Zobrazeno 1 - 10
of 15
pro vyhledávání: '"MESH: Electroretinography"'
Autor:
Christoph Kernstock, Ditta Zobor, Anne Kurtenbach, Francesca Simonelli, Susanne Kohl, Stephanie Hipp, José-Alain Sahel, Marko Hawlina, Isabelle Audo, Saddek Mohand-Said, Crystel Bonnet, Christine Petit, Eberhart Zrenner, Katarina Stingl, Gesa Hahn, Francesco Testa, Ana Fakin
Publikováno v:
Documenta Ophthalmologica
Documenta Ophthalmologica, 2019, 139 (2), pp.151-160. ⟨10.1007/s10633-019-09704-8⟩
Documenta Ophthalmologica, Springer Verlag, 2019, 139 (2), pp.151-160. ⟨10.1007/s10633-019-09704-8⟩
Documenta Ophthalmologica, 2019, 139 (2), pp.151-160. ⟨10.1007/s10633-019-09704-8⟩
Documenta Ophthalmologica, Springer Verlag, 2019, 139 (2), pp.151-160. ⟨10.1007/s10633-019-09704-8⟩
Purpose: Usher syndrome (USH) is a multisensory deficiency involving vision, hearing and the vestibular system. The purpose of this study is to report on the functional data (i.e. electroretinography, visual fields, visual acuity) of patients with re
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4df813b327a4ef628f079aff04267f7b
https://pubmed.ncbi.nlm.nih.gov/31267413
https://pubmed.ncbi.nlm.nih.gov/31267413
Autor:
Stéphane Grégoire, Lionel Bretillon, Catherine Creuzot-Garcher, Niyazi Acar, Bertrand Bardet, Emilie Simon, Alain M. Bron
Publikováno v:
Experimental Eye Research
Experimental Eye Research, Elsevier, 2011, 93 (5), pp.628-35. ⟨10.1016/j.exer.2011.07.016⟩
Experimental Eye Research, Elsevier, 2011, 93 (5), pp.628-35. 〈10.1016/j.exer.2011.07.016〉
Experimental Eye Research, Elsevier, 2011, 93 (5), pp.628-35. ⟨10.1016/j.exer.2011.07.016⟩
Experimental Eye Research, Elsevier, 2011, 93 (5), pp.628-35. 〈10.1016/j.exer.2011.07.016〉
International audience; Age-related macular degeneration (AMD) may be partially prevented by dietary habits privileging the consumption of ω3 long chain polyunsaturated fatty acids (ω3s) while lowering linoleic acid (LA) intake. The present study a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ba98cdfac86ba9431efd44472ebdf87e
https://doi.org/10.1016/j.exer.2011.07.016
https://doi.org/10.1016/j.exer.2011.07.016
Autor:
Testa, Francesco, Melillo, Paolo, Bonnet, Crystel, Marcelli, Vincenzo, de Benedictis, Antonella, Colucci, Raffaella, Gallo, Beatrice, Kurtenbach, Anne, Rossi, Settimio, Marciano, Elio, AURICCHIO, ALBERTO, Petit, Christine, Zrenner, Eberhart, Simonelli, Francesca, MARCIANO, ELIO
Publikováno v:
RETINA
RETINA, Lippincott, Williams & Wilkins, 2017, 37 (8), pp.1581-1590. ⟨10.1097/IAE.0000000000001389⟩
RETINA. The Journal of Retinal and Vitreous Diseases
RETINA. The Journal of Retinal and Vitreous Diseases, 2017, 37 (8), pp.1581-1590. ⟨10.1097/IAE.0000000000001389⟩
RETINA, Lippincott, Williams & Wilkins, 2017, 37 (8), pp.1581-1590. ⟨10.1097/IAE.0000000000001389⟩
RETINA. The Journal of Retinal and Vitreous Diseases
RETINA. The Journal of Retinal and Vitreous Diseases, 2017, 37 (8), pp.1581-1590. ⟨10.1097/IAE.0000000000001389⟩
Purpose: To evaluate differences in the visual phenotype and natural history of Usher syndrome caused by mutations in MYO7A or USH2A, the most commonly affected genes of Usher syndrome Type I (USH1) and Type II (USH2), respectively.Methods: Eighty-ei
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::99848b4d30d4d74bd061287b8a7428c2
https://hal-pasteur.archives-ouvertes.fr/pasteur-03219649
https://hal-pasteur.archives-ouvertes.fr/pasteur-03219649
Loss of CRB2 in the mouse retina mimics human retinitis pigmentosa due to mutations in the CRB1 gene
