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Year Number of Results
2002 5
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2005 3
2006 2
2007 3
2008 2
2009 3
2010 4
2011 4
2012 4
2013 6
2014 5
2015 6
2016 6
2017 7
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2024 2

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82 results

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Page 1
Genome sequencing with comprehensive variant calling identifies structural variants and repeat expansions in a large fraction of individuals with ataxia and/or neuromuscular disorders.
Ek M, Nilsson D, Engvall M, Malmgren H, Thonberg H, Pettersson M, Anderlid BM, Hammarsjö A, Helgadottir HT, Arnardottir S, Naess K, Nennesmo I, Paucar M, Hjartarson HT, Press R, Solders G, Sejersen T, Lindstrand A, Kvarnung M. Ek M, et al. Among authors: nennesmo i. Front Neurol. 2023 May 18;14:1170005. doi: 10.3389/fneur.2023.1170005. eCollection 2023. Front Neurol. 2023. PMID: 37273706 Free PMC article.
Single-cell profiling of muscle-infiltrating T cells in idiopathic inflammatory myopathies.
Argyriou A, Horuluoglu B, Galindo-Feria AS, Diaz-Boada JS, Sijbranda M, Notarnicola A, Dani L, van Vollenhoven A, Ramsköld D, Nennesmo I, Dastmalchi M, Lundberg IE, Diaz-Gallo LM, Chemin K. Argyriou A, et al. Among authors: nennesmo i. EMBO Mol Med. 2023 Oct 11;15(10):e17240. doi: 10.15252/emmm.202217240. Epub 2023 Jul 31. EMBO Mol Med. 2023. PMID: 37522383 Free PMC article.
PARKIN is not required to sustain OXPHOS function in adult mammalian tissues.
Filograna R, Gerlach J, Choi HN, Rigoni G, Barbaro M, Oscarson M, Lee S, Tiklova K, Ringnér M, Koolmeister C, Wibom R, Riggare S, Nennesmo I, Perlmann T, Wredenberg A, Wedell A, Motori E, Svenningsson P, Larsson NG. Filograna R, et al. Among authors: nennesmo i. NPJ Parkinsons Dis. 2024 Apr 29;10(1):93. doi: 10.1038/s41531-024-00707-0. NPJ Parkinsons Dis. 2024. PMID: 38684669 Free PMC article.
Creating the Pick's disease International Consortium: Association study of MAPT H2 haplotype with risk of Pick's disease.
Valentino RR, Scotton WJ, Roemer SF, Lashley T, Heckman MG, Shoai M, Martinez-Carrasco A, Tamvaka N, Walton RL, Baker MC, Macpherson HL, Real R, Soto-Beasley AI, Mok K, Revesz T, Warner TT, Jaunmuktane Z, Boeve BF, Christopher EA, DeTure M, Duara R, Graff-Radford NR, Josephs KA, Knopman DS, Koga S, Murray ME, Lyons KE, Pahwa R, Parisi JE, Petersen RC, Whitwell J, Grinberg LT, Miller B, Schlereth A, Seeley WW, Spina S, Grossman M, Irwin DJ, Lee EB, Suh E, Trojanowski JQ, Van Deerlin VM, Wolk DA, Connors TR, Dooley PM, Frosch MP, Oakley DH, Aldecoa I, Balasa M, Gelpi E, Borrego-Écija S, de Eugenio Huélamo RM, Gascon-Bayarri J, Sánchez-Valle R, Sanz-Cartagena P, Piñol-Ripoll G, Molina-Porcel L, Bigio EH, Flanagan ME, Gefen T, Rogalski EJ, Weintraub S, Redding-Ochoa J, Chang K, Troncoso JC, Prokop S, Newell KL, Ghetti B, Jones M, Richardson A, Robinson AC, Roncaroli F, Snowden J, Allinson K, Green O, Rowe JB, Singh P, Beach TG, Serrano GE, Flowers XE, Goldman JE, Heaps AC, Leskinen SP, Teich AF, Black SE, Keith JL, Masellis M, Bodi I, King A, Sarraj SA, Troakes C, Halliday GM, Hodges JR, Kril JJ, Kwok JB, Piguet O, Gearing M, Arzberger T, Roeber S, Attems J, Morris CM, Thomas AJ, Ever… See abstract for full author list ➔ Valentino RR, et al. Among authors: nennesmo i. medRxiv [Preprint]. 2023 Apr 24:2023.04.17.23288471. doi: 10.1101/2023.04.17.23288471. medRxiv. 2023. Update in: Lancet Neurol. 2024 May;23(5):487-499. doi: 10.1016/S1474-4422(24)00083-8. PMID: 37163045 Free PMC article. Updated. Preprint.
