Ngozi Oluonye
London, ENG, United Kingdom
Last Updated: 09/26/2026
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Found 10 publications
Gene therapy in children with AIPL1-associated severe retinal dystrophy: an open-label, first-in-human interventional study.
Journal: Lancet (London, England)
Published: October 03, 2024
Incidence, aetiology and neurodisability associated with severe microcephaly: a national surveillance study.
Journal: Archives of disease in childhood
Published: July 26, 2022
Real-world clinical and molecular management of 50 prospective patients with microphthalmia, anophthalmia and/or ocular coloboma.
Journal: The British journal of ophthalmology
Published: June 24, 2022
Prospective study of pediatric patients presenting with idiopathic infantile nystagmus-Management and molecular diagnostics.
Journal: Frontiers in genetics
Published: June 24, 2022
Pathogenic NR2F1 variants cause a developmental ocular phenotype recapitulated in a mutant mouse model.
Journal: Brain communications
Published: May 10, 2021
Prognostic value of transient pattern visual evoked potentials in children with cerebral visual impairment.
Journal: Developmental medicine and child neurology
Published: December 21, 2020
Congenital cataract: a guide to genetic and clinical management.
Journal: Therapeutic advances in rare disease
Published: April 10, 2020
Juvenile Batten Disease (CLN3): Detailed Ocular Phenotype, Novel Observations, Delayed Diagnosis, Masquerades, and Prospects for Therapy.
Journal: Ophthalmology. Retina
Published: November 04, 2019
Showing 1-10 of 10
Last Updated: 09/26/2026