Coscas G - Search Results

1

Five novel missense mutations of the rhodopsin gene in autosomal dominant retinitis pigmentosa.

Souied E, Gerber S, Rozet JM, Bonneau D, Dufier JL, Ghazi I, Philip N, Soubrane G, Coscas G, Munnich A, et al. Souied E, et al. Among authors: coscas g. Hum Mol Genet. 1994 Aug;3(8):1433-4. doi: 10.1093/hmg/3.8.1433. Hum Mol Genet. 1994. PMID: 7987331 No abstract available.

2

Retinitis punctata albescens associated with the Arg135Trp mutation in the rhodopsin gene.

Souied E, Soubrane G, Benlian P, Coscas GJ, Gerber S, Munnich A, Kaplan J. Souied E, et al. Among authors: coscas gj. Am J Ophthalmol. 1996 Jan;121(1):19-25. doi: 10.1016/s0002-9394(14)70530-6. Am J Ophthalmol. 1996. PMID: 8554077

3

Two novel missense mutations in the peripherin/RDS gene in two unrelated French patients with autosomal dominant retinitis pigmentosa.

Souied EH, Rozet JM, Gerber S, Dufier JL, Soubrane G, Coscas G, Munnich A, Kaplan J. Souied EH, et al. Among authors: coscas g. Eur J Ophthalmol. 1998 Apr-Jun;8(2):98-101. doi: 10.1177/112067219800800208. Eur J Ophthalmol. 1998. PMID: 9673478

4

Exclusion of the apoE gene in autosomal dominant retinitis pigmentosa.

Souied EH, Benlian P, Rozet JM, Gerber S, Lagarde JP, Coscas G, Soubrane G, Duffier JL, Munnich A, Kaplan J. Souied EH, et al. Among authors: coscas g. Vision Res. 1998 Dec;38(24):3829-31. doi: 10.1016/s0042-6989(98)00176-x. Vision Res. 1998. PMID: 10211375 Free article.

5

[Retinitis pigmentosa].

Souied E, Kaplan J, Soubrane G, Coscas G. Souied E, et al. Among authors: coscas g. J Fr Ophtalmol. 1997;20(6):461-86. J Fr Ophtalmol. 1997. PMID: 9296044 Review. French. No abstract available.

6

A novel ABCR nonsense mutation responsible for late-onset fundus flavimaculatus.

Souied EH, Ducroq D, Rozet JM, Gerber S, Perrault I, Sterkers M, Benhamou N, Munnich A, Coscas G, Soubrane G, Kaplan J. Souied EH, et al. Among authors: coscas g. Invest Ophthalmol Vis Sci. 1999 Oct;40(11):2740-4. Invest Ophthalmol Vis Sci. 1999. PMID: 10509673

7

The ABCR gene: a major disease gene in macular and peripheral retinal degenerations with onset from early childhood to the elderly.

Rozet JM, Gerber S, Souied E, Ducroq D, Perrault I, Ghazi I, Soubrane G, Coscas G, Dufier JL, Munnich A, Kaplan J. Rozet JM, et al. Among authors: coscas g. Mol Genet Metab. 1999 Oct;68(2):310-5. doi: 10.1006/mgme.1999.2925. Mol Genet Metab. 1999. PMID: 10527682 Review. No abstract available.

8

ABCR gene analysis in familial exudative age-related macular degeneration.

Souied EH, Ducroq D, Rozet JM, Gerber S, Perrault I, Munnich A, Coscas G, Soubrane G, Kaplan J. Souied EH, et al. Among authors: coscas g. Invest Ophthalmol Vis Sci. 2000 Jan;41(1):244-7. Invest Ophthalmol Vis Sci. 2000. PMID: 10634626

9

Age-related macular degeneration in grandparents of patients with Stargardt disease: genetic study.

Souied EH, Ducroq D, Gerber S, Ghazi I, Rozet JM, Perrault I, Munnich A, Dufier JL, Coscas G, Soubrane G, Kaplan J. Souied EH, et al. Among authors: coscas g. Am J Ophthalmol. 1999 Aug;128(2):173-8. doi: 10.1016/s0002-9394(99)00145-2. Am J Ophthalmol. 1999. PMID: 10458172

10

Macular dystrophy, diabetes, and deafness associated with a large mitochondrial DNA deletion.

Souied EH, Salès MJ, Soubrane G, Coscas G, Bigorie B, Kaplan J, Munnich A, Rötig A. Souied EH, et al. Among authors: coscas g. Am J Ophthalmol. 1998 Jan;125(1):100-3. doi: 10.1016/s0002-9394(99)80243-8. Am J Ophthalmol. 1998. PMID: 9437322

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