Leber's Hereditary Optic Neuropathy - Case Discussion.

Cristina Culea, Bogdana Tăbăcaru, Simona Stanca, Horia Tudor Stanca

Open access · bronzeAbstract readCase Reports

In one paragraph

Article in Romanian journal of ophthalmology. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it

0cells of the map it votes in

7citing papers in PubMed

0.4field-weighted citation impact, top 38% of its field

1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

7 citing papers in PubMed, 9 citations in OpenAlex.

Leber Hereditary Optic Neuropathy Caused by the Rare MT-ND1 m.3394T>C Mutation: A Case With Favorable Visual Prognosis and a Literature Review.Cureus · 2026
Article
Establishment of human Leber's hereditary optic neuropathy model using iPSC-derived retinal organoids.Frontiers in cellular neuroscience · 2025
Article
Central Serous Chorioretinopathy Associated with Corticosteroid Use in a Patient with Leber Hereditary Optic Neuropathy: A Case Report.Medicina (Kaunas, Lithuania) · 2024
Article
LHON needs to be genetically diagnosed and the idebenone effect quantified.Romanian journal of ophthalmology
Article
Further advances in the diagnosis and treatment of Leber's Hereditary Optic Neuropathy - a review.Romanian journal of ophthalmology
Review
Leber Hereditary Optic Neuropathy-Associated Novel Mutation inCase reports in ophthalmology
Article
Leber's Hereditary Optic Neuropathy - Reply Letter to the Editor.Romanian journal of ophthalmology
Article

4 · The record

Corrections and comments

Commented on by
LHON needs to be genetically diagnosed and the idebenone effect quantified.

5 · Who and what money

Authors and funding

4 authors at 1 institution in 1 country.

Cristina Culea"Prof. Dr. Agrippa Ionescu" Clinical Emergency Hospital, Bucharest, Romania.

Bogdana Tăbăcaru"Prof. Dr. Agrippa Ionescu" Clinical Emergency Hospital, Bucharest, Romania.

Simona Stanca"Carol Davila" University of Medicine and Pharmacy Bucharest, Romania.

Horia Tudor Stanca"Prof. Dr. Agrippa Ionescu" Clinical Emergency Hospital, Bucharest, Romania.

Carol Davila University of Medicine and Pharmacy · RO

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

Visual AcuityFluorescein AngiographyFundus OculiHumansMaleNerve FibersOptic Atrophy, Hereditary, LeberOptic NerveRetinal Ganglion CellsTomography, Optical CoherenceVisual FieldsYoung Adultabsence of relative afferent pupillary defectidebenonematernal inheritancepattern of nerve fiber damageselective vulnerability of the optic nerve and the retinal ganglion cells

Identifiers

PMID31198903

PMCPMC6531774

OpenAlexW2941246333

What OpenQuestion holds

Textmetadata

LicenceCC BY

Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.