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Acta Ophthalmologica
|
September 27, 2021
Artificial vision: the effectiveness of the OrCam in patients with advanced inherited retinal dystrophies
Xuan-Thanh-An Nguyen, Jan Koopman, Maria M van Genderen, et al.
Documenta Ophthalmologica. Advances in Ophthalmology
|
September 28, 2011
An extended 15 Hz ERG protocol (2): data of normal subjects and patients with achromatopsia, CSNB1, and CSNB2
Mieke M C Bijveld, Frans C C Riemslag, Astrid M L Kappers, et al.
International Journal of Molecular Sciences
|
April 28, 2023
Retinitis Pigmentosa: Current Clinical Management and Emerging Therapies
Xuan-Thanh-An Nguyen, Lude Moekotte, Astrid S Plomp, et al.
Ophthalmology
|
August 12, 2018
The Phenotypic Spectrum of Albinism
Charlotte C Kruijt, Gerard C de Wit, Arthur A Bergen, et al.
Acta Ophthalmologica
|
March 20, 2020
Electroretinogram abnormalities in non-infectious uveitis often persist
Anna H Brouwer, Gerard C de Wit, Ninette H Ten Dam, et al.
American Journal of Ophthalmology Case Reports
|
May 17, 2024
Leber's hereditary optic neuropathy like disease in <i>MT-ATP6</i> variant m.8969G>A
Cansu de Muijnck, Mary J van Schooneveld, Astrid S Plomp, et al.
American Journal of Ophthalmology
|
June 8, 2019
Prolonged Cone b-Wave on Electroretinography Is Associated with Severity of Inflammation in Noninfectious Uveitis
Anna H Brouwer, Gerard C de Wit, Ninette H Ten Dam, et al.
Journal of Inherited Metabolic Disease
|
February 3, 2018
Timing of cognitive decline in CLN3 disease
Willemijn F E Kuper, Claudia van Alfen, Roeliene H Rigterink, et al.
Acta Ophthalmologica
|
January 28, 2025
Reference values for the Teller Acuity Cards II (TAC II) in infants and preverbal children, a meta-analysis
Catelijne M Neijzen, Femke M de Wit, Ymkje M Hettinga, et al.
Early Human Development
|
June 1, 2023
Visual impairment due to retinopathy of prematurity and concomitant disabilities in the Netherlands
Kasia Trzcionkowska, Jacqueline U M Termote, Maria M van Genderen, et al.
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of 8
Search research articles
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Showing results (11-20 of 74) with videos related to
Sort By:
Page
of 8
Acta Ophthalmologica
|
September 27, 2021
Artificial vision: the effectiveness of the OrCam in patients with advanced inherited retinal dystrophies
Xuan-Thanh-An Nguyen, Jan Koopman, Maria M van Genderen, et al.
Documenta Ophthalmologica. Advances in Ophthalmology
|
September 28, 2011
An extended 15 Hz ERG protocol (2): data of normal subjects and patients with achromatopsia, CSNB1, and CSNB2
Mieke M C Bijveld, Frans C C Riemslag, Astrid M L Kappers, et al.
International Journal of Molecular Sciences
|
April 28, 2023
Retinitis Pigmentosa: Current Clinical Management and Emerging Therapies
Xuan-Thanh-An Nguyen, Lude Moekotte, Astrid S Plomp, et al.
Ophthalmology
|
August 12, 2018
The Phenotypic Spectrum of Albinism
Charlotte C Kruijt, Gerard C de Wit, Arthur A Bergen, et al.
Acta Ophthalmologica
|
March 20, 2020
Electroretinogram abnormalities in non-infectious uveitis often persist
Anna H Brouwer, Gerard C de Wit, Ninette H Ten Dam, et al.
American Journal of Ophthalmology Case Reports
|
May 17, 2024
Leber's hereditary optic neuropathy like disease in <i>MT-ATP6</i> variant m.8969G>A
Cansu de Muijnck, Mary J van Schooneveld, Astrid S Plomp, et al.
American Journal of Ophthalmology
|
June 8, 2019
Prolonged Cone b-Wave on Electroretinography Is Associated with Severity of Inflammation in Noninfectious Uveitis
Anna H Brouwer, Gerard C de Wit, Ninette H Ten Dam, et al.
Journal of Inherited Metabolic Disease
|
February 3, 2018
Timing of cognitive decline in CLN3 disease
Willemijn F E Kuper, Claudia van Alfen, Roeliene H Rigterink, et al.
Acta Ophthalmologica
|
January 28, 2025
Reference values for the Teller Acuity Cards II (TAC II) in infants and preverbal children, a meta-analysis
Catelijne M Neijzen, Femke M de Wit, Ymkje M Hettinga, et al.
Early Human Development
|
June 1, 2023
Visual impairment due to retinopathy of prematurity and concomitant disabilities in the Netherlands
Kasia Trzcionkowska, Jacqueline U M Termote, Maria M van Genderen, et al.
Page
of 8