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Items: 1 to 50 of 702

1.

The development of white matter structural changes during the process of deterioration of the visual field.

Hofstetter S, Sabbah N, Mohand-Saïd S, Sahel JA, Habas C, Safran AB, Amedi A.

Sci Rep. 2019 Feb 14;9(1):2085. doi: 10.1038/s41598-018-38430-5.

PMID:
30765782
2.

Immune Response and Intraocular Inflammation in Patients With Leber Hereditary Optic Neuropathy Treated With Intravitreal Injection of Recombinant Adeno-Associated Virus 2 Carrying the ND4 Gene: A Secondary Analysis of a Phase 1/2 Clinical Trial.

Bouquet C, Vignal Clermont C, Galy A, Fitoussi S, Blouin L, Munk MR, Valero S, Meunier S, Katz B, Sahel JA, Thomasson N.

JAMA Ophthalmol. 2019 Feb 7. doi: 10.1001/jamaophthalmol.2018.6902. [Epub ahead of print]

PMID:
30730541
3.

Gene therapy for retinal dystrophy.

Sahel JA, Dalkara D.

Nat Med. 2019 Feb;25(2):198-199. doi: 10.1038/s41591-019-0346-1. No abstract available.

PMID:
30718907
4.

Classification of disease severity in retinitis pigmentosa.

Iftikhar M, Lemus M, Usmani B, Campochiaro PA, Sahel JA, Scholl HPN, Shah SMA.

Br J Ophthalmol. 2019 Jan 31. pii: bjophthalmol-2018-313669. doi: 10.1136/bjophthalmol-2018-313669. [Epub ahead of print]

PMID:
30705041
5.

In vivo laser Doppler holography of the human retina.

Puyo L, Paques M, Fink M, Sahel JA, Atlan M.

Biomed Opt Express. 2018 Aug 6;9(9):4113-4129. doi: 10.1364/BOE.9.004113. eCollection 2018 Sep 1.

6.

Six-Month Safety and Efficacy of the Intelligent Retinal Implant System II Device in Retinitis Pigmentosa.

Muqit MMK, Velikay-Parel M, Weber M, Dupeyron G, Audemard D, Corcostegui B, Sahel J, Le Mer Y.

Ophthalmology. 2018 Dec 24. pii: S0161-6420(18)32685-X. doi: 10.1016/j.ophtha.2018.11.010. [Epub ahead of print] No abstract available.

PMID:
30591229
7.

Optogenetic Light Sensors in Human Retinal Organoids.

Garita-Hernandez M, Guibbal L, Toualbi L, Routet F, Chaffiol A, Winckler C, Harinquet M, Robert C, Fouquet S, Bellow S, Sahel JA, Goureau O, Duebel J, Dalkara D.

Front Neurosci. 2018 Nov 2;12:789. doi: 10.3389/fnins.2018.00789. eCollection 2018.

8.

Facing hatred.

Sahel JA.

Science. 2018 Nov 9;362(6415):621. doi: 10.1126/science.aav9391. No abstract available.

PMID:
30409862
9.

Effects of corneal injury on ciliary nerve fibre activity and corneal nociception in mice: A behavioural and electrophysiological study.

Joubert F, Acosta MDC, Gallar J, Fakih D, Sahel JA, Baudouin C, Bodineau L, Mélik Parsadaniantz S, Réaux-Le Goazigo A.

Eur J Pain. 2019 Mar;23(3):589-602. doi: 10.1002/ejp.1332. Epub 2018 Nov 16.

PMID:
30370980
10.

Whole exome sequencing resolves complex phenotype and identifies CC2D2A mutations underlying non-syndromic rod-cone dystrophy.

Méjécase C, Hummel A, Mohand-Saïd S, Andrieu C, El Shamieh S, Antonio A, Condroyer C, Boyard F, Foussard M, Blanchard S, Letexier M, Saraiva JP, Sahel JA, Zeitz C, Audo I.

Clin Genet. 2019 Feb;95(2):329-333. doi: 10.1111/cge.13453. Epub 2018 Nov 4.

PMID:
30267408
11.

Defined Xeno-free and Feeder-free Culture Conditions for the Generation of Human iPSC-derived Retinal Cell Models.

Slembrouck-Brec A, Nanteau C, Sahel JA, Goureau O, Reichman S.

J Vis Exp. 2018 Sep 6;(139). doi: 10.3791/57795.

PMID:
30247478
12.

Translational Retinal Research and Therapies.

Hardcastle AJ, Sieving PA, Sahel JA, Jacobson SG, Cideciyan AV, Flannery JG, Beltran WA, Aguirre GD.

