Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Maria M van Genderen

Showing results (21-30 of 74) with videos related to

Pageof 8
Sort By:
European Journal of Medical Genetics|October 13, 2007
Proportional growth failure and oculocutaneous albinism in a girl with a 6.87 Mb deletion of region 15q26.2-->qterMartin Poot, Marc J Eleveld, Ruben van 't Slot, et al.
Documenta Ophthalmologica. Advances in Ophthalmology|September 28, 2011
An extended 15 Hz ERG protocol (1): the contributions of primary and secondary rod pathways and the cone pathwayMieke M C Bijveld, Astrid M L Kappers, Frans C C Riemslag, et al.
Molecular Genetics & Genomic Medicine|April 6, 2019
The identification of a RNA splice variant in TULP1 in two siblings with early-onset photoreceptor dystrophySanne K Verbakel, Zeinab Fadaie, B Jeroen Klevering, et al.
Acta Ophthalmologica|May 1, 2016
Quantification of visual function assessment using remote eye tracking in children: validity and applicabilityMarlou J G Kooiker, Johan J M Pel, Hélène J M Verbunt, et al.
Plos One|May 10, 2013
Assessment of night vision problems in patients with congenital stationary night blindnessMieke M C Bijveld, Maria M van Genderen, Frank P Hoeben, et al.
Investigative Ophthalmology & Visual Science|October 3, 2013
Ultrastructural localization of GPR179 and the impact of mutant forms on retinal function in CSNB1 patients and a mouse modelJan Klooster, Maria M van Genderen, Minzhong Yu, et al.
Genes|May 25, 2024
Mutations in <i>NSUN3</i>, a Mitochondrial Methyl Transferase Gene, Cause Inherited Optic NeuropathyCansu de Muijnck, Jacoline B Ten Brink, Hugoline G de Haan, et al.
Investigative Ophthalmology & Visual Science|October 4, 2023
CRB1-Associated Retinal Dystrophy Patients Have Expanded Lewis Glycoantigen-Positive T CellsLude Moekotte, Jonas J W Kuiper, Sanne Hiddingh, 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|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.
Pageof 8

Showing results (21-30 of 74) with videos related to

Sort By:
Pageof 8
European Journal of Medical Genetics|October 13, 2007
Proportional growth failure and oculocutaneous albinism in a girl with a 6.87 Mb deletion of region 15q26.2-->qterMartin Poot, Marc J Eleveld, Ruben van 't Slot, et al.
Documenta Ophthalmologica. Advances in Ophthalmology|September 28, 2011
An extended 15 Hz ERG protocol (1): the contributions of primary and secondary rod pathways and the cone pathwayMieke M C Bijveld, Astrid M L Kappers, Frans C C Riemslag, et al.
Molecular Genetics & Genomic Medicine|April 6, 2019
The identification of a RNA splice variant in TULP1 in two siblings with early-onset photoreceptor dystrophySanne K Verbakel, Zeinab Fadaie, B Jeroen Klevering, et al.
Acta Ophthalmologica|May 1, 2016
Quantification of visual function assessment using remote eye tracking in children: validity and applicabilityMarlou J G Kooiker, Johan J M Pel, Hélène J M Verbunt, et al.
Plos One|May 10, 2013
Assessment of night vision problems in patients with congenital stationary night blindnessMieke M C Bijveld, Maria M van Genderen, Frank P Hoeben, et al.
Investigative Ophthalmology & Visual Science|October 3, 2013
Ultrastructural localization of GPR179 and the impact of mutant forms on retinal function in CSNB1 patients and a mouse modelJan Klooster, Maria M van Genderen, Minzhong Yu, et al.
Genes|May 25, 2024
Mutations in <i>NSUN3</i>, a Mitochondrial Methyl Transferase Gene, Cause Inherited Optic NeuropathyCansu de Muijnck, Jacoline B Ten Brink, Hugoline G de Haan, et al.
Investigative Ophthalmology & Visual Science|October 4, 2023
CRB1-Associated Retinal Dystrophy Patients Have Expanded Lewis Glycoantigen-Positive T CellsLude Moekotte, Jonas J W Kuiper, Sanne Hiddingh, 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|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.
Pageof 8