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Herman E Talsma

Showing results (1-10 of 11) with videos related to

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Documenta Ophthalmologica. Advances in Ophthalmology|February 18, 2026
Keeping kids engaged: the effects of superimposed single-line cartoons on pattern reversal VEPsHerman E Talsma, Frank P Hoeben, Maria M van Genderen, et al.
Documenta Ophthalmologica. Advances in Ophthalmology|June 3, 2025
Nystagmus characteristics and their impact on pattern-reversal VEP in patients with albinismHerman E Talsma, Gerard C de Wit, Charlotte C Kruijt, et al.
Investigative Ophthalmology & Visual Science|December 22, 2023
Nystagmus Characteristics in Albinism: Unveiling the Link to Foveal Hypoplasia and Visual AcuityHerman E Talsma, Charlotte C Kruijt, Gerard C de Wit, et al.
Investigative Ophthalmology & Visual Science|September 28, 2019
The Detection Of Misrouting In Albinism: Evaluation of Different VEP Procedures in a Heterogeneous CohortCharlotte C Kruijt, Gerard C de Wit, Herman E Talsma, et al.
Acta Ophthalmologica|October 19, 2020
Recognizing differentiating clinical signs of CLN3 disease (Batten disease) at presentationWillemijn F E Kuper, Herman E Talsma, Mary J van Schooneveld, et al.
Genes|February 2, 2018
Autosomal Recessive NRL Mutations in Patients with Enhanced S-Cone SyndromeKarin W Littink, Patricia T Y Stappers, Frans C C Riemslag, et al.
Genes|August 23, 2017
A Rare Form of Retinal Dystrophy Caused by Hypomorphic Nonsense Mutations in CEP290Susanne Roosing, Frans P M Cremers, Frans C C Riemslag, et al.
Genes|March 10, 2018
Correction: Littink, K. W.; et al. Autosomal Recessive NRL Mutations in Patients with Enhanced S-Cone Syndrome. Genes 2018, 9, 68Karin W Littink, Patricia T Y Stappers, Frans C C Riemslag, et al.
American Journal of Medical Genetics. Part A|May 3, 2021
Beyond nephronophthisis: Retinal dystrophy in the absence of kidney dysfunction in childhood expands the clinical spectrum of CEP83 deficiencyBram C F Veldman, Willemijn F E Kuper, Marc Lilien, et al.
Acta Ophthalmologica|February 2, 2021
Defining inclusion criteria and endpoints for clinical trials: a prospective cross-sectional study in CRB1-associated retinal dystrophiesMays Talib, Mary J van Schooneveld, Jan Wijnholds, et al.
Pageof 2

Showing results (1-10 of 11) with videos related to

Sort By:
Pageof 2
Documenta Ophthalmologica. Advances in Ophthalmology|February 18, 2026
Keeping kids engaged: the effects of superimposed single-line cartoons on pattern reversal VEPsHerman E Talsma, Frank P Hoeben, Maria M van Genderen, et al.
Documenta Ophthalmologica. Advances in Ophthalmology|June 3, 2025
Nystagmus characteristics and their impact on pattern-reversal VEP in patients with albinismHerman E Talsma, Gerard C de Wit, Charlotte C Kruijt, et al.
Investigative Ophthalmology & Visual Science|December 22, 2023
Nystagmus Characteristics in Albinism: Unveiling the Link to Foveal Hypoplasia and Visual AcuityHerman E Talsma, Charlotte C Kruijt, Gerard C de Wit, et al.
Investigative Ophthalmology & Visual Science|September 28, 2019
The Detection Of Misrouting In Albinism: Evaluation of Different VEP Procedures in a Heterogeneous CohortCharlotte C Kruijt, Gerard C de Wit, Herman E Talsma, et al.
Acta Ophthalmologica|October 19, 2020
Recognizing differentiating clinical signs of CLN3 disease (Batten disease) at presentationWillemijn F E Kuper, Herman E Talsma, Mary J van Schooneveld, et al.
Genes|February 2, 2018
Autosomal Recessive NRL Mutations in Patients with Enhanced S-Cone SyndromeKarin W Littink, Patricia T Y Stappers, Frans C C Riemslag, et al.
Genes|August 23, 2017
A Rare Form of Retinal Dystrophy Caused by Hypomorphic Nonsense Mutations in CEP290Susanne Roosing, Frans P M Cremers, Frans C C Riemslag, et al.
Genes|March 10, 2018
Correction: Littink, K. W.; et al. Autosomal Recessive NRL Mutations in Patients with Enhanced S-Cone Syndrome. Genes 2018, 9, 68Karin W Littink, Patricia T Y Stappers, Frans C C Riemslag, et al.
American Journal of Medical Genetics. Part A|May 3, 2021
Beyond nephronophthisis: Retinal dystrophy in the absence of kidney dysfunction in childhood expands the clinical spectrum of CEP83 deficiencyBram C F Veldman, Willemijn F E Kuper, Marc Lilien, et al.
Acta Ophthalmologica|February 2, 2021
Defining inclusion criteria and endpoints for clinical trials: a prospective cross-sectional study in CRB1-associated retinal dystrophiesMays Talib, Mary J van Schooneveld, Jan Wijnholds, et al.
Pageof 2