Transl Vis Sci Technol. 2018 Sep 13;7(5):8. doi: 10.1167/tvst.7.5.8. eCollection 2018 Sep.

13.

Correlation Between Visual Function and Performance of Simulated Daily Living Activities in Glaucomatous Patients.

Lombardi M, Zenouda A, Azoulay-Sebban L, Lebrisse M, Gutman E, Brasnu E, Hamard P, Sahel JA, Baudouin C, Labbé A.

J Glaucoma. 2018 Nov;27(11):1017-1024. doi: 10.1097/IJG.0000000000001066.

PMID:
30157061
14.

High loop rate adaptive optics flood illumination ophthalmoscope with structured illumination capability.

Gofas-Salas E, Mecê P, Petit C, Jarosz J, Mugnier LM, Montmerle Bonnefois A, Grieve K, Sahel J, Paques M, Meimon S.

Appl Opt. 2018 Jul 10;57(20):5635-5642. doi: 10.1364/AO.57.005635.

PMID:
30118075
15.

Characterization and Transplantation of CD73-Positive Photoreceptors Isolated from Human iPSC-Derived Retinal Organoids.

Gagliardi G, Ben M'Barek K, Chaffiol A, Slembrouck-Brec A, Conart JB, Nanteau C, Rabesandratana O, Sahel JA, Duebel J, Orieux G, Reichman S, Goureau O.

Stem Cell Reports. 2018 Sep 11;11(3):665-680. doi: 10.1016/j.stemcr.2018.07.005. Epub 2018 Aug 9.

16.

A Comparison of the Dexamethasone Implant (Ozurdex®) and Inferior Fornix-based sub-Tenon Triamcinolone Acetonide for Treatment of Inflammatory Ocular Diseases.

Errera MH, Westcott M, Benesty J, Falah S, Smadja J, Orès R, Pratas AC, Sedira N, Bensemlali A, Héron E, Goldschmidt P, Bodaghi B, Sahel JA.

Ocul Immunol Inflamm. 2018 Aug 6:1-11. doi: 10.1080/09273948.2018.1501492. [Epub ahead of print]

PMID:
30081675
17.

Expanding the Mutation Spectrum in ABCA4: Sixty Novel Disease Causing Variants and Their Associated Phenotype in a Large French Stargardt Cohort.

Nassisi M, Mohand-Saïd S, Dhaenens CM, Boyard F, Démontant V, Andrieu C, Antonio A, Condroyer C, Foussard M, Méjécase C, Eandi CM, Sahel JA, Zeitz C, Audo I.

Int J Mol Sci. 2018 Jul 27;19(8). pii: E2196. doi: 10.3390/ijms19082196.

18.

Inherited Retinal Degenerations: Current Landscape and Knowledge Gaps.

Duncan JL, Pierce EA, Laster AM, Daiger SP, Birch DG, Ash JD, Iannaccone A, Flannery JG, Sahel JA, Zack DJ, Zarbin MA; and the Foundation Fighting Blindness Scientific Advisory Board.

Transl Vis Sci Technol. 2018 Jul 18;7(4):6. doi: 10.1167/tvst.7.4.6. eCollection 2018 Jul. No abstract available.

19.

Usher Syndrome and Color Vision.

Kurtenbach A, Hahn G, Kernstock C, Hipp S, Zobor D, Stingl K, Kohl S, Bonnet C, Mohand-Saïd S, Sliesoraityte I, Sahel JA, Audo I, Fakin A, Hawlina M, Testa F, Simonelli F, Petit C, Zrenner E.

Curr Eye Res. 2018 Oct;43(10):1295-1301. doi: 10.1080/02713683.2018.1501804. Epub 2018 Jul 30.

PMID:
30012035
20.

Scotopic Microperimetric Assessment of Rod Function in Stargardt Disease (SMART) Study: Design and Baseline Characteristics (Report No. 1).

Strauss RW, Kong X, Bittencourt MG, Ho A, Jha A, Schönbach EM, Ahmed MI, Muñoz B, Ervin AM, Michaelides M, Birch DG, Sahel JA, Sunness JS, Zrenner E, Bagheri S, Ip M, Sadda S, West S, Scholl HPN; for the SMART Study Group.

Ophthalmic Res. 2019;61(1):36-43. doi: 10.1159/000488711. Epub 2018 Jun 25.

PMID:
29940588
21.

Visual brain plasticity induced by central and peripheral visual field loss.

Sanda N, Cerliani L, Authié CN, Sabbah N, Sahel JA, Habas C, Safran AB, Thiebaut de Schotten M.

