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B

Bader, Ingrid and Brandau, Oliver and Achatz, Helene and Apfelstedt-Sylla, Eckart and Hergersberg, Martin and Lorenz, Birgit and Wissinger, Bernd and Wittwer, Bärbel and Rudolph, Günther and Meindl, Alfons and Meitinger, Thomas (2003) X-linked retinitis pigmentosa: RPGR mutations in most families with definite X linkage and clustering of mutations in a short sequence stretch of Exon ORF15. INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 44 (4). pp. 1458-1463. ISSN 0146-0404

Bunse, A. and Bock, M. and Lorenz, B. and Gabel, V. P. (2001) Photodynamic therapy in age-related macular degeneration: Functional results. In: Association for Research in Vision and Ophthalmology - Annual Meeting 2001, April 29 - May 4, 2001, Fort Lauderdale, Florida.

E

Elflein, H. M. and Brueckner, C. and Preising, M. N. and Wegscheider, E. and Lorenz, B. (2004) Telemedicine based digital widefield retinal imaging for screening of retinopathy of prematurity: Present status of the Regensburg Telemedicine Project. In: Annual Meeting of the Association for Research in Vision and Ophthalmology, April 24-29, 2004, Ft Lauderdale, FL.

Elflein, H. M. and Lorenz, B. (2005) Acute severe retinopathy of prematurity (ROP) in VLBW twin sisters: Anterior and posterior segment findings as seen with serial digital wide field imaging. In: Meeting of the Association for Research in Vision and Ophthalmology (ARVO 2005), May 01-05, 2005, Ft Lauderdale, FL.

Elflein, H. M. and Lorenz, B. and Preising, M. N. and Pisinger, G. (2002) Telemedicine in acute ROP: A multicenter study using a digital retinal imaging system. In: Annual Meeting of the Association-for-Research-in-Vision-and-Ophthalmology, MAY 05-10, 2002, FT LAUDERDALE, FLORIDA.

F

Fassbender, B. and Kretschmann, U. and Wegscheider, E. and Kohl, S. and Wissinger, B. and Lorenz, B. (2001) Genotype-phenotype-correlation In patients with achromatopsia. In: Association for Research in Vision and Ophthalmology - Annual Meeting 2001, April 29 - May 4, 2001, Fort Lauderdale, Florida.

Fasser, C. and Preising, M. N. and Lorenz, B. (2005) Retina International's Scientific Newsletter (RISN) - A web resource for genetics of retinal disorders. In: Meeting of the Association for Research in Vision and Ophthalmology (ARVO 2005), May 01-05, 2005, Ft Lauderdale, FL.

Friedburg, Christoph and Wissinger, Bernd and Schambeck, Maria and Bonin, Michael and Kohl, Susanne and Lorenz, Birgit (2011) Long-Term Follow-Up of the Human Phenotype in Three Siblings with Cone Dystrophy Associated with a Homozygous p.G461R Mutation of KCNV2. INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 52 (12). pp. 8621-8629. ISSN 0146-0404, 1552-5783

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Gal, A. and von Brederlow, B. and Rudolph, G. and Lorenz, B. and Bolz, H. (2002) Identification and in vitro expression of novel CDH23 mutations of patients with Usher syndrome type 1D. In: Annual Meeting of the Association-for-Research-in-Vision-and-Ophthalmology, MAY 05-10, 2002, FT LAUDERDALE, FLORIDA.

Gerth, C. and Gehrig, A. and Weber, B. H. F. and Lorenz, B. (2000) Unexpected genetic findings in a patient with Stargardt macular dystrophy. In: Association for Research in Vision and Ophthalmology - Annual Meeting 2000, April 30 - May 5, 2000, Fort Lauderdale, Florida.

H

Hoffmann, MB and Lorenz, B and Preising, M and Seufert, PS (2006) Assessment of cortical visual field representations with multifocal VEPs in control subjects, patients with albinism, and female carriers of ocular albinism. INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 47 (7). pp. 3195-3201. ISSN 0146-0404

Hoffmann, Michael B. and Lorenz, Birgit and Morland, Anthony B. and Schmidtborn, Linda C. (2005) Misrouting of the optic nerves in albinism: Estimation of the extent with visual evoked potentials. INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 46 (10). pp. 3892-3898. ISSN 0146-0404

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Janke, B. and Lorenz, B. and Preising, M. N. (2004) Alternative Splicing in AIPL1 – Implications On Function And The Mutational Spectrum. In: Annual Meeting of the Association for Research in Vision and Ophthalmology, April 24-29, 2004, Ft Lauderdale, FL.

