Bellmann C - Search Results

1

Localized retinal electrophysiological and fundus autofluorescence imaging abnormalities in maternal inherited diabetes and deafness.

Bellmann C, Neveu MM, Scholl HP, Hogg CR, Rath PP, Jenkins S, Bird AC, Holder GE. Bellmann C, et al. Invest Ophthalmol Vis Sci. 2004 Jul;45(7):2355-60. doi: 10.1167/iovs.03-1090. Invest Ophthalmol Vis Sci. 2004. PMID: 15223817

2

An early-onset autosomal dominant macular dystrophy (MCDR3) resembling North Carolina macular dystrophy maps to chromosome 5.

Michaelides M, Johnson S, Tekriwal AK, Holder GE, Bellmann C, Kinning E, Woodruff G, Trembath RC, Hunt DM, Moore AT. Michaelides M, et al. Among authors: bellmann c. Invest Ophthalmol Vis Sci. 2003 May;44(5):2178-83. doi: 10.1167/iovs.02-1094. Invest Ophthalmol Vis Sci. 2003. PMID: 12714659

3

Photopic and scotopic fine matrix mapping of retinal areas of increased fundus autofluorescence in patients with age-related maculopathy.

Scholl HP, Bellmann C, Dandekar SS, Bird AC, Fitzke FW. Scholl HP, et al. Among authors: bellmann c. Invest Ophthalmol Vis Sci. 2004 Feb;45(2):574-83. doi: 10.1167/iovs.03-0495. Invest Ophthalmol Vis Sci. 2004. PMID: 14744901

4

Fundus autofluorescence imaging compared with different confocal scanning laser ophthalmoscopes.

Bellmann C, Rubin GS, Kabanarou SA, Bird AC, Fitzke FW. Bellmann C, et al. Br J Ophthalmol. 2003 Nov;87(11):1381-6. doi: 10.1136/bjo.87.11.1381. Br J Ophthalmol. 2003. PMID: 14609839 Free PMC article.

5

An autosomal dominant bull's-eye macular dystrophy (MCDR2) that maps to the short arm of chromosome 4.

Michaelides M, Johnson S, Poulson A, Bradshaw K, Bellmann C, Hunt DM, Moore AT. Michaelides M, et al. Among authors: bellmann c. Invest Ophthalmol Vis Sci. 2003 Apr;44(4):1657-62. doi: 10.1167/iovs.02-0941. Invest Ophthalmol Vis Sci. 2003. PMID: 12657606

6

Potential diagnostic dilemmas using the multifocal electroretinogram in intermittent exotropia.

Bellmann C, Neveu MM, Kousoulides L, Sloper JJ, Bird AC, Holder GE. Bellmann C, et al. Br J Ophthalmol. 2004 Sep;88(9):1223-4. doi: 10.1136/bjo.2003.040584. Br J Ophthalmol. 2004. PMID: 15317720 Free PMC article. No abstract available.

7

Juvenile neuronal ceroid lipofuscinosis (Batten disease) CLN3 mutation (Chrom 16p11.2) with different phenotypes in a sibling pair and low intensity in vivo autofluorescence.

Mantel I, Brantley MA Jr, Bellmann C, Robson AG, Holder GE, Taylor A, Anderson G, Moore AT. Mantel I, et al. Among authors: bellmann c. Klin Monbl Augenheilkd. 2004 May;221(5):427-30. doi: 10.1055/s-2004-812819. Klin Monbl Augenheilkd. 2004. PMID: 15162299

8

Fixation stability using central and pericentral fixation targets in patients with age-related macular degeneration.

Bellmann C, Feely M, Crossland MD, Kabanarou SA, Rubin GS. Bellmann C, et al. Ophthalmology. 2004 Dec;111(12):2265-70. doi: 10.1016/j.ophtha.2004.06.019. Ophthalmology. 2004. PMID: 15582084

9

Gaze changes with binocular versus monocular viewing in age-related macular degeneration.

Kabanarou SA, Crossland MD, Bellmann C, Rees A, Culham LE, Rubin GS. Kabanarou SA, et al. Among authors: bellmann c. Ophthalmology. 2006 Dec;113(12):2251-8. doi: 10.1016/j.ophtha.2006.06.028. Epub 2006 Sep 25. Ophthalmology. 2006. PMID: 16996593

10

Patterns of increased in vivo fundus autofluorescence in the junctional zone of geographic atrophy of the retinal pigment epithelium associated with age-related macular degeneration.

Holz FG, Bellmann C, Margaritidis M, Schütt F, Otto TP, Völcker HE. Holz FG, et al. Among authors: bellmann c. Graefes Arch Clin Exp Ophthalmol. 1999 Feb;237(2):145-52. doi: 10.1007/s004170050209. Graefes Arch Clin Exp Ophthalmol. 1999. PMID: 9987631

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