Որոնման արդյունքները - Saddek Mohand‐Saïd
- Ցուցադրվում են 1 - 20 արդյունքները 37
- Գնացեք Հաջորդ էջ
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Neurodegenerative and Neuroprotective Effects of Tumor Necrosis Factor (TNF) in Retinal Ischemia: Opposite Roles of TNF Receptor 1 and TNF Receptor 2 Valérie Fontaine, Saddek Mohand‐Saïd, Noëlle Hanoteau, Céline Fuchs, Klaus Pfizenmaier, Ulrich Eisel
Հրապարակվել է 2002Artigo -
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Functional Cone Rescue by RdCVF Protein in a Dominant Model of Retinitis Pigmentosa Ying Yang, Saddek Mohand‐Saïd, Aude Danan, Manuel Simonutti, Valérie Fontaine, Emmanuelle Clérin, Serge Picaud, Thierry Léveillard, José‐Alain Sahel
Հրապարակվել է 2009Artigo -
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Normal retina releases a diffusible factor stimulating cone survival in the retinal degeneration mouse Saddek Mohand‐Saïd, Alain Deudon-Combe, David G. Hicks, Manuel Simonutti, Valérie Forster, Anne-Claire Fintz, Thierry Léveillard, H. Dreyfus, José‐Alain Sahel
Հրապարակվել է 1998Artigo -
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Safety of Intravitreal Gene Therapy for Treatment of Subjects with Leber Hereditary Optic Neuropathy due to Mutations in the Mitochondrial ND4 Gene: The REVEAL Study Catherine Vignal, Jean‐François Girmens, Isabelle Audo, Saddek Mohand Saïd, Marie‐Hélène Errera, Lise Plaine, Denis O’Shaughnessy, Magali Taiel, José‐Alain Sahel
Հրապարակվել է 2021Artigo -
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<i>MERTK</i> mutation update in inherited retinal diseases Isabelle Audo, Saddek Mohand‐Saïd, Élise Boulanger-Scemama, Xavier Zanlonghi, Christel Condroyer, Vanessa Démontant, Fiona Boyard, Aline Antonio, Cécile Méjécase, Saïd El Shamieh, José‐Alain Sahel, Christina Zeitz
Հրապարակվել է 2018Revisão -
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EYS is a major gene for rod-cone dystrophies in France Isabelle Audo, José‐Alain Sahel, Saddek Mohand‐Saïd, Marie‐Elise Lancelot, Aline Antonio, Veselina Moskova‐Doumanova, Emeline F. Nandrot, Jordan Doumanov, Isabel Barragán, Guillermo Antiñolo, Shomi S. Bhattacharya, Christina Zeitz
Հրապարակվել է 2010Artigo -
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Evaluation of Retinal Function and Flicker Light-Induced Retinal Vascular Response in Normotensive Patients with Diabetes without Retinopathy A. Lecleire–Collet, Isabelle Audo, Mounir Aout, Jean‐François Girmens, R. Sofroni, Ali Erginay, Jean‐François Le Gargasson, Saddek Mohand‐Saïd, T. Méas, Pierre-Jean Guillausseau, Éric Vicaut, Michel Pâques, Pascale Massin
Հրապարակվել է 2011Artigo -
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Development and application of a next-generation-sequencing (NGS) approach to detect known and novel gene defects underlying retinal diseases Isabelle Audo, Kinga M. Bujakowska, Thierry Léveillard, Saddek Mohand‐Saïd, Marie‐Elise Lancelot, Aurore Germain, Aline Antonio, Christelle Michiels, Jean‐Paul Saraiva, Mélanie Letexier, José‐Alain Sahel, Shomi S. Bhattacharya, Christina Zeitz
Հրապարակվել է 2012Artigo -
