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Documenta Ophthalmologica. Advances in Ophthalmology
|
August 12, 2016
Transfer characteristics of subretinal visual implants: corneally recorded implant responses
K Stingl, K U Bartz-Schmidt, A Braun, et al.
Eye (London, England)
|
February 9, 2010
A preliminary trial to determine whether prevention of dark adaptation affects the course of early diabetic retinopathy
G B Arden, M K Gündüz, A Kurtenbach, et al.
Investigative Ophthalmology & Visual Science
|
June 8, 1999
Direct visual resolution of gene copy number in the human photopigment gene array
S Wolf, L T Sharpe, H J Schmidt, et al.
Ophthalmology
|
January 11, 2001
Retinal prosthesis: an encouraging first decade with major challenges ahead
J F Rizzo, J Wyatt, M Humayun, et al.
Human Mutation
|
January 1, 1994
Mutations in the human peripherin/RDS gene associated with autosomal dominant retinitis pigmentosa
G Grüning, J M Millan, M Meins, et al.
Journal of Medical Genetics
|
April 10, 2009
GPR98 mutations cause Usher syndrome type 2 in males
I Ebermann, M H J Wiesen, E Zrenner, et al.
The American Journal of Clinical Nutrition
|
May 8, 1999
Biochemical but not clinical vitamin A deficiency results from mutations in the gene for retinol binding protein
H K Biesalski, J Frank, S C Beck, et al.
Human Molecular Genetics
|
August 25, 2000
Mutations in the CNGB3 gene encoding the beta-subunit of the cone photoreceptor cGMP-gated channel are responsible for achromatopsia (ACHM3) linked to chromosome 8q21
S Kohl, B Baumann, M Broghammer, et al.
American Journal of Human Genetics
|
November 1, 1993
Genetic heterogeneity among blue-cone monochromats
J Nathans, I H Maumenee, E Zrenner, et al.
Der Ophthalmologe : Zeitschrift Der Deutschen Ophthalmologischen Gesellschaft
|
February 22, 2012
[What can blind patients see in daily life with the subretinal Alpha IMS implant? Current overview from the clinical trial in Tübingen]
K Stingl, K U Bartz-Schmidt, D Besch, et al.
Page
of 29
Search research articles
Search
Showing results (261-270 of 284) with videos related to
Sort By:
Page
of 29
Documenta Ophthalmologica. Advances in Ophthalmology
|
August 12, 2016
Transfer characteristics of subretinal visual implants: corneally recorded implant responses
K Stingl, K U Bartz-Schmidt, A Braun, et al.
Eye (London, England)
|
February 9, 2010
A preliminary trial to determine whether prevention of dark adaptation affects the course of early diabetic retinopathy
G B Arden, M K Gündüz, A Kurtenbach, et al.
Investigative Ophthalmology & Visual Science
|
June 8, 1999
Direct visual resolution of gene copy number in the human photopigment gene array
S Wolf, L T Sharpe, H J Schmidt, et al.
Ophthalmology
|
January 11, 2001
Retinal prosthesis: an encouraging first decade with major challenges ahead
J F Rizzo, J Wyatt, M Humayun, et al.
Human Mutation
|
January 1, 1994
Mutations in the human peripherin/RDS gene associated with autosomal dominant retinitis pigmentosa
G Grüning, J M Millan, M Meins, et al.
Journal of Medical Genetics
|
April 10, 2009
GPR98 mutations cause Usher syndrome type 2 in males
I Ebermann, M H J Wiesen, E Zrenner, et al.
The American Journal of Clinical Nutrition
|
May 8, 1999
Biochemical but not clinical vitamin A deficiency results from mutations in the gene for retinol binding protein
H K Biesalski, J Frank, S C Beck, et al.
Human Molecular Genetics
|
August 25, 2000
Mutations in the CNGB3 gene encoding the beta-subunit of the cone photoreceptor cGMP-gated channel are responsible for achromatopsia (ACHM3) linked to chromosome 8q21
S Kohl, B Baumann, M Broghammer, et al.
American Journal of Human Genetics
|
November 1, 1993
Genetic heterogeneity among blue-cone monochromats
J Nathans, I H Maumenee, E Zrenner, et al.
Der Ophthalmologe : Zeitschrift Der Deutschen Ophthalmologischen Gesellschaft
|
February 22, 2012
[What can blind patients see in daily life with the subretinal Alpha IMS implant? Current overview from the clinical trial in Tübingen]
K Stingl, K U Bartz-Schmidt, D Besch, et al.
Page
of 29