Works matching AU van Genderen, Maria M.

Results: 21

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

Published in:

Documenta Ophthalmologica, 2025, v. 150, p. 1, doi. 10.1007/s10633-025-10033-2

By:

van Genderen, Maria M.;
Talsma, Herman E.

Publication type:

Article

A Case of Unexpected Adult-Onset Neurologic Decline in CLN3-Associated Retinal Degeneration.

Published in:

2017

By:

Kuper, Willemijn F. E.;
van Alfen, Claudia;
van Eck, Linda;
van den Broek, Brigitte T. A.;
Huisman, Albert;
van Genderen, Maria M.;
van Hasselt, Peter M.

Publication type:

journal article

Reference values for the Teller Acuity Cards II (TAC II) in infants and preverbal children, a meta‐analysis.

Published in:

Acta Ophthalmologica (1755375X), 2025, v. 103, n. 4, p. 479, doi. 10.1111/aos.17447

By:

Neijzen, Catelijne M.;
de Wit, Femke M.;
Hettinga, Ymkje M.;
de Boer, Joke H.;
van Genderen, Maria M.;
de Wit, Gerard C.

Publication type:

Article

Quality of life in patients with CRB1‐associated retinal dystrophies: A longitudinal study.

Published in:

Acta Ophthalmologica (1755375X), 2024, v. 102, n. 4, p. 469, doi. 10.1111/aos.15769

By:

Karuntu, Jessica S.;
Nguyen, Xuan‐Thanh‐An;
Talib, Mays;
van Schooneveld, Mary J.;
Wijnholds, Jan;
van Genderen, Maria M.;
Schalij‐Delfos, Nicoline E.;
Klaver, Caroline C. W.;
Meester‐Smoor, Magda A.;
van den Born, L. Ingeborgh;
Hoyng, Carel B.;
Thiadens, Alberta A. H. J.;
Bergen, Arthur A.;
van Nispen, Ruth M. A.;
Boon, Camiel J. F.

Publication type:

Article

Artificial vision: the effectiveness of the OrCam in patients with advanced inherited retinal dystrophies.

Published in:

Acta Ophthalmologica (1755375X), 2022, v. 100, n. 4, p. e986, doi. 10.1111/aos.15001

By:

Nguyen, Xuan‐Thanh‐An;
Koopman, Jan;
van Genderen, Maria M.;
Stam, Henk L.M.;
Boon, Camiel J.F.

Publication type:

Article

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

Published in:

2018

By:

Littink, Karin W.;
Stappers, Patricia T.Y.;
Riemslag, Frans C.C.;
Talsma, Herman E.;
van Genderen, Maria M.;
Cremers, Frans P.M.;
Collin, Rob W.J.;
van den Born, L. Ingeborgh

Publication type:

Correction Notice

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

Published in:

Genes, 2018, v. 9, n. 2, p. 68, doi. 10.3390/genes9020068

By:

Littink, Karin W.;
Stappers, Patricia T. Y.;
Riemslag, Frans C. C.;
Talsma, Herman E.;
van Genderen, Maria M.;
Cremers, Frans P. M.;
Collin, Rob W. J.;
van den Born, L. Ingeborgh

Publication type:

Article

Retinitis Pigmentosa: Current Clinical Management and Emerging Therapies.

Published in:

International Journal of Molecular Sciences, 2023, v. 24, n. 8, p. 7481, doi. 10.3390/ijms24087481

By:

Nguyen, Xuan-Thanh-An;
Moekotte, Lude;
Plomp, Astrid S.;
Bergen, Arthur A.;
van Genderen, Maria M.;
Boon, Camiel J. F.

Publication type:

Article

Effects of DTL electrode position on the amplitude and implicit time of the electroretinogram.

Published in:

Documenta Ophthalmologica, 2020, v. 140, n. 3, p. 201, doi. 10.1007/s10633-019-09733-3

By:

Brouwer, Anna H.;
de Wit, Gerard C.;
de Boer, Joke H.;
van Genderen, Maria M.

Publication type:

Article

Reply to: Pitfalls in the genetic testing of the OPN1LW-OPN1MW gene cluster in human subjects.

Published in:

NPJ Genomic Medicine, 2024, v. 9, n. 1, p. 1, doi. 10.1038/s41525-024-00409-9

By:

Haer-Wigman, Lonneke;
den Ouden, Amber;
Derks, Ronny;
van Genderen, Maria M.;
Lugtenberg, Dorien;
Verheij, Joke;
Vijzelaar, Raymon;
Yntema, Helger G.;
Vissers, Lisenka E. L. M.;
Neveling, Kornelia

Publication type:

Article

Diagnostic analysis of the highly complex OPN1LW/OPN1MW gene cluster using long-read sequencing and MLPA.

