Per Zetterstrom
Umea, AC 90187, Sweden
Last Updated: 09/26/2026
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Found 19 publications
Seeds from ALS patients homozygous for the SOD1 D90A mutation transmit two types of SOD1 aggregation and motor neuron disease.
Journal: Acta neuropathologica
Published: June 16, 2026
N-Truncated Superoxide Dismutase-1 in Cerebrospinal Fluid Is Folded and Active.
Journal: Journal of neurochemistry
Published: November 17, 2025
Heterogeneous phenotype and cardiovascular comorbidities in Swedish patients with spinobulbar muscular atrophy.
Journal: Journal of neurology
Published: October 13, 2025
Pathology of three ALS patients with FUS variants, including one likely benign Q23L variant lacking FUS inclusions.
Journal: Human molecular genetics
Published: April 17, 2025
SOD1 Protein Content in Human Central Nervous System and Peripheral Tissues.
Journal: Journal of neurochemistry
Published: April 09, 2025
Diverse effects of coexpression of human SOD1 variants on motor neuron disease.
Journal: Human molecular genetics
Published: February 13, 2025
Specific analysis of SOD1 enzymatic activity in CSF from ALS patients with and without SOD1 mutations.
Journal: Neurobiology of disease
Published: August 08, 2024
The motor system is exceptionally vulnerable to absence of the ubiquitously expressed superoxide dismutase-1.
Journal: Brain communications
Published: August 27, 2022
Mutant SOD1 aggregates formed in vitro and in cultured cells are polymorphic and differ from those arising in the CNS.
Journal: Journal of neurochemistry
Published: March 31, 2022
Aggregate-selective antibody attenuates seeded aggregation but not spontaneously evolving disease in SOD1 ALS model mice.
Journal: Acta neuropathologica communications
Published: July 12, 2020
Phenotype in an Infant with SOD1 Homozygous Truncating Mutation.
Journal: The New England journal of medicine
Published: July 18, 2019
Last Updated: 09/26/2026