Christian Hamel

Christian Hamel

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Generation of a human iPSC line, INMi003-A, with a missense mutation in CRX associated with autosomal dominant cone-rod dystrophy.

Stem Cell Res 2019 07 7;38:101478. Epub 2019 Jun 7.

Inserm U1051, Institute for Neurosciences of Montpellier, Montpellier, France; University of Montpellier, Montpellier, France. Electronic address:

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http://dx.doi.org/10.1016/j.scr.2019.101478DOI Listing
July 2019

Generation of a human iPSC line, INMi004-A, with a point mutation in CRX associated with autosomal dominant Leber congenital amaurosis.

Stem Cell Res 2019 07 3;38:101476. Epub 2019 Jun 3.

Inserm U1051, Institute for Neurosciences of Montpellier, Montpellier, France; University of Montpellier, Montpellier, France. Electronic address:

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https://linkinghub.elsevier.com/retrieve/pii/S18735061193010
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http://dx.doi.org/10.1016/j.scr.2019.101476DOI Listing
July 2019

Natural models for retinitis pigmentosa: progressive retinal atrophy in dog breeds.

Hum Genet 2019 May 23;138(5):441-453. Epub 2019 Mar 23.

University of Rennes, CNRS, IGDR (Institut de génétique et développement de Rennes)-UMR6290, 35000, Rennes, France.

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http://dx.doi.org/10.1007/s00439-019-01999-6DOI Listing
May 2019

Pathogenicity of novel atypical variants leading to choroideremia as determined by functional analyses.

Hum Mutat 2019 01 8;40(1):31-35. Epub 2018 Nov 8.

Laboratoire de Génétique Moléculaire, CHU de Montpellier, Université de Montpellier, Montpellier, France.

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http://dx.doi.org/10.1002/humu.23671DOI Listing
January 2019

Generation of an iPSC line, INMi001-A, carrying the two most common USH2A mutations from a compound heterozygote with non-syndromic retinitis pigmentosa.

Stem Cell Res 2018 12 10;33:228-232. Epub 2018 Nov 10.

Inserm U1051, Institute for Neurosciences of Montpellier, Montpellier, France; University of Montpellier, Montpellier, France. Electronic address:

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http://dx.doi.org/10.1016/j.scr.2018.11.004DOI Listing
December 2018

Generation of a human iPSC line, INMi002-A, carrying the most prevalent USH2A variant associated with Usher syndrome type 2.

Stem Cell Res 2018 12 16;33:247-250. Epub 2018 Nov 16.

Inserm U1051, Institute for Neurosciences of Montpellier, Montpellier, France; University of Montpellier, Montpellier, France. Electronic address:

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https://linkinghub.elsevier.com/retrieve/pii/S18735061183027
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http://dx.doi.org/10.1016/j.scr.2018.11.007DOI Listing
December 2018

mutations: A novel phenotype associating severe optic atrophy and spastic paraplegia.

Neurol Genet 2018 Apr 20;4(2):e225. Epub 2018 Mar 20.

Department of Neurology (C.M., B.C.), Gui de Chauliac Montpellier University Hospital; EA7402 Institut Universitaire de Recherche Clinique (C.M., L.L., M.K., C.G.), and Laboratoire de Génétique Moléculaire, University Hospital; Maladies Sensorielles Génétiques (C.H., M.Q., C.D., E.S.), CHRU; INSERM U1051 (C.H., M.Q., C.D., E.S.), Institute for Neurosciences of Montpellier; Université Montpellier (C.H., M.Q., C.D., E.S.), France; INSERM UMR 1141 (D.C., P.R.), PROTECT, INSERM, Université Paris Diderot, Sorbonne Paris Cité, France.

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http://dx.doi.org/10.1212/NXG.0000000000000225DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5860906PMC
April 2018

Novel splice-site mutation in TTLL5 causes cone dystrophy in a consanguineous family.

Mol Vis 2017 18;23:131-139. Epub 2017 Mar 18.

Sorbonne Universités, UPMC Univ Paris 06, INSERM U968, CNRS UMR 7210, Institut de la Vision, 17 rue Moreau, Paris, France.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5360453PMC
February 2018

OPA1 gene therapy prevents retinal ganglion cell loss in a Dominant Optic Atrophy mouse model.

