Goran Solders
Stockholm, AB, Sweden
Last Updated: 09/26/2026
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Found 15 publications
Spinocerebellar ataxia type 4 is caused by a GGC expansion in the ZFHX3 gene and is associated with prominent dysautonomia and motor neuron signs.
Journal: Journal of internal medicine
Published: July 08, 2024
Genome sequencing with comprehensive variant calling identifies structural variants and repeat expansions in a large fraction of individuals with ataxia and/or neuromuscular disorders.
Journal: Frontiers in neurology
Published: February 20, 2023
Parkinson's disease with restless legs syndrome-an in vivo corneal confocal microscopy study.
Journal: NPJ Parkinson's disease
Published: July 28, 2020
Broader phenotypic traits and widespread brain hypometabolism in spinocerebellar ataxia 27.
Journal: Journal of internal medicine
Published: March 01, 2020
Pallidal Deep Brain Stimulation in DYT6 Dystonia: Clinical Outcome and Predictive Factors for Motor Improvement.
Journal: Journal of clinical medicine
Published: October 29, 2019
Polyneuropathy in Gaucher disease type 1 and 3 - a descriptive case series.
Journal: Scientific reports
Published: June 19, 2019
The cerebellar phenotype of Charcot-Marie-Tooth neuropathy type 4C.
Journal: Cerebellum & ataxias
Published: May 26, 2019
Involuntary movements, vocalizations and cognitive decline.
Journal: Parkinsonism & related disorders
Published: May 08, 2019
Altered CSF levels of monoamines in hereditary spastic paraparesis 10: A case series.
Journal: Neurology. Genetics
Published: February 06, 2019
WITHDRAWN: Novel Xp21.1 deletion associated with unusual features in a large McLeod syndrome kindred.
Journal: Parkinsonism & related disorders
Published: June 16, 2018
Late-onset limb-girdle muscular dystrophy caused by GMPPB mutations.
Journal: Neuromuscular disorders : NMD
Published: November 24, 2016
Last Updated: 09/26/2026