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Journal of Medical Genetics
|
September 22, 2001
Clustering and frequency of mutations in the retinal guanylate cyclase (GUCY2D) gene in patients with dominant cone-rod dystrophies
A M Payne, A G Morris, S M Downes, et al.
Ophthalmic Surgery, Lasers & Imaging Retina
|
July 7, 2023
New Imaging Technology for Simultaneous Multiwavelength-UWF Fundus Fluorescein Angiography and Indocyanine Green Angiography With Navigated Central and Peripheral SS-OCT
Francisco Javier Valentin Bravo, William Ayliffe, Sebastian Francis Eduardo Stanga, et al.
Retina (Philadelphia, Pa.)
|
December 3, 2009
"Cone dystrophy with supernormal rod electroretinogram": a comprehensive genotype/phenotype study including fundus autofluorescence and extensive electrophysiology
Anthony G Robson, Andrew R Webster, Michel Michaelides, et al.
Cells
|
August 26, 2023
The Role of Inflammation in Age-Related Macular Degeneration-Therapeutic Landscapes in Geographic Atrophy
Grace A Borchert, Hoda Shamsnajafabadi, Monica L Hu, et al.
International Journal of Radiation Oncology, Biology, Physics
|
February 25, 1999
Immediate side effects of stereotactic radiotherapy and radiosurgery
M Werner-Wasik, S Rudoler, P E Preston, et al.
Genes
|
December 30, 2025
Expanding the Genetic Spectrum in <i>IMPG1</i> and <i>IMPG2</i> Retinopathy
Saoud Al-Khuzaei, Ahmed K Shalaby, Jing Yu, et al.
The British Journal of Ophthalmology
|
July 22, 2017
Pigmentary retinopathy, rod-cone dysfunction and sensorineural deafness associated with a rare mitochondrial tRNA<sup>Lys</sup> (m.8340G>A) gene variant
Jaidip S Gill, Steven A Hardy, Emma L Blakely, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)
|
November 16, 2001
Autosomal dominant cone-rod dystrophy with mutations in the guanylate cyclase 2D gene encoding retinal guanylate cyclase-1
S M Downes, A M Payne, R E Kelsell, et al.
Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia
|
November 23, 2020
Auditory-perceptual voice and speech evaluation in ATP1A3 positive patients
Mary E Moya-Mendez, Lyndsay L Madden, Kathryn W Ruckart, et al.
Frontiers in Neuroscience
|
July 16, 2024
Age-related macular degeneration: suitability of optogenetic therapy for geographic atrophy
Grace A Borchert, Hoda Shamsnajafabadi, Benjamin W J Ng, et al.
Page
of 30
Search research articles
Search
Showing results (211-220 of 295) with videos related to
Sort By:
Page
of 30
Journal of Medical Genetics
|
September 22, 2001
Clustering and frequency of mutations in the retinal guanylate cyclase (GUCY2D) gene in patients with dominant cone-rod dystrophies
A M Payne, A G Morris, S M Downes, et al.
Ophthalmic Surgery, Lasers & Imaging Retina
|
July 7, 2023
New Imaging Technology for Simultaneous Multiwavelength-UWF Fundus Fluorescein Angiography and Indocyanine Green Angiography With Navigated Central and Peripheral SS-OCT
Francisco Javier Valentin Bravo, William Ayliffe, Sebastian Francis Eduardo Stanga, et al.
Retina (Philadelphia, Pa.)
|
December 3, 2009
"Cone dystrophy with supernormal rod electroretinogram": a comprehensive genotype/phenotype study including fundus autofluorescence and extensive electrophysiology
Anthony G Robson, Andrew R Webster, Michel Michaelides, et al.
Cells
|
August 26, 2023
The Role of Inflammation in Age-Related Macular Degeneration-Therapeutic Landscapes in Geographic Atrophy
Grace A Borchert, Hoda Shamsnajafabadi, Monica L Hu, et al.
International Journal of Radiation Oncology, Biology, Physics
|
February 25, 1999
Immediate side effects of stereotactic radiotherapy and radiosurgery
M Werner-Wasik, S Rudoler, P E Preston, et al.
Genes
|
December 30, 2025
Expanding the Genetic Spectrum in <i>IMPG1</i> and <i>IMPG2</i> Retinopathy
Saoud Al-Khuzaei, Ahmed K Shalaby, Jing Yu, et al.
The British Journal of Ophthalmology
|
July 22, 2017
Pigmentary retinopathy, rod-cone dysfunction and sensorineural deafness associated with a rare mitochondrial tRNA<sup>Lys</sup> (m.8340G>A) gene variant
Jaidip S Gill, Steven A Hardy, Emma L Blakely, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)
|
November 16, 2001
Autosomal dominant cone-rod dystrophy with mutations in the guanylate cyclase 2D gene encoding retinal guanylate cyclase-1
S M Downes, A M Payne, R E Kelsell, et al.
Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia
|
November 23, 2020
Auditory-perceptual voice and speech evaluation in ATP1A3 positive patients
Mary E Moya-Mendez, Lyndsay L Madden, Kathryn W Ruckart, et al.
Frontiers in Neuroscience
|
July 16, 2024
Age-related macular degeneration: suitability of optogenetic therapy for geographic atrophy
Grace A Borchert, Hoda Shamsnajafabadi, Benjamin W J Ng, et al.
Page
of 30