B. Arnaud

发表

Macroglial alterations after isolated optic nerve sheath fenestration in rabbit.

Max Villain, Alain Privat, G. Alonso, 2002, Investigative ophthalmology & visual science.

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

C. Hamel, X. Zanlonghi, I. Meunier, 2009, American journal of ophthalmology.

RRH, Encoding the RPE-Expressed Opsin-Like Peropsin, Is Not Mutated in Retinitis Pigmentosa and Allied Diseases

C. Hamel, A. Sénéćhal, B. Arnaud, 2007, Ophthalmic genetics.

The protein truncation test (PTT) as a method of detection for choroideremia mutations.

M. Claustres, C. Bareil, J. Demaille, 1997, Experimental eye research.

A complex allele (1064delTC and IVS2 + 22ins7) in the peripherin/RDS gene in retinitis pigmentosa with macular dystrophy.

M. Claustres, C. Bareil, J. Demaille, 1997, Ophthalmic genetics.

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

B. Arnaud, C. Arndt, D. Audemard, 2007, Journal francais d'ophtalmologie.

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

E. Laurent, P. Brabet, C. Hamel, 2006, American journal of ophthalmology.

Novel Mutations in MYO7A and USH2A in Usher Syndrome

C. Hamel, B. Arnaud, C. Maubaret, 2005, Ophthalmic genetics.

BIGH3 (TGFBI) Arg124 mutations influence the amyloid conversion of related peptides in vitro.

À. Argilés, J. Demaille, A. Chavanieu, 2002, European journal of biochemistry.

Experimental model of optic nerve sheath fenestration Histology, ultrastructure, and glial immunocytochemistry

A. Privat, M. Villain, F. Sandillon, 1995 .

Dural carotid cavernous fistulas (seven cases) Diagnosis and treatment

G. Bourbotte, B. Arnaud, B. Bordat, 1991 .

Retinal Electrophysiological Results in Patients Receiving Lamotrigine Monotherapy

P. Derambure, S. Defoort-Dhellemmes, B. Arnaud, 2005, Epilepsia.

[Palpebral Merkel cell tumors apropos of 3 cases].

B. Arnaud, G. Dupeyron, K. Zaghloul, 1989, Bulletin des societes d'ophtalmologie de France.

Keratographic analysis of a family with keratoconus in identical twins

B. Arnaud, C. Schmitt-Bernard, C. Schneider, 2000, Journal of cataract and refractive surgery.

Keratectasia induced by laser in situ keratomileusis in keratoconus.

B. Arnaud, C. Schmitt-Bernard, C. Lesage, 2000, Journal of refractive surgery.

Lattice corneal dystrophy.

M. Claustres, À. Argilés, J. Demaille, 2000, Ophthalmology.

[Accuracy of videokeratographic quantitative criteria for detection of keratoconus suspects in families with keratoconus].

B. Arnaud, C. Schmitt-Bernard, S. Claude, 2004, Journal francais d'ophtalmologie.

[Arterial occlusion associated with toxoplasmic chorioretinitis].

B. Arnaud, S. Pakalin, 1990, Journal francais d'ophtalmologie.

BIGH3 exon 14 mutations lead to intermediate type I/IIIA of lattice corneal dystrophies.

M. Claustres, À. Argilés, J. Demaille, 2000, Investigative ophthalmology & visual science.

Merkel cell palpebral tumors Three cases

B. Arnaud, G. Barnéon, K. Zaghloul, 1989 .

The trochlear nerve: anatomy by microdissection

F. Bonnel, F. Segnarbieux, M. Villain, 2005, Surgical and Radiologic Anatomy.

Retinal dystrophies caused by mutations inRPE65: assessment of visual functions

C. Hamel, B. Arnaud, C. Bazalgette, 2001, The British journal of ophthalmology.

Autosomal recessive retinal dystrophy associated with two novel mutations in the RPE65 gene

M. Claustres, C. Bareil, C. Hamel, 1998, European Journal of Human Genetics.

Mutations in RPE65 cause Leber's congenital amaurosis

E. Zrenner, M. Claustres, C. Bareil, 1997, Nature Genetics.

Segregation of a mutation in CNGB1 encoding the β-subunit of the rod cGMP-gated channel in a family with autosomal recessive retinitis pigmentosa

M. Claustres, C. Bareil, J. Demaille, 2001, Human Genetics.

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

C. Pusch, N. Blin, Martina Broghammer, 2003, American journal of ophthalmology.

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

M. Claustres, C. Bareil, C. Hamel, 2000, Journal francais d'ophtalmologie.

Missense mutation in the gene encoding the α subunit of rod transducin in the Nougaret form of congenital stationary night blindness

T. Dryja, L. B. Hahn, B. Arnaud, 1996, Nature Genetics.

Nuclear gene OPA1, encoding a mitochondrial dynamin-related protein, is mutated in dominant optic atrophy

J. Grosgeorge, C. Turc‐Carel, G. Lenaers, 2000, Nature Genetics.

The Franchebois antral balloon: Its use in stabilizing fractures of the orbital floor

B. Arnaud, G. Dupeyron, C. Malrieu, 1989 .

[Spontaneous hyphema caused by Ginkgo biloba extract].

B. Arnaud, C. Schmitt-Bernard, C. Schneider, 2002, Journal francais d'ophtalmologie.

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

G. Lenaers, A. Barakat, C. Hamel, 2006, Investigative ophthalmology & visual science.

Primary orbital liposarcoma:Clinicopathologic case report and review of the literature

P. Baldet, B. Arnaud, P. Malan, 1983 .

[Thrombosis of the central vein of the retina or its branches and spasmophilia: preliminary notes].

B. Arnaud, C. Boudet, B. Bullier, 1972, Bulletin des societes d'ophtalmologie de France.

[Blue nevus localized in the limbus: anatomical evolution and therapeutic approach].

B. Arnaud, C. Boudet, L. Navarre, 1977, Bulletin des societes d'ophtalmologie de France.

Effect of acetazolamide on ocular hemodynamics in pseudotumor cerebri associated with inflammatory bowel disease.

A. Harris, D. Greenfield, G. Pageaux, 2002, American journal of ophthalmology.

Port-wine stains of eyelids and face: Argon laser therapy

B. Arnaud, G. Barnéon, G. Dupeyron, 1985 .

Superior oblique muscle injuries in orbital roof fractures

B. Arnaud, J. Fuentes, C. Merlier, 1983 .

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

B. Arnaud, C. Bazalgette, Cécile Le Sage, 2002, Journal of cataract and refractive surgery.

Rod and cone function in the Nougaret form of stationary night blindness.

M. Sandberg, T. Dryja, E. Berson, 1998, A M A Archives of Ophthalmology.

Molecular analysis of the rhodopsin gene in southern France: identification of the first duplication responsible for retinitis pigmentosa, c.998999ins4.

M. Claustres, N. Pallares-Ruiz, C. Bareil, 1999, Ophthalmic genetics.

[Optic nerve sheath decompression in optic neuropathy complicating idiopathic intracranial hypertension: a new focus].

J. Adenis, M. Villain, E. Candon, 2003, Journal francais d'ophtalmologie.