Результати пошуку - Anthony G. Robson
- Показ 1 - 20 результатів із 52
- На наступну сторінку
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Electrodiagnostic tests of the visual pathway and applications in neuro-ophthalmology за авторством Antonio Calcagni, M. Neveu, Neringa Jurkutė, Anthony G. Robson
Опубліковано 2024Revisão -
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ISCEV extended protocol for the dark-adapted red flash ERG за авторством Dorothy Thompson, Kaoru Fujinami, Ido Perlman, Ruth Hamilton, Anthony G. Robson
Опубліковано 2018Artigo -
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ISCEV extended protocol for the S-cone ERG за авторством Ido Perlman, Mineo Kondo, Enid Chelva, Anthony G. Robson, Graham E. Holder
Опубліковано 2019Artigo -
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ISCEV Standard for clinical electro-oculography (2017 update) за авторством Paul A. Constable, Michael Bach, Laura J. Frishman, Brett G. Jeffrey, Anthony G. Robson
Опубліковано 2017Artigo -
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ISCEV standard for clinical pattern electroretinography (2024 update) за авторством Dorothy Thompson, Michael Bach, J. Jason McAnany, Maja Šuštar Habjan, Suresh Viswanáthan, Anthony G. Robson
Опубліковано 2024Artigo -
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ISCEV extended protocol for the photopic On–Off ERG за авторством Maja Šuštar, Graham E. Holder, Jan Kremers, Claire S. Barnes, Bo Lei, Naheed W. Khan, Anthony G. Robson
Опубліковано 2018Artigo -
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Enhanced S-Cone Syndrome за авторством Emanuel R. de Carvalho, Anthony G. Robson, Gavin Arno, Camiel J. F. Boon, Andrew Webster, Michel Michaelides
Опубліковано 2020Artigo -
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Phenotype and Progression of Retinal Degeneration Associated With Nullizigosity of <i>ABCA4</i> за авторством Ana Fakin, Anthony G. Robson, Kaoru Fujinami, Anthony T. Moore, Michel Michaelides, John Chiang, Graham E. Holder, Andrew R. Webster
Опубліковано 2016Artigo -
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The Effect on Retinal Structure and Function of 15 Specific <i>ABCA4</i> Mutations: A Detailed Examination of 82 Hemizygous Patients за авторством Ana Fakin, Anthony G. Robson, John Chiang, Kaoru Fujinami, Anthony T. Moore, Michel Michaelides, Graham E. Holder, Andrew R. Webster
Опубліковано 2016Artigo -
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ISCEV guide to visual electrodiagnostic procedures за авторством Anthony G. Robson, Josefin Nilsson, Shiying Li, Subhadra Jalali, Anne B. Fulton, A Tormene, Graham E. Holder, Scott E. Brodie
Опубліковано 2018Artigo -
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Ophthalmological Manifestations of Oculocutaneous and Ocular Albinism: Current Perspectives за авторством M. Neveu, Srikanta Kumar Padhy, Srishti Raksheeth Ramamurthy, Brijesh Takkar, Subhadra Jalali, Deepika CP, Tapas Ranjan Padhi, Anthony G. Robson
Опубліковано 2022Revisão -
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Functional characteristics of patients with retinal dystrophy that manifest abnormal parafoveal annuli of high density fundus autofluorescence; a review and update за авторством Anthony G. Robson, Michel Michaelides, Zubin Saihan, Alan C. Bird, Andrew R. Webster, Anthony T. Moore, Fred W. Fitzke, Graham E. Holder
Опубліковано 2007Revisão -
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Leber Congenital Amaurosis Associated with Mutations in CEP290, Clinical Phenotype, and Natural History in Preparation for Trials of Novel Therapies за авторством Leo Sheck, Wayne I. L. Davies, Phillip Moradi, Anthony G. Robson, Neruban Kumaran, Alki Liasis, Andrew R. Webster, Anthony T. Moore, Michel Michaelides
Опубліковано 2018Artigo -
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Photoreceptor Structure in<i>GNAT2</i>-Associated Achromatopsia за авторством Michalis Georgiou, Navjit Singh, Thomas Kane, Anthony G. Robson, Angelos Kalitzeos, Nashila Hirji, Andrew R. Webster, Alfredo Dubra, Joseph Carroll, Michel Michaelides
Опубліковано 2020Artigo -
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Autosomal Recessive Bestrophinopathy за авторством Giuseppe Casalino, Kamron Khan, Monica Armengol, Genevieve Wright, Nikolas Pontikos, Michalis Georgiou, Andrew R. Webster, Anthony G. Robson, Parampal S. Grewal, Michel Michaelides
Опубліковано 2020Artigo
Інструменти для пошуку:
Пов'язані теми
Medicine
Ophthalmology
Retinal
Biology
Genetics
Electroretinography
Gene
Optometry
Pathology
Internal medicine
Phenotype
Visual acuity
Erg
Fundus (uterus)
Neuroscience
Computer science
Electrophysiology
Retinitis pigmentosa
Clinical electrophysiology
Mutation
Retinal degeneration
Biochemistry
Optics
Physics
ABCA4
Macular degeneration
Missense mutation
Pediatrics
Retina
Stargardt disease