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2011 4
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Page 1
Insight and Recommendations for Fragile X-Premutation-Associated Conditions from the Fifth International Conference on FMR1 Premutation.
Tassone F, Protic D, Allen EG, Archibald AD, Baud A, Brown TW, Budimirovic DB, Cohen J, Dufour B, Eiges R, Elvassore N, Gabis LV, Grudzien SJ, Hall DA, Hessl D, Hogan A, Hunter JE, Jin P, Jiraanont P, Klusek J, Kooy RF, Kraan CM, Laterza C, Lee A, Lipworth K, Losh M, Loesch D, Lozano R, Mailick MR, Manolopoulos A, Martinez-Cerdeno V, McLennan Y, Miller RM, Montanaro FAM, Mosconi MW, Potter SN, Raspa M, Rivera SM, Shelly K, Todd PK, Tutak K, Wang JY, Wheeler A, Winarni TI, Zafarullah M, Hagerman RJ. Tassone F, et al. Among authors: mclennan y. Cells. 2023 Sep 21;12(18):2330. doi: 10.3390/cells12182330. Cells. 2023. PMID: 37759552 Free PMC article. Review.
Fragile x syndrome.
McLennan Y, Polussa J, Tassone F, Hagerman R. McLennan Y, et al. Curr Genomics. 2011 May;12(3):216-24. doi: 10.2174/138920211795677886. Curr Genomics. 2011. PMID: 22043169 Free PMC article.
Fragile X syndrome and associated disorders: Clinical aspects and pathology.
Salcedo-Arellano MJ, Dufour B, McLennan Y, Martinez-Cerdeno V, Hagerman R. Salcedo-Arellano MJ, et al. Among authors: mclennan y. Neurobiol Dis. 2020 Mar;136:104740. doi: 10.1016/j.nbd.2020.104740. Epub 2020 Jan 10. Neurobiol Dis. 2020. PMID: 31927143 Free PMC article. Review.
Cerebral Microbleeds in Fragile X-Associated Tremor/Ataxia Syndrome.
Salcedo-Arellano MJ, Wang JY, McLennan YA, Doan M, Cabal-Herrera AM, Jimenez S, Wolf-Ochoa MW, Sanchez D, Juarez P, Tassone F, Durbin-Johnson B, Hagerman RJ, Martínez-Cerdeño V. Salcedo-Arellano MJ, et al. Among authors: mclennan ya. Mov Disord. 2021 Aug;36(8):1935-1943. doi: 10.1002/mds.28559. Epub 2021 Mar 24. Mov Disord. 2021. PMID: 33760253 Free PMC article.
Brain Metabolomics in Fragile X-Associated Tremor/Ataxia Syndrome (FXTAS).
Salcedo-Arellano MJ, Johnson MD, McLennan YA, Hwang YH, Juarez P, McBride EL, Pantoja AP, Durbin-Johnson B, Tassone F, Hagerman RJ, Martínez-Cerdeño V. Salcedo-Arellano MJ, et al. Among authors: mclennan ya. Cells. 2023 Aug 23;12(17):2132. doi: 10.3390/cells12172132. Cells. 2023. PMID: 37681866 Free PMC article.
Hypermobile Ehlers-Danlos syndrome (hEDS) phenotype in fragile X premutation carriers: case series.
Tassanakijpanich N, McKenzie FJ, McLennan YA, Makhoul E, Tassone F, Jasoliya MJ, Romney C, Petrasic IC, Napalinga K, Buchanan CB, Hagerman P, Hagerman R, Casanova EL. Tassanakijpanich N, et al. Among authors: mclennan ya. J Med Genet. 2022 Jul;59(7):687-690. doi: 10.1136/jmedgenet-2020-107609. Epub 2021 Jun 30. J Med Genet. 2022. PMID: 34193467 Free PMC article.
23 results