Autor:
Jan Wijnholds, Naoyuki Tanimoto, Mariyam Murtaza, André Le Bivic, Lucie P. Pellissier, Susanne C. Beck, Iswariyaraja Sridevi Gurubaran, Christiaan N. Levelt, Fabrice Richard, Bokyung Park, Gesine Huber, Alicia Sanz Sanz, Mathias W. Seeliger, P. Rashbass, Marina Garcia Garrido, Celso Henrique Alves
Publikováno v:
Human Molecular Genetics, 22, 35-50. Oxford University Press
Human Molecular Genetics; Vol 22
Human Molecular Genetics
Human Molecular Genetics, 2013, 22 (1), pp.35-50. ⟨10.1093/hmg/dds398⟩
Human Molecular Genetics, Oxford University Press (OUP), 2013, 22 (1), pp.35-50. ⟨10.1093/hmg/dds398⟩
Human Molecular Genetics; Vol 22
Human Molecular Genetics
Human Molecular Genetics, 2013, 22 (1), pp.35-50. ⟨10.1093/hmg/dds398⟩
Human Molecular Genetics, Oxford University Press (OUP), 2013, 22 (1), pp.35-50. ⟨10.1093/hmg/dds398⟩
International audience; In humans, the Crumbs homolog-1 (CRB1) gene is mutated in progressive types of autosomal recessive retinitis pigmentosa and Leber congenital amaurosis. However, there is no clear genotype-phenotype correlation for CRB1 mutatio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2c6a00cd12f66bfe693da064f70bc347
https://pubmed.ncbi.nlm.nih.gov/23001562
https://pubmed.ncbi.nlm.nih.gov/23001562
Autor:
Nicholas Sitaras, Florian Sennlaub, Daya R. Varma, Elsa Kermorvant-Duchemin, Joseph A. Mancini, Pierre Hardy, Emilie Picard, Allison Dorfman, Pierre Lachapelle, Jean-Sébastien Joyal, Mikheil Djavari, Przemyslaw Sapieha, Swathi Seshadri, Sylvain Chemtob, Martine Blais, Anna Polosa, Zhuo Shao
Publikováno v:
Investigative Ophthalmology & Visual Science
Investigative Ophthalmology & Visual Science, Association for Research in Vision and Ophthalmology, 2011, 52 (9), pp.6238. ⟨10.1167/iovs.10-6742⟩
Investigative Ophthalmology & Visual Science, 2011, 52 (9), pp.6238. ⟨10.1167/iovs.10-6742⟩
Investigative Ophthalmology & Visual Science, Association for Research in Vision and Ophthalmology, 2011, 52 (9), pp.6238. ⟨10.1167/iovs.10-6742⟩
Investigative Ophthalmology & Visual Science, 2011, 52 (9), pp.6238. ⟨10.1167/iovs.10-6742⟩
International audience; Purpose: Retinopathy of prematurity (ROP) is a major cause of visual handicap in the pediatric population. To date, this disorder is thought to stem from deficient retinal vascularization. Intriguingly, functional electrophysi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::24c42a72248ba7a38249fd9d82f3ea17
https://doi.org/10.1167/iovs.10-6742
https://doi.org/10.1167/iovs.10-6742
Autor:
Frederic Gaillard, Ian M. MacDonald, Silvina C. Mema, Paul R. Freund, Sharee Kuny, Janet R. Sparrow, Yves Sauve, Kang Zhang
Publikováno v:
Investigative Ophthalmology & Visual Science
Investigative Ophthalmology & Visual Science, Association for Research in Vision and Ophthalmology, 2010, 51 (4), pp.2248-62. ⟨10.1167/iovs.09-4718⟩
Investigative Ophthalmology & Visual Science, Association for Research in Vision and Ophthalmology, 2010, 51 (4), pp.2248-62. ⟨10.1167/iovs.09-4718⟩
IF : 3,58); International audience; Purpose. To investigate the impact of progressive age-related photoreceptor degeneration on retinal integrity in Stargardt-like macular dystrophy (STGD3). Methods. The structural design of the inner retina of the E
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ef00efbcc291b9195effe78af48640bb
https://hal.archives-ouvertes.fr/hal-00582487
https://hal.archives-ouvertes.fr/hal-00582487
Autor:
