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E Weidle

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

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Klinische Monatsblatter Fur Augenheilkunde|March 1, 1983
[Tyrosinosis with hepatolenticular degeneration (Wilson's disease)]H J Thiel, E Weidle
Klinische Monatsblatter Fur Augenheilkunde|October 1, 1993
[Unilateral type III (Hida) lattice stromal corneal dystrophy]B Seitz, E Weidle, G O Naumann
Klinische Monatsblatter Fur Augenheilkunde|June 10, 2009
[Mutational analysis of VSX-1 in one patient with posterior polymorphous corneal dystrophy and in three families with hereditary Fuchs endothelial dystrophy]I Clausen, E Weidle, G Duncker, et al.
Klinische Monatsblatter Fur Augenheilkunde|August 1, 1988
[Anesthesia for eye operations in mitochondrial encephalomyelopathy]T Fritz, K Wessel, E Weidle, et al.
Klinische Monatsblatter Fur Augenheilkunde|August 18, 2015
[TGC Repeats in Intron 2 of the TCF4 Gene have a Good Predictive Power Regarding to Fuchs Endothelial Corneal Dystrophy]M Luther, C Grünauer-Kloevekorn, E Weidle, et al.
American Journal of Ophthalmology|March 1, 1983
Nine cases of cavernous hemangioma of the retinaE Messmer, H Laqua, A Wessing, et al.
Klinische Monatsblatter Fur Augenheilkunde|December 29, 2005
[Molecular genetic analysis of the BIGH3 gene in lattice type I (Biber-Haab-Dimmer) and granular type II (Avellino) corneal dystrophy: is indirect mutation analysis for hot spots recommended?]C Grünauer-Kloevekorn, S Bräutigam, M Wolter-Roessler, et al.
Klinische Monatsblatter Fur Augenheilkunde|October 26, 2006
[Molecular genetic and histopathological examinations for genotype-phenotype analysis in patients with TGFBI-linked corneal dystrophy]C Grünauer-Kloevekorn, S Braeutigam, E Weidle, et al.
The British Journal of Ophthalmology|November 13, 2008
TGFBI (BIGH3) gene mutations in German families: two novel mutations associated with unique clinical and histopathological findingsC Gruenauer-Kloevekorn, I Clausen, E Weidle, et al.
Science Advances|May 4, 2022
Characterization of a vaccine-elicited human antibody with sequence homology to VRC01-class antibodies that binds the C1C2 gp120 domainMatthew D Gray, Junli Feng, Connor E Weidle, et al.
Pageof 2

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

Sort By:
Pageof 2
Klinische Monatsblatter Fur Augenheilkunde|March 1, 1983
[Tyrosinosis with hepatolenticular degeneration (Wilson's disease)]H J Thiel, E Weidle
Klinische Monatsblatter Fur Augenheilkunde|October 1, 1993
[Unilateral type III (Hida) lattice stromal corneal dystrophy]B Seitz, E Weidle, G O Naumann
Klinische Monatsblatter Fur Augenheilkunde|June 10, 2009
[Mutational analysis of VSX-1 in one patient with posterior polymorphous corneal dystrophy and in three families with hereditary Fuchs endothelial dystrophy]I Clausen, E Weidle, G Duncker, et al.
Klinische Monatsblatter Fur Augenheilkunde|August 1, 1988
[Anesthesia for eye operations in mitochondrial encephalomyelopathy]T Fritz, K Wessel, E Weidle, et al.
Klinische Monatsblatter Fur Augenheilkunde|August 18, 2015
[TGC Repeats in Intron 2 of the TCF4 Gene have a Good Predictive Power Regarding to Fuchs Endothelial Corneal Dystrophy]M Luther, C Grünauer-Kloevekorn, E Weidle, et al.
American Journal of Ophthalmology|March 1, 1983
Nine cases of cavernous hemangioma of the retinaE Messmer, H Laqua, A Wessing, et al.
Klinische Monatsblatter Fur Augenheilkunde|December 29, 2005
[Molecular genetic analysis of the BIGH3 gene in lattice type I (Biber-Haab-Dimmer) and granular type II (Avellino) corneal dystrophy: is indirect mutation analysis for hot spots recommended?]C Grünauer-Kloevekorn, S Bräutigam, M Wolter-Roessler, et al.
Klinische Monatsblatter Fur Augenheilkunde|October 26, 2006
[Molecular genetic and histopathological examinations for genotype-phenotype analysis in patients with TGFBI-linked corneal dystrophy]C Grünauer-Kloevekorn, S Braeutigam, E Weidle, et al.
The British Journal of Ophthalmology|November 13, 2008
TGFBI (BIGH3) gene mutations in German families: two novel mutations associated with unique clinical and histopathological findingsC Gruenauer-Kloevekorn, I Clausen, E Weidle, et al.
Science Advances|May 4, 2022
Characterization of a vaccine-elicited human antibody with sequence homology to VRC01-class antibodies that binds the C1C2 gp120 domainMatthew D Gray, Junli Feng, Connor E Weidle, et al.
Pageof 2