Stefan L. Marklund
Umea, AC 90187, Sweden
Last Updated: 09/26/2026
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Found 56 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
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
A novel homozygous p.Ser69Pro SOD1 mutation causes severe young-onset ALS with decreased enzyme activity.
Journal: Journal of neurology
Published: August 26, 2022
Widespread CNS pathology in amyotrophic lateral sclerosis homozygous for the D90A SOD1 mutation.
Journal: Acta neuropathologica
Published: July 07, 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
Alteration of Mitochondrial Integrity as Upstream Event in the Pathophysiology of SOD1-ALS.
Journal: Cells
Published: February 18, 2022
Infantile SOD1 deficiency syndrome caused by a homozygous SOD1 variant with absence of enzyme activity.
Journal: Brain : a journal of neurology
Published: June 21, 2021
Last Updated: 09/26/2026