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Ophthalmic Genetics|October 23, 2019
Presence of corneal crystals confirms an unusual presentation of Bietti's retinal dystrophyWon Kyung Song, Penny Clouston, Robert E MacLarenCerebellum (London, England)|November 14, 2019
Infantile Onset of Spinocerebellar Ataxia Type 5 (SCA-5) in a 6 Month Old with Ataxic Cerebral PalsyGillian Rea, Sandya Tirupathi, Jonathan Williams, et al.Ocular Immunology and Inflammation|October 18, 2017
Two Novel CAPN5 Variants Associated with Mild and Severe Autosomal Dominant Neovascular Inflammatory Vitreoretinopathy PhenotypesNadia M Randazzo, Morag E Shanks, Penny Clouston, et al.Ophthalmic Genetics|December 2, 2017
A splice-site variant in FLVCR1 produces retinitis pigmentosa without posterior column ataxiaImran H Yusuf, Morag E Shanks, Penny Clouston, et al.BMJ Case Reports|March 24, 2012
Fragile XE: an important differential diagnosisVenkataraman Krishnan, Penny Clouston, Mark Crocker, et al.Vision (Basel, Switzerland)|April 24, 2026
OCT and Autofluorescence Phenotypic Features in Autosomal Dominant <i>RHO</i>-Associated Retinitis Pigmentosa VariantsChristina Karakosta, Saoud Al-Khuzaei, Penny Clouston, et al.Genes|December 21, 2018
Exploring the Variable Phenotypes of RPGR Carrier Females in Assessing their Potential for Retinal Gene TherapyAnika Nanda, Anna P Salvetti, Penny Clouston, et al.Ophthalmic Genetics|May 22, 2018
Slowly progressive retinitis pigmentosa caused by two novel mutations in the MAK geneJoanna Monika Gray, Harry Otway Orlans, Morag Shanks, et al.American Journal of Ophthalmology|February 8, 2019
The Location of Exon 4 Mutations in RP1 Raises Challenges for Genetic Counseling and Gene TherapyAnika Nanda, Michelle E McClements, Penny Clouston, et al.American Journal of Ophthalmology Case Reports|November 17, 2022
Compound dominant-null heterozygosity in a family with <i>RP1</i>-related retinal dystrophyThomas M W Buckley, Jasmina Cehajic-Kapetanovic, Morag Shanks, et al.Pageof 4