Sci Rep 2018 02 6;8(1):2468. Epub 2018 Feb 6.

UMR INSERM U1051/Université Montpellier - Institut des Neurosciences de Montpellier, 34091, Montpellier, France.

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http://dx.doi.org/10.1038/s41598-018-20838-8DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5802757PMC
February 2018

AP4 deficiency: A novel form of neurodegeneration with brain iron accumulation?

Neurol Genet 2018 Feb 24;4(1):e217. Epub 2018 Jan 24.

Département de Neuropédiatrie (A.R., B.E., P.M., F.R.), CHU Gui de Chauliac, Montpellier; Institut des Neurosciences de Montpellier (A.R., N.H., G.M., C.P.H.), INSERM U1051, Université de Montpellier; Service de Neuroradiologie (C.-J.R., N.L.), CHU Gui de Chauliac, Montpellier; Equipe MitoLab (M.C., G.L.), UMR CNRS 6015-INSERM 1083, Institut MitoVasc, University of Angers, France; Department of Medical Genetics (C. Goizet), Hopital Pellegrin, Bordeaux University Hospital; MRGM Laboratory (C. Goizet), INSERM U1211, University of Bordeaux; Laboratoire de Génétique Moléculaire (C. Guissart), CHU de Montpellier; U1046 INSERM (P.M., F.R.), UMR9214 CNRS, Université de Montpellier; Department of Neurology (C.M.), University Hospital Gui de Chauliac, Montpellier; Centre de Référence des Malformations et Maladies Congénitales du Cervelet (L.B.), Service de Génétique, Hôpital Armand Trousseau, AP-HP, Paris, France; Wellcome Trust Centre for Mitochondrial Research (R.H.), Institute of Genetic Medicine, Newcastle University, United Kingdom; and Centre of Reference for Genetic Sensory Diseases (C.P.H.), Montpellier, France.

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http://dx.doi.org/10.1212/NXG.0000000000000217DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5820597PMC
February 2018

LEBER CONGENITAL AMAUROSIS WITH LARGE RETINAL PIGMENT CLUMPS CAUSED BY COMPOUND HETEROZYGOUS MUTATIONS IN KCNJ13.

Retin Cases Brief Rep 2017 Summer;11(3):221-226

*Maladies Sensorielles Génétiques, CHRU, Montpellier, France; †INSERM U1051, Institute for Neurosciences of Montpellier, Montpellier, France; ‡Université Montpellier, Montpellier, France; §Laboratory of Genetics in Ophthalmology, INSERM UMR 1163, Paris, France; and ¶Paris Descartes-Sorbonne Paris Cité University, Imagine Institute, Paris, France.

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http://dx.doi.org/10.1097/ICB.0000000000000326DOI Listing
January 2018

Cone dystrophy or macular dystrophy associated with novel autosomal dominant mutations.

Mol Vis 2017 3;23:198-209. Epub 2017 Apr 3.

Institut National de la Santé et de la Recherche Médicale, U1051, Institute for Neurosciences of Montpellier, Montpellier, France.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5389339PMC
January 2018

Spatially Resolved Spectral Sensitivities as a Potential Read-out Parameter in Clinical Gene Therapeutic Trials.

Ophthalmic Res 2017 12;58(4):194-202. Epub 2017 Jul 12.

Department of Ophthalmology, Justus Liebig University Giessen, Giessen, Germany.

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http://dx.doi.org/10.1159/000477257DOI Listing
November 2017

Pathogenicity of a novel missense variant associated with choroideremia and its impact on gene replacement therapy.

Hum Mol Genet 2017 09;26(18):3573-3584

Inserm U1051, Institute for Neurosciences of Montpellier, Montpellier, France.

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http://dx.doi.org/10.1093/hmg/ddx244DOI Listing
September 2017

Adaptive optics: a tool for screening hydroxychloroquine-induced maculopathy?

Acta Ophthalmol 2017 08 2;95(5):e424-e425. Epub 2016 Nov 2.

Department of Ophthalmology, Gui De Chauliac Hospital, Montpellier, France.

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http://dx.doi.org/10.1111/aos.13276DOI Listing
August 2017

Targeted Metabolomics Reveals Early Dominant Optic Atrophy Signature in Optic Nerves of Opa1delTTAG/+ Mice.

