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Daniela Vaideanu

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Clinical Ophthalmology (Auckland, N.Z.)|June 25, 2014
Progressive retinal detachment secondary to juxtapapillary microholes in association with type 3 posterior staphylomasChristiana B Dinah, Daniela Vaideanu-Collins, David Hw Steel
Molecular Vision|June 28, 2012
Common TGFβ2, BMP4, and FOXC1 variants are not associated with primary open-angle glaucomaSoo Park, Yalda Jamshidi, Daniela Vaideanu, et al.
Clinical Ophthalmology (Auckland, N.Z.)|August 12, 2009
Visual and refractive outcome of one-site phacotrabeculectomy compared with temporal approach phacoemulsificationDaniela Vaideanu, Kaveri Mandal, Anthony Hildreth, et al.
Survey of Ophthalmology|April 29, 2006
A review of anterior segment dysgenesesFaisal Idrees, Daniela Vaideanu, Scott G Fraser, et al.
Ophthalmic Epidemiology|April 19, 2014
Rate of diabetic vitrectomy in a defined geographical part of North East EnglandDaniela Vaideanu, Sukhpal Singh Sandhu, Jonathan Ling, et al.
Investigative Ophthalmology & Visual Science|October 28, 2008
Genetic risk for primary open-angle glaucoma determined by LMX1B haplotypesSoo Park, Yalda Jamshidi, Daniela Vaideanu, et al.
Clinical Kidney Journal|June 14, 2016
A wide spectrum of phenotypes in a family with renal coloboma syndrome caused by a PAX2 mutationJennifer Adam, Andrew C Browning, Daniela Vaideanu, et al.
European Journal of Ophthalmology|February 7, 2017
Diabetic macular edema outcomes in eyes treated with fluocinolone acetonide 0.2 µg/d intravitreal implant: real-world UK experienceIbraheem El-Ghrably, David H W Steel, Maged Habib, et al.
European Journal of Ophthalmology|September 30, 2020
Comparison between different techniques for treatment of submacular haemorrhage due to Age-Related Macular DegenerationLyudmila Kishikova, Ahmed Abdelwahab A Saad, Daniela Vaideanu-Collins, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|January 4, 2006
A novel homeobox mutation in the PITX2 gene in a family with Axenfeld-Rieger syndrome associated with brain, ocular, and dental phenotypesFaisal Idrees, Agnes Bloch-Zupan, Samantha L Free, et al.
Pageof 2

Showing results (1-10 of 11) with videos related to

Sort By:
Pageof 2
Clinical Ophthalmology (Auckland, N.Z.)|June 25, 2014
Progressive retinal detachment secondary to juxtapapillary microholes in association with type 3 posterior staphylomasChristiana B Dinah, Daniela Vaideanu-Collins, David Hw Steel
Molecular Vision|June 28, 2012
Common TGFβ2, BMP4, and FOXC1 variants are not associated with primary open-angle glaucomaSoo Park, Yalda Jamshidi, Daniela Vaideanu, et al.
Clinical Ophthalmology (Auckland, N.Z.)|August 12, 2009
Visual and refractive outcome of one-site phacotrabeculectomy compared with temporal approach phacoemulsificationDaniela Vaideanu, Kaveri Mandal, Anthony Hildreth, et al.
Survey of Ophthalmology|April 29, 2006
A review of anterior segment dysgenesesFaisal Idrees, Daniela Vaideanu, Scott G Fraser, et al.
Ophthalmic Epidemiology|April 19, 2014
Rate of diabetic vitrectomy in a defined geographical part of North East EnglandDaniela Vaideanu, Sukhpal Singh Sandhu, Jonathan Ling, et al.
Investigative Ophthalmology & Visual Science|October 28, 2008
Genetic risk for primary open-angle glaucoma determined by LMX1B haplotypesSoo Park, Yalda Jamshidi, Daniela Vaideanu, et al.
Clinical Kidney Journal|June 14, 2016
A wide spectrum of phenotypes in a family with renal coloboma syndrome caused by a PAX2 mutationJennifer Adam, Andrew C Browning, Daniela Vaideanu, et al.
European Journal of Ophthalmology|February 7, 2017
Diabetic macular edema outcomes in eyes treated with fluocinolone acetonide 0.2 µg/d intravitreal implant: real-world UK experienceIbraheem El-Ghrably, David H W Steel, Maged Habib, et al.
European Journal of Ophthalmology|September 30, 2020
Comparison between different techniques for treatment of submacular haemorrhage due to Age-Related Macular DegenerationLyudmila Kishikova, Ahmed Abdelwahab A Saad, Daniela Vaideanu-Collins, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|January 4, 2006
A novel homeobox mutation in the PITX2 gene in a family with Axenfeld-Rieger syndrome associated with brain, ocular, and dental phenotypesFaisal Idrees, Agnes Bloch-Zupan, Samantha L Free, et al.
Pageof 2