Bradshaw K - Search Results

1

Mutations in the CACNA1F and NYX genes in British CSNBX families.

Zito I, Allen LE, Patel RJ, Meindl A, Bradshaw K, Yates JR, Bird AC, Erskine L, Cheetham ME, Webster AR, Poopalasundaram S, Moore AT, Trump D, Hardcastle AJ. Zito I, et al. Among authors: bradshaw k. Hum Mutat. 2003 Feb;21(2):169. doi: 10.1002/humu.9106. Hum Mutat. 2003. PMID: 12552565

2

Genotype-phenotype correlation in British families with X linked congenital stationary night blindness.

Allen LE, Zito I, Bradshaw K, Patel RJ, Bird AC, Fitzke F, Yates JR, Trump D, Hardcastle AJ, Moore AT. Allen LE, et al. Among authors: bradshaw k. Br J Ophthalmol. 2003 Nov;87(11):1413-20. doi: 10.1136/bjo.87.11.1413. Br J Ophthalmol. 2003. PMID: 14609846 Free PMC article.

3

Abnormalities of the scotopic threshold response correlated with gene mutation in X-linked retinoschisis and congenital stationary night blindness.

Bradshaw K, Newman D, Allen L, Moore A. Bradshaw K, et al. Doc Ophthalmol. 2003 Sep;107(2):155-64. doi: 10.1023/a:1026245931580. Doc Ophthalmol. 2003. PMID: 14661905

4

A comparison of ERG abnormalities in XLRS and XLCSNB.

Bradshaw K, Allen L, Trump D, Hardcastle A, George N, Moore A. Bradshaw K, et al. Doc Ophthalmol. 2004 Mar;108(2):135-45. doi: 10.1023/b:doop.0000036786.22179.44. Doc Ophthalmol. 2004. PMID: 15455796

5

Identification of novel RPGR ORF15 mutations in X-linked progressive cone-rod dystrophy (XLCORD) families.

Ebenezer ND, Michaelides M, Jenkins SA, Audo I, Webster AR, Cheetham ME, Stockman A, Maher ER, Ainsworth JR, Yates JR, Bradshaw K, Holder GE, Moore AT, Hardcastle AJ. Ebenezer ND, et al. Among authors: bradshaw k. Invest Ophthalmol Vis Sci. 2005 Jun;46(6):1891-8. doi: 10.1167/iovs.04-1482. Invest Ophthalmol Vis Sci. 2005. PMID: 15914600

6

Is optic nerve fibre mis-routing a feature of congenital stationary night blindness?

Ung T, Allen LE, Moore AT, Trump D, Zito I, Hardcastle AJ, Yates J, Bradshaw K. Ung T, et al. Among authors: bradshaw k. Doc Ophthalmol. 2005 Nov;111(3):169-78. doi: 10.1007/s10633-005-5503-9. Epub 2006 Mar 6. Doc Ophthalmol. 2005. PMID: 16523234

7

X-linked cone dysfunction syndrome with myopia and protanopia.

Michaelides M, Johnson S, Bradshaw K, Holder GE, Simunovic MP, Mollon JD, Moore AT, Hunt DM. Michaelides M, et al. Among authors: bradshaw k. Ophthalmology. 2005 Aug;112(8):1448-54. doi: 10.1016/j.ophtha.2005.02.021. Ophthalmology. 2005. PMID: 15953640

8

Cone-rod dystrophy, intrafamilial variability, and incomplete penetrance associated with the R172W mutation in the peripherin/RDS gene.

Michaelides M, Holder GE, Bradshaw K, Hunt DM, Moore AT. Michaelides M, et al. Among authors: bradshaw k. Ophthalmology. 2005 Sep;112(9):1592-8. doi: 10.1016/j.ophtha.2005.04.004. Ophthalmology. 2005. PMID: 16019073

9

Mutations of the XLRS1 gene cause abnormalities of photoreceptor as well as inner retinal responses of the ERG.

Bradshaw K, George N, Moore A, Trump D. Bradshaw K, et al. Doc Ophthalmol. 1999;98(2):153-73. doi: 10.1023/a:1002432919073. Doc Ophthalmol. 1999. PMID: 10947001

10

A clinical and molecular genetic study of a rare dominantly inherited syndrome (MRCS) comprising of microcornea, rod-cone dystrophy, cataract, and posterior staphyloma.

Reddy MA, Francis PJ, Berry V, Bradshaw K, Patel RJ, Maher ER, Kumar R, Bhattacharya SS, Moore AT. Reddy MA, et al. Among authors: bradshaw k. Br J Ophthalmol. 2003 Feb;87(2):197-202. doi: 10.1136/bjo.87.2.197. Br J Ophthalmol. 2003. PMID: 12543751 Free PMC article. Clinical Trial.

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