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Page 1
Stress in Parents of Children With Genetically Determined Leukoencephalopathies: A Pilot Study.
Dermer E, Spahr A, Tran LT, Mirchi A, Pelletier F, Guerrero K, Ahmed S, Brais B, Braverman N, Buhas D, Chandratre S, Chenier S, Chrestian N, Desmeules M, Dilenge ME, Laflamme J, Larbrisseau A, Legault G, Lim KY, Maftei C, Major P, Malvey-Dorn E, Marois P, Mitchell J, Nadeau A, Osterman B, Paradis I, Pohl D, Reggin J, Riou E, Roedde G, Rossignol E, Sébire G, Shevell M, Srour M, Sylvain M, Tarnopolsky M, Venkateswaran S, Sullivan M, Bernard G. Dermer E, et al. Among authors: chenier s. J Child Neurol. 2020 Nov;35(13):901-907. doi: 10.1177/0883073820938645. Epub 2020 Jul 28. J Child Neurol. 2020. PMID: 32720856
Biallelic Loss-of-Function Variants in AIMP1 Cause a Rare Neurodegenerative Disease.
Accogli A, Guerrero K, D'Agostino MD, Tran L, Cieuta-Walti C, Thiffault I, Chénier S, Schwartzentruber J, Majewski J; Care4Rare Canada Consortium; Bernard G. Accogli A, et al. Among authors: chenier s. J Child Neurol. 2019 Feb;34(2):74-80. doi: 10.1177/0883073818811223. Epub 2018 Nov 28. J Child Neurol. 2019. PMID: 30486714
Copy number variation in genetic epilepsy with febrile seizures plus.
Fortin O, Vincelette C, Chénier S, Ghais A, Shevell MI, Simard-Tremblay E, Myers KA. Fortin O, et al. Among authors: chenier s. Eur J Paediatr Neurol. 2020 Jul;27:111-115. doi: 10.1016/j.ejpn.2020.05.005. Epub 2020 Jun 20. Eur J Paediatr Neurol. 2020. PMID: 32595013
Experience of Parents of Children with Genetically Determined Leukoencephalopathies Regarding the Adapted Health Care Services During the COVID-19 Pandemic.
Amir Yazdani P, St-Jean ML, Matovic S, Spahr A, Tran LT, Boucher RM, Poulin C, Osterman B, Srour M, Rosenblatt B, Chenier S, Soucy JF, Laberge AM, Braverman N, D'Agostino MD, Nguyen CE, Morsa M, Bernard G. Amir Yazdani P, et al. Among authors: chenier s. J Child Neurol. 2022 Mar;37(4):237-245. doi: 10.1177/08830738211065317. Epub 2022 Jan 5. J Child Neurol. 2022. PMID: 34986037 Free PMC article.
The Experience of Parents of Children With Genetically Determined Leukoencephalopathies With the Health Care System: A Qualitative Study.
Yazdani PA, St-Jean ML, Matovic S, Spahr A, Tran LT, Boucher RM, Poulin C, Osterman B, Srour M, Rosenblatt B, Chénier S, Soucy JF, Laberge AM, D'Agostino MD, Nguyen CE, Morsa M, Bernard G. Yazdani PA, et al. Among authors: chenier s. J Child Neurol. 2023 Apr;38(5):329-335. doi: 10.1177/08830738231176672. Epub 2023 May 24. J Child Neurol. 2023. PMID: 37225698 Free PMC article.
Diagnosis of late-onset Pompe disease and other muscle disorders by next-generation sequencing.
Lévesque S, Auray-Blais C, Gravel E, Boutin M, Dempsey-Nunez L, Jacques PE, Chenier S, Larue S, Rioux MF, Al-Hertani W, Nadeau A, Mathieu J, Maranda B, Désilets V, Waters PJ, Keutzer J, Austin S, Kishnani P. Lévesque S, et al. Among authors: chenier s. Orphanet J Rare Dis. 2016 Jan 25;11:8. doi: 10.1186/s13023-016-0390-6. Orphanet J Rare Dis. 2016. PMID: 26809617 Free PMC article.
Molecular diagnosis of muscular diseases in outpatient clinics: A Canadian perspective.
Thuriot F, Gravel E, Buote C, Doyon M, Lapointe E, Marcoux L, Larue S, Nadeau A, Chénier S, Waters PJ, Jacques PÉ, Gravel S, Lévesque S. Thuriot F, et al. Among authors: chenier s. Neurol Genet. 2020 Mar 13;6(2):e408. doi: 10.1212/NXG.0000000000000408. eCollection 2020 Apr. Neurol Genet. 2020. PMID: 32337335 Free PMC article.
Novel pathogenic SMAD2 variants in five families with arterial aneurysm and dissection: further delineation of the phenotype.
Cannaerts E, Kempers M, Maugeri A, Marcelis C, Gardeitchik T, Richer J, Micha D, Beauchesne L, Timmermans J, Vermeersch P, Meyten N, Chénier S, van de Beek G, Peeters N, Alaerts M, Schepers D, Van Laer L, Verstraeten A, Loeys B. Cannaerts E, et al. Among authors: chenier s. J Med Genet. 2019 Apr;56(4):220-227. doi: 10.1136/jmedgenet-2018-105304. Epub 2018 Jul 2. J Med Genet. 2019. PMID: 29967133
Comparison of genome-wide array genomic hybridization platforms for the detection of copy number variants in idiopathic mental retardation.
Tucker T, Montpetit A, Chai D, Chan S, Chénier S, Coe BP, Delaney A, Eydoux P, Lam WL, Langlois S, Lemyre E, Marra M, Qian H, Rouleau GA, Vincent D, Michaud JL, Friedman JM. Tucker T, et al. Among authors: chenier s. BMC Med Genomics. 2011 Mar 25;4:25. doi: 10.1186/1755-8794-4-25. BMC Med Genomics. 2011. PMID: 21439053 Free PMC article.
40 results