Brain Struct Funct. 2018 Jun 23. doi: 10.1007/s00429-018-1700-7. [Epub ahead of print]

22.

Detailed genetic characteristics of an international large cohort of patients with Stargardt disease: ProgStar study report 8.

Fujinami K, Strauss RW, Chiang JP, Audo IS, Bernstein PS, Birch DG, Bomotti SM, Cideciyan AV, Ervin AM, Marino MJ, Sahel JA, Mohand-Said S, Sunness JS, Traboulsi EI, West S, Wojciechowski R, Zrenner E, Michaelides M, Scholl HPN; On behalf of the ProgStar Study Group; ProgStar Study Group.

Br J Ophthalmol. 2018 Jun 20. pii: bjophthalmol-2018-312064. doi: 10.1136/bjophthalmol-2018-312064. [Epub ahead of print]

23.

Restoring vision.

Roska B, Sahel JA.

Nature. 2018 May;557(7705):359-367. doi: 10.1038/s41586-018-0076-4. Epub 2018 May 16. Review.

PMID:
29769667
24.

Phenotypic Characteristics of a French Cohort of Patients with X-Linked Retinoschisis.

Orès R, Mohand-Said S, Dhaenens CM, Antonio A, Zeitz C, Augstburger E, Andrieu C, Sahel JA, Audo I.

Ophthalmology. 2018 Oct;125(10):1587-1596. doi: 10.1016/j.ophtha.2018.03.057. Epub 2018 May 5.

PMID:
29739629
25.

Maintaining Cone Function in Rod-Cone Dystrophies.

Sahel JA, Léveillard T.

Adv Exp Med Biol. 2018;1074:499-509. doi: 10.1007/978-3-319-75402-4_62.

PMID:
29721982
26.

Dietary, environmental, and genetic risk factors of Extensive Macular Atrophy with Pseudodrusen, a severe bilateral macular atrophy of middle-aged patients.

Douillard A, Picot MC, Delcourt C, Defoort-Dhellemmes S, Marzouka NA, Lacroux A, Zanlonghi X, Drumare I, Jozefowicz E, Bocquet B, Baudoin C, Perez-Roustit S, Arsène S, Gissot V, Devin F, Arndt C, Wolff B, Mauget-Faÿsse M, Quaranta M, Mura T, Deplanque D, Oubraham H, Cohen SY, Gastaud P, Zambrowski O, Creuzot-Garcher C, Saïd SM, Sahel JA, Souied E, Milazzo S, Garavito RB, Kalatzis V, Puech B, Hamel C, Audo I, Meunier I.

Sci Rep. 2018 May 1;8(1):6840. doi: 10.1038/s41598-018-25003-9.

27.

MERTK mutation update in inherited retinal diseases.

Audo I, Mohand-Said S, Boulanger-Scemama E, Zanlonghi X, Condroyer C, Démontant V, Boyard F, Antonio A, Méjécase C, El Shamieh S, Sahel JA, Zeitz C.

Hum Mutat. 2018 Jul;39(7):887-913. doi: 10.1002/humu.23431. Epub 2018 May 23.

28.

Multimodal imaging including semiquantitative short-wavelength and near-infrared autofluorescence in achromatopsia.

Matet A, Kohl S, Baumann B, Antonio A, Mohand-Said S, Sahel JA, Audo I.

Sci Rep. 2018 Apr 4;8(1):5665. doi: 10.1038/s41598-018-23919-w.

29.

In vivo high resolution human corneal imaging using full-field optical coherence tomography.

Mazlin V, Xiao P, Dalimier E, Grieve K, Irsch K, Sahel JA, Fink M, Boccara AC.

Biomed Opt Express. 2018 Jan 10;9(2):557-568. doi: 10.1364/BOE.9.000557. eCollection 2018 Feb 1.

30.

Chronic exposure to tumor necrosis factor alpha induces retinal pigment epithelium cell dedifferentiation.

Touhami S, Beguier F, Augustin S, Charles-Messance H, Vignaud L, Nandrot EF, Reichman S, Forster V, Mathis T, Sahel JA, Bodaghi B, Guillonneau X, Sennlaub F.

J Neuroinflammation. 2018 Mar 16;15(1):85. doi: 10.1186/s12974-018-1106-8.

31.

Light action spectrum on oxidative stress and mitochondrial damage in A2E-loaded retinal pigment epithelium cells.

Marie M, Bigot K, Angebault C, Barrau C, Gondouin P, Pagan D, Fouquet S, Villette T, Sahel JA, Lenaers G, Picaud S.

Cell Death Dis. 2018 Feb 19;9(3):287. doi: 10.1038/s41419-018-0331-5.

