Herman E. Talsma

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

Karin W. Littink, Patricia Stappers, Frans C. C. Riemslag et al. · Genes · 2018 · 46 citations · Full text

Life Sciences, Genetics, Ophthalmology +14

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

Xuan‐Thanh‐An Nguyen, Mays Talib, Mary J. van Schooneveld et al. · American Journal of Ophthalmology · 2021 · 40 citations · Full text

Health Professions, Ophthalmology, Optometry +17

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

Susanne Roosing, Frans P.M. Cremers, Frans C. C. Riemslag et al. · Genes · 2017 · 28 citations · Full text

Medicine, Genetics, Ophthalmology +17

Defining inclusion criteria and endpoints for clinical trials: a prospective cross‐sectional study in <i>CRB1</i>‐associated retinal dystrophies

Mays Talib, Mary J. van Schooneveld, Jan Wijnholds et al. · Acta Ophthalmologica · 2021 · 23 citations · Full text

Medicine, Ophthalmology, Optometry +17

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

Charlotte C. Kruijt, Gerard C. de Wit, Herman E. Talsma et al. · Investigative Ophthalmology & Visual Science · 2019 · 21 citations · Full text

Medicine, Ophthalmology, Optometry +17