Published in:

NPJ Genomic Medicine, 2022, v. 7, n. 1, p. 1, doi. 10.1038/s41525-022-00334-9

By:

Haer-Wigman, Lonneke;
den Ouden, Amber;
van Genderen, Maria M.;
Kroes, Hester Y.;
Verheij, Joke;
Smailhodzic, Dzenita;
Hoekstra, Attje S.;
Vijzelaar, Raymon;
Blom, Jan;
Derks, Ronny;
Tjon-Pon-Fong, Menno;
Yntema, Helger G.;
Nelen, Marcel R.;
Vissers, Lisenka E.L.M.;
Lugtenberg, Dorien;
Neveling, Kornelia

Publication type:

Article

A Retrospective, Nationwide, Multicenter Study on Diagnosis and Treatment Outcome of Pediatric Optic Pathway/Hypothalamic Gliomas Including Analysis of Risk Factors for Progression After Systemic Anticancer Therapy.

Published in:

Cancers, 2025, v. 17, n. 5, p. 716, doi. 10.3390/cancers17050716

By:

Bennebroek, Carlien A. M.;
van Zwol, Judith;
Montauban van Swijndregt, Maartje C.;
Porro, Giorgio L.;
Oostenbrink, Rianne;
Dittrich, Anne T. M.;
Pott, Jan W.;
Meijer, Lisethe;
Janssen, Etienne J. M.;
Klinkenberg, Sylvia;
Bauer, Noel J.;
Notting, Irene C.;
van Genderen, Maria M.;
Tanck, Michael W.;
de Graaf, Pim;
Saeed, Peerooz;
Schouten-van Meeteren, Antoinette Y. N.

Publication type:

Article

Impact of Bevacizumab on Visual Function, Tumor Size, and Toxicity in Pediatric Progressive Optic Pathway Glioma: A Retrospective Nationwide Multicentre Study.

Published in:

Cancers, 2022, v. 14, n. 24, p. 6087, doi. 10.3390/cancers14246087

By:

Bennebroek, Carlien A. M.;
van Zwol, Judith;
Porro, Giorgio L.;
Oostenbrink, Rianne;
Dittrich, Anne T. M.;
Groot, Annabel L. W.;
Pott, Jan W.;
Janssen, Etienne J. M.;
Bauer, Noël J.;
van Genderen, Maria M.;
Saeed, Peerooz;
Lequin, Maarten H.;
de Graaf, Pim;
Schouten-van Meeteren, Antoinette Y. N.

Publication type:

Article

CVI Experience toolbox: Simulation of visual processing difficulties.

Published in:

British Journal of Visual Impairment, 2019, v. 37, n. 3, p. 248, doi. 10.1177/0264619619869044

By:

Pilon-Kamsteeg, Florine;
Dekker-Pap, Marjoke J;
de Wit, Gerard C;
van Genderen, Maria M

Publication type:

Article

In childhood, a different electrode placement improves the recording of pattern reversal visual evoked potentials.

Published in:

Journal of Physiology, 2023, v. 601, n. 10, p. 1703, doi. 10.1113/JP284400

By:

van Genderen, Maria M.

Publication type:

Article

The impact of an eye drop booklet on distress in children when receiving eye drops.

Published in:

Strabismus (09273972), 2020, v. 28, n. 2, p. 67, doi. 10.1080/09273972.2020.1752264

By:

Pilon, Florine;
Veen, Heleen;
Kef, Sabina;
van Genderen, Maria M.

Publication type:

Article

Crowding Ratio in Young Normally Sighted Children.

Published in:

Strabismus (09273972), 2012, v. 20, n. 2, p. 49, doi. 10.3109/09273972.2012.680233

By:

Dekker, Marjoke J.;
Pilon, Florine;
Bijveld, Mieke M. C.;
de Wit, Gerard C.;
van Genderen, Maria M.

Publication type:

Article

Assessment of Night Vision Problems in Patients with Congenital Stationary Night Blindness

Published in:

PLoS ONE, 2013, v. 8, n. 5, p. 1, doi. 10.1371/journal.pone.0062927

By:

Bijveld, Mieke M. C.;
van Genderen, Maria M.;
Hoeben, Frank P.;
Katzin, Amir A.;
van Nispen, Ruth M. A.;
Riemslag, Frans C. C.;
Kappers, Astrid M. L.

Publication type:

Article

Mutations in NSUN3 , a Mitochondrial Methyl Transferase Gene, Cause Inherited Optic Neuropathy.

Published in:

2024

By:

de Muijnck, Cansu;
Brink, Jacoline B. ten;
de Haan, Hugoline G.;
Rodenburg, Richard J.;
Wolf, Nicole I.;
Bergen, Arthur A.;
Boon, Camiel J. F.;
van Genderen, Maria M.

Publication type:

Case Study

Visual Impairment and Blindness in People with Intellectual Disabilities: A Systematic Review.

Published in:

Optometry & Visual Performance, 2020, v. 8, n. 3, p. 109

By:

Kroezen, Marieke;
den Akker, Natalie van;
van Genderen, Maria M.;
Wolkorte, Ria

Publication type:

Article

The identification of a RNA splice variant in TULP1 in two siblings with early‐onset photoreceptor dystrophy.

Published in:

Molecular Genetics & Genomic Medicine, 2019, v. 7, n. 6, p. N.PAG, doi. 10.1002/mgg3.660

By:

Verbakel, Sanne K.;
Fadaie, Zeinab;
Klevering, B. Jeroen;
van Genderen, Maria M.;
Feenstra, Ilse;
Cremers, Frans P. M.;
Hoyng, Carel B.;
Roosing, Susanne

Publication type:

Article