Preising MN - Search Results

1

In vivo assessment of retinal vascular wall dimensions.

Fischer MD, Huber G, Feng Y, Tanimoto N, Mühlfriedel R, Beck SC, Tröger E, Kernstock C, Preising MN, Lorenz B, Hammes HP, Seeliger MW. Fischer MD, et al. Among authors: preising mn. Invest Ophthalmol Vis Sci. 2010 Oct;51(10):5254-9. doi: 10.1167/iovs.09-5139. Epub 2010 May 5. Invest Ophthalmol Vis Sci. 2010. PMID: 20445120

2

IRPA scientific newsletter--a new website to integrate data on hereditary retinal disorders.

Preising M, Lorenz B. Preising M, et al. Ophthalmic Genet. 1998 Dec;19(4):213-4. doi: 10.1076/opge.19.4.213.2314. Ophthalmic Genet. 1998. PMID: 9895247 No abstract available.

3

Early-onset severe rod-cone dystrophy in young children with RPE65 mutations.

Lorenz B, Gyürüs P, Preising M, Bremser D, Gu S, Andrassi M, Gerth C, Gal A. Lorenz B, et al. Invest Ophthalmol Vis Sci. 2000 Aug;41(9):2735-42. Invest Ophthalmol Vis Sci. 2000. PMID: 10937591

4

Deletion in the OA1 gene in a family with congenital X linked nystagmus.

Preising M, Op de Laak JP, Lorenz B. Preising M, et al. Br J Ophthalmol. 2001 Sep;85(9):1098-103. doi: 10.1136/bjo.85.9.1098. Br J Ophthalmol. 2001. PMID: 11520764 Free PMC article.

5

In search for increased prevalence rates of strabismus and microstrabismus in two Bavarian districts, Oberpfalz and Niederbayern, to spot populations for gene identification.

Zitzlsperger M, Salzberger M, Lorenz B, Preising M. Zitzlsperger M, et al. Strabismus. 2002 Jun;10(2):163-8. doi: 10.1076/stra.10.2.163.8129. Strabismus. 2002. PMID: 12221496

6

CYP1B1 gene analysis in primary congenital glaucoma in Indonesian and European patients.

Sitorus R, Ardjo SM, Lorenz B, Preising M. Sitorus R, et al. J Med Genet. 2003 Jan;40(1):e9. doi: 10.1136/jmg.40.1.e9. J Med Genet. 2003. PMID: 12525557 Free PMC article. No abstract available.

7

Causes of blindness at the "Wiyata Guna" School for the Blind, Indonesia.

Sitorus R, Preising M, Lorenz B. Sitorus R, et al. Br J Ophthalmol. 2003 Sep;87(9):1065-8. doi: 10.1136/bjo.87.9.1065. Br J Ophthalmol. 2003. PMID: 12928266 Free PMC article.

8

Phenotypic variability in three carriers from a family with choroideremia and a frameshift mutation 1388delCCinsG in the REP-1 gene.

Rudolph G, Preising M, Kalpadakis P, Haritoglou C, Lang GE, Lorenz B. Rudolph G, et al. Ophthalmic Genet. 2003 Dec;24(4):203-14. doi: 10.1076/opge.24.4.203.17232. Ophthalmic Genet. 2003. PMID: 14566650

9

Analysis of three genes in Leber congenital amaurosis in Indonesian patients.

Sitorus RS, Lorenz B, Preising MN. Sitorus RS, et al. Among authors: preising mn. Vision Res. 2003 Dec;43(28):3087-93. doi: 10.1016/j.visres.2003.08.008. Vision Res. 2003. PMID: 14611946 Free article.

10

Fundus autofluorescence in carriers of X-linked recessive retinitis pigmentosa associated with mutations in RPGR, and correlation with electrophysiological and psychophysical data.

Wegscheider E, Preising MN, Lorenz B. Wegscheider E, et al. Among authors: preising mn. Graefes Arch Clin Exp Ophthalmol. 2004 Jun;242(6):501-11. doi: 10.1007/s00417-004-0891-1. Epub 2004 May 29. Graefes Arch Clin Exp Ophthalmol. 2004. PMID: 15173948

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