Ales Dudesek
Rostock, MV, Germany
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 18 publications
Apheresis for the treatment of relapses in MS and NMOSD: reduced antibody reactivities, gene expression changes and potential clinical response indicators.
Journal: Frontiers in immunology
Published: November 20, 2024
Differential gene expression in B cells and T helper cells following high-dose glucocorticoid therapy for multiple sclerosis relapse.
Journal: Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie
Published: March 05, 2024
Transcriptome alterations in peripheral blood B cells of patients with multiple sclerosis receiving immune reconstitution therapy.
Journal: Journal of neuroinflammation
Published: October 12, 2022
Evolution of Clinical Outcome Measures and Biomarkers in Sporadic Adult-Onset Degenerative Ataxia.
Journal: Movement disorders : official journal of the Movement Disorder Society
Published: September 12, 2022
Endoplasmic reticulum-stress and unfolded protein response-activation in immune-mediated necrotizing myopathy.
Journal: Brain pathology (Zurich, Switzerland)
Published: September 02, 2021
Frequency and risk factors of antibody-induced secondary failure of botulinum neurotoxin therapy.
Journal: Neurology
Published: September 10, 2019
Characterization of Cerebellar Atrophy and Resting State Functional Connectivity Patterns in Sporadic Adult-Onset Ataxia of Unknown Etiology (SAOA).
Journal: Cerebellum (London, England)
Published: August 19, 2019
Prominent White Matter Involvement in Multiple System Atrophy of Cerebellar Type.
Journal: Movement disorders : official journal of the Movement Disorder Society
Published: August 04, 2019
A genetic variant associated with multiple sclerosis inversely affects the expression of CD58 and microRNA-548ac from the same gene.
Journal: PLoS genetics
Published: June 14, 2018
A simplified ultrasonography-guided approach for neurotoxin injection into the obliquus capitis inferior muscle in spasmodic torticollis.
Journal: Journal of neural transmission (Vienna, Austria : 1996)
Published: December 04, 2017
A novel heterozygous variant in ERLIN2 causes autosomal dominant pure hereditary spastic paraplegia.
A novel heterozygous variant in ERLIN2 causes autosomal dominant pure hereditary spastic paraplegia.
Journal: European journal of neurology
Published: July 21, 2017
Last Updated: 09/26/2026