Euvgeni Vlodavsky
Haifa, HA, Israel
Last Updated: 09/26/2026
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Found 11 publications
Primary ectopic meningioma of the brachial plexus: A case report and literature review.
Journal: Surgical neurology international
Published: September 30, 2025
Sengers syndrome caused by biallelic TIMM29 variants and RNAi silencing in Drosophila orthologue recapitulates the human phenotype.
Journal: Human genomics
Published: November 01, 2024
A novel loss-of-function mutation in LACC1 underlies hereditary juvenile arthritis with extended intra-familial phenotypic heterogeneity.
Journal: Rheumatology (Oxford, England)
Published: October 04, 2020
Heparanase promotes glioma progression via enhancing CD24 expression.
Journal: International journal of cancer
Published: October 29, 2018
Deficiency of HTRA2/Omi is associated with infantile neurodegeneration and 3-methylglutaconic aciduria.
Journal: Journal of medical genetics
Published: March 26, 2016
Erratum to: Autosomal recessive lissencephaly with cerebellar hypoplasia is associated with a loss-of-function mutation in CDK5.
Journal: Human genetics
Published: January 23, 2015
KRAS mutation positive mucinous adenocarcinoma originating in mature ovarian teratoma: case report and review of literature.
Journal: Pathology international
Published: September 12, 2013
Computerized morphometry as an aid in distinguishing recurrent versus nonrecurrent meningiomas.
Journal: Analytical and quantitative cytology and histology
Published: October 08, 2011
Showing 1-11 of 11
Last Updated: 09/26/2026