Invest Ophthalmol Vis Sci 2017 02;58(2):812-820

Pôle de Recherche et d'Enseignement en Médecine Mitochondriale (PREMMi), Institut MITOVASC, Université d'Angers, Angers, France 2Département de Biochimie et Génétique, Centre Hospitalier Universitaire, Angers, France.

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http://dx.doi.org/10.1167/iovs.16-21116DOI Listing
February 2017

The Clinical Phenotype of CNGA3-Related Achromatopsia: Pretreatment Characterization in Preparation of a Gene Replacement Therapy Trial.

Invest Ophthalmol Vis Sci 2017 02;58(2):821-832

Center for Ophthalmology, University of Tübingen, Tübingen, Germany 7Werner Reichardt Center for Integrative Neuroscience, University of Tübingen, Tübingen, Germany.

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http://dx.doi.org/10.1167/iovs.16-20427DOI Listing
February 2017

Pattern dystrophy in a female carrier of RP2 mutation.

Ophthalmic Genet 2016 12 17;37(4):453-455. Epub 2016 Feb 17.

a Genetics of Sensory Diseases, CHU , Montpellier , France.

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http://dx.doi.org/10.3109/13816810.2015.1081253DOI Listing
December 2016

Martinique Crinkled Retinal Pigment Epitheliopathy: Clinical Stages and Pathophysiologic Insights.

Ophthalmology 2016 10 26;123(10):2196-204. Epub 2016 Jul 26.

Institute for Neurosciences of Montpellier U1051, University of Montpellier - University Hospital, Genetics of Sensory Diseases, Montpellier, France. Electronic address:

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http://dx.doi.org/10.1016/j.ophtha.2016.06.028DOI Listing
October 2016

Primary leptomeningeal melanocytic tumour with a plaque-like blue nevus in a patient with ocular albinism.

Eur J Dermatol 2016 Oct;26(5):496-498

Department of Biopathology, University Hospital, 80 av Augustin Fliche, 34295 Montpellier Cedex 5,, Tumorotheque of Biopathology, University Hospital, 80 av Augustin Fliche, 34295, Montpellier Cedex 5, France.

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http://dx.doi.org/10.1684/ejd.2016.2828DOI Listing
October 2016

WFS1 in Optic Neuropathies: Mutation Findings in Nonsyndromic Optic Atrophy and Assessment of Clinical Severity.

Ophthalmology 2016 09 7;123(9):1989-98. Epub 2016 Jul 7.

Maladies Sensorielles Génétiques, CHRU, Montpellier, France; INSERM U1051, Institute for Neurosciences of Montpellier, Montpellier, France; Université Montpellier, Montpellier, France. Electronic address:

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http://dx.doi.org/10.1016/j.ophtha.2016.05.036DOI Listing
September 2016

Clinical Evaluation and Cone Alterations in Choroideremia.

Ophthalmology 2016 08 15;123(8):1830-1832. Epub 2016 Mar 15.

Genetics of Sensory Diseases, CHU de Montpellier, Montpellier, France; INSERM U1051, Institute for Neurosciences of Montpellier, Montpellier, France; Université Montpellier, Montpellier, France. Electronic address:

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http://dx.doi.org/10.1016/j.ophtha.2016.02.025DOI Listing
August 2016

Confirmation of TENM3 involvement in autosomal recessive colobomatous microphthalmia.

Am J Med Genet A 2016 07 22;170(7):1895-8. Epub 2016 Apr 22.

CHU Toulouse, Service de Génétique Médicale, Hôpital Purpan, Toulouse, France.

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http://dx.doi.org/10.1002/ajmg.a.37667DOI Listing
July 2016

OPA1-related disorders: Diversity of clinical expression, modes of inheritance and pathophysiology.

Neurobiol Dis 2016 Jun 23;90:20-6. Epub 2015 Aug 23.

Centre Hospitalier Universitaire, Département de Biochimie et Génétique, Angers, France; UMR CNRS 6214-INSERM 1083, Université d'Angers, Angers, France. Electronic address:

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http://dx.doi.org/10.1016/j.nbd.2015.08.015DOI Listing
June 2016

Biallelic Mutations in GNB3 Cause a Unique Form of Autosomal-Recessive Congenital Stationary Night Blindness.

