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ARVO Annual Meeting Abstract June 2024

Myopia Progression in Children with Stickler Syndrome: a Longitudinal Cohort Study

Nisha Nixon; Kelly Hoi Lee Cheng; Allan Richards; Howard Martin; Martin Snead; Brinda Muthusamy

Invest. Ophthalmol. Vis. Sci.. 2024; 65(7):166.

ARVO Annual Meeting Abstract June 2024

RNA-seq suggests integrins as a potential therapeutic target in epiretinal membrane pathogenesis

Thomas Nixon; Mel Maranian; Anton Enright; Allan Richards; Howard Martin; Martin Snead

Invest. Ophthalmol. Vis. Sci.. 2024; 65(7):6651.

ARVO Annual Meeting Abstract July 2018

BMP4 loss of function mutation is a cause of autosomal dominant Stickler syndrome with associated renal dysplasia in one family

Thomas Ralph William Nixon; Allan Richards; Laura Towns; Richard Sandford; Martin Snead

Invest. Ophthalmol. Vis. Sci.. 2018; 59(9):6041.

ARVO Annual Meeting Abstract June 2013

The efficacy and safety of prophylactic cryotherapy in preventing retinal detachment in type 1 Stickler syndrome

Gregory Fincham; Laura Pasea; Christopher Carroll; Annie McNinch; Arabella Poulson; Allan Richards; John Scott; Martin Snead

Invest. Ophthalmol. Vis. Sci.. 2013; 54(15):2848.

Retina February 2005

A Novel Mutation of COL2A1 Resulting in Dominantly Inherited Rhegmatogenous Retinal Detachment

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Allan J. Richards; Sarah Meredith; Arabella Poulson; Philip Bearcroft; Graeme Crossland; David M. Baguley; John D. Scott; Martin P. Snead
TAGS: family, mutation, rhegmatogenous retinal detachment, stickler syndrome, phenotype, rna splicing
Invest. Ophthalmol. Vis. Sci.. 2005; 46(2):663-668. https://doi.org/10.1167/iovs.04-1017

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