Monique Cordonnier
Brussels, BRU 1070, Belgium
Last Updated: 09/26/2026
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Found 20 publications
Novel OPN1LW/OPN1MW Exon 3 Haplotype-Associated Splicing Defect in Patients with X-Linked Cone Dysfunction.
Journal: International journal of molecular sciences
Published: June 02, 2022
Evaluation of the Blinq Vision Screener in the Detection of Amblyopia and Strabismus in Children.
Journal: Translational vision science & technology
Published: April 13, 2022
Diagnosis and classification of optic neuritis.
Journal: The Lancet. Neurology
Published: June 28, 2021
Congenital stationary night blindness in a patient with mild learning disability due to a compound heterozygous microdeletion of 15q13 and a missense mutation in TRPM1.
Journal: Ophthalmic genetics
Published: March 11, 2021
Post-surgical left oculomotor nerve neuromyotonia: Cause or coincidence?
Journal: European journal of ophthalmology
Published: November 04, 2020
Atypical case of acute unilateral complete external ophthalmoplegia.
Journal: Journal francais d'ophtalmologie
Published: September 01, 2020
Management of congenital lacrimal gland agenesis in a patient with blepharophimosis-ptosis-epicanthus inversus syndrome (BPES).
Journal: Journal francais d'ophtalmologie
Published: April 22, 2020
Salzmann's nodular degeneration in a patient with Kartagener syndrome.
Journal: Journal francais d'ophtalmologie
Published: March 22, 2020
Three cases of molecularly confirmed Knobloch syndrome.
Journal: Ophthalmic genetics
Published: March 18, 2020
Identification of a novel GRM6 mutation in a previously described consanguineous family with complete congenital stationary night blindness.
Journal: Ophthalmic genetics
Published: May 08, 2019
Sixth cranial nerve neuromyotonia mimicking intermittent Duane syndrome type II: case report.
Journal: Acta neurologica Belgica
Published: May 31, 2016
Last Updated: 09/26/2026