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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.
DNA methylation in Friedreich ataxia silences expression of frataxin isoform E.
Rodden LN, Gilliam KM, Lam C, Rojsajjakul T, Mesaros C, Dionisi C, Pook M, Pandolfo M, Lynch DR, Blair IA, Bidichandani SI. Rodden LN, et al. Among authors: bidichandani si. Sci Rep. 2022 Mar 23;12(1):5031. doi: 10.1038/s41598-022-09002-5. Sci Rep. 2022. PMID: 35322126 Free PMC article.
Friedreich ataxia- pathogenesis and implications for therapies.
Delatycki MB, Bidichandani SI. Delatycki MB, et al. Among authors: bidichandani si. Neurobiol Dis. 2019 Dec;132:104606. doi: 10.1016/j.nbd.2019.104606. Epub 2019 Sep 5. Neurobiol Dis. 2019. PMID: 31494282 Free article. Review.
Friedreich Ataxia.
Bidichandani SI, Delatycki MB. Bidichandani SI, et al. 1998 Dec 18 [updated 2017 Jun 1]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. 1998 Dec 18 [updated 2017 Jun 1]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. PMID: 20301458 Free Books & Documents. Review.
FXN Promoter Silencing in the Humanized Mouse Model of Friedreich Ataxia.
Chutake YK, Costello WN, Lam CC, Parikh AC, Hughes TT, Michalopulos MG, Pook MA, Bidichandani SI. Chutake YK, et al. Among authors: bidichandani si. PLoS One. 2015 Sep 22;10(9):e0138437. doi: 10.1371/journal.pone.0138437. eCollection 2015. PLoS One. 2015. PMID: 26393353 Free PMC article.
48 results