Am J Hum Genet 2016 05 7;98(5):1011-1019. Epub 2016 Apr 7.

Department of Ophthalmology, The Hospital for Sick Children, Toronto, ON M5G 1X8, Canada; Program in Genetics and Genome Biology, The Hospital for Sick Children, Toronto, ON M5G 0A4, Canada; Department of Ophthalmology, University of Toronto, 340 College Street, Toronto, ON M5T 3A9, Canada. Electronic address:

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http://dx.doi.org/10.1016/j.ajhg.2016.03.021DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4867910PMC
May 2016

Whole USH2A Gene Sequencing Identifies Several New Deep Intronic Mutations.

Hum Mutat 2016 Feb 23;37(2):184-93. Epub 2015 Nov 23.

Laboratoire de Génétique de Maladies Rares EA 7402, Université de Montpellier, Montpellier, France.

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http://dx.doi.org/10.1002/humu.22926DOI Listing
February 2016

A novel mutation of AFG3L2 might cause dominant optic atrophy in patients with mild intellectual disability.

Front Genet 2015 19;6:311. Epub 2015 Oct 19.

Institut des Neurosciences de Montpellier, U1051 de l'INSERM, Université de Montpellier Montpellier, France ; PREMMi, CNRS UMR 6214 - INSERM U1083, Département de Biochimie et Génétique, Université d'Angers, CHU d'Angers Angers, France.

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http://dx.doi.org/10.3389/fgene.2015.00311DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4609881PMC
November 2015

Autosomal recessive retinitis pigmentosa with RP1 mutations is associated with myopia.

Br J Ophthalmol 2015 Oct 16;99(10):1360-5. Epub 2015 Apr 16.

Maladies Sensorielles Génétiques, CHRU, Montpellier, France INSERM U1051, Institute for Neurosciences of Montpellier, Montpellier, France Université Montpellier 1, Montpellier, France Université Montpellier 2, Montpellier, France.

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http://dx.doi.org/10.1136/bjophthalmol-2014-306224DOI Listing
October 2015

How can we prevent myopia progression?

Eur J Ophthalmol 2015 Jul-Aug;25(4):280-5. Epub 2015 Feb 3.

1 Department of Ophthalmology, Gui De Chauliac Hospital, Montpellier - France.

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http://dx.doi.org/10.5301/ejo.5000571DOI Listing
September 2015

Predominantly Cone-System Dysfunction as Rare Form of Retinal Degeneration in Patients With Molecularly Confirmed Bardet-Biedl Syndrome.

Am J Ophthalmol 2015 Aug 15;160(2):364-372.e1. Epub 2015 May 15.

Service de Génétique Médicale, Institut de Génétique Médicale d'Alsace, Centre de Référence pour les Affections Rares en Génétique Ophtalmologique (CARGO), Strasbourg, France; Laboratoire de Génétique Médicale, Institut de Génétique Médicale d'Alsace, INSERM U1112, Faculté de Médecine, Université de Strasbourg, Strasbourg, France. Electronic address:

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http://dx.doi.org/10.1016/j.ajo.2015.05.007DOI Listing
August 2015

Mutation in NDUFA13/GRIM19 leads to early onset hypotonia, dyskinesia and sensorial deficiencies, and mitochondrial complex I instability.

Hum Mol Genet 2015 Jul 21;24(14):3948-55. Epub 2015 Apr 21.

Institut des Neurosciences de Montpellier, Université de Montpellier I et II, BP 74103, 34 091 Montpellier Cedex 5, France, Service de Neuropédiatrie, CHU Gui de Chauliac, 34 295 Montpellier, France,

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http://dx.doi.org/10.1093/hmg/ddv133DOI Listing
July 2015

Proof of concept for AAV2/5-mediated gene therapy in iPSC-derived retinal pigment epithelium of a choroideremia patient.

Mol Ther Methods Clin Dev 2014 2;1:14011. Epub 2014 Apr 2.

Inserm U1051, Institute for Neurosciences of Montpellier , Montpellier, France ; University of Montpellier 1 , Montpellier, France ; University of Montpellier 2 , Montpellier, France.

