Mirella S. Barboni

Mária Str. 39
Budapest, BU 1085, Hungary

Last Updated: 09/26/2026

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Found 55 publications

Correction: ISCEV extended protocol for the photoreceptor directed ERG using full-field silent substitution stimuli.

Correction: ISCEV extended protocol for the photoreceptor directed ERG using full-field silent substitution stimuli.

Journal: Documenta ophthalmologica. Advances in ophthalmology

Published: March 26, 2026

ISCEV extended protocol for the photoreceptor directed ERG using full-field silent substitution stimuli.

ISCEV extended protocol for the photoreceptor directed ERG using full-field silent substitution stimuli.

Journal: Documenta ophthalmologica. Advances in ophthalmology

Published: February 03, 2026

Bilateral perifoveal macular ischemia in non-proliferative Duchenne muscular dystrophy-associated retinopathy: a case report.

Bilateral perifoveal macular ischemia in non-proliferative Duchenne muscular dystrophy-associated retinopathy: a case report.

Journal: Documenta ophthalmologica. Advances in ophthalmology

Published: January 27, 2026

Selective i-wave attenuation in unilateral high myopia.

Selective i-wave attenuation in unilateral high myopia.

Journal: Documenta ophthalmologica. Advances in ophthalmology

Published: January 25, 2026

Biofeedback Fixation Training in the Rehabilitation of Patients with Geographic Atrophy.

Biofeedback Fixation Training in the Rehabilitation of Patients with Geographic Atrophy.

Journal: Life (Basel, Switzerland)

Published: November 28, 2025

Dystrophin-gene mutation location influences severity of electroretinogram defects in mouse models of Duchenne muscular dystrophy.

Dystrophin-gene mutation location influences severity of electroretinogram defects in mouse models of Duchenne muscular dystrophy.

Journal: BMC medicine

Published: November 28, 2025

Disease progression in IMPDH1 gene-associated rod-cone dystrophy caused by a rare p.Thr244Pro heterozygous variant.

Disease progression in IMPDH1 gene-associated rod-cone dystrophy caused by a rare p.Thr244Pro heterozygous variant.

Journal: Documenta ophthalmologica. Advances in ophthalmology

Published: November 18, 2025

CDHR1-Associated Retinal Dystrophies: Expanding the Clinical and Genetic Spectrum with a Hungarian Cohort.

CDHR1-Associated Retinal Dystrophies: Expanding the Clinical and Genetic Spectrum with a Hungarian Cohort.

Journal: Genes

Published: November 17, 2025

Applicability of Electroretinography Measurements in Congenital PAX6-Related Aniridia.

Applicability of Electroretinography Measurements in Congenital PAX6-Related Aniridia.

Journal: Investigative ophthalmology & visual science

Published: November 14, 2025

De novo and inherited dominant variants in U4 and U6 snRNA genes cause retinitis pigmentosa.

De novo and inherited dominant variants in U4 and U6 snRNA genes cause retinitis pigmentosa.

Journal: Nature genetics

Published: June 02, 2025

The reproducibility of handheld ERGs recorded with skin electrode and natural pupils.

The reproducibility of handheld ERGs recorded with skin electrode and natural pupils.

Journal: Documenta ophthalmologica. Advances in ophthalmology

Published: May 16, 2025

De novo and inherited dominant variants in U4 and U6 snRNAs cause retinitis pigmentosa.

De novo and inherited dominant variants in U4 and U6 snRNAs cause retinitis pigmentosa.

Journal: medRxiv : the preprint server for health sciences

Published: January 20, 2025

Showing 1-12 of 55

Last Updated: 09/26/2026