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

Year Number of Results
1993 1
1994 5
1995 2
1996 1
1997 3
1998 3
1999 1
2000 2
2001 2
2002 1
2004 7
2005 1
2006 4
2007 8
2008 2
2009 2
2010 2
2011 1
2012 1
2013 1
2014 2
2015 1
2016 1
2017 1
2019 1
2021 2
2022 1
2023 1
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Search Results

53 results
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Page 1
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's ataxia: autosomal recessive disease caused by an intronic GAA triplet repeat expansion.
Campuzano V, Montermini L, Moltò MD, Pianese L, Cossée M, Cavalcanti F, Monros E, Rodius F, Duclos F, Monticelli A, Zara F, Cañizares J, Koutnikova H, Bidichandani SI, Gellera C, Brice A, Trouillas P, De Michele G, Filla A, De Frutos R, Palau F, Patel PI, Di Donato S, Mandel JL, Cocozza S, Koenig M, Pandolfo M. Campuzano V, et al. Among authors: bidichandani si. Science. 1996 Mar 8;271(5254):1423-7. doi: 10.1126/science.271.5254.1423. Science. 1996. PMID: 8596916
Friedreich Ataxia.
Bidichandani SI, Delatycki MB. Bidichandani SI, et al. 1998 Dec 18 [updated 2017 Jun 1]. In: Adam MP, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2023. 1998 Dec 18 [updated 2017 Jun 1]. In: Adam MP, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2023. PMID: 20301458 Free Books & Documents. Review.
Frataxin fracas.
Cossée M, Campuzano V, Koutnikova H, Fischbeck K, Mandel JL, Koenig M, Bidichandani SI, Patel PI, Moltè MD, Cañizares J, De Frutos R, Pianese L, Cavalcanti F, Monticelli A, Cocozza S, Montermini L, Pandolfo M. Cossée M, et al. Among authors: bidichandani si. Nat Genet. 1997 Apr;15(4):337-8. doi: 10.1038/ng0497-337. Nat Genet. 1997. PMID: 9090376 No abstract available.
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.
Funding agencies and disease organizations: resources and recommendations to facilitate ALS clinical research.
Chad DA, Bidichandani S, Bruijn L, Capra JD, Dickie B, Ferguson J, Figlewicz D, Forsythe M, Kaufmann P, Kirshner A, Monti W. Chad DA, et al. Among authors: bidichandani s. Amyotroph Lateral Scler Frontotemporal Degener. 2013 May;14 Suppl 1:62-6. doi: 10.3109/21678421.2013.778588. Amyotroph Lateral Scler Frontotemporal Degener. 2013. PMID: 23678881 Review.
FXN gene methylation determines carrier status in Friedreich ataxia.
Lam C, Gilliam KM, Rodden LN, Schadt KA, Lynch DR, Bidichandani S. Lam C, et al. Among authors: bidichandani s. J Med Genet. 2023 Jan 12:jmedgenet-2022-108742. doi: 10.1136/jmg-2022-108742. Online ahead of print. J Med Genet. 2023. PMID: 36635061 Free article.
Acidic proline-rich protein Db and caries in young children.
Zakhary GM, Clark RM, Bidichandani SI, Owen WL, Slayton RL, Levine M. Zakhary GM, et al. Among authors: bidichandani si. J Dent Res. 2007 Dec;86(12):1176-80. doi: 10.1177/154405910708601207. J Dent Res. 2007. PMID: 18037651
53 results