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http://dx.doi.org/10.1038/mtm.2014.11DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4362346PMC
May 2015

[Genetic ocular diseases].

Rev Prat 2015 Apr;65(4):467-70

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April 2015

Neuroradiological findings expand the phenotype of OPA1-related mitochondrial dysfunction.

J Neurol Sci 2015 Feb 13;349(1-2):154-60. Epub 2015 Jan 13.

INSERM, U-1051, Institut des Neurosciences, Montpellier, France; CHU Montpellier, Centre of Reference for Genetic Sensory Diseases, Montpellier, France.

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http://dx.doi.org/10.1016/j.jns.2015.01.008DOI Listing
February 2015

A truncated form of rod photoreceptor PDE6 β-subunit causes autosomal dominant congenital stationary night blindness by interfering with the inhibitory activity of the γ-subunit.

PLoS One 2014 23;9(4):e95768. Epub 2014 Apr 23.

Inserm U1051, Institute for Neurosciences of Montpellier, Montpellier, France; University of Montpellier 1, Montpellier, France; University of Montpellier 2, Montpellier, France.

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http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0095768PLOS
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3997432PMC
January 2015

Novel insights into the molecular pathogenesis of CYP4V2-associated Bietti's retinal dystrophy.

Mol Genet Genomic Med 2015 Jan 15;3(1):14-29. Epub 2014 Sep 15.

McGill Ocular Genetics Laboratory, Departments of Paediatric Surgery, Human Genetics and Ophthalmology, Montreal Children's Hospital, McGill University Health Centre Montreal, Quebec, Canada.

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http://dx.doi.org/10.1002/mgg3.109DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4299712PMC
January 2015

Impairment of visual function and retinal ER stress activation in Wfs1-deficient mice.

PLoS One 2014 13;9(5):e97222. Epub 2014 May 13.

INSERM U1051, Institut des Neurosciences de Montpellier, France and Université de Montpellier I et II, Montpellier, France.

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http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0097222PLOS
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4019519PMC
December 2014

Frequency and clinical pattern of vitelliform macular dystrophy caused by mutations of interphotoreceptor matrix IMPG1 and IMPG2 genes.

Ophthalmology 2014 Dec 29;121(12):2406-14. Epub 2014 Jul 29.

Centre de Référence Maladies Sensorielles Génétiques, Hôpital Gui de Chauliac, Montpellier, France; Montpellier University, Montpellier, France; Institute for Neurosciences, INSERM, Montpellier, France.

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http://dx.doi.org/10.1016/j.ophtha.2014.06.028DOI Listing
December 2014

[Inherited retinal dystrophies: contributions of molecular genetics].

Biol Aujourdhui 2013 10;207(2):73-85. Epub 2013 Oct 10.

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http://www.biologie-journal.org/10.1051/jbio/2013007
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http://dx.doi.org/10.1051/jbio/2013007DOI Listing
July 2014

Homozygosity mapping in autosomal recessive retinitis pigmentosa families detects novel mutations.

Mol Vis 2013 8;19:2487-500. Epub 2013 Dec 8.

INSERM U. 1051, Institute for Neurosciences of Montpellier, Montpellier, France ; Université Montpellier 1, Montpellier, France ; Université Montpellier 2, Montpellier, France.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3857159PMC
July 2014

A missense mutation in the splicing factor gene DHX38 is associated with early-onset retinitis pigmentosa with macular coloboma.

J Med Genet 2014 Jul 15;51(7):444-8. Epub 2014 Apr 15.

Faculty of Science, Department of Biosciences, COMSATS Institute of Information Technology, Islamabad, Pakistan Department of Human Genetics, Radboud University Medical Center, Nijmegen, The Netherlands Radboud Institute for Molecular Life Sciences, Radboud University Nijmegen, Nijmegen, The Netherlands.

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http://dx.doi.org/10.1136/jmedgenet-2014-102316DOI Listing
July 2014

Long-term follow-up of a randomized controlled trial of Lichtenstein's operation versus mesh plug repair for inguinal hernia.

