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P M Cremers

Showing results (61-70 of 307) with videos related to

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Archives of Ophthalmology (Chicago, Ill. : 1960)|August 19, 2007
Clinical and genetic heterogeneity in multifocal vitelliform dystrophyCamiel J F Boon, B Jeroen Klevering, Anneke I den Hollander, et al.
Ophthalmology|March 28, 2012
Clinical and genetic characteristics of late-onset Stargardt's diseaseSarah C Westeneng-van Haaften, Camiel J F Boon, Frans P M Cremers, et al.
Ophthalmology|September 17, 2019
Highly Variable Disease Courses in Siblings with Stargardt DiseaseDyon Valkenburg, Esmee H Runhart, Nathalie M Bax, et al.
Investigative Ophthalmology & Visual Science|May 24, 2022
Identification of a Complex Allele in IMPG2 as a Cause of Adult-Onset Vitelliform Macular DystrophyIrene Vázquez-Domínguez, Catherina H Z Li, Zeinab Fadaie, et al.
Current Issues in Molecular Biology|March 27, 2024
Autosomal Recessive Rod-Cone Dystrophy with Mild Extra-Ocular Manifestations Due to a Splice-Affecting Variant in <i>BBS9</i>Iris Deitch, Sofia Itskov, Daan Panneman, et al.
International Journal of Molecular Sciences|June 19, 2024
Novel and Recurrent Copy Number Variants in <i>ABCA4</i>-Associated RetinopathyZelia Corradi, Claire-Marie Dhaenens, Olivier Grunewald, et al.
Ophthalmology|February 27, 2009
Central areolar choroidal dystrophyCamiel J F Boon, B Jeroen Klevering, Frans P M Cremers, et al.
Molecular Vision|October 19, 2012
A novel crumbs homolog 1 mutation in a family with retinitis pigmentosa, nanophthalmos, and optic disc drusenCodrut C Paun, Benjamin J Pijl, Anna M Siemiatkowska, et al.
Cerebral Cortex (New York, N.Y. : 1991)|September 9, 2025
Cortical response to transient and long-term visual field lossMarco Ninghetto, Georgios A Keliris, Kamil Szulborski, et al.
European Journal of Human Genetics : EJHG|October 21, 2004
Microarray-based mutation analysis of the ABCA4 (ABCR) gene in autosomal recessive cone-rod dystrophy and retinitis pigmentosaB Jeroen Klevering, Suzanne Yzer, Klaus Rohrschneider, et al.
Pageof 31

Showing results (61-70 of 307) with videos related to

Sort By:
Pageof 31
Archives of Ophthalmology (Chicago, Ill. : 1960)|August 19, 2007
Clinical and genetic heterogeneity in multifocal vitelliform dystrophyCamiel J F Boon, B Jeroen Klevering, Anneke I den Hollander, et al.
Ophthalmology|March 28, 2012
Clinical and genetic characteristics of late-onset Stargardt's diseaseSarah C Westeneng-van Haaften, Camiel J F Boon, Frans P M Cremers, et al.
Ophthalmology|September 17, 2019
Highly Variable Disease Courses in Siblings with Stargardt DiseaseDyon Valkenburg, Esmee H Runhart, Nathalie M Bax, et al.
Investigative Ophthalmology & Visual Science|May 24, 2022
Identification of a Complex Allele in IMPG2 as a Cause of Adult-Onset Vitelliform Macular DystrophyIrene Vázquez-Domínguez, Catherina H Z Li, Zeinab Fadaie, et al.
Current Issues in Molecular Biology|March 27, 2024
Autosomal Recessive Rod-Cone Dystrophy with Mild Extra-Ocular Manifestations Due to a Splice-Affecting Variant in <i>BBS9</i>Iris Deitch, Sofia Itskov, Daan Panneman, et al.
International Journal of Molecular Sciences|June 19, 2024
Novel and Recurrent Copy Number Variants in <i>ABCA4</i>-Associated RetinopathyZelia Corradi, Claire-Marie Dhaenens, Olivier Grunewald, et al.
Ophthalmology|February 27, 2009
Central areolar choroidal dystrophyCamiel J F Boon, B Jeroen Klevering, Frans P M Cremers, et al.
Molecular Vision|October 19, 2012
A novel crumbs homolog 1 mutation in a family with retinitis pigmentosa, nanophthalmos, and optic disc drusenCodrut C Paun, Benjamin J Pijl, Anna M Siemiatkowska, et al.
Cerebral Cortex (New York, N.Y. : 1991)|September 9, 2025
Cortical response to transient and long-term visual field lossMarco Ninghetto, Georgios A Keliris, Kamil Szulborski, et al.
European Journal of Human Genetics : EJHG|October 21, 2004
Microarray-based mutation analysis of the ABCA4 (ABCR) gene in autosomal recessive cone-rod dystrophy and retinitis pigmentosaB Jeroen Klevering, Suzanne Yzer, Klaus Rohrschneider, et al.
Pageof 31