Inner Retinal Dysfunction in the Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay

por Borruat, François-Xavier, Holder, Graham E., Bremner, Fion
Publicado 2017

Quality Control Procedures and Baseline Values for Electroretinography, Perimetry, Color Vision, and Visual Acuity in an International Multicenter Study: Observations from a Safety...

por Zrenner, Eberhart, Holder, Graham E., Schiefer, Ulrich, Wild, John M.
Publicado 2020

Three-Year Changes in Visual Function in the Placebo Group of a Randomized Double-Blind International Multicenter Safety Study: Analysis of Electroretinography, Perimetry, Color Vi...

por Zrenner, Eberhart, Holder, Graham E., Schiefer, Ulrich, Wild, John M.
Publicado 2022

The clinical features of retinal disease due to a dominant mutation in RPE65

por Hull, Sarah, Mukherjee, Rajarshi, Holder, Graham E., Moore, Anthony T., Webster, Andrew R.
Publicado 2016

ISCEV standard for clinical pattern electroretinography—2007 update

por Holder, Graham E., Brigell, Mitchell G., Hawlina, Marko, Meigen, Thomas, Vaegan, Bach, Michael
Publicado 2007

ISCEV extended protocol for the photopic On–Off ERG

por Sustar, Maja, Holder, Graham E., Kremers, Jan, Barnes, Claire S., Lei, Bo, Khan, Naheed W., Robson, Anthony G.
Publicado 2018

Clinical characteristics of early retinal disease due to CDHR1 mutation

por Ba-Abbad, Rola, Sergouniotis, Panagiotis I., Plagnol, Vincent, Robson, Anthony G., Michaelides, Michel, Holder, Graham E., Webster, Andrew R.
Publicado 2013

Isolated rod dysfunction associated with a novel genotype of CNGB1

por Ba-Abbad, Rola, Holder, Graham E., Robson, Anthony G., Neveu, Magella M., Waseem, Naushin, Arno, Gavin, Webster, Andrew R.
Publicado 2019

Functional characteristics of patients with retinal dystrophy that manifest abnormal parafoveal annuli of high density fundus autofluorescence; a review and update

por Robson, Anthony G., Michaelides, Michel, Saihan, Zubin, Bird, Alan C., Webster, Andrew R., Moore, Anthony T., Fitzke, Fred W., Holder, Graham E.
Publicado 2007

Blue cone monochromacy: Causative mutations and associated phenotypes

por Gardner, Jessica C., Michaelides, Michel, Holder, Graham E., Kanuga, Naheed, Webb, Tom R., Mollon, John D., Moore, Anthony T., Hardcastle, Alison J.
Publicado 2009

ISCEV guide to visual electrodiagnostic procedures

por Robson, Anthony G., Nilsson, Josefin, Li, Shiying, Jalali, Subhadra, Fulton, Anne B., Tormene, Alma Patrizia, Holder, Graham E., Brodie, Scott E.
Publicado 2018

Autosomal dominant Best disease with an unusual electrooculographic light rise and risk of angle-closure glaucoma: a clinical and molecular genetic study

por Low, Sancy, Davidson, Alice E., Holder, Graham E., Hogg, Chris R., Bhattacharya, Shomi S., Black, Graeme C., Foster, Paul J., Webster, Andrew R.
Publicado 2011

Unilateral BEST1-Associated Retinopathy

por Arora, Rashi, Khan, Kamron, Kasilian, Melissa L., Strauss, Rupert W., Holder, Graham E., Robson, Anthony G., Thompson, Dorothy A., Moore, Anthony T., Michaelides, Michel
Publicado 2016

A rare de novo nonsense mutation in OTX2 causes early onset retinal dystrophy and pituitary dysfunction

por Henderson, Robert H., Williamson, Kathleen A., Kennedy, Joanna S., Webster, Andrew R., Holder, Graham E., Robson, Anthony G., FitzPatrick, David R., van Heyningen, Veronica, Moore, Anthony T.
Publicado 2009

Somatosensory Evoked Potentials and Central Motor Conduction Times in children with dystonia and their correlation with outcomes from Deep Brain Stimulation of the Globus pallidus...

por McClelland, Verity M., Fialho, Doreen, Flexney-Briscoe, Denise, Holder, Graham E., Elze, Markus C., Gimeno, Hortensia, Siddiqui, Ata, Mills, Kerry, Selway, Richard, Lin, Jean-Pierre
Publicado 2018

A detailed phenotypic assessment of individuals affected by MFRP-related oculopathy

por Mukhopadhyay, Rajarshi, Sergouniotis, Panagiotis I., Mackay, Donna S., Day, Alexander C., Wright, Genevieve, Devery, Sophie, Leroy, Bart P., Robson, Anthony G., Holder, Graham E., Li, Zheng, Webster, Andrew R.
Publicado 2010

Clinical and Molecular Characteristics of Childhood-Onset Stargardt Disease

por Fujinami, Kaoru, Zernant, Jana, Chana, Ravinder K., Wright, Genevieve A., Tsunoda, Kazushige, Ozawa, Yoko, Tsubota, Kazuo, Robson, Anthony G., Holder, Graham E., Allikmets, Rando, Michaelides, Michel, Moore, Anthony T.
Publicado 2014

Novel mutations in MERTK associated with childhood onset rod-cone dystrophy

por Mackay, Donna S., Henderson, Robert H., Sergouniotis, Panagiotis I., Li, Zheng, Moradi, Phillip, Holder, Graham E., Waseem, Naushin, Bhattacharya, Shomi S., Aldahmesh, Mohammed A., Alkuraya, Fowzan S., Meyer, Brian, Webster, Andrew R., Moore, Anthony T.
Publicado 2010

A randomised controlled trial investigating the effect of n-3 long-chain polyunsaturated fatty acid supplementation on cognitive and retinal function in cognitively healthy older p...

por Dangour, Alan D, Clemens, Felicity, Elbourne, Diana, Fasey, Nicky, Fletcher, Astrid E, Hardy, Pollyanna, Holder, Graham E, Huppert, Felicia A, Knight, Rosemary, Letley, Louise, Richards, Marcus, Truesdale, Ann, Vickers, Madge, Uauy, Ricardo
Publicado 2006

RDH12 retinopathy: novel mutations and phenotypic description

por Mackay, Donna S., Dev Borman, Arundhati, Moradi, Phillip, Henderson, Robert H., Li, Zheng, Wright, Genevieve A., Waseem, Naushin, Gandra, Mamatha, Thompson, Dorothy A., Bhattacharya, Shomi S., Holder, Graham E., Webster, Andrew R., Moore, Anthony T.
Publicado 2011