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Results: 1-25/44
Authors:
MARLHENS F
GRIFFOIN JM
BAREIL C
ARNAUD B
CLAUSTRES M
HAMEL CP
Citation: F. Marlhens et al., AUTOSOMAL RECESSIVE RETINAL DYSTROPHY ASSOCIATED WITH 2 NOVEL MUTATIONS IN THE RPE65 GENE, European journal of human genetics, 6(5), 1998, pp. 527-531
Authors:
BEAUFRERE L
GIRARDET A
ARNAUD B
CLAUSTRES M
TUFFERY S
Citation: L. Beaufrere et al., MOLECULAR DIAGNOSIS OF CHOROIDEREMIA, Journal francais d'ophtalmologie, 21(5), 1998, pp. 345-350
Authors:
SCHMITTBERNARD CF
BAREIL C
HAMEL CP
BEAUFRERE L
ARNAUD B
CLAUSTRES M
DEMEEUS A
Citation: Cf. Schmittbernard et al., GENETIC-ANALYSIS IN A FAMILY WITH X-LINKE D INCOMPLETE TYPE OF CONGENITAL STATIONARY NIGHTBLINDNESS (CSNBI), Journal francais d'ophtalmologie, 21(4), 1998, pp. 251-256
Authors:
SCHMITTBERNARD CF
ARNAUD B
Citation: Cf. Schmittbernard et B. Arnaud, AIRBAG-INDUCED EYE INJURIES, Journal francais d'ophtalmologie, 21(3), 1998, pp. 220-222
Authors:
DUPIN O
COMPEYRE S
TRINQUAND C
PERSI L
ARNAUD B
Citation: O. Dupin et al., INTEREST OF CONJUNCTIVAL PROVOCATION TEST (CPT) FOR THE EVALUATION OFTHE ACTIVITY OF 2 CONCENTRATIONS OF ANTIALLERGIC EYEDROPS, MEQUITAZINE, Journal francais d'ophtalmologie, 21(1), 1998, pp. 12-18
Authors:
SANDBERG MA
PAWLYK BS
DAN J
ARNAUD B
DRYJA TP
BERSON EL
Citation: Ma. Sandberg et al., ROD AND CONE FUNCTION IN THE NOUGARET FORM OF STATIONARY NIGHT BLINDNESS, Archives of ophthalmology, 116(7), 1998, pp. 867-872
Authors:
BAREIL C
HAMEL C
ARNAUD B
DEMAILLE J
CLAUSTRES M
Citation: C. Bareil et al., A COMPLEX ALLELE (1064DELTC AND IVS2+22INS7) IN THE PERIPHERIN RDS GENE IN RETINITIS-PIGMENTOSA WITH MACULAR DYSTROPHY/, Ophthalmic genetics, 18(3), 1997, pp. 129-138
Authors:
MARLHENS F
BAREIL C
GRIFFOIN JM
ZRENNER E
AMALRIC P
ELIAOU C
LIU SY
HARRIS E
REDMOND TM
ARNAUD B
CLAUSTRES M
HAMEL CP
Citation: F. Marlhens et al., MUTATIONS IN RPE65 CAUSE LEBERS CONGENITAL AMAUROSIS, Nature genetics, 17(2), 1997, pp. 139-141
Authors:
SCHMITTBERNARD CF
VILLAIN M
BEAUFRERE L
ARNAUD B
Citation: Cf. Schmittbernard et al., TRAUMA AFTER RADIAL KERATOTOMY AND PHOTOREFRACTIVE KERATECTOMY, Journal of cataract and refractive surgery, 23(5), 1997, pp. 803-804
Authors:
SCHMITTBERNARD CF
ARNAUD B
Citation: Cf. Schmittbernard et B. Arnaud, ENDOTHELIAL-CELL LOSS LINKED TO PHACOEMUL SIFICATION - CLARIFICATION, Journal francais d'ophtalmologie, 20(8), 1997, pp. 628-639
Authors:
BEAUFRERE L
TUFFERY S
HAMEL C
BAREIL C
ARNAUD B
DEMAILLE J
CLAUSTRES M
Citation: L. Beaufrere et al., RAPID GENETIC DIAGNOSIS IN CARRIER FEMALES RELATED TO SUBJECTS WITH CHOROIDEREMIA, Journal francais d'ophtalmologie, 20(7), 1997, pp. 534-538
Authors:
ARNAUD B
TRINQUAND C
BRON A
DUPEYRON G
GASTAUD P
GRANGE JD
LEREBELLER MJ
LIGEON P
MATHIS A
METGE P
MISSOTTEN L
MOUILLON M
OHRLOFF C
QUEGUINER P
RIDINGS B
Citation: B. Arnaud et al., DOUBLE-MASKED STUDY ON 3 PARALLEL GROUPS OF 2 0.1-PERCENT INDOMETHACIN FORMULATIONS AND 0.1-PERCENT DICLOFENAC IN THE PREVENTION AND CONTROL OF INFLAMMATION SECONDARY TO CATARACT-SURGERY, Journal francais d'ophtalmologie, 20(3), 1997, pp. 183-188
Authors:
SANBERG MA
PAWLYK BS
ARNAUD B
DRYJA TP
BERSON EL
