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

Year Number of Results
2002 5
2003 1
2004 1
2005 1
2006 2
2007 2
2008 1
2009 2
2010 1
2011 1
2012 6
2013 2
2014 5
2015 4
2016 1
2017 5
2018 10
2019 6
2020 5
2021 3
2024 1

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58 results

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Page 1
Exome-wide rare variant analysis in familial essential tremor.
Diez-Fairen M, Houle G, Ortega-Cubero S, Bandres-Ciga S, Alvarez I, Carcel M, Ibañez L, Fernandez MV, Budde JP, Trotta JR, Tonda R, Chong JX, Bamshad MJ, Nickerson DA; University of Washington Center for Mendelian Genomics (UWCMG); Aguilar M, Tartari JP, Gironell A, García-Martín E, Agundez JA, Alonso-Navarro H, Jimenez-Jimenez FJ, Fernandez M, Valldeoriola F, Marti MJ, Tolosa E, Coria F, Pastor MA, Vilariño-Güell C, Rajput A, Dion PA, Cruchaga C, Rouleau GA, Pastor P. Diez-Fairen M, et al. Among authors: tolosa e. Parkinsonism Relat Disord. 2021 Jan;82:109-116. doi: 10.1016/j.parkreldis.2020.11.021. Epub 2020 Nov 24. Parkinsonism Relat Disord. 2021. PMID: 33279834 Free PMC article.
Galloping tongue syndrome in a PRRT2 mutation carrier.
Vilas D, Marcé-Grau A, Macaya A, Valls-Solé J, Tolosa E. Vilas D, et al. Among authors: tolosa e. Neurol Genet. 2019 Nov 11;5(6):e377. doi: 10.1212/NXG.0000000000000377. eCollection 2019 Dec. Neurol Genet. 2019. PMID: 31872056 Free PMC article. No abstract available.
Cutaneous autonomic denervation in Parkinson's disease.
Navarro-Otano J, Casanova-Mollà J, Morales M, Valls-Solé J, Tolosa E. Navarro-Otano J, et al. Among authors: tolosa e. J Neural Transm (Vienna). 2015 Aug;122(8):1149-55. doi: 10.1007/s00702-014-1355-3. Epub 2014 Dec 24. J Neural Transm (Vienna). 2015. PMID: 25536890
Lack of Asymmetry of Nigrostriatal Dopaminergic Function in Healthy Subjects.
Garrido A, Iranzo A, Stefani A, Serradell M, Muñoz-Lopetegi A, Marrero P, Högl B, Gaig C, Santamaria J, Tolosa E, Poewe W; Sleep Innsbruck Barcelona (SINBAR) Group. Garrido A, et al. Among authors: tolosa e. Mov Disord. 2020 Jun;35(6):1072-1076. doi: 10.1002/mds.28019. Epub 2020 Mar 6. Mov Disord. 2020. PMID: 32141653
MicroRNA Deregulation in Blood Serum Identifies Multiple System Atrophy Altered Pathways.
Pérez-Soriano A, Bravo P, Soto M, Infante J, Fernández M, Valldeoriola F, Muñoz E, Compta Y, Tolosa E, Garrido A, Ezquerra M, Fernández-Santiago R, Martí MJ; Catalan MSA registry (CMSAR). Pérez-Soriano A, et al. Among authors: tolosa e. Mov Disord. 2020 Oct;35(10):1873-1879. doi: 10.1002/mds.28143. Epub 2020 Jul 20. Mov Disord. 2020. PMID: 32687224
Regional Overlap of Pathologies in Lewy Body Disorders.
Colom-Cadena M, Grau-Rivera O, Planellas L, Cerquera C, Morenas E, Helgueta S, Muñoz L, Kulisevsky J, Martí MJ, Tolosa E, Clarimon J, Lleó A, Gelpi E. Colom-Cadena M, et al. Among authors: tolosa e. J Neuropathol Exp Neurol. 2017 Mar 1;76(3):216-224. doi: 10.1093/jnen/nlx002. J Neuropathol Exp Neurol. 2017. PMID: 28395086
Neuropathology of prodromal Lewy body disease.
Iranzo A, Gelpi E, Tolosa E, Molinuevo JL, Serradell M, Gaig C, Santamaria J. Iranzo A, et al. Among authors: tolosa e. Mov Disord. 2014 Mar;29(3):410-5. doi: 10.1002/mds.25825. Epub 2014 Jan 31. Mov Disord. 2014. PMID: 24488760
58 results