 [updated 2020 Sep 24]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2025. 2015 Mar 12 [updated 2020 Sep 24]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2025. PMID: 25763452 Free Books & Documents. Review.
Classification of GBA1 variants and their impact on Parkinson's disease: an in silico score analysis.
Lanore A, Tesson C, Basset A, Lejeune FX, Cogan G, Mangone G, Sambin S, Bertille N, Anheim M, Arnulf I, Ansquer S, Brandel JP, Brefel-Courbon C, Defebvre L, Drapier S, Eusebsio A, Fabbri M, Giordana C, Hainque E, Lehericy S, Marques A, Moreau C, Moro E, Ory F, Rolland AS, Thobois S, Vidailhet M, Devos D, Mariani LL, Lesage S, Brice A, Corvol JC; Predistim study group; Iceberg study group; NSPark study group. Lanore A, et al. NPJ Parkinsons Dis. 2025 Aug 2;11(1):226. doi: 10.1038/s41531-025-01060-6. NPJ Parkinsons Dis. 2025. PMID: 40753162 Free PMC article.
Subcutaneous Apomorphine Infusion Initiation Is Associated with Impulse Control Disorder Attenuation in Advanced Parkinson's Disease Patients: Insights from the French NS-Park Cohort.
Desjardins C, Bastos PAD, Lanore A, Brefel-Courbon C, Benatru I, Giordana C, de Maindreville AD, Castelnovo G, Remy P, Defebvre L, Thiriez C, Prange S, Houeto JL, Foubert AS, Ory-Magne F, Barbosa RP, Bertille N, Corvol JC, Rascol O, Fabbri M; NS‐Part Cohort study group. Desjardins C, et al. Mov Disord Clin Pract. 2025 Jul 17. doi: 10.1002/mdc3.70240. Online ahead of print. Mov Disord Clin Pract. 2025. PMID: 40671628
Congenital mirror movements are associated with defective polymerisation of RAD51.
Trouillard O, Dupaigne P, Dunoyer M, Doulazmi M, Herlin MK, Frismand S, Riou A, Legros V, Chevreux G, Veaute X, Busso D, Fouquet C, Saint-Martin C, Méneret A, Trembleau A, Dusart I, Dubacq C, Roze E. Trouillard O, et al. Among authors: dunoyer m. J Med Genet. 2023 Nov;60(11):1116-1126. doi: 10.1136/jmg-2023-109189. Epub 2023 Jun 12. J Med Genet. 2023. PMID: 37308287
NeuroQ: A neurophobia screening tool assesses how roleplay challenges neurophobia.
McGovern E, Louapre C, Cassereau J, Flamand-Roze C, Corsetti E, Jegatheesan P, Bendetowicz D, Giron C, Dunoyer M, Villain N, Renaud MC, Sauleau P, Michel L, Vérin M, Worbe Y, Falissard B, Roze E. McGovern E, et al. Among authors: dunoyer m. J Neurol Sci. 2021 Feb 15;421:117320. doi: 10.1016/j.jns.2021.117320. Epub 2021 Jan 20. J Neurol Sci. 2021. PMID: 33518377 Free article.
Validation of the French Translation of the Movement Disorder Society Non-Motor Symptoms Scale (MDS-NMS) in Parkinson's Disease.
Desjardins C, Grimaldi S, Luo S, Yu L, Goetz CG, Stebbins GT, Martinez-Martin P, Kurtis MM, Mestre TA, Sanchez-Ferro A, Tosin MHS, Balestrino R, Lin CR, Gasca-Salas C, Witjas T, Colin O, Maltete D, Defebvre L, Giordana C, Charif M, Thiriez C, Laurencin C, Tir M, Dupont G, Remy P, Tranchant C, Drapier S, Samier A, Benatru I, Sambin S, Corvol JC, Kelifi F, Fabbri M, Rascol O; NS‐Part Cohort study group and the MDS COA Translation Steering Committee. Desjardins C, et al. Mov Disord Clin Pract. 2025 Sep 1. doi: 10.1002/mdc3.70323. Online ahead of print. Mov Disord Clin Pract. 2025. PMID: 40888151 No abstract available.
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