32.

Safety of rAAV2/2-ND4 Gene Therapy for Leber Hereditary Optic Neuropathy.

Vignal C, Uretsky S, Fitoussi S, Galy A, Blouin L, Girmens JF, Bidot S, Thomasson N, Bouquet C, Valero S, Meunier S, Combal JP, Gilly B, Katz B, Sahel JA.

Ophthalmology. 2018 Jun;125(6):945-947. doi: 10.1016/j.ophtha.2017.12.036. Epub 2018 Feb 14. No abstract available.

33.

Cone degeneration is triggered by the absence of USH1 proteins but prevented by antioxidant treatments.

Trouillet A, Dubus E, Dégardin J, Estivalet A, Ivkovic I, Godefroy D, García-Ayuso D, Simonutti M, Sahly I, Sahel JA, El-Amraoui A, Petit C, Picaud S.

Sci Rep. 2018 Jan 31;8(1):1968. doi: 10.1038/s41598-018-20171-0.

34.

AUTOSOMAL DOMINANT VITREORETINOCHOROIDOPATHY: When Molecular Genetic Testing Helps Clinical Diagnosis.

Boulanger-Scemama E, Sahel JA, Mohand-Said S, Antonio A, Condroyer C, Zeitz C, Audo I.

Retina. 2018 Jan 23. doi: 10.1097/IAE.0000000000002041. [Epub ahead of print]

PMID:
29370033
35.

Noninvasive gene delivery to foveal cones for vision restoration.

Khabou H, Garita-Hernandez M, Chaffiol A, Reichman S, Jaillard C, Brazhnikova E, Bertin S, Forster V, Desrosiers M, Winckler C, Goureau O, Picaud S, Duebel J, Sahel JA, Dalkara D.

JCI Insight. 2018 Jan 25;3(2). pii: 96029. doi: 10.1172/jci.insight.96029. [Epub ahead of print]

36.

Increase in Ocular Syphilis Cases at Ophthalmologic Reference Center, France, 2012-2015.

Pratas AC, Goldschmidt P, Lebeaux D, Aguilar C, Ermak N, Benesty J, Charlier C, Benveniste E, Merabet L, Sedira N, Hope-Rapp E, Chaumeil C, Bodaghi B, Héron E, Sahel JA, Lortholary O, Errera MH.

Emerg Infect Dis. 2018 Feb;24(2):193-200. doi: 10.3201/eid2402.171167.

37.

MRI of the Optic Nerves and Chiasm in Patients With Leber Hereditary Optic Neuropathy.

Blanc C, Heran F, Habas C, Bejot Y, Sahel J, Vignal-Clermont C.

J Neuroophthalmol. 2018 Dec;38(4):434-437. doi: 10.1097/WNO.0000000000000621.

PMID:
29300239
38.

Human ESC-derived retinal epithelial cell sheets potentiate rescue of photoreceptor cell loss in rats with retinal degeneration.

Ben M'Barek K, Habeler W, Plancheron A, Jarraya M, Regent F, Terray A, Yang Y, Chatrousse L, Domingues S, Masson Y, Sahel JA, Peschanski M, Goureau O, Monville C.

Sci Transl Med. 2017 Dec 20;9(421). pii: eaai7471. doi: 10.1126/scitranslmed.aai7471.

PMID:
29263231
39.

Mutations in TUBB4B Cause a Distinctive Sensorineural Disease.

Luscan R, Mechaussier S, Paul A, Tian G, Gérard X, Defoort-Dellhemmes S, Loundon N, Audo I, Bonnin S, LeGargasson JF, Dumont J, Goudin N, Garfa-Traoré M, Bras M, Pouliet A, Bessières B, Boddaert N, Sahel JA, Lyonnet S, Kaplan J, Cowan NJ, Rozet JM, Marlin S, Perrault I.

Am J Hum Genet. 2017 Dec 7;101(6):1006-1012. doi: 10.1016/j.ajhg.2017.10.010. Epub 2017 Nov 30.

40.

AFLIBERCEPT AFTER RANIBIZUMAB INTRAVITREAL INJECTIONS IN EXUDATIVE AGE-RELATED MACULAR DEGENERATION: The ARI2 Study.

Blanco-Garavito R, Jung C, Uzzan J, Quaranta-ElMaftouhi M, Coscas F, Sahel J, Korobelnik JF, Béchet S, Querques G, Souied EH.

Retina. 2018 Dec;38(12):2285-2292. doi: 10.1097/IAE.0000000000001928.

41.

A novel nonsense variant in REEP6 is involved in a sporadic rod-cone dystrophy case.

