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

Year Number of Results
2002 5
2003 5
2004 10
2005 6
2006 10
2007 7
2008 5
2009 12
2010 9
2011 7
2012 13
2013 14
2014 9
2015 9
2016 8
2017 10
2018 8
2019 7
2020 10
2021 5
2022 7
2023 3
2024 1

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164 results

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Page 1
Neurology: Genetics Year in Review.
Pulst S, Pandolfo M, Roos R, Milone M, Jayadev S. Pulst S, et al. Among authors: pandolfo m. Neurol Genet. 2021 Feb 5;7(1):e556. doi: 10.1212/NXG.0000000000000556. eCollection 2021 Feb. Neurol Genet. 2021. PMID: 33889725 Free PMC article. No abstract available.
Friedreich ataxia.
Pandolfo M. Pandolfo M. Arch Neurol. 2008 Oct;65(10):1296-303. doi: 10.1001/archneur.65.10.1296. Arch Neurol. 2008. PMID: 18852343 Review.
Genetics of epilepsy.
Pandolfo M. Pandolfo M. Semin Neurol. 2011 Nov;31(5):506-18. doi: 10.1055/s-0031-1299789. Epub 2012 Jan 21. Semin Neurol. 2011. PMID: 22266888 Review.
Pediatric epilepsy genetics.
Pandolfo M. Pandolfo M. Curr Opin Neurol. 2013 Apr;26(2):137-45. doi: 10.1097/WCO.0b013e32835f19da. Curr Opin Neurol. 2013. PMID: 23449174 Review.
Genetic architecture of subcortical brain structures in 38,851 individuals.
Satizabal CL, Adams HHH, Hibar DP, White CC, Knol MJ, Stein JL, Scholz M, Sargurupremraj M, Jahanshad N, Roshchupkin GV, Smith AV, Bis JC, Jian X, Luciano M, Hofer E, Teumer A, van der Lee SJ, Yang J, Yanek LR, Lee TV, Li S, Hu Y, Koh JY, Eicher JD, Desrivières S, Arias-Vasquez A, Chauhan G, Athanasiu L, Rentería ME, Kim S, Hoehn D, Armstrong NJ, Chen Q, Holmes AJ, den Braber A, Kloszewska I, Andersson M, Espeseth T, Grimm O, Abramovic L, Alhusaini S, Milaneschi Y, Papmeyer M, Axelsson T, Ehrlich S, Roiz-Santiañez R, Kraemer B, Håberg AK, Jones HJ, Pike GB, Stein DJ, Stevens A, Bralten J, Vernooij MW, Harris TB, Filippi I, Witte AV, Guadalupe T, Wittfeld K, Mosley TH, Becker JT, Doan NT, Hagenaars SP, Saba Y, Cuellar-Partida G, Amin N, Hilal S, Nho K, Mirza-Schreiber N, Arfanakis K, Becker DM, Ames D, Goldman AL, Lee PH, Boomsma DI, Lovestone S, Giddaluru S, Le Hellard S, Mattheisen M, Bohlken MM, Kasperaviciute D, Schmaal L, Lawrie SM, Agartz I, Walton E, Tordesillas-Gutierrez D, Davies GE, Shin J, Ipser JC, Vinke LN, Hoogman M, Jia T, Burkhardt R, Klein M, Crivello F, Janowitz D, Carmichael O, Haukvik UK, Aribisala BS, Schmidt H, Strike LT, Cheng CY, Risacher SL, Pütz B, Fleisch… See abstract for full author list ➔ Satizabal CL, et al. Among authors: pandolfo m. Nat Genet. 2019 Nov;51(11):1624-1636. doi: 10.1038/s41588-019-0511-y. Epub 2019 Oct 21. Nat Genet. 2019. PMID: 31636452 Free PMC article.
Friedreich ataxia.
Pandolfo M. Pandolfo M. Handb Clin Neurol. 2012;103:275-94. doi: 10.1016/B978-0-444-51892-7.00017-6. Handb Clin Neurol. 2012. PMID: 21827895 No abstract available.
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. Among authors: pandolfo m. 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.
Frataxin overexpressing mice.
Miranda CJ, Santos MM, Ohshima K, Tessaro M, Sequeiros J, Pandolfo M. Miranda CJ, et al. Among authors: pandolfo m. FEBS Lett. 2004 Aug 13;572(1-3):281-8. doi: 10.1016/j.febslet.2004.07.022. FEBS Lett. 2004. PMID: 15304363 Free article.
Frataxin knockin mouse.
Miranda CJ, Santos MM, Ohshima K, Smith J, Li L, Bunting M, Cossée M, Koenig M, Sequeiros J, Kaplan J, Pandolfo M. Miranda CJ, et al. Among authors: pandolfo m. FEBS Lett. 2002 Feb 13;512(1-3):291-7. doi: 10.1016/s0014-5793(02)02251-2. FEBS Lett. 2002. PMID: 11852098 Free article.
164 results