Eve Shlik-Oiglane

2 L. Puusepa Street
Tartu, 51014, Estonia

Last Updated: 09/26/2026

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Found 17 publications

Long-Term Outcomes After Childhood Stroke.

Long-Term Outcomes After Childhood Stroke.

Journal: Pediatric reports

Published: February 27, 2026

Exploratory analysis of epilepsy biomarkers using untargeted metabolomics across multiple cohorts.

Exploratory analysis of epilepsy biomarkers using untargeted metabolomics across multiple cohorts.

Journal: Frontiers in neurology

Published: August 12, 2025

Biallelic Variants in the DARS2 Gene as a Novel Cause of Axonal Charcot-Marie-Tooth Disease.

Biallelic Variants in the DARS2 Gene as a Novel Cause of Axonal Charcot-Marie-Tooth Disease.

Journal: Annals of neurology

Published: April 01, 2025

TTN-Related Muscular Dystrophies, LGMD, and TMD, in an Estonian Family Caused by the Finnish Founder Variant.

TTN-Related Muscular Dystrophies, LGMD, and TMD, in an Estonian Family Caused by the Finnish Founder Variant.

Journal: Neurology. Genetics

Published: March 21, 2024

The Birth Prevalence of Spinal Muscular Atrophy: A Population Specific Approach in Estonia.

The Birth Prevalence of Spinal Muscular Atrophy: A Population Specific Approach in Estonia.

Journal: Frontiers in genetics

Published: October 17, 2021

PEHO syndrome caused by compound heterozygote variants in ZNHIT3 gene.

PEHO syndrome caused by compound heterozygote variants in ZNHIT3 gene.

Journal: European journal of medical genetics

Published: March 12, 2019

A retrospective analysis of the prevalence of imprinting disorders in Estonia from 1998 to 2016.

A retrospective analysis of the prevalence of imprinting disorders in Estonia from 1998 to 2016.

Journal: European journal of human genetics : EJHG

Published: January 21, 2019

Incidence of Childhood Epilepsy in Estonia.

Incidence of Childhood Epilepsy in Estonia.

Journal: Journal of child neurology

Published: June 05, 2018

Diverse phenotype in patients with complex I deficiency due to mutations in NDUFB11.

Diverse phenotype in patients with complex I deficiency due to mutations in NDUFB11.

Journal: European journal of medical genetics

Published: April 08, 2018

Epilepsy after perinatal stroke with different vascular subtypes.

Epilepsy after perinatal stroke with different vascular subtypes.

Journal: Epilepsia open

Published: January 12, 2018

Effectiveness of whole exome sequencing in unsolved patients with a clinical suspicion of a mitochondrial disorder in Estonia.

Effectiveness of whole exome sequencing in unsolved patients with a clinical suspicion of a mitochondrial disorder in Estonia.

Journal: Molecular genetics and metabolism reports

Published: December 09, 2017

Genetic and phenotypic heterogeneity suggest therapeutic implications in SCN2A-related disorders.

Genetic and phenotypic heterogeneity suggest therapeutic implications in SCN2A-related disorders.

Journal: Brain : a journal of neurology

Published: November 08, 2016

Showing 1-12 of 17

Last Updated: 09/26/2026