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Cellular Reprogramming
|
May 14, 2013
Human induced pluripotent stem cells as a tool to model a form of Leber congenital amaurosis
Céline Lustremant, Walter Habeler, Alexandra Plancheron, et al.
Retinal Cases & Brief Reports
|
May 26, 2017
RETINOCHOROIDAL ANASTOMOSIS ASSOCIATED WITH ENHANCED S-CONE SYNDROME
Jennyfer Zerbib, Rocio Blanco Garavito, Sylvie Gerber, et al.
Biomed Research International
|
February 19, 2015
Cone dystrophy in patient with homozygous RP1L1 mutation
Sachiko Kikuchi, Shuhei Kameya, Kiyoko Gocho, et al.
Acta Ophthalmologica
|
August 5, 2022
Extensive myelinated retinal nerve fibres and bilateral foveal hypoplasia: A specific clinical entity
Gabriel Hallali, Sjoukje E Loudon, Anthony G Robson, et al.
Ophthalmic Research
|
August 1, 2015
Threshold levels of visual field and acuity loss related to significant decreases in the quality of life and emotional states of patients with retinitis pigmentosa
Line Azoulay, Philippe Chaumet-Riffaud, Steven Jaron, et al.
Ophthalmology
|
April 7, 2024
Extensive Macular Atrophy with Pseudodrusen-like appearance: Progression Kinetics and Late-Stage Findings
Alessio Antropoli, Lorenzo Bianco, Christel Condroyer, et al.
Ophthalmology
|
May 10, 2018
Phenotypic Characteristics of a French Cohort of Patients with X-Linked Retinoschisis
Raphaëlle Orès, Saddek Mohand-Said, Claire-Marie Dhaenens, et al.
Scientific Reports
|
August 21, 2019
TRPM1 Mutations are the Most Common Cause of Autosomal Recessive Congenital Stationary Night Blindness (CSNB) in the Palestinian and Israeli Populations
Alaa AlTalbishi, Lina Zelinger, Christina Zeitz, et al.
International Journal of Molecular Sciences
|
April 30, 2021
A New Mouse Model for Complete Congenital Stationary Night Blindness Due to <i>Gpr179</i> Deficiency
Elise Orhan, Marion Neuillé, Miguel de Sousa Dias, et al.
Investigative Ophthalmology & Visual Science
|
December 3, 2019
Peripapillary Sparing With Near Infrared Autofluorescence Correlates With Electroretinographic Findings in Patients With Stargardt Disease
Marco Nassisi, Saddek Mohand-Saïd, Camille Andrieu, et al.
Page
of 24
Search research articles
Search
Showing results (61-70 of 234) with videos related to
Sort By:
Page
of 24
Cellular Reprogramming
|
May 14, 2013
Human induced pluripotent stem cells as a tool to model a form of Leber congenital amaurosis
Céline Lustremant, Walter Habeler, Alexandra Plancheron, et al.
Retinal Cases & Brief Reports
|
May 26, 2017
RETINOCHOROIDAL ANASTOMOSIS ASSOCIATED WITH ENHANCED S-CONE SYNDROME
Jennyfer Zerbib, Rocio Blanco Garavito, Sylvie Gerber, et al.
Biomed Research International
|
February 19, 2015
Cone dystrophy in patient with homozygous RP1L1 mutation
Sachiko Kikuchi, Shuhei Kameya, Kiyoko Gocho, et al.
Acta Ophthalmologica
|
August 5, 2022
Extensive myelinated retinal nerve fibres and bilateral foveal hypoplasia: A specific clinical entity
Gabriel Hallali, Sjoukje E Loudon, Anthony G Robson, et al.
Ophthalmic Research
|
August 1, 2015
Threshold levels of visual field and acuity loss related to significant decreases in the quality of life and emotional states of patients with retinitis pigmentosa
Line Azoulay, Philippe Chaumet-Riffaud, Steven Jaron, et al.
Ophthalmology
|
April 7, 2024
Extensive Macular Atrophy with Pseudodrusen-like appearance: Progression Kinetics and Late-Stage Findings
Alessio Antropoli, Lorenzo Bianco, Christel Condroyer, et al.
Ophthalmology
|
May 10, 2018
Phenotypic Characteristics of a French Cohort of Patients with X-Linked Retinoschisis
Raphaëlle Orès, Saddek Mohand-Said, Claire-Marie Dhaenens, et al.
Scientific Reports
|
August 21, 2019
TRPM1 Mutations are the Most Common Cause of Autosomal Recessive Congenital Stationary Night Blindness (CSNB) in the Palestinian and Israeli Populations
Alaa AlTalbishi, Lina Zelinger, Christina Zeitz, et al.
International Journal of Molecular Sciences
|
April 30, 2021
A New Mouse Model for Complete Congenital Stationary Night Blindness Due to <i>Gpr179</i> Deficiency
Elise Orhan, Marion Neuillé, Miguel de Sousa Dias, et al.
Investigative Ophthalmology & Visual Science
|
December 3, 2019
Peripapillary Sparing With Near Infrared Autofluorescence Correlates With Electroretinographic Findings in Patients With Stargardt Disease
Marco Nassisi, Saddek Mohand-Saïd, Camille Andrieu, et al.
Page
of 24