Snjolaug Arnardottir
Stockholm, AB 17165, Sweden
Last Updated: 09/26/2026
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Found 9 publications
MRPS22 variants alter mitochondrial ribosome assembly in patients with leukodystrophy, movement disorder and intellectual impairment.
Journal: Human molecular genetics
Published: December 09, 2025
Novel Clinical Insights From a Swedish RFC1 Spectrum Disorder Cohort.
Journal: European journal of neurology
Published: August 17, 2025
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
EULAR/ACR classification criteria for adult and juvenile idiopathic inflammatory myopathies and their major subgroups: a methodology report.
Journal: RMD open
Published: June 01, 2017
2017 European League Against Rheumatism/American College of Rheumatology classification criteria for adult and juvenile idiopathic inflammatory myopathies and their major subgroups.
Journal: Annals of the rheumatic diseases
Published: March 14, 2017
2017 European League Against Rheumatism/American College of Rheumatology Classification Criteria for Adult and Juvenile Idiopathic Inflammatory Myopathies and Their Major Subgroups.
Journal: Arthritis & rheumatology (Hoboken, N.J.)
Published: March 14, 2017
A heterozygous 21-bp deletion in CAPN3 causes dominantly inherited limb girdle muscular dystrophy.
Journal: Brain : a journal of neurology
Published: January 12, 2016
Autoantibodies to cytosolic 5'-nucleotidase 1A in inclusion body myositis.
Journal: Annals of neurology
Published: August 16, 2012
Effects of immunosuppressive treatment on interleukin-15 and interleukin-15 receptor α expression in muscle tissue of patients with polymyositis or dermatomyositis.
Journal: Annals of the rheumatic diseases
Published: January 24, 2012
Showing 1-9 of 9
Last Updated: 09/26/2026