Arvydas Gelzinis

Eiveniu Str. 2
Kaunas, KU LT50161, Lithuania

Last Updated: 09/26/2026

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Found 8 publications

Recruiting children and young people with vision impairment for clinical research - experience from the SeeMyLife study.

Recruiting children and young people with vision impairment for clinical research - experience from the SeeMyLife study.

Journal: BMC medical research methodology

Published: February 03, 2026

First Case in Lithuania of an Autosomal Recessive Mutation in the DNAJC30 Gene as a Cause of Leber's Hereditary Optic Neuropathy.

First Case in Lithuania of an Autosomal Recessive Mutation in the DNAJC30 Gene as a Cause of Leber's Hereditary Optic Neuropathy.

Journal: Genes

Published: June 30, 2025

Myopia Control in Caucasian Children with 0.01% Atropine Eye Drops: 1-Year Follow-Up Study.

Myopia Control in Caucasian Children with 0.01% Atropine Eye Drops: 1-Year Follow-Up Study.

Journal: Medicina (Kaunas, Lithuania)

Published: May 02, 2024

Efficacy and Safety of 0.03% Atropine Eye Drops in Controlling Myopia Progression: A One-Year Prospective Clinical Study.

Efficacy and Safety of 0.03% Atropine Eye Drops in Controlling Myopia Progression: A One-Year Prospective Clinical Study.

Journal: Journal of clinical medicine

Published: April 17, 2024

The Effectiveness and Tolerability of Atropine Eye Drops for Myopia Control in Non-Asian Regions.

The Effectiveness and Tolerability of Atropine Eye Drops for Myopia Control in Non-Asian Regions.

Journal: Journal of clinical medicine

Published: January 10, 2023

Neurotrophic Keratitis Due to Congenital Corneal Anesthesia with Deafness, Hypotonia, Intellectual Disability, Face Abnormality and Metabolic Disorder: A New Syndrome?

Neurotrophic Keratitis Due to Congenital Corneal Anesthesia with Deafness, Hypotonia, Intellectual Disability, Face Abnormality and Metabolic Disorder: A New Syndrome?

Journal: Medicina (Kaunas, Lithuania)

Published: April 16, 2022

A Typical Case Presentation with Spontaneous Visual Recovery in Patient Diagnosed with Leber Hereditary Optic Neuropathy due to Rare Point Mutation in MT-ND4 Gene (m.11253T>C) and Literature Review.

A Typical Case Presentation with Spontaneous Visual Recovery in Patient Diagnosed with Leber Hereditary Optic Neuropathy due to Rare Point Mutation in MT-ND4 Gene (m.11253T>C) and Literature Review.

Journal: Medicina (Kaunas, Lithuania)

Published: February 17, 2021

Inherited macular dystrophies and differential diagnostics.

Inherited macular dystrophies and differential diagnostics.

Journal: Medicina (Kaunas, Lithuania)

Published: November 22, 2012

Showing 1-8 of 8

Last Updated: 09/26/2026