Fitzke FW - Search Results

1

Clinical features of codon 172 RDS macular dystrophy: similar phenotype in 12 families.

Downes SM, Fitzke FW, Holder GE, Payne AM, Bessant DA, Bhattacharya SS, Bird AC. Downes SM, et al. Among authors: fitzke fw. Arch Ophthalmol. 1999 Oct;117(10):1373-83. doi: 10.1001/archopht.117.10.1373. Arch Ophthalmol. 1999. PMID: 10532447

2

Autofluorescence imaging of choroidal neovascularization due to age-related macular degeneration.

Dandekar SS, Jenkins SA, Peto T, Scholl HP, Sehmi KS, Fitzke FW, Bird AC, Webster AR. Dandekar SS, et al. Among authors: fitzke fw. Arch Ophthalmol. 2005 Nov;123(11):1507-13. doi: 10.1001/archopht.123.11.1507. Arch Ophthalmol. 2005. PMID: 16286612

3

Phenotype of retinitis pigmentosa associated with the Ser50Thr mutation in the NRL gene.

Bessant DA, Holder GE, Fitzke FW, Payne AM, Bhattacharya SS, Bird AC. Bessant DA, et al. Among authors: fitzke fw. Arch Ophthalmol. 2003 Jun;121(6):793-802. doi: 10.1001/archopht.121.6.793. Arch Ophthalmol. 2003. PMID: 12796249

4

Acute macular neuroretinopathy.

Miller MH, Spalton DJ, Fitzke FW, Bird AC. Miller MH, et al. Among authors: fitzke fw. Ophthalmology. 1989 Feb;96(2):265-9. doi: 10.1016/s0161-6420(89)32906-x. Ophthalmology. 1989. PMID: 2704546

5

Distribution of fundus autofluorescence with a scanning laser ophthalmoscope.

von Rückmann A, Fitzke FW, Bird AC. von Rückmann A, et al. Among authors: fitzke fw. Br J Ophthalmol. 1995 May;79(5):407-12. doi: 10.1136/bjo.79.5.407. Br J Ophthalmol. 1995. PMID: 7612549 Free PMC article.

6

Autosomal dominant pattern dystrophy of the retina associated with a 4-base pair insertion at codon 140 in the peripherin/RDS gene.

Kim RY, Dollfus H, Keen TJ, Fitzke FW, Arden GB, Bhattacharya SS, Bird AC. Kim RY, et al. Among authors: fitzke fw. Arch Ophthalmol. 1995 Apr;113(4):451-5. doi: 10.1001/archopht.1995.01100040067029. Arch Ophthalmol. 1995. PMID: 7710395

7

Ocular findings associated with a 3 base pair deletion in the peripherin-RDS gene in autosomal dominant retinitis pigmentosa.

Wroblewski JJ, Wells JA 3rd, Eckstein A, Fitzke FW, Jubb C, Keen TJ, Inglehearn CF, Bhattacharya SS, Arden GB, Jay MR, et al. Wroblewski JJ, et al. Among authors: fitzke fw. Br J Ophthalmol. 1994 Nov;78(11):831-6. doi: 10.1136/bjo.78.11.831. Br J Ophthalmol. 1994. PMID: 7848979 Free PMC article.

8

Chromosome 19q cone-rod retinal dystrophy. Ocular phenotype.

Evans K, Duvall-Young J, Fitzke FW, Arden GB, Bhattacharya SS, Bird AC. Evans K, et al. Among authors: fitzke fw. Arch Ophthalmol. 1995 Feb;113(2):195-201. doi: 10.1001/archopht.1995.01100020079033. Arch Ophthalmol. 1995. PMID: 7864751

9

Ocular manifestations in autosomal dominant retinitis pigmentosa with a Lys-296-Glu rhodopsin mutation at the retinal binding site.

Owens SL, Fitzke FW, Inglehearn CF, Jay M, Keen TJ, Arden GB, Bhattacharya SS, Bird AC. Owens SL, et al. Among authors: fitzke fw. Br J Ophthalmol. 1994 May;78(5):353-8. doi: 10.1136/bjo.78.5.353. Br J Ophthalmol. 1994. PMID: 8025068 Free PMC article.

10

Symptomatic abnormalities of dark adaptation in patients with age-related Bruch's membrane change.

Steinmetz RL, Haimovici R, Jubb C, Fitzke FW, Bird AC. Steinmetz RL, et al. Among authors: fitzke fw. Br J Ophthalmol. 1993 Sep;77(9):549-54. doi: 10.1136/bjo.77.9.549. Br J Ophthalmol. 1993. PMID: 8218049 Free PMC article.

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