Méjécase C, Mohand-Saïd S, El Shamieh S, Antonio A, Condroyer C, Blanchard S, Letexier M, Saraiva JP, Sahel JA, Audo I, Zeitz C.

Clin Genet. 2018 Mar;93(3):707-711. doi: 10.1111/cge.13171.

PMID:
29120066
42.

Further Insights into the Ciliary Gene and Protein KIZ and Its Murine Ortholog PLK1S1 Mutated in Rod-Cone Dystrophy.

El Shamieh S, Méjécase C, Bertelli M, Terray A, Michiels C, Condroyer C, Fouquet S, Sadoun M, Clérin E, Liu B, Léveillard T, Goureau O, Sahel JA, Audo I, Zeitz C.

Genes (Basel). 2017 Oct 18;8(10). pii: E277. doi: 10.3390/genes8100277.

43.

Establishment of an induced pluripotent stem (iPS) cell line from dermal fibroblasts of an asymptomatic patient with dominant PRPF31 mutation.

Terray A, Fort V, Slembrouck A, Nanteau C, Sahel JA, Reichman S, Audo I, Goureau O.

Stem Cell Res. 2017 Dec;25:26-29. doi: 10.1016/j.scr.2017.10.007. Epub 2017 Oct 7.

44.

Generation of an induced pluripotent stem cell (iPSC) line from a patient with autosomal dominant retinitis pigmentosa due to a mutation in the NR2E3 gene.

Terray A, Slembrouck A, Nanteau C, Chondroyer C, Zeitz C, Sahel JA, Audo I, Reichman S, Goureau O.

Stem Cell Res. 2017 Oct;24:1-4. doi: 10.1016/j.scr.2017.08.003. Epub 2017 Aug 5.

45.

Otx2-Genetically Modified Retinal Pigment Epithelial Cells Rescue Photoreceptors after Transplantation.

Kole C, Klipfel L, Yang Y, Ferracane V, Blond F, Reichman S, Millet-Puel G, Clérin E, Aït-Ali N, Pagan D, Camara H, Delyfer MN, Nandrot EF, Sahel JA, Goureau O, Léveillard T.

Mol Ther. 2018 Jan 3;26(1):219-237. doi: 10.1016/j.ymthe.2017.09.007. Epub 2017 Sep 8.

46.

A novel duplication of PRMD13 causes North Carolina macular dystrophy: overexpression of PRDM13 orthologue in drosophila eye reproduces the human phenotype.

Manes G, Joly W, Guignard T, Smirnov V, Berthemy S, Bocquet B, Audo I, Zeitz C, Sahel J, Cazevieille C, Sénéchal A, Deleuze JF, Blanché-Koch H, Boland A, Carroll P, Geneviève D, Zanlonghi X, Arndt C, Hamel CP, Defoort-Dhellemmes S, Meunier I.

Hum Mol Genet. 2017 Nov 15;26(22):4367-4374. doi: 10.1093/hmg/ddx322.

47.

Cell Motility as Contrast Agent in Retinal Explant Imaging With Full-Field Optical Coherence Tomography.

Thouvenin O, Boccara C, Fink M, Sahel J, Pâques M, Grieve K.

Invest Ophthalmol Vis Sci. 2017 Sep 1;58(11):4605-4615. doi: 10.1167/iovs.17-22375.

PMID:
28892117
48.

Taurine Promotes Retinal Ganglion Cell Survival Through GABAB Receptor Activation.

Hadj-Saïd W, Fradot V, Ivkovic I, Sahel JA, Picaud S, Froger N.

Adv Exp Med Biol. 2017;975 Pt 2:687-701. doi: 10.1007/978-94-024-1079-2_54.

PMID:
28849492
49.

A New Promoter Allows Optogenetic Vision Restoration with Enhanced Sensitivity in Macaque Retina.

Chaffiol A, Caplette R, Jaillard C, Brazhnikova E, Desrosiers M, Dubus E, Duhamel L, Macé E, Marre O, Benoit P, Hantraye P, Bemelmans AP, Bamberg E, Duebel J, Sahel JA, Picaud S, Dalkara D.

Mol Ther. 2017 Nov 1;25(11):2546-2560. doi: 10.1016/j.ymthe.2017.07.011. Epub 2017 Jul 20.

50.

Adaptive Gaze Strategies for Locomotion with Constricted Visual Field.

Authié CN, Berthoz A, Sahel JA, Safran AB.

Front Hum Neurosci. 2017 Jul 27;11:387. doi: 10.3389/fnhum.2017.00387. eCollection 2017.

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