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Items: 1 to 20 of 211

1.

Visual Acuity after Retinal Gene Therapy for Choroideremia.

Edwards TL, Jolly JK, Groppe M, Barnard AR, Cottriall CL, Tolmachova T, Black GC, Webster AR, Lotery AJ, Holder GE, Xue K, Downes SM, Simunovic MP, Seabra MC, MacLaren RE.

N Engl J Med. 2016 Apr 27. [Epub ahead of print]

PMID:
27120491
2.

Nonsyndromic Retinal Dystrophy due to Bi-Allelic Mutations in the Ciliary Transport Gene IFT140.

Hull S, Owen N, Islam F, Tracey-White D, Plagnol V, Holder GE, Michaelides M, Carss K, Raymond FL, Rozet JM, Ramsden SC, Black GC, Perrault I, Sarkar A, Moosajee M, Webster AR, Arno G, Moore AT.

Invest Ophthalmol Vis Sci. 2016 Mar 1;57(3):1053-62. doi: 10.1167/iovs.15-17976.

PMID:
26968735
3.

Preserved visual function in retinal dystrophy due to hypomorphic RPE65 mutations.

Hull S, Holder GE, Robson AG, Mukherjee R, Michaelides M, Webster AR, Moore AT.

Br J Ophthalmol. 2016 Feb 23. pii: bjophthalmol-2015-308019. doi: 10.1136/bjophthalmol-2015-308019. [Epub ahead of print]

PMID:
26906952
4.

The ophthalmic presentation of Hermansky-Pudlak syndrome 6.

Hull S, Arno G, Holder GE, Plagnol V, Gomez K, Liesner R, Webster AR, Moore AT.

Br J Ophthalmol. 2016 Jan 28. pii: bjophthalmol-2015-308067. doi: 10.1136/bjophthalmol-2015-308067. [Epub ahead of print]

PMID:
26823395
5.

Disease Expression in Autosomal Recessive Retinal Dystrophy Associated With Mutations in the DRAM2 Gene.

Sergouniotis PI, McKibbin M, Robson AG, Bolz HJ, De Baere E, Müller PL, Heller R, El-Asrag ME, Van Schil K, Plagnol V, Toomes C; Uk Inherited Retinal Disease Consortium, Ali M, Holder GE, Charbel Issa P, Leroy BP, Inglehearn CF, Webster AR.

Invest Ophthalmol Vis Sci. 2015 Dec;56(13):8083-90. doi: 10.1167/iovs.15-17604.

PMID:
26720460
6.

Mutations in CACNA2D4 Cause Distinctive Retinal Dysfunction in Humans.

Ba-Abbad R, Arno G, Carss K, Stirrups K, Penkett CJ, Moore AT, Michaelides M, Raymond FL, Webster AR, Holder GE.

Ophthalmology. 2016 Mar;123(3):668-671.e2. doi: 10.1016/j.ophtha.2015.09.045. Epub 2015 Nov 7. No abstract available.

PMID:
26560832
7.

Electroretinogram assessment of children with sensorineural hearing loss: implications for screening.

West SK, Hindocha M, Hogg CR, Holder GE, Moore AT, Reddy MA.

J AAPOS. 2015 Oct;19(5):450-4. doi: 10.1016/j.jaapos.2015.08.001.

PMID:
26486028
8.

Erratum to: ISCEV Standard for full-field clinical electroretinography (2015 update).

McCulloch DL, Marmor MF, Brigell MG, Hamilton R, Holder GE, Tzekov R, Bach M.

Doc Ophthalmol. 2015 Aug;131(1):81-3. doi: 10.1007/s10633-015-9504-z. No abstract available.

PMID:
26059396
9.

Congenital high myopia and central macular atrophy: a report of 3 families.

Hull S, Kalhoro A, Marr J, Thompson DA, Holder GE, Robson AG, Moore AT.

Eye (Lond). 2015 Jul;29(7):936-42. doi: 10.1038/eye.2015.53. Epub 2015 May 22.

10.

Ocular manifestations of microcephaly with or without chorioretinopathy, lymphedema or intellectual disability (MCLID) syndrome associated with mutations in KIF11.

Balikova I, Robson AG, Holder GE, Ostergaard P, Mansour S, Moore AT.

Acta Ophthalmol. 2016 Feb;94(1):92-8. doi: 10.1111/aos.12759. Epub 2015 May 21.

PMID:
25996076
11.

Predominantly Cone-System Dysfunction as Rare Form of Retinal Degeneration in Patients With Molecularly Confirmed Bardet-Biedl Syndrome.

