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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2002 1
2005 1
2006 1
2008 3
2009 1
2010 2
2011 2
2012 3
2013 1
2014 1
2015 2
2016 1
2018 2
2019 1
2021 1
2022 2
2024 0

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Page 1
Clinical management guidelines for Friedreich ataxia: best practice in rare diseases.
Corben LA, Collins V, Milne S, Farmer J, Musheno A, Lynch D, Subramony S, Pandolfo M, Schulz JB, Lin K, Delatycki MB; Clinical Management Guidelines Writing Group. Corben LA, et al. Orphanet J Rare Dis. 2022 Nov 12;17(1):415. doi: 10.1186/s13023-022-02568-3. Orphanet J Rare Dis. 2022. PMID: 36371255 Free PMC article.
Epigenetic therapy for Friedreich ataxia.
Soragni E, Miao W, Iudicello M, Jacoby D, De Mercanti S, Clerico M, Longo F, Piga A, Ku S, Campau E, Du J, Penalver P, Rai M, Madara JC, Nazor K, O'Connor M, Maximov A, Loring JF, Pandolfo M, Durelli L, Gottesfeld JM, Rusche JR. Soragni E, et al. Ann Neurol. 2014 Oct;76(4):489-508. doi: 10.1002/ana.24260. Epub 2014 Sep 16. Ann Neurol. 2014. PMID: 25159818 Free PMC article. Clinical Trial.
Translating HDAC inhibitors in Friedreich's ataxia.
Soragni E, Gottesfeld JM. Soragni E, et al. Expert Opin Orphan Drugs. 2016;4(9):961-970. doi: 10.1080/21678707.2016.1215910. Epub 2016 Jul 31. Expert Opin Orphan Drugs. 2016. PMID: 28392990 Free PMC article.
A non-synonymous single nucleotide polymorphism in SIRT6 predicts neurological severity in Friedreich ataxia.
Rodden LN, Rummey C, Dong YN, Lagedrost S, Regner S, Brocht A, Bushara K, Delatycki MB, Gomez CM, Mathews K, Murray S, Perlman S, Ravina B, Subramony SH, Wilmot G, Zesiewicz T, Bolotta A, Domissy A, Jespersen C, Ji B, Soragni E, Gottesfeld JM, Lynch DR. Rodden LN, et al. Among authors: soragni e. Front Mol Biosci. 2022 Sep 5;9:933788. doi: 10.3389/fmolb.2022.933788. eCollection 2022. Front Mol Biosci. 2022. PMID: 36133907 Free PMC article.
24 results