Search research articles
Contact Us
Filters
Showing results (51-60 of 56) with videos related to
Page
of 6
Sort By:
You have reached the last page of results.
This site can display upto 56 results.
Investigative Ophthalmology & Visual Science
|
January 25, 2017
Mutation Spectrum of the ABCA4 Gene in 335 Stargardt Disease Patients From a Multicenter German Cohort-Impact of Selected Deep Intronic Variants and Common SNPs
Heidi L Schulz, Felix Grassmann, Ulrich Kellner, et al.
Plos One
|
June 20, 2020
Real-world outcomes with ranibizumab in branch retinal vein occlusion: The prospective, global, LUMINOUS study
Ian Pearce, Andreas Clemens, Michael H Brent, et al.
Der Ophthalmologe : Zeitschrift Der Deutschen Ophthalmologischen Gesellschaft
|
October 28, 2018
[Baseline diagnostics and initial treatment decision for anti-vascular endothelial growth factor treatment in retinal diseases : Comparison between results by study physician and reading centers (ORCA/OCEAN study)]
Christian K Brinkmann, Petrus Chang, Tina Schick, et al.
Kidney International
|
June 21, 2021
NPHP1 gene-associated nephronophthisis is associated with an occult retinopathy
Johannes Birtel, Georg Spital, Marius Book, et al.
Canadian Journal of Ophthalmology. Journal Canadien D'Ophtalmologie
|
June 13, 2012
Three-year visual and anatomic results of administrating intravitreal bevacizumab in inflammatory ocular neovascularization
Ahmad M Mansour, J Fernando Arevalo, Christine Fardeau, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
April 21, 2020
Resolving the dark matter of ABCA4 for 1054 Stargardt disease probands through integrated genomics and transcriptomics
Mubeen Khan, Stéphanie S Cornelis, Marta Del Pozo-Valero, et al.
Page
of 6
Search research articles
Search
Showing results (51-60 of 56) with videos related to
Sort By:
Page
of 6
You have reached the last page of results.
This site can display upto 56 results.
Investigative Ophthalmology & Visual Science
|
January 25, 2017
Mutation Spectrum of the ABCA4 Gene in 335 Stargardt Disease Patients From a Multicenter German Cohort-Impact of Selected Deep Intronic Variants and Common SNPs
Heidi L Schulz, Felix Grassmann, Ulrich Kellner, et al.
Plos One
|
June 20, 2020
Real-world outcomes with ranibizumab in branch retinal vein occlusion: The prospective, global, LUMINOUS study
Ian Pearce, Andreas Clemens, Michael H Brent, et al.
Der Ophthalmologe : Zeitschrift Der Deutschen Ophthalmologischen Gesellschaft
|
October 28, 2018
[Baseline diagnostics and initial treatment decision for anti-vascular endothelial growth factor treatment in retinal diseases : Comparison between results by study physician and reading centers (ORCA/OCEAN study)]
Christian K Brinkmann, Petrus Chang, Tina Schick, et al.
Kidney International
|
June 21, 2021
NPHP1 gene-associated nephronophthisis is associated with an occult retinopathy
Johannes Birtel, Georg Spital, Marius Book, et al.
Canadian Journal of Ophthalmology. Journal Canadien D'Ophtalmologie
|
June 13, 2012
Three-year visual and anatomic results of administrating intravitreal bevacizumab in inflammatory ocular neovascularization
Ahmad M Mansour, J Fernando Arevalo, Christine Fardeau, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
April 21, 2020
Resolving the dark matter of ABCA4 for 1054 Stargardt disease probands through integrated genomics and transcriptomics
Mubeen Khan, Stéphanie S Cornelis, Marta Del Pozo-Valero, et al.
Page
of 6