Scheidecker S, Hull S, Perdomo Y, Studer F, Pelletier V, Muller J, Stoetzel C, Schaefer E, Defoort-Dhellemmes S, Drumare I, Holder GE, Hamel CP, Webster AR, Moore AT, Puech B, Dollfus HJ.

Am J Ophthalmol. 2015 Aug;160(2):364-372.e1. doi: 10.1016/j.ajo.2015.05.007. Epub 2015 May 15.

PMID:
25982971
12.

Short Communication: Contribution of Voltage-Gated Sodium Channels to the Rabbit Cone Electroretinograms.

Becker S, Jayaram H, Holder GE, Limb GA.

Curr Eye Res. 2016 Apr;41(4):569-73. doi: 10.3109/02713683.2015.1029134. Epub 2015 May 14.

PMID:
25974324
13.

Long-term effect of gene therapy on Leber's congenital amaurosis.

Bainbridge JW, Mehat MS, Sundaram V, Robbie SJ, Barker SE, Ripamonti C, Georgiadis A, Mowat FM, Beattie SG, Gardner PJ, Feathers KL, Luong VA, Yzer S, Balaggan K, Viswanathan A, de Ravel TJ, Casteels I, Holder GE, Tyler N, Fitzke FW, Weleber RG, Nardini M, Moore AT, Thompson DA, Petersen-Jones SM, Michaelides M, van den Born LI, Stockman A, Smith AJ, Rubin G, Ali RR.

N Engl J Med. 2015 May 14;372(20):1887-97. doi: 10.1056/NEJMoa1414221. Epub 2015 May 4.

14.

Increased Expression of CD169 on Blood Monocytes and Its Regulation by Virus and CD8 T Cells in Macaque Models of HIV Infection and AIDS.

Kim WK, McGary CM, Holder GE, Filipowicz AR, Kim MM, Beydoun HA, Cai Y, Liu X, Sugimoto C, Kuroda MJ.

AIDS Res Hum Retroviruses. 2015 Jul;31(7):696-706. doi: 10.1089/AID.2015.0003. Epub 2015 May 11.

PMID:
25891017
15.

Author reply: To PMID 24480711.

Halford S, Liew G, Mackay DS, Sergouniotis PI, Holt R, Broadgate S, Volpi EV, Ocaka L, Robson AG, Holder GE, Moore AT, Michaelides M, Webster AR.

Ophthalmology. 2015 Apr;122(4):e22. doi: 10.1016/j.ophtha.2014.08.041. No abstract available.

PMID:
25797088
16.

Lack of Interphotoreceptor Retinoid Binding Protein Caused by Homozygous Mutation of RBP3 Is Associated With High Myopia and Retinal Dystrophy.

Arno G, Hull S, Robson AG, Holder GE, Cheetham ME, Webster AR, Plagnol V, Moore AT.

Invest Ophthalmol Vis Sci. 2015 Apr;56(4):2358-65. doi: 10.1167/iovs.15-16520.

PMID:
25766589
17.

Pointwise linear regression analysis of serial Humphrey visual fields and a correlation with electroretinography in birdshot chorioretinopathy.

Arya B, Westcott M, Robson AG, Holder GE, Pavesio C.

Br J Ophthalmol. 2015 Jul;99(7):973-8. doi: 10.1136/bjophthalmol-2014-306003. Epub 2015 Jan 30.

PMID:
25637598
18.

ISCEV Standard for full-field clinical electroretinography (2015 update).

McCulloch DL, Marmor MF, Brigell MG, Hamilton R, Holder GE, Tzekov R, Bach M.

Doc Ophthalmol. 2015 Feb;130(1):1-12. doi: 10.1007/s10633-014-9473-7. Epub 2014 Dec 14. Erratum in: Doc Ophthalmol. 2015 Aug;131(1):81-3.

PMID:
25502644
19.

Clinical and molecular characteristics of childhood-onset Stargardt disease.

Fujinami K, Zernant J, Chana RK, Wright GA, Tsunoda K, Ozawa Y, Tsubota K, Robson AG, Holder GE, Allikmets R, Michaelides M, Moore AT.

Ophthalmology. 2015 Feb;122(2):326-34. doi: 10.1016/j.ophtha.2014.08.012. Epub 2014 Oct 12.

20.

The phenotypic variability of retinal dystrophies associated with mutations in CRX, with report of a novel macular dystrophy phenotype.

Hull S, Arno G, Plagnol V, Chamney S, Russell-Eggitt I, Thompson D, Ramsden SC, Black GC, Robson A, Holder GE, Moore AT, Webster AR.

Invest Ophthalmol Vis Sci. 2014 Sep 30;55(10):6934-44. doi: 10.1167/iovs.14-14715.

PMID:
25270190
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