To the Editors of the Medical and Physical Journal

por Holder, H. E.
Publicado 1803

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

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

Uniparental disomy as a mechanism for CERS3‐mutated autosomal recessive congenital ichthyosis

por Polubothu, S., Glover, M., Holder, S.E., Kinsler, V.A.
Publicado 2018

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

The use of nanoparticles for targeted drug delivery in non-small cell lung cancer

por Holder, Jessica E., Ferguson, Christopher, Oliveira, Elisabete, Lodeiro, Carlos, Trim, Carol M., Byrne, Lee J., Bertolo, Emilia, Wilson, Cornelia M.
Publicado 2023

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

The pattern of retinal ganglion cell dysfunction in Leber hereditary optic neuropathy

por Majander, A., Robson, A.G., João, C., Holder, G.E., Chinnery, P.F., Moore, A.T., Votruba, M., Stockman, A., Yu-Wai-Man, P.
Publicado 2017

Proliferation of Perivascular Macrophages Contributes to the Development of Encephalitic Lesions in HIV-Infected Humans and in SIV-Infected Macaques

por Filipowicz, Adam R., McGary, Christopher M., Holder, Gerard E., Lindgren, Allison A., Johnson, Edward M., Sugimoto, Chie, Kuroda, Marcelo J., Kim, Woong-Ki
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

Complete Genome Sequence of Vibrio gazogenes ATCC 43942

por Gummadidala, Phani M., Holder, Michael E., O’Brien, Jacqueline L., Ajami, Nadim J., Petrosino, Joseph F., Mitra, Chandrani, Chen, Yung Pin, Decho, Alan W., Chanda, Anindya
Publicado 2017