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Showing results (771-780 of 1,112) with videos related to

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Investigative Ophthalmology & Visual Science|September 8, 2018
Clinical Characterization of 66 Patients With Congenital Retinal Disease Due to the Deep-Intronic c.2991+1655A>G Mutation in CEP290Dyon Valkenburg, Caroline van Cauwenbergh, Birgit Lorenz, et al.
American Journal of Ophthalmology|June 1, 2014
Lipids, lipid genes, and incident age-related macular degeneration: the three continent age-related macular degeneration consortiumRonald Klein, Chelsea E Myers, Gabriëlle H S Buitendijk, et al.
Investigative Ophthalmology & Visual Science|January 24, 2012
A genetic epidemiologic study of candidate genes involved in the optic nerve head morphologyAndrea C Gasten, Wishal D Ramdas, Linda Broer, et al.
Retina (Philadelphia, Pa.)|March 13, 2018
CLINICAL AND GENETIC CHARACTERISTICS OF MALE PATIENTS WITH RPGR-ASSOCIATED RETINAL DYSTROPHIES: A Long-Term Follow-up StudyMays Talib, Mary J van Schooneveld, Alberta A Thiadens, et al.
Progress in Retinal and Eye Research|May 7, 2018
A new perspective on lipid research in age-related macular degenerationElisabeth M van Leeuwen, Eszter Emri, Benedicte M J Merle, et al.
Prostate Cancer and Prostatic Diseases|May 4, 2021
Clinical use of the SelectMDx urinary-biomarker test with or without mpMRI in prostate cancer diagnosis: a prospective, multicenter study in biopsy-naïve menRianne J Hendriks, Marloes M G van der Leest, Bas Israël, et al.
Ophthalmology|March 2, 2016
Visual Prognosis in USH2A-Associated Retinitis Pigmentosa Is Worse for Patients with Usher Syndrome Type IIa Than for Those with Nonsyndromic Retinitis PigmentosaLaurence H M Pierrache, Bas P Hartel, Erwin van Wijk, et al.
Human Mutation|May 12, 2017
Haplotype reference consortium panel: Practical implications of imputations with large reference panelsAdriana I Iglesias, Sven J van der Lee, Pieter W M Bonnemaijer, et al.
Kidney International|August 19, 2020
A systematic review and participant-level meta-analysis found little association of retinal microvascular caliber with reduced kidney functionWeng Kit Lye, Euan Paterson, Christopher C Patterson, et al.
Investigative Ophthalmology & Visual Science|March 27, 2019
Macular Dystrophy and Cone-Rod Dystrophy Caused by Mutations in the RP1 Gene: Extending the RP1 Disease SpectrumSanne K Verbakel, Ramon A C van Huet, Anneke I den Hollander, et al.
Pageof 112

Showing results (771-780 of 1,112) with videos related to

Sort By:
Pageof 112
Investigative Ophthalmology & Visual Science|September 8, 2018
Clinical Characterization of 66 Patients With Congenital Retinal Disease Due to the Deep-Intronic c.2991+1655A>G Mutation in CEP290Dyon Valkenburg, Caroline van Cauwenbergh, Birgit Lorenz, et al.
American Journal of Ophthalmology|June 1, 2014
Lipids, lipid genes, and incident age-related macular degeneration: the three continent age-related macular degeneration consortiumRonald Klein, Chelsea E Myers, Gabriëlle H S Buitendijk, et al.
Investigative Ophthalmology & Visual Science|January 24, 2012
A genetic epidemiologic study of candidate genes involved in the optic nerve head morphologyAndrea C Gasten, Wishal D Ramdas, Linda Broer, et al.
Retina (Philadelphia, Pa.)|March 13, 2018
CLINICAL AND GENETIC CHARACTERISTICS OF MALE PATIENTS WITH RPGR-ASSOCIATED RETINAL DYSTROPHIES: A Long-Term Follow-up StudyMays Talib, Mary J van Schooneveld, Alberta A Thiadens, et al.
Progress in Retinal and Eye Research|May 7, 2018
A new perspective on lipid research in age-related macular degenerationElisabeth M van Leeuwen, Eszter Emri, Benedicte M J Merle, et al.
Prostate Cancer and Prostatic Diseases|May 4, 2021
Clinical use of the SelectMDx urinary-biomarker test with or without mpMRI in prostate cancer diagnosis: a prospective, multicenter study in biopsy-naïve menRianne J Hendriks, Marloes M G van der Leest, Bas Israël, et al.
Ophthalmology|March 2, 2016
Visual Prognosis in USH2A-Associated Retinitis Pigmentosa Is Worse for Patients with Usher Syndrome Type IIa Than for Those with Nonsyndromic Retinitis PigmentosaLaurence H M Pierrache, Bas P Hartel, Erwin van Wijk, et al.
Human Mutation|May 12, 2017
Haplotype reference consortium panel: Practical implications of imputations with large reference panelsAdriana I Iglesias, Sven J van der Lee, Pieter W M Bonnemaijer, et al.
Kidney International|August 19, 2020
A systematic review and participant-level meta-analysis found little association of retinal microvascular caliber with reduced kidney functionWeng Kit Lye, Euan Paterson, Christopher C Patterson, et al.
Investigative Ophthalmology & Visual Science|March 27, 2019
Macular Dystrophy and Cone-Rod Dystrophy Caused by Mutations in the RP1 Gene: Extending the RP1 Disease SpectrumSanne K Verbakel, Ramon A C van Huet, Anneke I den Hollander, et al.
Pageof 112