Dhillon H, Agarkar S, Vijaya L, Bhende M, Baskaran M, Jaichandran V
Indian J Ophthalmol. 2023; 71(11):3438-3445.
PMID: 37870002
PMC: 10752321.
DOI: 10.4103/IJO.IJO_3259_22.
Aher A, McKeefry D, Parry N, Maguire J, Murray I, Tsai T
Doc Ophthalmol. 2017; 136(1):27-43.
PMID: 29134295
DOI: 10.1007/s10633-017-9619-5.
Hamilton R, Graham K
Doc Ophthalmol. 2016; 133(1):11-9.
PMID: 27394667
DOI: 10.1007/s10633-016-9554-x.
Smirnov V, Drumare I, Bouacha I, Puech B, Defoort-Dhellemmes S
Doc Ophthalmol. 2015; 131(2):149-58.
PMID: 26138751
DOI: 10.1007/s10633-015-9508-8.
Huang J, Zhao H, Yang Y, Huang H, Yao Y, Wang Z
BMC Ophthalmol. 2015; 15:50.
PMID: 25956877
PMC: 4440277.
DOI: 10.1186/s12886-015-0030-2.
Retinal nerve fibre layer, ganglion cell layer and choroid thinning in migraine with aura.
Ekinci M, Ceylan E, Cagatay H, Keles S, Huseyinoglu N, Tanyildiz B
BMC Ophthalmol. 2014; 14:75.
PMID: 24885597
PMC: 4229806.
DOI: 10.1186/1471-2415-14-75.
X-linked cone dystrophy and colour vision deficiency arising from a missense mutation in a hybrid L/M cone opsin gene.
McClements M, Davies W, Michaelides M, Carroll J, Rha J, Mollon J
Vision Res. 2013; 80:41-50.
PMID: 23337435
PMC: 3594517.
DOI: 10.1016/j.visres.2012.12.012.
Clinical and genetic characterization of a Danish family with North Carolina macular dystrophy.
Rosenberg T, Roos B, Johnsen T, Bech N, Scheetz T, Larsen M
Mol Vis. 2010; 16:2659-68.
PMID: 21179233
PMC: 3002954.
Clinical applications of photopic negative response (PhNR) for the treatment of glaucoma and diabetic retinopathy.
Kim H, Park J, Ohn Y
Korean J Ophthalmol. 2010; 24(2):89-95.
PMID: 20379458
PMC: 2851008.
DOI: 10.3341/kjo.2010.24.2.89.
Molecular modeling of retinoschisin with functional analysis of pathogenic mutations from human X-linked retinoschisis.
Sergeev Y, Caruso R, Meltzer M, Smaoui N, MacDonald I, Sieving P
Hum Mol Genet. 2010; 19(7):1302-13.
PMID: 20061330
PMC: 2838538.
DOI: 10.1093/hmg/ddq006.
Identification of novel mutations in X-linked retinitis pigmentosa families and implications for diagnostic testing.
Neidhardt J, Glaus E, Lorenz B, Netzer C, Li Y, Schambeck M
Mol Vis. 2008; 14:1081-93.
PMID: 18552978
PMC: 2426717.
Evidence of a possible impact of the menstrual cycle on the reproducibility of scotopic ERGs in women.
Brule J, Lavoie M, Casanova C, Lachapelle P, Hebert M
Doc Ophthalmol. 2007; 114(3):125-34.
PMID: 17273847
DOI: 10.1007/s10633-007-9045-1.
Congenital cataract and macular hypoplasia in humans associated with a de novo mutation in CRYAA and compound heterozygous mutations in P.
Graw J, Klopp N, Illig T, Preising M, Lorenz B
Graefes Arch Clin Exp Ophthalmol. 2006; 244(8):912-9.
PMID: 16453125
DOI: 10.1007/s00417-005-0234-x.
Effect of optimal dietary therapy upon visual function in children with long-chain 3-hydroxyacyl CoA dehydrogenase and trifunctional protein deficiency.
Gillingham M, Weleber R, Neuringer M, Connor W, Mills M, van Calcar S
Mol Genet Metab. 2005; 86(1-2):124-33.
PMID: 16040264
PMC: 2694051.
DOI: 10.1016/j.ymgme.2005.06.001.
Neuro-ophthalmologic and electroretinographic findings in pantothenate kinase-associated neurodegeneration (formerly Hallervorden-Spatz syndrome).
Egan R, Weleber R, Hogarth P, Gregory A, Coryell J, Westaway S
Am J Ophthalmol. 2005; 140(2):267-74.
PMID: 16023068
PMC: 2169522.
DOI: 10.1016/j.ajo.2005.03.024.
Sampling and interpolation of the a-wave of the electroretinogram.
Robson J, Frishman L
Doc Ophthalmol. 2004; 108(3):171-9.
PMID: 15573940
DOI: 10.1007/s10633-004-4443-0.
Genotype-phenotype correlation in a family with Arg135Leu rhodopsin retinitis pigmentosa.
Oh K, Oh D, Weleber R, Stone E, Parikh A, White J
Br J Ophthalmol. 2004; 88(12):1533-7.
PMID: 15548806
PMC: 1772449.
DOI: 10.1136/bjo.2004.043653.
Congenital stationary night blindness and a "Schubert-Bornschein" type electrophysiology in a family with dominant inheritance.
Kabanarou S, Holder G, Fitzke F, Bird A, Webster A
Br J Ophthalmol. 2004; 88(8):1018-22.
PMID: 15258017
PMC: 1772254.
DOI: 10.1136/bjo.2003.033555.
Performance of the DTL electrode compared to the jet contact lens electrode in clinical testing.
Yin H, Pardue M
Doc Ophthalmol. 2004; 108(1):77-86.
PMID: 15104170
DOI: 10.1023/b:doop.0000018395.78512.4e.
Central serous chorioretinopathy associated with retinitis pigmentosa.
Dorenboim Y, Rehany U, Rumelt S
Graefes Arch Clin Exp Ophthalmol. 2004; 242(4):346-9.
PMID: 14997320
DOI: 10.1007/s00417-003-0819-1.