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Goran Solders

Explore the profile of Goran Solders including associated specialties, affiliations and a list of published articles. Areas
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Articles 24
Citations 256
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Recent Articles
1.
Paucar M, Nilsson D, Engvall M, Laffita-Mesa J, Soderhall C, Skorpil M, et al.
J Intern Med . 2024 Jul; 296(3):234-248. PMID: 38973251
Background: Spinocerebellar ataxia 4 (SCA4), characterized in 1996, features adult-onset ataxia, polyneuropathy, and linkage to chromosome 16q22.1; its underlying mutation has remained elusive. Objective: To explore the radiological and neuropathological...
2.
Ek M, Nilsson D, Engvall M, Malmgren H, Thonberg H, Pettersson M, et al.
Front Neurol . 2023 Jun; 14:1170005. PMID: 37273706
Introduction: Neuromuscular disorders (NMDs) have a heterogeneous etiology. A genetic diagnosis is key to personalized healthcare and access to targeted treatment for the affected individuals. Methods: In this study, 861...
3.
Andreasson M, Lagali N, Badian R, Utheim T, Scarpa F, Colonna A, et al.
NPJ Parkinsons Dis . 2021 Jan; 7(1):4. PMID: 33402694
Small fiber neuropathy (SFN) has been suggested as a trigger of restless legs syndrome (RLS). An increased prevalence of peripheral neuropathy has been demonstrated in Parkinson's disease (PD). We aimed...
4.
Paucar M, Dahl N, Engvall M, Svenningsson P, Solders G
Lakartidningen . 2020 Mar; 117. PMID: 32154899
Ataxias constitute a group of heterogeneous diseases with overlapping symptoms. The clinical investigation should primarily seek for treatable conditions such as neurometabolic disorders and autoimmune diseases. Rapid progression is often...
5.
Danielsson A, Carecchio M, Cif L, Koy A, Lin J, Solders G, et al.
J Clin Med . 2019 Dec; 8(12). PMID: 31817799
Pallidal deep brain stimulation is an established treatment in dystonia. Available data on the effect in DYT-THAP1 dystonia (also known as DYT6 dystonia) are scarce and long-term follow-up studies are...
6.
Andreasson M, Solders G, Bjorkvall C, Machaczka M, Svenningsson P
Sci Rep . 2019 Oct; 9(1):15358. PMID: 31653957
Polyneuropathy (PNP) has been reported to be a possible phenotypic feature in Gaucher disease type 1 (GD1), while less is known about PNP in type 3 (GD3). We performed a...
7.
Andreasson M, Lagerstedt-Robinson K, Samuelsson K, Solders G, Blennow K, Paucar M, et al.
Neurol Genet . 2019 Aug; 5(4):e344. PMID: 31403080
Objective: To perform a comprehensive clinical characterization and biochemical CSF profile analyses in 2 Swedish families with hereditary spastic paraparesis (HSP) 10 (SPG10) caused by 2 different mutations in the...
8.
Skott H, Muntean-Firanescu C, Samuelsson K, Verrecchia L, Svenningsson P, Malmgren H, et al.
Cerebellum Ataxias . 2019 Jul; 6:9. PMID: 31346473
Background: Friedreich ataxia (FRDA) is the most common familial ataxia syndrome in Central and Southern Europe but rare in Scandinavia. Biallelic mutations in SH3 domain and tetratricopeptide repeats 2 (...
9.
Sveinsson O, Udd B, Svenningsson P, Gassner C, Engstrom C, Laffita-Mesa J, et al.
Parkinsonism Relat Disord . 2019 Jun; 79:135-137. PMID: 31153763
No abstract available.
10.
Af Edholm K, Lidman C, Andersson S, Solders G, Paucar M
Neurology . 2019 Feb; 92(6):e622-e625. PMID: 30718330
No abstract available.