Trump D - Search Results

1

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. Among authors: trump d. Doc Ophthalmol. 2004 Mar;108(2):135-45. doi: 10.1023/b:doop.0000036786.22179.44. Doc Ophthalmol. 2004. PMID: 15455796

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: trump d. 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

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: trump d. Doc Ophthalmol. 2005 Nov;111(3):169-78. doi: 10.1007/s10633-005-5503-9. Epub 2006 Mar 6. Doc Ophthalmol. 2005. PMID: 16523234

4

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. Among authors: trump d. Doc Ophthalmol. 1999;98(2):153-73. doi: 10.1023/a:1002432919073. Doc Ophthalmol. 1999. PMID: 10947001

5

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: trump d. Hum Mutat. 2003 Feb;21(2):169. doi: 10.1002/humu.9106. Hum Mutat. 2003. PMID: 12552565

6

Congenital stationary night blindness associated with mutations in GRM6 encoding glutamate receptor MGluR6.

O'Connor E, Allen LE, Bradshaw K, Boylan J, Moore AT, Trump D. O'Connor E, et al. Among authors: trump d. Br J Ophthalmol. 2006 May;90(5):653-4. doi: 10.1136/bjo.2005.086678. Br J Ophthalmol. 2006. PMID: 16622103 Free PMC article. No abstract available.

7

X-linked retinoschisis: clinical phenotype and RS1 genotype in 86 UK patients.

Pimenides D, George ND, Yates JR, Bradshaw K, Roberts SA, Moore AT, Trump D. Pimenides D, et al. Among authors: trump d. J Med Genet. 2005 Jun;42(6):e35. doi: 10.1136/jmg.2004.029769. J Med Genet. 2005. PMID: 15937075 Free PMC article.

8

Temperature sensitive oculocutaneous albinism associated with missense changes in the tyrosinase gene.

Wang T, Waters CT, Jakins T, Yates JR, Trump D, Bradshaw K, Moore AT. Wang T, et al. Among authors: trump d. Br J Ophthalmol. 2005 Oct;89(10):1383-4. doi: 10.1136/bjo.2005.070243. Br J Ophthalmol. 2005. PMID: 16170149 Free PMC article. No abstract available.

9

Identification of XLRS1 gene mutation (608C > T) in a Portuguese family with juvenile retinoschisis.

Teixeira C, Rocha-Sousa A, Trump D, Brandão E, Falcão-Reis F. Teixeira C, et al. Among authors: trump d. Eur J Ophthalmol. 2005 Sep-Oct;15(5):638-40. Eur J Ophthalmol. 2005. PMID: 16167295

10

Molecular pathology of X linked retinoschisis: mutations interfere with retinoschisin secretion and oligomerisation.

Wang T, Zhou A, Waters CT, O'Connor E, Read RJ, Trump D. Wang T, et al. Among authors: trump d. Br J Ophthalmol. 2006 Jan;90(1):81-6. doi: 10.1136/bjo.2005.078048. Br J Ophthalmol. 2006. PMID: 16361673 Free PMC article.

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