Ann Surg 2014 May;259(5):966-72

*Division of General and Visceral Surgery and †Institute for Clinical Epidemiology and Biostatistics, University Hospital Basel, Basel, Switzerland ‡Division of Visceral Surgery and Medicine, University Hospital Bern, Bern, Switzerland §Division of Visceral Surgery, Cantonal Hospital Olten, Olten, Switzerland ¶Division of Visceral Surgery, Cantonal Hospital Lucerne, Lucerne, Switzerland ‖Division of Visceral Surgery, Kreiskrankenhaus Lörrach, Lörrach, Germany **Division of General Surgery, Gesundheitszentrum Wetzikon, Wetzikon, Switzerland.

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http://pdfs.journals.lww.com/annalsofsurgery/2014/05000/Long
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http://content.wkhealth.com/linkback/openurl?sid=WKPTLP:land
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http://dx.doi.org/10.1097/SLA.0000000000000297DOI Listing
May 2014

Gene discovery and prevalence in inherited retinal dystrophies.

C R Biol 2014 Mar 4;337(3):160-6. Epub 2014 Mar 4.

Inserm U.1051, institut des neurosciences de Montpellier, hôpital Saint-Éloi, BP 74103, 80, rue Augustin-Fliche, 34091 Montpellier cedex 5, France. Electronic address:

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http://dx.doi.org/10.1016/j.crvi.2013.12.001DOI Listing
March 2014

Clinical utility gene card for: Achromatopsia - update 2013.

Eur J Hum Genet 2013 Nov 13;21(11). Epub 2013 Mar 13.

Molecular Genetics Laboratory, Department for Ophthalmology, Institute for Ophthalmic Research, University Tuebingen, Tuebingen, Germany.

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http://dx.doi.org/10.1038/ejhg.2013.44DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3798849PMC
November 2013

Early-onset foveal involvement in retinitis punctata albescens with mutations in RLBP1.

JAMA Ophthalmol 2013 Oct;131(10):1314-23

Genetics of Sensory Diseases, Centre Hospitalier Régional Universitaire de Montpellier, Montpellier, France.

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http://dx.doi.org/10.1001/jamaophthalmol.2013.4476DOI Listing
October 2013

Choroideremia: towards a therapy.

Am J Ophthalmol 2013 Sep 28;156(3):433-437.e3. Epub 2013 Jun 28.

Department of Ophthalmology, University of Alberta, Edmonton, Canada. Electronic address:

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http://dx.doi.org/10.1016/j.ajo.2013.05.009DOI Listing
September 2013

The human OPA1delTTAG mutation induces premature age-related systemic neurodegeneration in mouse.

Brain 2012 Dec;135(Pt 12):3599-613

Institut des Neurosciences de Montpellier, INSERM U1051, Université Montpellier I et II CHU St Eloi, 80, rue Auguste Fliche, 34091 Montpellier Cedex 5, France.

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http://dx.doi.org/10.1093/brain/aws303DOI Listing
December 2012

Characterization of pupil responses to blue and red light stimuli in autosomal dominant retinitis pigmentosa due to NR2E3 mutation.

Invest Ophthalmol Vis Sci 2012 Aug 15;53(9):5562-9. Epub 2012 Aug 15.

Neuro-Ophthalmology Unit, Hôpital Ophtalmique Jules Gonin, University of Lausanne, Lausanne, Switzerland.

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http://iovs.arvojournals.org/article.aspx?doi=10.1167/iovs.1
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http://dx.doi.org/10.1167/iovs.12-10230DOI Listing
August 2012

Dominant optic atrophy.

Orphanet J Rare Dis 2012 Jul 9;7:46. Epub 2012 Jul 9.

Institut des Neurosciences de Montpellier, U1051 de l'INSERM, Université de Montpellier I et II, BP 74103, F-34091 Montpellier cedex 05, France.

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http://dx.doi.org/10.1186/1750-1172-7-46DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3526509PMC
July 2012

Mutational analysis of the RB1 gene in Moroccan patients with retinoblastoma.

Mol Vis 2011 30;17:3541-7. Epub 2011 Dec 30.

Laboratoire de Génétique Humaine et Biologie Moléculaire, Institut Pasteur du Maroc, Casablanca, Morocco.

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http://www.molvis.org/molvis/v17/a380/mv-v17-a380-abidi.pdf
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3250372PMC
April 2012