Moore AT - Search Results

1

Clinical characteristics of ocular angiomatosis in von Hippel-Lindau disease and correlation with germline mutation.

Webster AR, Maher ER, Moore AT. Webster AR, et al. Among authors: moore at. Arch Ophthalmol. 1999 Mar;117(3):371-8. doi: 10.1001/archopht.117.3.371. Arch Ophthalmol. 1999. PMID: 10088816

2

Von Hippel-Lindau disease.

Maher ER, Moore AT. Maher ER, et al. Among authors: moore at. Br J Ophthalmol. 1992 Dec;76(12):743-5. doi: 10.1136/bjo.76.12.743. Br J Ophthalmol. 1992. PMID: 1486078 Free PMC article. Review. No abstract available.

3

Ophthalmological screening for von Hippel-Lindau disease.

Moore AT, Maher ER, Rosen P, Gregor Z, Bird AC. Moore AT, et al. Eye (Lond). 1991;5 ( Pt 6):723-8. doi: 10.1038/eye.1991.133. Eye (Lond). 1991. PMID: 1800174

4

Clinical features and natural history of von Hippel-Lindau disease.

Maher ER, Yates JR, Harries R, Benjamin C, Harris R, Moore AT, Ferguson-Smith MA. Maher ER, et al. Among authors: moore at. Q J Med. 1990 Nov;77(283):1151-63. doi: 10.1093/qjmed/77.2.1151. Q J Med. 1990. PMID: 2274658

5

Ischaemic retinopathy occurring in patients receiving bone marrow allografts and campath-1G: a clinicopathological study.

Webster AR, Anderson JR, Richards EM, Moore AT. Webster AR, et al. Among authors: moore at. Br J Ophthalmol. 1995 Jul;79(7):687-91. doi: 10.1136/bjo.79.7.687. Br J Ophthalmol. 1995. PMID: 7662637 Free PMC article.

6

Clinical features and molecular genetics of Von Hippel-Lindau disease.

Maher ER, Webster AR, Moore AT. Maher ER, et al. Among authors: moore at. Ophthalmic Genet. 1995 Sep;16(3):79-84. doi: 10.3109/13816819509059966. Ophthalmic Genet. 1995. PMID: 8556282 Review.

7

Phenotypic expression in von Hippel-Lindau disease: correlations with germline VHL gene mutations.

Maher ER, Webster AR, Richards FM, Green JS, Crossey PA, Payne SJ, Moore AT. Maher ER, et al. Among authors: moore at. J Med Genet. 1996 Apr;33(4):328-32. doi: 10.1136/jmg.33.4.328. J Med Genet. 1996. PMID: 8730290 Free PMC article.

8

An analysis of phenotypic variation in the familial cancer syndrome von Hippel-Lindau disease: evidence for modifier effects.

Webster AR, Richards FM, MacRonald FE, Moore AT, Maher ER. Webster AR, et al. Among authors: moore at. Am J Hum Genet. 1998 Oct;63(4):1025-35. doi: 10.1086/302037. Am J Hum Genet. 1998. PMID: 9758595 Free PMC article.

9

A clinical and molecular genetic analysis of solitary ocular angioma.

Webster AR, Maher ER, Bird AC, Gregor ZJ, Moore AT. Webster AR, et al. Among authors: moore at. Ophthalmology. 1999 Mar;106(3):623-9. doi: 10.1016/S0161-6420(99)90127-6. Ophthalmology. 1999. PMID: 10080225

10

Incidence and significance of congenital hypertrophy of the retinal pigment epithelium (CHRPE) in familial adenomatous polyposis coli (FAPC).

Moore AT, Maher ER, Koch DJ, Charles SJ. Moore AT, et al. Ophthalmic Paediatr Genet. 1992 Jun;13(2):67-71. doi: 10.3109/13816819209087606. Ophthalmic Paediatr Genet. 1992. PMID: 1323091

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