A decade in search of myopia genes von Jacobi, Felix K, Pusch, Carsten M

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The complete form of X-linked congenital stationary night blindness is caused by mutations in a gene encoding a leucine-rich repeat protein von Meindl, Alfons, Pusch, Carsten M, Zeitz, Christina, Brandau, Oliver, Pesch, Katrin, Achatz, Helene, Feil, Silke, Scharfe, Curt, Maurer, Johannes, Jacobi, Felix K, Pinckers, Alfred, Andreasson, Sten, Hardcastle, Alison, Wissinger, Bernd, Berger, Wolfgang

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Refinement of the MYP3 locus on human chromosome 12 in a German family with Mendelian autosomal dominant high-grade myopia by SNP array mapping von Nürnberg, Gudrun, Jacobi, Felix, Broghammer, Martina, Becker, Christian, Blin, Nikolaus, Nürnberg, Peter, Stephani, Ulrich, Pusch, Carsten

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Multifocal intraocular lens implantation in prepresbyopic patients with unilateral cataract von JACOBI, Philipp C, DIETLEIN, Thomas S, LÜKE, Christoph, JACOBI, Felix K

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Scleral fixation of secondary foldable multifocal intraocular lens implants in children and young adults von Jacobi, Philipp C, Dietlein, Thomas S, Jacobi, Felix K

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Long-term endothelial cell loss following phacoemulsification through a temporal clear corneal incision von Burkhard Dick, H., Kohnen, Thomas, Jacobi, Felix K., Jacobi, Karl W.

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Ten novel ORF15 mutations confirm mutational hot spot in the RPGR gene in European patients with X-linked retinitis pigmentosa von Pusch, Carsten M., Broghammer, Martina, Jurklies, Bernhard, Besch, Dorothea, Jacobi, Felix K.

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Multifocal intraocular lens implantation in patients with traumatic cataract von Jacobi, Philipp C, Dietlein, Thomas S, Lueke, Cristoph, Jacobi, Felix K

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Population haplotypes of exon ORF15 of the retinitis pigmentosa GTPase regulator gene in Germany : implications for screening for inherited retinal disorders von Karra, Daniela, Jacobi, Felix K, Broghammer, Martina, Blin, Nikolaus, Pusch, Carsten M

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Cataract surgery under topical anesthesia in patients with coexisting glaucoma von Jacobi, Philipp C, Dietlein, Thomas S, Jacobi, Felix K

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Silicone intraocular lens implantation in children: preliminary results von Pavlovic, Sima, Jacobi, Felix K, Graef, Michael, Jacobi, Karl W

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Phenotypic expression of the complete type of X-linked congenital stationary night blindness in patients with different mutations in the NYX gene von JACOBI, Felix K, ANDREASSON, Sten, LANGROVA, Hana, MEINDL, Alfons, ZRENNER, Eberhart, APFELSTEDT-SYLLA, Eckart, PUSCH, Carsten M

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A Comparative Study of Topical vs Retrobulbar Anesthesia in Complicated Cataract Surgery von Jacobi, Philipp C, Dietlein, Thomas S, Jacobi, Felix K

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Bilateral Implantation of Asymmetrical Diffractive Multifocal Intraocular Lenses von Jacobi, Felix K, Kammann, Jochen, Jacobi, Karl W, Großkopf, Ute, Walden, Karin

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Segregation Patterns and Heteroplasmy Prevalence in Leber's Hereditary Optic Neuropathy von Jacobi, Felix K, Leo-Kottler, Beate, Mittelviefhaus, Karin, Zrenner, Eberhart, Meyer, Jens, Pusch, Carsten M, Wissinger, Bernd

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Pseudophakic retinal detachment in high axial myopia von Jacobi, Felix K., Hessemer, Volker

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Ten novel ORF15 mutations confirm mutational hot spot in theRPGR gene in European patients with X-linked retinitis pigmentosa von Pusch, Carsten M., Broghammer, Martina, Jurklies, Bernhard, Besch, Dorothea, Jacobi, Felix K.

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Physical mapping and exclusion of GPR34 as the causative gene for congenital stationary night blindness type 1 von JACOBI, F. K, BROGHAMMER, M, PESCH, K, ZRENNER, E, BERGER, W, MEINDL, A, PUSCH, C. M

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Temporal pars plana vitrectomy for submacular surgery von Jacobi, F K, Pavlovic, S

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Reply von Jacobi, Felix K., Dick, Burkhard H., Bohle, Rainer M.

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