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Number of items at this level: 7.

H

Hartl, Janine (2011) Funktionelle Auswirkungen bei X-chromosomaler Retinoschisis – Untersuchungen bei Patienten mit nachgewiesener Mutation im XLRS1-Gen. PhD, Universität Regensburg

L

Lorenz, Birgit and Lenk-Schaefer, Marlis (2006) Pediatric ophthalmology in Germany. Journal of AAPOS : the official publication of the American Association for Pediatric Ophthalmology and Strabismus / American Association for Pediatric Ophthalmology and Strabismus 10 (1), pp. 1-3.

S

Sand, Philipp G and Langguth, Berthold and Kleinjung, Tobias (2011) Deep resequencing of the voltage-gated potassium channel subunit KCNE3 gene in chronic tinnitus. Behavioral and brain functions : BBF 7, p. 39.

W

Wilscher, Stephanie (2010) Statische und kinetische Gesichtsfelduntersuchung bei Kindern mittels verschiedener Strategien. PhD, Universität Regensburg

Willer, Mario (2009) Molekulargenetische Untersuchungen zur Expression von Sequenzveränderungen im REP-1-Gen bei heterozygoten Trägerinnen. PhD, Universität Regensburg

Wabbels, B. and Preising, M. N. and Kretschmann, U. and Demmler, A. and Lorenz, B. (2006) Genotype-phenotype correlation and longitudinal course in ten families with Best vitelliform macular dystrophy. Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv für klinische und experimentelle Ophthalmologie 244 (11), pp. 1453-1466.

Wabbels, Bettina and Demmler, Anke and Paunescu, Karina and Wegscheider, Erika and Preising, Markus N. and Lorenz, Birgit (2006) Fundus autofluorescence in children and teenagers with hereditary retinal diseases. Graefe's archive for clinical and experimental ophthalmology 244 (1), pp. 36-45.

This list was generated on Sat Nov 22 17:45:01 2014 CET.
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