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Progression of Friedreich ataxia: quantitative characterization over 5 years.
Patel M, Isaacs CJ, Seyer L, Brigatti K, Gelbard S, Strawser C, Foerster D, Shinnick J, Schadt K, Yiu EM, Delatycki MB, Perlman S, Wilmot GR, Zesiewicz T, Mathews K, Gomez CM, Yoon G, Subramony SH, Brocht A, Farmer J, Lynch DR. Patel M, et al. Among authors: yiu em. Ann Clin Transl Neurol. 2016 Jul 25;3(9):684-94. doi: 10.1002/acn3.332. eCollection 2016 Sep. Ann Clin Transl Neurol. 2016. PMID: 27648458 Free PMC article.
A longitudinal study of the Friedreich Ataxia Impact Scale.
Tai G, Yiu EM, Corben LA, Delatycki MB. Tai G, et al. Among authors: yiu em. J Neurol Sci. 2015 May 15;352(1-2):53-7. doi: 10.1016/j.jns.2015.03.024. Epub 2015 Mar 21. J Neurol Sci. 2015. PMID: 25840637
An open-label trial in Friedreich ataxia suggests clinical benefit with high-dose resveratrol, without effect on frataxin levels.
Yiu EM, Tai G, Peverill RE, Lee KJ, Croft KD, Mori TA, Scheiber-Mojdehkar B, Sturm B, Praschberger M, Vogel AP, Rance G, Stephenson SE, Sarsero JP, Stockley C, Lee CY, Churchyard A, Evans-Galea MV, Ryan MM, Lockhart PJ, Corben LA, Delatycki MB. Yiu EM, et al. J Neurol. 2015 May;262(5):1344-53. doi: 10.1007/s00415-015-7719-2. Epub 2015 Apr 7. J Neurol. 2015. PMID: 25845763 Clinical Trial.
Consensus clinical management guidelines for Friedreich ataxia.
Corben LA, Lynch D, Pandolfo M, Schulz JB, Delatycki MB; Clinical Management Guidelines Writing Group. Corben LA, et al. Orphanet J Rare Dis. 2014 Nov 30;9:184. doi: 10.1186/s13023-014-0184-7. Orphanet J Rare Dis. 2014. PMID: 25928624 Free PMC article. Review.
Compound heterozygous FXN mutations and clinical outcome in friedreich ataxia.
Galea CA, Huq A, Lockhart PJ, Tai G, Corben LA, Yiu EM, Gurrin LC, Lynch DR, Gelbard S, Durr A, Pousset F, Parkinson M, Labrum R, Giunti P, Perlman SL, Delatycki MB, Evans-Galea MV. Galea CA, et al. Among authors: yiu em. Ann Neurol. 2016 Mar;79(3):485-95. doi: 10.1002/ana.24595. Ann Neurol. 2016. PMID: 26704351
132 results