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

Year Number of Results
2005 2
2006 2
2008 4
2009 4
2010 1
2012 2
2013 1
2014 1
2017 2
2018 2
2022 2
2023 1
2024 0

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21 results

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Page 1
Episodic ataxia type 2 (EA2) with interictal myokymia and focal dystonia.
Nielsen EN, Ásbjörnsdóttir B, Møller LB, Nielsen JE, Lindquist SG. Nielsen EN, et al. Among authors: lindquist sg. Cold Spring Harb Mol Case Stud. 2022 Oct 28;8(6):a006236. doi: 10.1101/mcs.a006236. Print 2022 Oct. Cold Spring Harb Mol Case Stud. 2022. PMID: 36307210 Free PMC article.
National clinical Genetic Networks - GENets - Establishment of expert collaborations in Denmark.
Lildballe DL, Frederiksen AL, Schönewolf-Greulich B, Brasch-Andersen C, Lautrup CK, Karstensen HG, Pedersen IS, Sunde L, Risom L, Rasmussen M, Bertelsen M, Andersen MK, Rendtorff ND, Gregersen PA, Tørring PM, Hammer-Hansen S, Boonen SE, Lindquist SG, Hammer TB, Diness BR. Lildballe DL, et al. Among authors: lindquist sg. Eur J Med Genet. 2023 Dec;66(12):104872. doi: 10.1016/j.ejmg.2023.104872. Epub 2023 Nov 13. Eur J Med Genet. 2023. PMID: 37967791
Six generations of CHMP2B-mediated Frontotemporal Dementia: Clinical features, predictive testing, progression, and survival.
Roos P, Johannsen P, Lindquist SG, Brown JM, Waldemar G, Duno M, Nielsen TT, Budtz-Jørgensen E, Gydesen S, Holm IE, Collinge J, Isaacs AM; Frontotemporal dementia Research in Jutland Association (FReJA) consortium; Nielsen JE. Roos P, et al. Among authors: lindquist sg. Acta Neurol Scand. 2022 May;145(5):529-540. doi: 10.1111/ane.13578. Epub 2022 Jan 8. Acta Neurol Scand. 2022. PMID: 34997757
TMEM106B and ApoE polymorphisms in CHMP2B-mediated frontotemporal dementia (FTD-3).
Rostgaard N, Roos P, Budtz-Jørgensen E, Johannsen P, Waldemar G, Nørremølle A, Lindquist SG, Gydesen S, Brown JM, Collinge J, Isaacs AM; FReJA collaboration; Nielsen TT, Nielsen JE. Rostgaard N, et al. Among authors: lindquist sg. Neurobiol Aging. 2017 Nov;59:221.e1-221.e7. doi: 10.1016/j.neurobiolaging.2017.06.026. Epub 2017 Jul 11. Neurobiol Aging. 2017. PMID: 28888721
Genotype-phenotype correlations, dystonia and disease progression in spinocerebellar ataxia type 14.
Chelban V, Wiethoff S, Fabian-Jessing BK, Haridy NA, Khan A, Efthymiou S, Becker EBE, O'Connor E, Hersheson J, Newland K, Hojland AT, Gregersen PA, Lindquist SG, Petersen MB, Nielsen JE, Nielsen M, Wood NW, Giunti P, Houlden H. Chelban V, et al. Among authors: lindquist sg. Mov Disord. 2018 Jul;33(7):1119-1129. doi: 10.1002/mds.27334. Epub 2018 Mar 30. Mov Disord. 2018. PMID: 29603387 Free PMC article.
Reduced CSF CART in dementia with Lewy bodies.
Schultz K, Wiehager S, Nilsson K, Nielsen JE, Lindquist SG, Hjermind LE, Andersen BB, Wallin A, Nilsson C, Petersén A. Schultz K, et al. Among authors: lindquist sg. Neurosci Lett. 2009 Apr 3;453(2):104-6. doi: 10.1016/j.neulet.2009.02.008. Epub 2009 Feb 10. Neurosci Lett. 2009. PMID: 19356602 Free article.
[Dementia--genetic aspects].
Lindquist SG, Waldemar G, Nielsen JE. Lindquist SG, et al. Ugeskr Laeger. 2006 Oct 2;168(40):3405-8. Ugeskr Laeger. 2006. PMID: 17032604 Danish.
A Swedish family with de novo alpha-synuclein A53T mutation: evidence for early cortical dysfunction.
Puschmann A, Ross OA, Vilariño-Güell C, Lincoln SJ, Kachergus JM, Cobb SA, Lindquist SG, Nielsen JE, Wszolek ZK, Farrer M, Widner H, van Westen D, Hägerström D, Markopoulou K, Chase BA, Nilsson K, Reimer J, Nilsson C. Puschmann A, et al. Among authors: lindquist sg. Parkinsonism Relat Disord. 2009 Nov;15(9):627-32. doi: 10.1016/j.parkreldis.2009.06.007. Epub 2009 Jul 25. Parkinsonism Relat Disord. 2009. PMID: 19632874 Free PMC article.
21 results