Items where Division is "Medicine > Abteilung für Pädiatrische Ophthalmologie, Strabismologie und Ophthalmogenetik" and Year is 2001

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Bassi, Maria Teresa and Bergen, Arthur A. B. and Bitoun, Pierre and Charles, Stephen J. and Clementi, Maurizio and Gosselin, Richard and Hurst, Jane and Lewis, Richard Alan and Lorenz, Birgit and Meitinger, Thomas and Messiaen, Ludwine and Ramesar, Rajkumar S. and Ballabio, Andrea and Schiaffino, M. Vittoria (2001) Diverse prevalence of large deletions within the OA1 gene in ocular albinism type 1 patients from Europe and North America. HUMAN GENETICS, 108 (1). pp. 51-54. ISSN 0340-6717

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.

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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.

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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, Birgit and Gampe, Elisabeth (2001) Analysis of 180 patients with sensory defect nystagmus (SDN) and congenital idiopathic nystagmus (CIN). KLINISCHE MONATSBLATTER FUR AUGENHEILKUNDE, 218 (1). pp. 3-12. ISSN 0023-2165, 1439-3999

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Motaref, Behnas and Lorenz, B. (2001) The role of ultrasound in the diagnosis and follow-up of orbital mucoceles. ULTRASCHALL IN DER MEDIZIN, 22 (2). pp. 100-103. ISSN 0172-4614

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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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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, Markus and de Laak, Jean-Paul Op and Lorenz, Birgit (2001) Deletion in the OA1 gene in a family with congenital X linked nystagmus. BRITISH JOURNAL OF OPHTHALMOLOGY, 85 (9). pp. 1098-1103. ISSN 0007-1161

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Wissinger, Bernd and Gamer, Daphne and Jaegle, Herbert and Giorda, Roberto and Marx, Tim and Mayer, Simone and Tippmann, Sabine and Broghammer, Martina and Jurklies, Bernhard and Rosenberg, Thomas and Jacobson, Samuel G. and Sener, E. Cumhur and Tatlipinar, Sinan and Hoyng, Carel B. and Castellan, Claudio and Bitoun, Pierre and Andreasson, Sten and Rudolph, Günter and Kellner, Ulrich and Lorenz, Birgit and Wolff, Gerhard and Verellen-Dumoulin, Christine and Schwartz, Marianne and Cremers, Frans P. M. and Apfelstedt-Sylla, Eckart and Zrenner, Eberhart and Salati, Roberto and Sharpe, Lindsay T. and Kohl, Susanne (2001) CNGA3 mutations in hereditary cone photoreceptor disorders. AMERICAN JOURNAL OF HUMAN GENETICS, 69 (4). pp. 722-737. ISSN 0002-9297, 1537-6605