Magella M Neveu
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Explore the profile of Magella M Neveu including associated specialties, affiliations and a list of published articles.
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25
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442
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Recent Articles
1.
Neveu M, Chong V, Empeslidis T, Scholl H, Robson A
Ophthalmic Res
. 2025 Feb;
:1-26.
PMID: 39980175
Background Electrodiagnostic tests (EDTs) provide non-invasive, objective and measurable indications of retinal and visual pathway function. These hold the promise of evaluating drug efficacy and disease progression over shorter periods...
2.
Allon G, Lin S, Robson A, Arno G, Neveu M, Hysi P, et al.
Invest Ophthalmol Vis Sci
. 2025 Feb;
66(2):50.
PMID: 39969478
Purpose: To report findings in GUCA1A-associated retinopathy, a rare autosomal-dominant retinopathy. Methods: Clinical features and investigations from molecularly confirmed patients at a large referral center were analyzed (retrospective cohort study)....
3.
Calcagni A, Neveu M, Jurkute N, Robson A
Eye (Lond)
. 2024 Jun;
38(12):2392-2405.
PMID: 38862643
This article describes the main visual electrodiagnostic tests relevant to neuro-ophthalmology practice, including the visual evoked potential (VEP), and the full-field, pattern and multifocal electroretinograms (ffERG; PERG; mfERG). The principles...
4.
Leo S, Neveu M, Yu-Wai-Man P, Mahroo O, Robson A
Doc Ophthalmol
. 2023 Oct;
147(3):165-177.
PMID: 37889400
Purpose: To compare the diagnostic accuracy of the photopic negative response (PhNR) elicited by red-blue (RB) and white-white (WW) stimuli, for detection of retinal ganglion cell (RGC) dysfunction in a...
5.
Neveu M, Padhy S, Ramamurthy S, Takkar B, Jalali S, Cp D, et al.
Clin Ophthalmol
. 2022 May;
16:1569-1587.
PMID: 35637898
Albinism describes a heterogeneous group of genetically determined disorders characterized by disrupted synthesis of melanin and a range of developmental ocular abnormalities. The main ocular features common to both oculocutaneous...
6.
Majander A, Jurkute N, Burte F, Brock K, Joao C, Huang H, et al.
Am J Ophthalmol
. 2022 Apr;
241:9-27.
PMID: 35469785
Objective: To evaluate the pattern of vision loss and genotype-phenotype correlations in WFS1-associated optic neuropathy (WON). Design: Multicenter cohort study. Methods: The study involved 37 patients with WON carrying pathogenic...
7.
Chan H, Schiff E, Tailor V, Malka S, Neveu M, Theodorou M, et al.
Genes (Basel)
. 2021 Apr;
12(4).
PMID: 33808351
Albinism encompasses a group of hereditary disorders characterized by reduced or absent ocular pigment and variable skin and/or hair involvement, with syndromic forms such as Hermansky-Pudlak syndrome and Chédiak-Higashi syndrome....
8.
Wright G, Georgiou M, Robson A, Ali N, Kalhoro A, Holthaus S, et al.
Ophthalmol Retina
. 2020 Jan;
4(4):433-445.
PMID: 31926949
Purpose: To characterize the retinal phenotype of juvenile neuronal ceroid lipofuscinosis (JNCL), highlight delayed and mistaken diagnosis, and propose an algorithm for early identification. Design: Retrospective case series. Participants: Eight...
9.
Ba-Abbad R, Holder G, Robson A, Neveu M, Waseem N, Arno G, et al.
Am J Ophthalmol Case Rep
. 2019 Apr;
14:83-86.
PMID: 30976726
Purpose: To describe the clinical and electrophysiological features of an unusual retinopathy in a patient with a novel genotype of , mutations in which are implicated in autosomal recessive retinitis...
10.
Unilateral Pigmented Paravenous Retinochoroidal Atrophy Associated With Presumed Ocular Tuberculosis
Fernandez-Sanz G, Carreno E, Mall S, Neveu M, Holder G, Thomas D
Ophthalmic Surg Lasers Imaging Retina
. 2017 Apr;
48(4):345-349.
PMID: 28419401
This report describes a case of unilateral pigmented paravenous retinochoroidal atrophy (PPRCA) in a patient with low-grade unilateral intermediate uveitis. A 31-year-old woman, previously diagnosed with intermediate uveitis in the...