Antemortem Prediction of Braak Stage.
Carlson JO, Gatz M, Pedersen NL, Graff C, Nennesmo I, Lindström AK, Gerritsen L. Carlson JO, et al. Among authors: nennesmo i. J Neuropathol Exp Neurol. 2015 Nov;74(11):1061-70. doi: 10.1097/NEN.0000000000000251. J Neuropathol Exp Neurol. 2015. PMID: 26469248 Free PMC article.
Spinocerebellar ataxia type 4 is caused by a GGC expansion in the ZFHX3 gene and is associated with prominent dysautonomia and motor neuron signs.
Paucar M, Nilsson D, Engvall M, Laffita-Mesa J, Söderhäll C, Skorpil M, Halldin C, Fazio P, Lagerstedt-Robinson K, Solders G, Angeria M, Varrone A, Risling M, Jiao H, Nennesmo I, Wedell A, Svenningsson P. Paucar M, et al. Among authors: nennesmo i. J Intern Med. 2024 Sep;296(3):234-248. doi: 10.1111/joim.13815. Epub 2024 Jul 7. J Intern Med. 2024. PMID: 38973251
[11 C]PBB3 binding in Aβ(-) or Aβ(+) corticobasal syndrome.
Cselényi Z, Wallin J, Tjerkoski J, Bloth B, Svensson S, Nennesmo I, Sunnemark D, Jelic V, Farde L, Svenningsson P. Cselényi Z, et al. Among authors: nennesmo i. Synapse. 2023 Jul;77(4):e22269. doi: 10.1002/syn.22269. Epub 2023 Apr 30. Synapse. 2023. PMID: 36951466 Free article.
Predominant Spastic Paraparesis Associated With the D178N Mutation in PRNP.
Thams S, Paucar M, Wingård L, Thonberg H, Smith C, Nennesmo I, Svenningsson P. Thams S, et al. Among authors: nennesmo i. Neurol Genet. 2021 Nov 3;7(6):e636. doi: 10.1212/NXG.0000000000000636. eCollection 2021 Dec. Neurol Genet. 2021. PMID: 34746379 Free PMC article. No abstract available.
Intra-mitochondrial Methylation Deficiency Due to Mutations in SLC25A26.
Kishita Y, Pajak A, Bolar NA, Marobbio CM, Maffezzini C, Miniero DV, Monné M, Kohda M, Stranneheim H, Murayama K, Naess K, Lesko N, Bruhn H, Mourier A, Wibom R, Nennesmo I, Jespers A, Govaert P, Ohtake A, Van Laer L, Loeys BL, Freyer C, Palmieri F, Wredenberg A, Okazaki Y, Wedell A. Kishita Y, et al. Among authors: nennesmo i. Am J Hum Genet. 2015 Nov 5;97(5):761-8. doi: 10.1016/j.ajhg.2015.09.013. Epub 2015 Oct 29. Am J Hum Genet. 2015. PMID: 26522469 Free PMC article.
Resolution of inflammation is altered in Alzheimer's disease.
Wang X, Zhu M, Hjorth E, Cortés-Toro V, Eyjolfsdottir H, Graff C, Nennesmo I, Palmblad J, Eriksdotter M, Sambamurti K, Fitzgerald JM, Serhan CN, Granholm AC, Schultzberg M. Wang X, et al. Among authors: nennesmo i. Alzheimers Dement. 2015 Jan;11(1):40-50.e1-2. doi: 10.1016/j.jalz.2013.12.024. Epub 2014 Feb 12. Alzheimers Dement. 2015. PMID: 24530025 Free PMC article.
82 results