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Identification and characterization of rod-derived cone viability factor Thierry Léveillard, Saddek Mohand‐Saïd, Olivier Lorentz, David Hicks, Anne-Claire Fintz, Emmanuelle Clérin, Manuel Simonutti, Valérie Forster, Nükhet Cavusoglu, Frédéric Chalmel, Pascal Dollé, Olivier Poch, George Ι. Lambrou, José‐Alain Sahel
Հրապարակվել է 2004Artigo -
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<i>CRB1</i> mutations in inherited retinal dystrophies Kinga M. Bujakowska, Isabelle Audo, Saddek Mohand‐Saïd, Marie‐Elise Lancelot, Aline Antonio, Aurore Germain, Thierry Léveillard, Mélanie Letexier, Jean‐Paul Saraiva, Christine Lonjou, Wassila Carpentier, José‐Alain Sahel, Shomi S. Bhattacharya, Christina Zeitz
Հրապարակվել է 2011Revisão -
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Incidence of Atrophic Lesions in Stargardt Disease in the Progression of Atrophy Secondary to Stargardt Disease (ProgStar) Study Rupert W. Strauß, Beatriz Muñoz, Alexander Ho, Anamika Jha, Michel Michaelides, Saddek Mohand‐Saïd, Artur V. Cideciyan, David G. Birch, Amir H Hariri, Muneeswar Gupta Nittala, Srinivas R. Sadda, Hendrik P. N. Scholl
Հրապարակվել է 2017Artigo -
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Retinal Phenotype of Patients With Isolated Retinal Degeneration Due to<i>CLN3</i>Pathogenic Variants in a French Retinitis Pigmentosa Cohort Vasily Smirnov, Marco Nassisi, Cyntia Solis Hernandez, Cécile Méjécase, Saïd El Shamieh, Christel Condroyer, Aline Antonio, Isabelle Meunier, Camille Andrieu, Sabine Defoort‐Dhellemmes, Saddek Mohand‐Saïd, José‐Alain Sahel, Isabelle Audo, Christina Zeitz
Հրապարակվել է 2021Artigo -
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Next-generation sequencing applied to a large French cone and cone-rod dystrophy cohort: mutation spectrum and new genotype-phenotype correlation Élise Boulanger-Scemama, Saïd El Shamieh, Vanessa Démontant, Christel Condroyer, Aline Antonio, Christelle Michiels, Fiona Boyard, Jean‐Paul Saraiva, Mélanie Letexier, Eric H. Souied, Saddek Mohand‐Saïd, José‐Alain Sahel, Christina Zeitz, Isabelle Audo
Հրապարակվել է 2015Artigo -
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Preliminary 6 month results from the argus<sup>tm</sup> ii epiretinal prosthesis feasibility study Mark S. Humayun, Jessy D. Dorn, Arvind Ahuja, Avi Caspi, E. Filley, Gislin Dagnelie, Joël Salzmann, Arturo Santos, John S. Duncan, Lyndon daCruz, Saddek Mohand‐Saïd, Dean Eliott, Matthew J. McMahon, R.J. Greenberg
Հրապարակվել է 2009Artigo -
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Test–Retest Variability of Functional and Structural Parameters in Patients with Stargardt Disease Participating in the SAR422459 Gene Therapy Trial Maria A. Parker, Dongseok Choi, Laura Erker, Mark E. Pennesi, Paul Yang, Elvira N. Chegarnov, Peter Steinkamp, Catherine L. Schlechter, Claire‐Marie Dhaenens, Saddek Mohand‐Saïd, Isabelle Audo, José‐Alain Sahel, Richard G. Weleber, David J. Wilson
Հրապարակվել է 2016Artigo
Որոնման գործիքներ:
Առնչվող խորագիր
Biology
Medicine
Genetics
Gene
Ophthalmology
Retinal
Phenotype
Retinitis pigmentosa
Biochemistry
Mutation
Macular degeneration
Neuroscience
Internal medicine
Retina
Retinal degeneration
Computer science
Missense mutation
Optometry
Visual acuity
ABCA4
Pathology
Stargardt disease
Blindness
Cell biology
Dystrophy
Endocrinology
Exome sequencing
Genotype
Retinal pigment epithelium
Sanger sequencing