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

Year Number of Results
2002 1
2003 3
2004 3
2006 2
2007 1
2015 2
2016 1
2017 1
2018 1
2019 6
2020 2
2021 1
2023 1
2024 0

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23 results

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Page 1
Involuntary movements, vocalizations and cognitive decline.
Sveinsson O, Udd B, Svenningsson P, Gassner C, Engström C, Laffita-Mesa J, Solders G, Hertegård S, Savitcheva I, Jung HH, Tolnay M, Frey BM, Paucar M. Sveinsson O, et al. Among authors: solders g. Parkinsonism Relat Disord. 2020 Oct;79:135-137. doi: 10.1016/j.parkreldis.2019.05.029. Epub 2019 May 29. Parkinsonism Relat Disord. 2020. PMID: 31153763 No abstract available.
The cerebellar phenotype of Charcot-Marie-Tooth neuropathy type 4C.
Skott H, Muntean-Firanescu C, Samuelsson K, Verrecchia L, Svenningsson P, Malmgren H, Cananau C, Espay AJ, Press R, Solders G, Paucar M. Skott H, et al. Among authors: solders g. Cerebellum Ataxias. 2019 Jul 15;6:9. doi: 10.1186/s40673-019-0103-8. eCollection 2019. Cerebellum Ataxias. 2019. PMID: 31346473 Free PMC article.
[Ataxia - a group of heterogeneous diseases].
Paucar M, Dahl N, Engvall M, Svenningsson P, Solders G. Paucar M, et al. Among authors: solders g. Lakartidningen. 2020 Mar 9;117:FX4F. Lakartidningen. 2020. PMID: 32154899 Free article. Swedish.
Parkinson's disease with restless legs syndrome-an in vivo corneal confocal microscopy study.
Andréasson M, Lagali N, Badian RA, Utheim TP, Scarpa F, Colonna A, Allgeier S, Bartschat A, Köhler B, Mikut R, Reichert KM, Solders G, Samuelsson K, Zetterberg H, Blennow K, Svenningsson P. Andréasson M, et al. Among authors: solders g. NPJ Parkinsons Dis. 2021 Jan 5;7(1):4. doi: 10.1038/s41531-020-00148-5. NPJ Parkinsons Dis. 2021. PMID: 33402694 Free PMC article.
Late-onset limb-girdle muscular dystrophy caused by GMPPB mutations.
Balcin H, Palmio J, Penttilä S, Nennesmo I, Lindfors M, Solders G, Udd B. Balcin H, et al. Among authors: solders g. Neuromuscul Disord. 2017 Jul;27(7):627-630. doi: 10.1016/j.nmd.2017.04.006. Epub 2017 Apr 18. Neuromuscul Disord. 2017. PMID: 28478914
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: solders g. Front Neurol. 2023 May 18;14:1170005. doi: 10.3389/fneur.2023.1170005. eCollection 2023. Front Neurol. 2023. PMID: 37273706 Free PMC article.
WITHDRAWN: Novel Xp21.1 deletion associated with unusual features in a large McLeod syndrome kindred.
Sveinsson O, Udd B, Svenningsson P, Gassner C, Engström C, Laffita-Mesa JM, Solders G, Hertegård S, Savitcheva I, Jung HH, Tolnay M, Frey BM, Paucar M. Sveinsson O, et al. Among authors: solders g. Parkinsonism Relat Disord. 2018 Oct 8:S1353-8020(18)30399-7. doi: 10.1016/j.parkreldis.2018.09.014. Online ahead of print. Parkinsonism Relat Disord. 2018. PMID: 30305234 No abstract available.
23 results