Sharp D - Search Results

1

Alström syndrome--an uncommon cause of early childhood retinal dystrophy.

Sheck L, Al-Taie R, Sharp D, Vincent A. Sheck L, et al. Among authors: sharp d. BMJ Case Rep. 2011 Aug 17;2011:bcr0620114388. doi: 10.1136/bcr.06.2011.4388. BMJ Case Rep. 2011. PMID: 22688943 Free PMC article.

2

Pseudodominance in two families with KCNV2 related retinopathy.

Kiray G, Rapata M, Sharp D, Vincent AL. Kiray G, et al. Among authors: sharp d. Am J Ophthalmol Case Rep. 2020 Feb 26;18:100625. doi: 10.1016/j.ajoc.2020.100625. eCollection 2020 Jun. Am J Ophthalmol Case Rep. 2020. PMID: 32154435 Free PMC article.

3

A novel rhodopsin point mutation, proline-170-histidine, associated with sectoral retinitis pigmentosa.

Shah SP, Wong F, Sharp DM, Vincent AL. Shah SP, et al. Ophthalmic Genet. 2014 Dec;35(4):241-7. doi: 10.3109/13816810.2014.924014. Epub 2014 Jun 11. Ophthalmic Genet. 2014. PMID: 24918165

4

Drug-induced optic neuropathy-TB or not TB.

Pradhan M, Sharp D, Best S, Vincent A, Vaphiades M. Pradhan M, et al. Among authors: sharp d. Surv Ophthalmol. 2010 Jul-Aug;55(4):378-85. doi: 10.1016/j.survophthal.2009.10.005. Epub 2010 Jan 18. Surv Ophthalmol. 2010. PMID: 20083290

5

Rhodopsin F45L Allele Does Not Cause Autosomal Dominant Retinitis Pigmentosa in a Large Caucasian Family.

Vincent AL, Carroll J, Fishman GA, Sauer A, Sharp D, Summerfelt P, Williams V, Dubis AM, Kohl S, Wong F. Vincent AL, et al. Among authors: sharp d. Transl Vis Sci Technol. 2013 Feb;2(2):4. doi: 10.1167/tvst.2.2.4. Epub 2013 Mar 13. Transl Vis Sci Technol. 2013. PMID: 24049715 Free PMC article.

6

Incidence, Risk Factors, and Outcomes of Rhegmatogenous Retinal Detachment after Intravitreal Injections of Anti-VEGF for Retinal Diseases: Data from the Fight Retinal Blindness! Registry.

Gabrielle PH, Nguyen V, Arnould L, Viola F, Zarranz-Ventura J, Barthelmes D, Creuzot-Garcher C, Gillies M; Fight Retinal Blindness! Study Group. Gabrielle PH, et al. Ophthalmol Retina. 2022 Nov;6(11):1044-1053. doi: 10.1016/j.oret.2022.05.008. Epub 2022 May 16. Ophthalmol Retina. 2022. PMID: 35589075 Free article.

7

Autoimmune retinopathy associated with carcinoid tumour of the small bowel.

Ogra S, Sharp D, Danesh-Meyer H. Ogra S, et al. Among authors: sharp d. J Clin Neurosci. 2014 Feb;21(2):358-60. doi: 10.1016/j.jocn.2013.07.002. Epub 2013 Oct 11. J Clin Neurosci. 2014. PMID: 24126040

8

A 5-year-old girl with decreased vision in the left eye.

Yap J, Sharp D, Dai S. Yap J, et al. Among authors: sharp d. Digit J Ophthalmol. 2015 May 9;21(2):1-7. doi: 10.5693/djo.03.2014.09.001. eCollection 2015. Digit J Ophthalmol. 2015. PMID: 27330462 Free PMC article. No abstract available.

9

Clinical manifestations of a unique X-linked retinal disorder in a large New Zealand family with a novel mutation in CACNA1F, the gene responsible for CSNB2.

Hope CI, Sharp DM, Hemara-Wahanui A, Sissingh JI, Lundon P, Mitchell EA, Maw MA, Clover GM. Hope CI, et al. Clin Exp Ophthalmol. 2005 Apr;33(2):129-36. doi: 10.1111/j.1442-9071.2005.00987.x. Clin Exp Ophthalmol. 2005. PMID: 15807819

10

Randomised controlled trial of prevention of falls in people aged > or =75 with severe visual impairment: the VIP trial.

Campbell AJ, Robertson MC, La Grow SJ, Kerse NM, Sanderson GF, Jacobs RJ, Sharp DM, Hale LA. Campbell AJ, et al. BMJ. 2005 Oct 8;331(7520):817. doi: 10.1136/bmj.38601.447731.55. Epub 2005 Sep 23. BMJ. 2005. PMID: 16183652 Free PMC article. Clinical Trial.

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