Herman E. Talsma

Zeist, UT, Netherlands

Last Updated: 09/26/2026

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Found 12 publications

Keeping kids engaged: the effects of superimposed single-line cartoons on pattern reversal VEPs.

Keeping kids engaged: the effects of superimposed single-line cartoons on pattern reversal VEPs.

Journal: Documenta ophthalmologica. Advances in ophthalmology

Published: October 24, 2025

Guest editorial: ISCEV Symposium 2025, Utrecht, The Netherlands.

Guest editorial: ISCEV Symposium 2025, Utrecht, The Netherlands.

Journal: Documenta ophthalmologica. Advances in ophthalmology

Published: May 15, 2025

Nystagmus characteristics and their impact on pattern-reversal VEP in patients with albinism.

Nystagmus characteristics and their impact on pattern-reversal VEP in patients with albinism.

Journal: Documenta ophthalmologica. Advances in ophthalmology

Published: January 08, 2025

Nystagmus Characteristics in Albinism: Unveiling the Link to Foveal Hypoplasia and Visual Acuity.

Nystagmus Characteristics in Albinism: Unveiling the Link to Foveal Hypoplasia and Visual Acuity.

Journal: Investigative ophthalmology & visual science

Published: December 22, 2023

CRB1-Associated Retinal Dystrophies: A Prospective Natural History Study in Anticipation of Future Clinical Trials.

CRB1-Associated Retinal Dystrophies: A Prospective Natural History Study in Anticipation of Future Clinical Trials.

Journal: American journal of ophthalmology

Published: March 01, 2021

Beyond nephronophthisis: Retinal dystrophy in the absence of kidney dysfunction in childhood expands the clinical spectrum of CEP83 deficiency.

Beyond nephronophthisis: Retinal dystrophy in the absence of kidney dysfunction in childhood expands the clinical spectrum of CEP83 deficiency.

Journal: American journal of medical genetics. Part A

Published: September 14, 2020

Recognizing differentiating clinical signs of CLN3 disease (Batten disease) at presentation.

Recognizing differentiating clinical signs of CLN3 disease (Batten disease) at presentation.

Journal: Acta ophthalmologica

Published: June 05, 2020

The Detection Of Misrouting In Albinism: Evaluation of Different VEP Procedures in a Heterogeneous Cohort.

The Detection Of Misrouting In Albinism: Evaluation of Different VEP Procedures in a Heterogeneous Cohort.

Journal: Investigative ophthalmology & visual science

Published: September 28, 2019

Defining inclusion criteria and endpoints for clinical trials: a prospective cross-sectional study in CRB1-associated retinal dystrophies.

Defining inclusion criteria and endpoints for clinical trials: a prospective cross-sectional study in CRB1-associated retinal dystrophies.

Journal: Acta ophthalmologica

Published: March 05, 2019

Correction: Littink, K. W.; et al. Autosomal Recessive NRL Mutations in Patients with Enhanced S-Cone Syndrome. Genes 2018, 9, 68.

Correction: Littink, K. W.; et al. Autosomal Recessive NRL Mutations in Patients with Enhanced S-Cone Syndrome. Genes 2018, 9, 68.

Journal: Genes

Published: March 02, 2018

Autosomal Recessive NRL Mutations in Patients with Enhanced S-Cone Syndrome.

Autosomal Recessive NRL Mutations in Patients with Enhanced S-Cone Syndrome.

Journal: Genes

Published: December 01, 2017

A Rare Form of Retinal Dystrophy Caused by Hypomorphic Nonsense Mutations in CEP290.

A Rare Form of Retinal Dystrophy Caused by Hypomorphic Nonsense Mutations in CEP290.

Journal: Genes

Published: June 30, 2017

Showing 1-12 of 12

Last Updated: 09/26/2026