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Year Number of Results
1980 1
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1992 6
1993 4
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1995 3
1996 1
1997 6
1998 4
1999 4
2000 2
2002 2
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81 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: 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.
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.
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: solders g. J Intern Med. 2024 Sep;296(3):234-248. doi: 10.1111/joim.13815. Epub 2024 Jul 7. J Intern Med. 2024. PMID: 38973251
Autonomic dysfunction in Alzheimer's disease.
Algotsson A, Viitanen M, Winblad B, Solders G. Algotsson A, et al. Among authors: solders g. Acta Neurol Scand. 1995 Jan;91(1):14-8. doi: 10.1111/j.1600-0404.1995.tb05836.x. Acta Neurol Scand. 1995. PMID: 7732768
Creatine treatment in MELAS.
Hagenfeldt L, von Döbeln U, Solders G, Kaijser L. Hagenfeldt L, et al. Among authors: solders g. Muscle Nerve. 1994 Oct;17(10):1236-7. Muscle Nerve. 1994. PMID: 7935543 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.
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
[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.
81 results