Serge Picaud, Emmanuelle Clérin, José-Alain Sahel, Saddek Mohand-Said, Thierry Léveillard, Ying Yang, Valérie Fontaine, Manuel Simonutti, Aude Danan
Publikováno v:
Molecular Therapy
Molecular Therapy, 2009, 17 (5), pp.787-95. ⟨10.1038/mt.2009.28⟩
Molecular Therapy, Cell Press, 2009, 17 (5), pp.787-95. ⟨10.1038/mt.2009.28⟩
Molecular Therapy, 2009, 17 (5), pp.787-95. ⟨10.1038/mt.2009.28⟩
Molecular Therapy, Cell Press, 2009, 17 (5), pp.787-95. ⟨10.1038/mt.2009.28⟩
International audience; In retinitis pigmentosa (RP), a majority of causative mutations affect genes solely expressed in rods; however, cone degeneration inevitably follows rod cell loss. Following transplantation and in vitro studies, we demonstrate
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::85dcb28b4862bc07c88b0a10e7318d1b
https://www.hal.inserm.fr/inserm-00464512/file/inserm-00464512_edited.pdf
https://www.hal.inserm.fr/inserm-00464512/file/inserm-00464512_edited.pdf
Autor:
Bernard Arnaud, Philippe Derambure, Carl Arndt, Jeremie Husson, Jean Claude Hache, Sabine Defoort-Dhellemmes
Publikováno v:
Epilepsia
Epilepsia, Wiley, 2005, 46 (7), pp.1055-60. ⟨10.1111/j.1528-1167.2005.43204.x⟩
Epilepsia, 2005, 46 (7), pp.1055-60. ⟨10.1111/j.1528-1167.2005.43204.x⟩
Epilepsia, Wiley, 2005, 46 (7), pp.1055-60. ⟨10.1111/j.1528-1167.2005.43204.x⟩
Epilepsia, 2005, 46 (7), pp.1055-60. ⟨10.1111/j.1528-1167.2005.43204.x⟩
Summary: Purpose: To evaluate the effects on vision in patients receiving lamotrigine (LTG) monotherapy. Methods: Twenty-four consecutive patients taking LTG for partial seizures were referred for a routine ophthalmologic examination including visual
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c5a7dd9c11ae73d7bc2529d8b58ca5cc
https://hal.archives-ouvertes.fr/hal-00346411
https://hal.archives-ouvertes.fr/hal-00346411
Autor:
Nicole Zsürger, Henriette Cordes, Joëlle Chabry, H. Laursen, Ann-Louise Bergström, Peter M. H. Heegaard
Publikováno v:
Journal of Biological Chemistry
Journal of Biological Chemistry, American Society for Biochemistry and Molecular Biology, 2005, 280 (24), pp.23114-21. ⟨10.1074/jbc.M500210200⟩
Journal of Biological Chemistry, American Society for Biochemistry and Molecular Biology, 2005, 280 (24), pp.23114-21. ⟨10.1074/jbc.M500210200⟩
One of the major pathological hallmarks of transmissible spongiform encephalopathies (TSEs) is the accumulation of a pathogenic (scrapie) isoform (PrP(Sc)) of the cellular prion protein (PrP(C)) primarily in the central nervous system. The synthetic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::707a28262cb8978d6e6e1752c638abc8
https://hal.archives-ouvertes.fr/hal-00171577
https://hal.archives-ouvertes.fr/hal-00171577
Autor:
Carlo Reggiani, Aram Megighian, Geertruy te Kronnie, Maria Giovanna Ducato, Rodolfo Costa, Mauro Agostino Zordan, Carine Chagneau, Michele Massironi, Jean-René Martin
Publikováno v:
Journal of Neurophysiology
Journal of Neurophysiology, American Physiological Society, 2005, 94 (2), pp.1074-1083. ⟨10.1152/jn.00954.2004⟩
Journal of Neurophysiology, American Physiological Society, 2005, 94 (2), pp.1074-1083. ⟨10.1152/jn.00954.2004⟩
Vertebrate CASK is a member of the membrane-associated guanylate kinase (MAGUK) family of proteins. CASK is present in the nervous system where it binds to neurexin, a transmembrane protein localized in the presynaptic membrane. The Drosophila homolo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::940e8ebab33ec3e099a2dce251085a2f
https://pubmed.ncbi.nlm.nih.gov/15872064
https://pubmed.ncbi.nlm.nih.gov/15872064