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Bernard Arnaud

universidade do estado do para (uepa)

16H指数
40论文数
2.9K被引数
收录论文 12
发表时间
Extensive Macular Atrophy with Pseudodrusen-like Appearance: A New Clinical Entity
err2009-04-01
err46
PREAI
errHamel, Christian P.; Meunier, Isabelle; Arndt, Carl; Ben Salah, Safouane; Lopez, Severine; Bazalgette, Christian; Bazalgette, Cecile; Zanlonghi, Xavier; Arnaud, Bernard; Defoort-Dellhemmes, Sabine; Puech, Bernard
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Homozygous deletion related to Alu repeats in RLBP1 causes retinitis punctata albescens
err2006-11-01
err38
errOAAI
errHumbert, Ghyslaine; Delettre, Cecile; Senechal, Audrey; Bazalgette, Cecile; Barakat, Abdelhamid; Bazalgette, Christian; Arnaud, Bernard; Lenaers, Guy; Hamel, Christian P.
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Screening genes of the retinoid metabolism:: Novel LRAT mutation in Leber congenital amaurosis
err2006-10-01
err38
PREAI
errSenechal, Audrey; Humbert, Ghyslaine; Surget, MarieOdile; Bazalgette, Cecile; Bazalgette, Christian; Arnaud, Bernard; Arndt, Carl; Laurent, Eric; Brabet, Philippe; Hamel, Christian P.
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Retinal electrophysiological results in patients receiving lamotrigine monotherapy
err2005-06-30
err12
PREAI
errArndt, CF; Husson, J; Derambure, P; Hache, TC; Arnaud, B; Defoort-Dhellemmes, T
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A novel CACNA1F mutation in a French family with the incomplete type of X-linked congenital stationary night blindness
err2003-05-01
err21
PREAI
errJacobi, FK; Hamel, CP; Arnaud, B; Blin, N; Broghammer, M; Jacobi, PC; Apfelstedt-Sylla, E; Pusch, CM
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Nuclear gene OPA1, encoding a mitochondrial dynamin-related protein, is mutated in dominant optic atrophy
err2000-10-01
err1.3K
PREAI
errDelettre, C; Lenaers, G; Griffoin, JM; Gigarel, N; Lorenzo, C; Belenguer, P; Pelloquin, L; Grosgeorge, J; Turc-Carel, C; Perret, E; Astarie-Dequeker, C; Lasquellec, L; Arnaud, B; Ducommun, B; Kaplan, J; Hamel, CP
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Lattice corneal dystrophy
err2000-09-01
err7
errOAAI
errSchmitt-Bernard, CF; Claustres, M; Arnaud, B; Demaille, J; Argiles, A
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Autosomal recessive retinal dystrophy associated with two novel mutations in the RPE65 gene
err1998-11-18
err58
errOAAI
errMarlhens, F; Griffoin, JM; Bareil, C; Arnaud, B; Claustres, M; Hamel, CP
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Mutations in RPE65 cause Leber's congenital amaurosis
err1997-10-01
err530
PREAI
errMarlhens, F; Bareil, C; Griffoin, JM; Zrenner, E; Amalric, P; Eliaou, C; Liu, SY; Harris, E; Redmond, TM; Arnaud, B; Claustres, M; Hamel, CP
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