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F W Fitzke

Showing results (91-100 of 135) with videos related to

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The British Journal of Ophthalmology|June 1, 1997
High spatial resolution automated perimetry in glaucomaM C Westcott, A I McNaught, D P Crabb, et al.
Ophthalmology|July 1, 1997
Effect of surgery on visual field progression in normal-tension glaucomaA Bhandari, D P Crabb, D Poinoosawmy, et al.
Der Ophthalmologe : Zeitschrift Der Deutschen Ophthalmologischen Gesellschaft|June 6, 2009
[In vivo imaging of retinal cell apoptosis following acute light exposure]S Schmitz-Valckenberg, L Guo, W Cheung, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|March 26, 1998
Clinical features in affected individuals from 21 pedigrees with dominant optic atrophyM Votruba, F W Fitzke, G E Holder, et al.
Documenta Ophthalmologica. Advances in Ophthalmology|October 26, 1999
Electrophysiological findings in dominant optic atrophy (DOA) linking to the OPA1 locus on chromosome 3q 28-qterG E Holder, M Votruba, A C Carter, et al.
European Journal of Ophthalmology|October 1, 1991
Corneal haze after excimer laser refractive surgery: objective measurements and functional implicationsC P Lohmann, D S Gartry, M K Muir, et al.
The British Journal of Ophthalmology|January 30, 1999
Simulating binocular visual field status in glaucomaD P Crabb, A C Viswanathan, A I McNaught, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|February 1, 1995
Chromosome 19q cone-rod retinal dystrophy. Ocular phenotypeK Evans, J Duvall-Young, F W Fitzke, et al.
The British Journal of Ophthalmology|February 1, 1995
Motion detection threshold and field progression in normal tension glaucomaK A Baez, A I McNaught, J G Dowler, et al.
The British Journal of Ophthalmology|January 25, 2005
A detailed study of the phenotype of an autosomal dominant cone-rod dystrophy (CORD7) associated with mutation in the gene for RIM1M Michaelides, G E Holder, D M Hunt, et al.
Pageof 14

Showing results (91-100 of 135) with videos related to

Sort By:
Pageof 14
The British Journal of Ophthalmology|June 1, 1997
High spatial resolution automated perimetry in glaucomaM C Westcott, A I McNaught, D P Crabb, et al.
Ophthalmology|July 1, 1997
Effect of surgery on visual field progression in normal-tension glaucomaA Bhandari, D P Crabb, D Poinoosawmy, et al.
Der Ophthalmologe : Zeitschrift Der Deutschen Ophthalmologischen Gesellschaft|June 6, 2009
[In vivo imaging of retinal cell apoptosis following acute light exposure]S Schmitz-Valckenberg, L Guo, W Cheung, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|March 26, 1998
Clinical features in affected individuals from 21 pedigrees with dominant optic atrophyM Votruba, F W Fitzke, G E Holder, et al.
Documenta Ophthalmologica. Advances in Ophthalmology|October 26, 1999
Electrophysiological findings in dominant optic atrophy (DOA) linking to the OPA1 locus on chromosome 3q 28-qterG E Holder, M Votruba, A C Carter, et al.
European Journal of Ophthalmology|October 1, 1991
Corneal haze after excimer laser refractive surgery: objective measurements and functional implicationsC P Lohmann, D S Gartry, M K Muir, et al.
The British Journal of Ophthalmology|January 30, 1999
Simulating binocular visual field status in glaucomaD P Crabb, A C Viswanathan, A I McNaught, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|February 1, 1995
Chromosome 19q cone-rod retinal dystrophy. Ocular phenotypeK Evans, J Duvall-Young, F W Fitzke, et al.
The British Journal of Ophthalmology|February 1, 1995
Motion detection threshold and field progression in normal tension glaucomaK A Baez, A I McNaught, J G Dowler, et al.
The British Journal of Ophthalmology|January 25, 2005
A detailed study of the phenotype of an autosomal dominant cone-rod dystrophy (CORD7) associated with mutation in the gene for RIM1M Michaelides, G E Holder, D M Hunt, et al.
Pageof 14