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Kretschmann, U. and Fassbender, B. and Preising, M. N. and Andrassi, M. and Rivera, A. and Weber, B. H. F. and Wegscheider, E. and Lorenz, B. (2001) Relation of function and morphology in the highly variable phenotype of X-linked retinoschisis. In: Association for Research in Vision and Ophthalmology - Annual Meeting 2001, April 29 - May 4, 2001, Fort Lauderdale, Florida.

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Lorenz, B. and Andrassi, M. and Fassbender, B. and Kretschmann, U. and Preising, M. N. (2001) Blue cone monochromacy. An underdiagnosed entity. In: Association for Research in Vision and Ophthalmology - Annual Meeting 2001, April 29 - May 4, 2001, Fort Lauderdale, Florida.

Lorenz, B. and Augustin, S. and Donaubauer, M. and Pisinger, G. and Elflein, H. and Preising, M. N. and Ells, A. L. (2004) Computerized reading of digital wide-field retinal images of prematures at risk for retinopathy of prematurity (ROP). In: Annual Meeting of the Association for Research in Vision and Ophthalmology, April 24-29, 2004, Ft Lauderdale, FL.

Lorenz, B. and Augustin, S. and Wegscheider, E. and Pisinger, G. and Fuchs, E. and Elflein, H. (2003) Telemedicine combined with a digital retinal imaging system. A new method for improved ROP screeening in premature children. In: Annual Meeting of the Association for Research in Vision and Ophthalmology, MAY, 2003, FT LAUDERDALE, FLORIDA.

Lorenz, B. and Gerth, C. and Bock, M. and Preising, M. (2000) Isolated foveal retinoschisis in a 7 year old girl. In: Association for Research in Vision and Ophthalmology - Annual Meeting 2000, April 30 - May 5, 2000, Fort Lauderdale, Florida.

Lorenz, Birgit and Gyürüs, P. and Preising, M. and Bremser, D. and Gu, S. M. and Andrassi, M. and Gerth, C. and Gal, A. (2000) Early-onset severe rod-cone dystrophy in young children with RPE65 mutations. INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 41 (9). pp. 2735-2742. ISSN 0146-0404

Lorenz, Birgit and Poliakov, Eugenia and Schambeck, Maria and Friedburg, Christoph and Preising, Markus N. and Redmond, T. Michael (2008) A Comprehensive Clinical and Biochemical Functional Study of a Novel RPE65 Hypomorphic Mutation. INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 49 (12). pp. 5235-5242. ISSN 0146-0404

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Ottmann, S. and Reich, M. and Lorenz, B. (2001) Comparison of early postoperative refraction versus predicted refraction in childhood pseudophakia resulting from 3 different formulas for calculating IOL-power. In: Association for Research in Vision and Ophthalmology - Annual Meeting 2001, April 29 - May 4, 2001, Fort Lauderdale, Florida.

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Paunescu, K. and Wabbels, B. and Wegscheider, E. and Drexler, W. and Preising, M. and Lorenz, B. (2004) Extending the phenotypical description of patients with early onset severe retinal degeneration (EOSRD) caused by RPE65-mutations. In: Annual Meeting of the Association for Research in Vision and Ophthalmology, April 24-29, 2004, Ft Lauderdale, FL.

Preising, M. N. and Op de Laak, J. P. and Sendtner, R. and Funck, S. and Lorenz, B. (2000) Elucidating the molecular genetic defect in a family with X-linked congenital nystagmus associated with macular hypoplasia. In: Association for Research in Vision and Ophthalmology - Annual Meeting 2000, April 30 - May 5, 2000, Fort Lauderdale, Florida.

Preising, M. N. and Pina, A.-L. and Elflein, H. and Schmidt-Kastner, R. and Wachtlin, J. and Kellner, U. and Lorenz, B. (2004) Exploration of two key genes controlling angiogenesis in patients with increased retinal vascularization. In: Annual Meeting of the Association for Research in Vision and Ophthalmology, April 24-29, 2004, Ft Lauderdale, FL.

