Arama Sonuçları - Saddek Mohand‐Saïd
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1
Simultaneous perception of prosthetic and natural vision in AMD patients Yazar: Daniel Palanker, Y. Le Mer, Saddek Mohand‐Saïd, José‐Alain Sahel
Baskı/Yayın Bilgisi 2022Artigo -
2
Neurodegenerative and Neuroprotective Effects of Tumor Necrosis Factor (TNF) in Retinal Ischemia: Opposite Roles of TNF Receptor 1 and TNF Receptor 2 Yazar: Valérie Fontaine, Saddek Mohand‐Saïd, Noëlle Hanoteau, Céline Fuchs, Klaus Pfizenmaier, Ulrich Eisel
Baskı/Yayın Bilgisi 2002Artigo -
3
Inherited retinal degenerations: therapeutic prospects Yazar: Marie‐Noëlle Delyfer, Thierry Léveillard, Saddek Mohand‐Saïd, David Hicks, Serge Picaud, José‐Alain Sahel
Baskı/Yayın Bilgisi 2004Revisão -
4
Photovoltaic Restoration of Central Vision in Atrophic Age-Related Macular Degeneration Yazar: Daniel Palanker, Y. Le Mer, Saddek Mohand‐Saïd, Mahiul M. K. Muqit, José‐Alain Sahel
Baskı/Yayın Bilgisi 2020Artigo -
5
Temporal Properties of Visual Perception on Electrical Stimulation of the Retina Yazar: Angelica Pérez Fornos, Jörg Sommerhalder, Lyndon da Cruz, José‐Alain Sahel, Saddek Mohand‐Saïd, Farhad Hafezi, Marco Pelizzone
Baskı/Yayın Bilgisi 2012Artigo -
6
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7
Functional Cone Rescue by RdCVF Protein in a Dominant Model of Retinitis Pigmentosa Yazar: Ying Yang, Saddek Mohand‐Saïd, Aude Danan, Manuel Simonutti, Valérie Fontaine, Emmanuelle Clérin, Serge Picaud, Thierry Léveillard, José‐Alain Sahel
Baskı/Yayın Bilgisi 2009Artigo -
8
Normal retina releases a diffusible factor stimulating cone survival in the retinal degeneration mouse Yazar: Saddek Mohand‐Saïd, Alain Deudon-Combe, David G. Hicks, Manuel Simonutti, Valérie Forster, Anne-Claire Fintz, Thierry Léveillard, H. Dreyfus, José‐Alain Sahel
Baskı/Yayın Bilgisi 1998Artigo -
9
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 Yazar: Catherine Vignal, Jean‐François Girmens, Isabelle Audo, Saddek Mohand Saïd, Marie‐Hélène Errera, Lise Plaine, Denis O’Shaughnessy, Magali Taiel, José‐Alain Sahel
Baskı/Yayın Bilgisi 2021Artigo -
10
<i>MERTK</i> mutation update in inherited retinal diseases Yazar: 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
Baskı/Yayın Bilgisi 2018Revisão -
11
EYS is a major gene for rod-cone dystrophies in France Yazar: 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
Baskı/Yayın Bilgisi 2010Artigo -
12
Evaluation of Retinal Function and Flicker Light-Induced Retinal Vascular Response in Normotensive Patients with Diabetes without Retinopathy Yazar: 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
Baskı/Yayın Bilgisi 2011Artigo -
13
Development and application of a next-generation-sequencing (NGS) approach to detect known and novel gene defects underlying retinal diseases Yazar: 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
Baskı/Yayın Bilgisi 2012Artigo -
14
Identification and characterization of rod-derived cone viability factor Yazar: 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
Baskı/Yayın Bilgisi 2004Artigo -
15
<i>CRB1</i> mutations in inherited retinal dystrophies Yazar: 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
Baskı/Yayın Bilgisi 2011Revisão -
16
Incidence of Atrophic Lesions in Stargardt Disease in the Progression of Atrophy Secondary to Stargardt Disease (ProgStar) Study Yazar: 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
Baskı/Yayın Bilgisi 2017Artigo -
17
Retinal Phenotype of Patients With Isolated Retinal Degeneration Due to<i>CLN3</i>Pathogenic Variants in a French Retinitis Pigmentosa Cohort Yazar: 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
Baskı/Yayın Bilgisi 2021Artigo -
18
Next-generation sequencing applied to a large French cone and cone-rod dystrophy cohort: mutation spectrum and new genotype-phenotype correlation Yazar: 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
Baskı/Yayın Bilgisi 2015Artigo -
19
Preliminary 6 month results from the argus<sup>tm</sup> ii epiretinal prosthesis feasibility study Yazar: 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
Baskı/Yayın Bilgisi 2009Artigo -
20
Test–Retest Variability of Functional and Structural Parameters in Patients with Stargardt Disease Participating in the SAR422459 Gene Therapy Trial Yazar: 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
Baskı/Yayın Bilgisi 2016Artigo
Arama Araçları:
İlgili Konular
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