Arnaud B - Search Results

1

Extensive macular atrophy with pseudodrusen-like appearance: a new clinical entity.

Hamel CP, Meunier I, Arndt C, Ben Salah S, Lopez S, Bazalgette C, Bazalgette C, Zanlonghi X, Arnaud B, Defoort-Dellhemmes S, Puech B. Hamel CP, et al. Among authors: arnaud b. Am J Ophthalmol. 2009 Apr;147(4):609-20. doi: 10.1016/j.ajo.2008.10.022. Epub 2009 Feb 1. Am J Ophthalmol. 2009. PMID: 19181301

2

Screening genes of the retinoid metabolism: novel LRAT mutation in leber congenital amaurosis.

Sénéchal A, Humbert G, Surget MO, Bazalgette C, Bazalgette C, Arnaud B, Arndt C, Laurent E, Brabet P, Hamel CP. Sénéchal A, et al. Among authors: arnaud b. Am J Ophthalmol. 2006 Oct;142(4):702-4. doi: 10.1016/j.ajo.2006.04.057. Am J Ophthalmol. 2006. PMID: 17011878

3

Homozygous deletion related to Alu repeats in RLBP1 causes retinitis punctata albescens.

Humbert G, Delettre C, Sénéchal A, Bazalgette C, Barakat A, Bazalgette C, Arnaud B, Lenaers G, Hamel CP. Humbert G, et al. Among authors: arnaud b. Invest Ophthalmol Vis Sci. 2006 Nov;47(11):4719-24. doi: 10.1167/iovs.05-1488. Invest Ophthalmol Vis Sci. 2006. PMID: 17065479

4

Retinal dystrophies caused by mutations in RPE65: assessment of visual functions.

Hamel CP, Griffoin JM, Lasquellec L, Bazalgette C, Arnaud B. Hamel CP, et al. Among authors: arnaud b. Br J Ophthalmol. 2001 Apr;85(4):424-7. doi: 10.1136/bjo.85.4.424. Br J Ophthalmol. 2001. PMID: 11264131 Free PMC article.

5

A novel CACNA1F mutation in a french family with the incomplete type of X-linked congenital stationary night blindness.

Jacobi FK, Hamel CP, Arnaud B, Blin N, Broghammer M, Jacobi PC, Apfelstedt-Sylla E, Pusch CM. Jacobi FK, et al. Among authors: arnaud b. Am J Ophthalmol. 2003 May;135(5):733-6. doi: 10.1016/s0002-9394(02)02109-8. Am J Ophthalmol. 2003. PMID: 12719097

6

RRH, encoding the RPE-expressed opsin-like peropsin, is not mutated in retinitis pigmentosa and allied diseases.

Ksantini M, Sénéchal A, Humbert G, Arnaud B, Hamel CP. Ksantini M, et al. Among authors: arnaud b. Ophthalmic Genet. 2007 Mar;28(1):31-7. doi: 10.1080/13816810701202052. Ophthalmic Genet. 2007. PMID: 17454745

7

[Molecular genetics of pigmentary retinopathies: identification of mutations in CHM, RDS, RHO, RPE65, USH2A and XLRS1 genes].

Hamel CP, Griffoin JM, Bazalgette C, Lasquellec L, Duval PA, Bareil C, Beaufrère L, Bonnet S, Eliaou C, Marlhens F, Schmitt-Bernard CF, Tuffery S, Claustres M, Arnaud B. Hamel CP, et al. Among authors: arnaud b. J Fr Ophtalmol. 2000 Dec;23(10):985-95. J Fr Ophtalmol. 2000. PMID: 11139690 French.

8

Accuracy of IRAS GT interferometer and potential acuity meter prediction of visual acuity after phacoemulsification: prospective comparative study.

Le Sage C, Bazalgette C, Arnaud B, Schmitt-Bernard CF. Le Sage C, et al. Among authors: arnaud b. J Cataract Refract Surg. 2002 Jan;28(1):131-8. doi: 10.1016/s0886-3350(01)01118-x. J Cataract Refract Surg. 2002. PMID: 11777722

9

[Quality of life in patients with wet age-related macular degeneration treated with photodynamic therapy].

Laouar K, Dupeyron G, Audemard D, Arnaud B, Arndt C. Laouar K, et al. Among authors: arnaud b. J Fr Ophtalmol. 2007 Mar;30(3):233-8. doi: 10.1016/s0181-5512(07)89583-0. J Fr Ophtalmol. 2007. PMID: 17417147 French.

10

Retinal electrophysiological results in patients receiving lamotrigine monotherapy.

Arndt CF, Husson J, Derambure P, Hache JC, Arnaud B, Defoort-Dhellemmes S. Arndt CF, et al. Among authors: arnaud b. Epilepsia. 2005 Jul;46(7):1055-60. doi: 10.1111/j.1528-1167.2005.43204.x. Epilepsia. 2005. PMID: 16026557 Free article.

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