Prevention of retinal detachment in Stickler syndrome: the Cambridge prophylactic cryotherapy protocol
Fincham, Gregory S, Pasea, Laura, Carroll, Christopher, McNinch, Annie M, Poulson, Arabella V, Richards, Allan J, Scott, John D, Snead, Martin P
Published in Ophthalmology (Rochester, Minn.) (01.08.2014)
Published in Ophthalmology (Rochester, Minn.) (01.08.2014)
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Journal Article
Posterior Vitreous Detachment and the Posterior Hyaloid Membrane
Fincham, Gregory S., James, Sean, Spickett, Carl, Hollingshead, Michael, Thrasivoulou, Christopher, Poulson, Arabella V., McNinch, Annie, Richards, Allan, Snead, David, Limb, Gloria A., Snead, Martin P.
Published in Ophthalmology (Rochester, Minn.) (01.02.2018)
Published in Ophthalmology (Rochester, Minn.) (01.02.2018)
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Journal Article
Alternative splicing modifies the effect of mutations in COL11A1 and results in recessive type 2 Stickler syndrome with profound hearing loss
Richards, Allan J, Fincham, Gregory S, McNinch, Annie, Hill, David, Poulson, Arabella V, Castle, Bruce, Lees, Melissa M, Moore, Anthony T, Scott, John D, Snead, Martin P
Published in Journal of medical genetics (01.11.2013)
Published in Journal of medical genetics (01.11.2013)
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Journal Article
Retinal Detachment and Prophylaxis in Type 1 Stickler Syndrome
Ang, Alan, FRCOphth, Poulson, Arabella V., FRCOphth, Goodburn, Sandy F., PhD, Richards, Allan J., PhD, Scott, John D., FRCOphth, Snead, Martin P., MD, FRCOphth
Published in Ophthalmology (Rochester, Minn.) (2008)
Published in Ophthalmology (Rochester, Minn.) (2008)
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Journal Article
Missense and silent mutations in COL2A1 result in Stickler syndrome but via different molecular mechanisms
Richards, Allan J., Laidlaw, Maureen, Meredith, Sarah P., Shankar, Pallavi, Poulson, Arabella V., Scott, John D., Snead, Martin P.
Published in Human mutation (01.06.2007)
Published in Human mutation (01.06.2007)
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Journal Article
Clinical characterisation and molecular analysis of Wagner syndrome
Meredith, Sarah P, Richards, Allan J, Flanagan, Declan W, Scott, John D, Poulson, Arabella V, Snead, Martin P
Published in British journal of ophthalmology (01.05.2007)
Published in British journal of ophthalmology (01.05.2007)
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Journal Article
Auditory dysfunction in type 2 Stickler Syndrome
Alexander, Philip, Gomersall, Philip, Stancel-Lewis, Jack, Fincham, Gregory Scott, Poulson, Arabella, Richards, Allan, McNinch, Annie, Baguley, David M., Snead, Martin
Published in European archives of oto-rhino-laryngology (01.07.2021)
Published in European archives of oto-rhino-laryngology (01.07.2021)
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Journal Article
Stickler syndrome and the vitreous phenotype: mutations in COL2A1 and COL11A1
Richards, Allan J, McNinch, Annie, Martin, Howard, Oakhill, Kim, Rai, Harjeet, Waller, Sarah, Treacy, Becky, Whittaker, Joanne, Meredith, Sarah, Poulson, Arabella, Snead, Martin P
Published in Human mutation (01.06.2010)
Published in Human mutation (01.06.2010)
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Journal Article
High efficiency of mutation detection in type 1 stickler syndrome using a two-stage approach: vitreoretinal assessment coupled with exon sequencing for screening COL2A1
Richards, Allan J., Laidlaw, Maureen, Whittaker, Joanne, Treacy, Becky, Rai, Harjeet, Bearcroft, Philip, Baguley, David M., Poulson, Arabella, Ang, Alan, Scott, John D., Snead, Martin P.
Published in Human mutation (01.07.2006)
Published in Human mutation (01.07.2006)
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Journal Article
A Novel Mutation of COL2A1 Resulting in Dominantly Inherited Rhegmatogenous Retinal Detachment
Richards, Allan J, Meredith, Sarah, Poulson, Arabella, Bearcroft, Philip, Crossland, Graeme, Baguley, David M, Scott, John D, Snead, Martin P
Published in Investigative ophthalmology & visual science (01.02.2005)
Published in Investigative ophthalmology & visual science (01.02.2005)
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Journal Article
An Autosomal Dominant Bull's-Eye Macular Dystrophy (MCDR2) that Maps to the Short Arm of Chromosome 4
Michaelides, Michel, Johnson, Samantha, Poulson, Arabella, Bradshaw, Keith, Bellmann, Caren, Hunt, David M, Moore, Anthony T
Published in Investigative ophthalmology & visual science (01.04.2003)
Published in Investigative ophthalmology & visual science (01.04.2003)
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Journal Article
Vitreous phenotype: A key diagnostic sign in Stickler syndrome types 1 and 2 complicated by double heterozygosity
Ang, Alan, Ung, Tsiang, Puvanachandra, Narman, Wilson, Louise, Howard, Frances, Ryalls, Michael, Richards, Allan, Meredith, Sarah, Laidlaw, Maureen, Poulson, Arabella, Scott, John, Snead, Martin
Published in American journal of medical genetics. Part A (15.03.2007)
Published in American journal of medical genetics. Part A (15.03.2007)
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Journal Article
Intraocular surgery for optic nerve disorders
Poulson, A V, Snead, D R J, Jacobs, P M, Ahmad, N, Snead, M P
Published in Eye (London) (01.11.2004)
Published in Eye (London) (01.11.2004)
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