R. Brennan

Pediatric retinal detachment in cutis aplasia and cutis marmorata telangiectasia

E. McLoone, M. Lagan, R. Brennan, 2012, European journal of ophthalmology.

Clinical and molecular genetic characterisation of a family segregating autosomal dominant retinitis pigmentosa and sensorineural deafness

F. Mansergh, P. Humphries, P. Kenna, 1997, The British journal of ophthalmology.

Visual impairment, severe visual impairment, and blindness in children in Britain (BCVIS2): a national observational study

Benjamin D. Moate, G. Dutton, M. Dattani, 2021, The Lancet. Child & adolescent health.

Repaglinide-induced factitious hypoglycemia.

P. Gorden, M. Skarulis, G. Csako, 2001, The Journal of clinical endocrinology and metabolism.

Mutational Analysis of the Rhodopsin Gene in Sector Retinitis Pigmentosa

C. Willoughby, G. Silvestri, C. Wolsley, 2015, Ophthalmic genetics.

Longitudinal Study of Retinal Nerve Fiber Layer Thickness and Ganglion Cell Complex in Traumatic Optic Neuropathy

T. Kamalden, Cathy Williams, C. K. Patel, 2017 .

Health, education, and social care provision after diagnosis of childhood visual disability

Manjula K Shenoy, Benjamin D. Moate, James K. Self, 2022, Developmental Medicine & Child Neurology.

Esotropia Outcomes and the Influence of Delay to Wearing Full Hypermetropic Correction.

J. Mallett, G. Adamson, J. Yeong, 2020, Journal of pediatric ophthalmology and strabismus.

Pediatric cataract surgery outcomes in Kano, Nigeria

N. Congdon, Ling Jin, R. Brennan, 2018 .