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Longitudinal and cross-sectional study of patients with early-onset severe retinal dystrophy associated with RPE65 mutations.
Graefes Arch Clin Exp Ophthalmol. 2005 May;243(5):417-26. doi: 10.1007/s00417-004-1020-x. Epub 2004 Nov 24.
Graefes Arch Clin Exp Ophthalmol. 2005.
PMID: 15565294
Genotype-phenotype correlation in a German family with a novel complex CRX mutation extending the open reading frame.
Paunescu K, Preising MN, Janke B, Wissinger B, Lorenz B.
Paunescu K, et al.
Ophthalmology. 2007 Jul;114(7):1348-1357.e1. doi: 10.1016/j.ophtha.2006.10.034. Epub 2007 Feb 22.
Ophthalmology. 2007.
PMID: 17320181
Review.
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Fundus autofluorescence in children and teenagers with hereditary retinal diseases.
Wabbels B, Demmler A, Paunescu K, Wegscheider E, Preising MN, Lorenz B.
Wabbels B, et al. Among authors: paunescu k.
Graefes Arch Clin Exp Ophthalmol. 2006 Jan;244(1):36-45. doi: 10.1007/s00417-005-0043-2. Epub 2005 Jul 21.
Graefes Arch Clin Exp Ophthalmol. 2006.
PMID: 16034607
Item in Clipboard
[Genetic and clinical heterogeneity in LCA patients. The end of uniformity].
Preising MN, Paunescu K, Friedburg C, Lorenz B.
Preising MN, et al. Among authors: paunescu k.
Ophthalmologe. 2007 Jun;104(6):490-8. doi: 10.1007/s00347-007-1533-x.
Ophthalmologe. 2007.
PMID: 17525851
German.
Item in Clipboard
[Genetics of osteoporosis].
Schütze N, Ebert R, Paunescu K, Jakob F.
Schütze N, et al. Among authors: paunescu k.
Dtsch Med Wochenschr. 2003 Jul 25;128(30):1609-14. doi: 10.1055/s-2003-40935.
Dtsch Med Wochenschr. 2003.
PMID: 12884150
German.
No abstract available.
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