Neringa Jurkute

Queen Square
London, ENG, United Kingdom

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 43 publications

Clinical and Genetic Spectrum of ACO2-Linked Dominant Optic Atrophy.

Clinical and Genetic Spectrum of ACO2-Linked Dominant Optic Atrophy.

Journal: JAMA ophthalmology

Published: April 09, 2026

Leber Hereditary Optic Neuropathy Caused by the Rare MT-ND1 m.3394T>C Mutation: A Case With Favorable Visual Prognosis and a Literature Review.

Leber Hereditary Optic Neuropathy Caused by the Rare MT-ND1 m.3394T>C Mutation: A Case With Favorable Visual Prognosis and a Literature Review.

Journal: Cureus

Published: February 03, 2026

Abnormal Splicing in the Final Intron of PRX Results in Dominant Congenital Cataract Without Neurological Phenotype.

Abnormal Splicing in the Final Intron of PRX Results in Dominant Congenital Cataract Without Neurological Phenotype.

Journal: Investigative ophthalmology & visual science

Published: November 13, 2025

Recessive variants in mitochondrial complex I nuclear subunits are an underrated cause of optic atrophy.

Recessive variants in mitochondrial complex I nuclear subunits are an underrated cause of optic atrophy.

Journal: Brain : a journal of neurology

Published: June 13, 2025

Recessive variants in mitochondrial Complex I nuclear subunits are an underrated cause of optic atrophy.

Recessive variants in mitochondrial Complex I nuclear subunits are an underrated cause of optic atrophy.

Journal: Brain : a journal of neurology

Published: June 13, 2025

Biallelic NSUN3 Variants Cause Diverse Phenotypic Spectrum Disease: From Isolated Optic Atrophy to Severe Early-Onset Mitochondrial Disorder.

Biallelic NSUN3 Variants Cause Diverse Phenotypic Spectrum Disease: From Isolated Optic Atrophy to Severe Early-Onset Mitochondrial Disorder.

Journal: Investigative ophthalmology & visual science

Published: June 04, 2025

Neuroretinal structure changes in infantile nephropathic cystinosis.

Neuroretinal structure changes in infantile nephropathic cystinosis.

Journal: Orphanet journal of rare diseases

Published: April 08, 2025

Diagnostic Value of Inter-Eye Difference Metrics on OCT for Myelin Oligodendrocyte Glycoprotein Antibody-Associated Optic Neuritis.

Diagnostic Value of Inter-Eye Difference Metrics on OCT for Myelin Oligodendrocyte Glycoprotein Antibody-Associated Optic Neuritis.

Journal: Neurology(R) neuroimmunology & neuroinflammation

Published: September 04, 2024

Candidate GRN Variant in Patient With Progressive Supranuclear Palsy.

Candidate GRN Variant in Patient With Progressive Supranuclear Palsy.

Journal: Journal of neuro-ophthalmology : the official journal of the North American Neuro-Ophthalmology Society

Published: June 24, 2024

Investigating Splice Defects in USH2A Using Targeted Long-Read Sequencing.

Investigating Splice Defects in USH2A Using Targeted Long-Read Sequencing.

Journal: Cells

Published: June 21, 2024

Electrodiagnostic tests of the visual pathway and applications in neuro-ophthalmology.

Electrodiagnostic tests of the visual pathway and applications in neuro-ophthalmology.

Journal: Eye (London, England)

Published: January 30, 2024

OPA1 Dominant Optic Atrophy: Pathogenesis and Therapeutic Targets.

OPA1 Dominant Optic Atrophy: Pathogenesis and Therapeutic Targets.

Journal: Journal of neuro-ophthalmology : the official journal of the North American Neuro-Ophthalmology Society

Published: November 17, 2023

Showing 1-12 of 43

Last Updated: 09/26/2026