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Page 1
Usher Syndrome on the Island of Ireland: A Genotype-Phenotype Review.
Stephenson KAJ, Whelan L, Zhu J, Dockery A, Wynne NC, Cairns RM, Kirk C, Turner J, Duignan ES, O'Byrne JJ, Silvestri G, Kenna PF, Farrar GJ, Keegan DJ. Stephenson KAJ, et al. Among authors: cairns rm. Invest Ophthalmol Vis Sci. 2023 Jul 3;64(10):23. doi: 10.1167/iovs.64.10.23. Invest Ophthalmol Vis Sci. 2023. PMID: 37466950 Free PMC article.
Target 5000: a standardized all-Ireland pathway for the diagnosis and management of inherited retinal degenerations.
Stephenson KAJ, Zhu J, Wynne N, Dockery A, Cairns RM, Duignan E, Whelan L, Malone CP, Dempsey H, Collins K, Routledge S, Pandey R, Crossan E, Turner J, O'Byrne JJ, Brady L, Silvestri G, Kenna PF, Farrar GJ, Keegan DJ. Stephenson KAJ, et al. Among authors: cairns rm. Orphanet J Rare Dis. 2021 May 5;16(1):200. doi: 10.1186/s13023-021-01841-1. Orphanet J Rare Dis. 2021. PMID: 33952326 Free PMC article.
Epilepsy.
CAIRNS RM. CAIRNS RM. Med Press. 1949 Jul 27;222(4):76-9. Med Press. 1949. PMID: 18133910 No abstract available.
Lesions of the facial nerve.
CAIRNS RM. CAIRNS RM. Med World. 1946 Sep 20;65:168-72. Med World. 1946. PMID: 20998954 No abstract available.
A CASE OF RITTER'S DISEASE.
Cairns RM. Cairns RM. Br Med J. 1923 Feb 3;1(3240):186. doi: 10.1136/bmj.1.3240.186. Br Med J. 1923. PMID: 20770997 Free PMC article. No abstract available.