Citation: Ma. Sanberg et al., ROD FUNCTION IN THE NOUGARET FORM OF STATIONARY NIGHT BLINDNESS (SNB), Investigative ophthalmology & visual science, 38(4), 1997, pp. 3294-3294
Authors:
SCHMITTBERNARD CF
BAREIL C
HAMEL C
ARNAUD B
CLAUSTRES M
DEMEEUS A
Citation: Cf. Schmittbernard et al., LINKAGE ANALYSIS IN A FAMILY WITH INCOMPLETE TYPE OF X-LINKED CONGENITAL STATIONARY NIGHT BLINDNESS (CSNB2), Investigative ophthalmology & visual science, 38(4), 1997, pp. 3685-3685
Authors:
BEAUFRERE L
TUFFERY S
HAMEL C
BAREIL C
ARNAUD B
DEMAILLE J
CLAUSTRES M
Citation: L. Beaufrere et al., THE PROTEIN TRUNCATION TEST AS METHOD OF DETECTION FOR CHOROIDEREMIA GENE-MUTATIONS, Investigative ophthalmology & visual science, 38(4), 1997, pp. 3704-3704
Authors:
VILLAIN M
SANDILLON F
MULLER A
CANDON E
ARNAUD B
PRIVAT A
Citation: M. Villain et al., GLIAL REACTIONS AND MENINGEAL SHEATH MODIFICATIONS IN EXPERIMENTAL OPTIC-NERVE SHEATH FENESTRATION, Investigative ophthalmology & visual science, 38(4), 1997, pp. 3090-3090
Authors:
PERSI L
DUPIN O
ARNAUD B
TRINQUAND C
MICHEL FB
BOUSQUET J
Citation: L. Persi et al., EFFICACY OF MEQUITAZINE IN COMPARISON WITH PLACEBO ASSESSED BY OCULARCHALLENGE WITH ALLERGEN IN ALLERGIC CONJUNCTIVITIS, Allergy, 52(4), 1997, pp. 451-454
Authors:
BEAUFRERE L
TUFFERY S
HAMEL C
BAREIL C
ARNAUD B
DEMAILLE J
CLAUSTRES M
Citation: L. Beaufrere et al., THE PROTEIN TRUNCATION TEST (PTT) AS A METHOD OF DETECTION FOR CHOROIDEREMIA MUTATIONS, Experimental Eye Research, 65(6), 1997, pp. 849-854
Authors:
VILLAIN M
TRINQUAND C
ARNAUD B
Citation: M. Villain et al., CORNEAL SENSITIVITY DEBATE, Archives of ophthalmology, 115(5), 1997, pp. 686-686
Authors:
BAREIL C
SCHMITTBERNARD CF
ARNAUD B
CLAUSTRES M
HAMEL C
DEMEEUS A
Citation: C. Bareil et al., LINKAGE AND CANDIDATE GENES ANALYSIS IN A FAMILY WITH X-LINKED INCOMPLETE TYPE CONGENITAL STATIONARY NIGHT BLINDNESS, American journal of human genetics, 61(4), 1997, pp. 1550-1550
Authors:
DRYJA TP
HAHN LB
REBOUL T
ARNAUD B
Citation: Tp. Dryja et al., MISSENSE MUTATION IN THE GENE ENCODING THE ALPHA-SUBUNIT OF ROD TRANSDUCIN IN THE NOUGARET FORM OF CONGENITAL STATIONARY NIGHT BLINDNESS, Nature genetics, 13(3), 1996, pp. 358-360
Authors:
BEAUFRERE L
TUFFERY S
HAMEL C
ARNAUD B
DEMAILLE J
CLAUSTRES M
Citation: L. Beaufrere et al., A NOVEL MUTATION (S558X) CAUSING CHOROIDEREMIA, Human mutation, 8(4), 1996, pp. 395-395
Authors:
SCHMITTBERNARD CF
VILLAIN M
BEAUFRERE L
ARNAUD B
Citation: Cf. Schmittbernard et al., OCULAR BILATERAL TRAUMA BY BLAST AFTER RE FRACTIVE SURGERY WITH THE 2CURRENT TECHNIQUES - COMPARATIVE ANATOMOCLINICAL ANALYSIS OF ONE CASE, Journal francais d'ophtalmologie, 19(4), 1996, pp. 287-291
Authors:
TRINQUAND C
RICHARD C
ARNAUD B
Citation: C. Trinquand et al., 3-ARM, DOUBLE-MASKED STUDY OF 2 OPHTHALMIC FORMULATIONS OF 0.1-PERCENT INDOMETHACIN AND 0.1-PERCENT DICLOFENAC IN CONTROLLING INFLAMMATION AFTER CATARACT-SURGERY, Investigative ophthalmology & visual science, 37(3), 1996, pp. 2719-2719
Authors:
HUSSELS IEM
HAHN LB
REBOUL T
ARNAUD B
DRYJA TP
Citation: Iem. Hussels et al., MISSENSE MUTATION IN THE GENE ENCODING THE ALPHA-SUBUNIT OF ROD TRANSDUCIN COSEGREGATES WITH NOUGARETS CONGENITAL NIGHT BLINDNESS, Investigative ophthalmology & visual science, 37(3), 1996, pp. 5240-5240