Russell-Eggitt IM[au] - Search Results

Year	Number of Results
1986	1
1989	1
1990	3
1991	2
1992	1
1993	1
1998	1
2000	3
2002	1
2003	2
2004	3
2005	3
2007	1
2008	1
2009	1
2022	0

1

Alström syndrome. Report of 22 cases and literature review.

Russell-Eggitt IM, Clayton PT, Coffey R, Kriss A, Taylor DS, Taylor JF. Russell-Eggitt IM, et al. Ophthalmology. 1998 Jul;105(7):1274-80. doi: 10.1016/S0161-6420(98)97033-6. Ophthalmology. 1998. PMID: 9663233 Review.

2

Temperature--a factor in ocular development?

Fielder AR, Levene MI, Russell-Eggitt IM, Weale RA. Fielder AR, et al. Among authors: russell eggitt im. Dev Med Child Neurol. 1986 Jun;28(3):279-84. doi: 10.1111/j.1469-8749.1986.tb03873.x. Dev Med Child Neurol. 1986. PMID: 3721069

3

The eye in the CHARGE association.

Russell-Eggitt IM, Blake KD, Taylor DS, Wyse RK. Russell-Eggitt IM, et al. Br J Ophthalmol. 1990 Jul;74(7):421-6. doi: 10.1136/bjo.74.7.421. Br J Ophthalmol. 1990. PMID: 2378857 Free PMC article.

4

X-linked cataract and Nance-Horan syndrome are allelic disorders.

Coccia M, Brooks SP, Webb TR, Christodoulou K, Wozniak IO, Murday V, Balicki M, Yee HA, Wangensteen T, Riise R, Saggar AK, Park SM, Kanuga N, Francis PJ, Maher ER, Moore AT, Russell-Eggitt IM, Hardcastle AJ. Coccia M, et al. Among authors: russell eggitt im. Hum Mol Genet. 2009 Jul 15;18(14):2643-55. doi: 10.1093/hmg/ddp206. Epub 2009 May 4. Hum Mol Genet. 2009. PMID: 19414485 Free PMC article.

5

Early proximal tubular dysfunction in Lowe's syndrome.

Laube GF, Russell-Eggitt IM, van't Hoff WG. Laube GF, et al. Among authors: russell eggitt im. Arch Dis Child. 2004 May;89(5):479-80. doi: 10.1136/adc.2003.031187. Arch Dis Child. 2004. PMID: 15102646 Free PMC article.

6

The achiasmia spectrum: congenitally reduced chiasmal decussation.

Sami DA, Saunders D, Thompson DA, Russell-Eggitt IM, Nischal KK, Jeffrey G, Dattani M, Clement RA, Liasis A, Taylor DS. Sami DA, et al. Among authors: russell eggitt im. Br J Ophthalmol. 2005 Oct;89(10):1311-7. doi: 10.1136/bjo.2005.068171. Br J Ophthalmol. 2005. PMID: 16170123 Free PMC article.

7

A novel mutation in the Connexin 46 gene causes autosomal dominant congenital cataract with incomplete penetrance.

Burdon KP, Wirth MG, Mackey DA, Russell-Eggitt IM, Craig JE, Elder JE, Dickinson JL, Sale MM. Burdon KP, et al. Among authors: russell eggitt im. J Med Genet. 2004 Aug;41(8):e106. doi: 10.1136/jmg.2004.018333. J Med Genet. 2004. PMID: 15286166 Free PMC article. No abstract available.

8

Vigabatrin-associated visual field defects in children.

Russell-Eggitt IM, Mackey DA, Taylor DS, Timms C, Walker JW. Russell-Eggitt IM, et al. Eye (Lond). 2000 Jun;14 ( Pt 3A):334-9. doi: 10.1038/eye.2000.83. Eye (Lond). 2000. PMID: 11026995

9

Investigation of crystallin genes in familial cataract, and report of two disease associated mutations.

Burdon KP, Wirth MG, Mackey DA, Russell-Eggitt IM, Craig JE, Elder JE, Dickinson JL, Sale MM. Burdon KP, et al. Among authors: russell eggitt im. Br J Ophthalmol. 2004 Jan;88(1):79-83. doi: 10.1136/bjo.88.1.79. Br J Ophthalmol. 2004. PMID: 14693780 Free PMC article.

10

Who's in CHARGE? Multidisciplinary management of patients with CHARGE association.

Blake KD, Russell-Eggitt IM, Morgan DW, Ratcliffe JM, Wyse RK. Blake KD, et al. Among authors: russell eggitt im. Arch Dis Child. 1990 Feb;65(2):217-23. doi: 10.1136/adc.65.2.217. Arch Dis Child. 1990. PMID: 2317068 Free PMC article.

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