Preising, M. N. and Rita, S. and Kellner, U. and Rosenberg, T. and Lorenz, B. (2002) Screening of three genes for Lebers Congenital Amaurosis - Novel mutations in AIPL1. In: Annual Meeting of the Association-for-Research-in-Vision-and-Ophthalmology, MAY 05-10, 2002, FT LAUDERDALE, FLORIDA.

Preising, M. N. and Rosenberg, T. and Kellner, U. and Meschede, D. and Brauer, U. and Lorenz, B. (2001) Mutation screening of RetGC1 and RPE65 in patients with LCA and RP. In: Association for Research in Vision and Ophthalmology - Annual Meeting 2001, April 29 - May 4, 2001, Fort Lauderdale, Florida.

Preising, M. N. and Sitorus, R. S. and Rosenberg, T. and Kellner, U. and Lorenz, B. (2003) Screening of NUB1 in patients with Leber Congenital Amaurosis. In: Annual Meeting of the Association for Research in Vision and Ophthalmology, MAY, 2003, FT LAUDERDALE, FLORIDA.

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Sitorus, R. S. and Preising, M. N. and Ardjo, S. M. and Lorenz, B. (2002) CYP1B1 mutations in patients with primary congenital glaucoma. In: Annual Meeting of the Association-for-Research-in-Vision-and-Ophthalmology, MAY 05-10, 2002, FT LAUDERDALE, FLORIDA.

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Wabbels, B. K. and Demmler, A. and Preising, M. and Lorenz, B. (2004) Fundus autofluorescence in patients with genetically determined best vitelliform macular dystrophy: Evaluation of genotype-phenotype correlation and longitudinal course. In: Annual Meeting of the Association for Research in Vision and Ophthalmology, April 24-29, 2004, Ft Lauderdale, FL.

Wabbels, B. K. and Wegscheider, E. and Preising, M. and Hamel, C. and Gal, A. and Lorenz, B. (2003) Absent or minimal fundus autofluorescence in patients with early onset retinal degeneration associated with the RPE65 genotype. In: Annual Meeting of the Association for Research in Vision and Ophthalmology, MAY, 2003, FT LAUDERDALE, FLORIDA.

Weber, B. H. F. and Apfelstedt-Sylla, E. and Lorenz, B. and Jurklies, B. and Rivera, A. (2000) Spectrum of ABCR mutations in a large series of German Stargardt disease patients. In: Association for Research in Vision and Ophthalmology - Annual Meeting 2000, April 30 - May 5, 2000, Fort Lauderdale, Florida.

Wegscheider, E. and Lorenz, B. and Bader, I. and Meitinger, T. and Meindl, A. (2002) Fundus autofluorescence in carriers for RP3 with known genotype. In: Annual Meeting of the Association-for-Research-in-Vision-and-Ophthalmology, MAY 05-10, 2002, FT LAUDERDALE, FLORIDA.

Wegscheider, E. and Poloschek, C. M. and Preising, M. N. and Lorenz, B. (2005) Fundus autofluorescence in carriers for choroideremia. In: Meeting of the Association for Research in Vision and Ophthalmology (ARVO 2005), May 01-05, 2005, Ft Lauderdale, FL.

Wegscheider, E. and Wabbels, B. and Lorenz, B. (2004) Retinitis pigmentosa and the rod ring in fundus autofluorescence. In: Annual Meeting of the Association for Research in Vision and Ophthalmology, April 24-29, 2004, Ft Lauderdale, FL.

Wegscheider, E. and Wabbels, B. and Schillinger, R. and Preising, M. and Hamel, C. and Lorenz, B. (2003) Rod or cone vision in young patients with early onset retinal degeneration associated with the RPE65 genotype? In: Annual Meeting of the Association for Research in Vision and Ophthalmology, MAY, 2003, FT LAUDERDALE, FLORIDA.

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Zernant, J. and Kulm, M. and Dharmaraj, S. and den Hollander, A. I. and Perrault, I. and Preising, Markus N. and Lorenz, Birgit and Kaplan, J. and Cremers, F. P. M. and Maumenee, I. and Koenekoop, R. K. and Allikmets, R. (2005) Genotyping microarray (disease chip) for Leber congenital amaurosis: Detection of modifier alleles. INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 46 (9). pp. 3052-3059. ISSN 0146-0404, 1552-5783