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المؤلفون: Kazushige Tsunoda, Camiel J. F. Boon, Ester Carreño, Xiao Liu, Rachel M. Huckfeldt, Mark E. Pennesi, Andrew R. Webster, Anthony G. Robson, Elise Héon, Gavin Arno, Susanne Kohl, Belen Jimenez-Rolando, Michel Michaelides, Carmen Ayuso, Omar A. Mahroo, Eyal Banin, Samer Khateb, Takaaki Hayashi, Bernd Wissinger, Arif O. Khan, Eberhart Zrenner, Alberta A H J Thiadens, Ajoy Vincent, Nikolas Pontikos, Maria Inmaculada Martin-Merida, Thales Antonio Cabral de Guimaraes, Xuan-Thanh-An Nguyen, Michalis Georgiou, Almudena Avila-Fernandez, Mauricio E Vargas, Emanuel R. de Carvalho, Shaun Michael Leo, Yu Fujinami-Yokokawa, Dror Sharon, Fadi Nasser, Kaoru Fujinami, Blanca Garcia-Sandoval
المساهمون: Ophthalmology, ANS - Complex Trait Genetics
المصدر: American journal of ophthalmology, 230, 1-11. Elsevier USA
American Journal of Ophthalmology, 230, 1-11. Elsevier Inc.
American Journal of Ophthalmology, 230. ELSEVIER SCIENCE INC
American Journal of Ophthalmologyمصطلحات موضوعية: medicine.medical_specialty, genetic structures, Fundus Oculi, Retina, Foveola, 03 medical and health sciences, chemistry.chemical_compound, 0302 clinical medicine, Retinal Diseases, Optical coherence tomography, Ophthalmology, medicine, Humans, Fluorescein Angiography, Outer nuclear layer, Retrospective Studies, 030304 developmental biology, 0303 health sciences, Retinal pigment epithelium, medicine.diagnostic_test, business.industry, Retinal, medicine.disease, eye diseases, Autofluorescence, Phenotype, medicine.anatomical_structure, chemistry, Potassium Channels, Voltage-Gated, 030221 ophthalmology & optometry, Original Article, sense organs, business, Tomography, Optical Coherence, Retinopathy
وصف الملف: application/pdf
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::25d64991d77208076740a746fc4a5daaTest
http://www.scopus.com/inward/record.url?scp=85108876875&partnerID=8YFLogxKTest -
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المؤلفون: Bernd Wissinger, Eberhart Zrenner, Nikolas Pontikos, Maria Inmaculada Martin-Merida, Xuan-Thanh-An Nguyen, Anthony G. Robson, Emanuel R. de Carvalho, Kazushige Tsunoda, Omar A. Mahroo, Alberta A H J Thiadens, Mauricio E Vargas, Fadi Nasser, Kaoru Fujinami, Gavin Arno, Rachel M. Huckfeldt, Ester Carreño, Thales Antonio Cabral de Guimaraes, Ayuso Carmen, Takaaki Hayashi, Michel Michaelides, Elise Héon, Xiao Liu, Dror Sharon, Ajoy Vincent, Mark E. Pennesi, Michalis Georgiou, Arif O. Khan, Andrew R. Webster, Yu Fujinami-Yokokawa, Gema Gordo, Eyal Banin, Shaun Michael Leo, Susanne Kohl, Belen Jimenez-Rolando, Camiel J. F. Boon, Samer Khateb
المساهمون: Ophthalmology, ANS - Complex Trait Genetics
المصدر: American journal of ophthalmology, 225, 95-107. Elsevier USA
American Journal of Ophthalmology, 225, 95-107. Elsevier Inc.
American Journal of Ophthalmology
American Journal of Ophthalmology, 225, 95-107. ELSEVIER SCIENCE INCمصطلحات موضوعية: Male, Visual acuity, Photophobia, genetic structures, Visual Acuity, 0302 clinical medicine, Child, Genetics, 0303 health sciences, medicine.diagnostic_test, High-Throughput Nucleotide Sequencing, Middle Aged, Phenotype, Potassium Channels, Voltage-Gated, Child, Preschool, Decreased Visual Acuity, Cohort, Female, Original Article, medicine.symptom, Erg, Retinitis Pigmentosa, Tomography, Optical Coherence, Retinopathy, Adult, Adolescent, Vision Disorders, Dark Adaptation, Refraction, Ocular, Nyctalopia, Retina, 03 medical and health sciences, Exome Sequencing, medicine, Electroretinography, Humans, Molecular Biology, Alleles, 030304 developmental biology, Aged, Retrospective Studies, Whole Genome Sequencing, business.industry, Infant, Newborn, Infant, medicine.disease, eye diseases, Ophthalmology, 030221 ophthalmology & optometry, business
وصف الملف: application/pdf
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::25c2d32445ffc5056e59894108f29ff3Test
http://www.scopus.com/inward/record.url?scp=85101977838&partnerID=8YFLogxKTest -
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المؤلفون: Samer Khateb, Tareq Jaouni, Michael Halpert, Hamzah Aweidah
المصدر: Case Reports in Ophthalmology
Case Reports in Ophthalmology, Vol 12, Iss 2, Pp 464-472 (2021)مصطلحات موضوعية: Pars plana, medicine.medical_specialty, Proliferative vitreoretinopathy, Visual acuity, genetic structures, medicine.medical_treatment, Vitrectomy, Case Report, Primary repair, Post-operative, Epiretinal membrane, Ophthalmology, Medicine, business.industry, Retinal detachment, RE1-994, medicine.disease, eye diseases, Macular function, medicine.anatomical_structure, Macular pucker, sense organs, medicine.symptom, business, Macular proliferative vitreoretinopathy, Premacular membrane
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2e496670352dc366b1234a839740b2ecTest
http://europepmc.org/articles/PMC8215993Test -
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المؤلفون: Itay Chowers, Khaled Safadi, Samer Khateb
المصدر: Acta Ophthalmologica. 99:892-897
مصطلحات موضوعية: Adult, Male, Pars plana, medicine.medical_specialty, Visual acuity, Adolescent, genetic structures, medicine.medical_treatment, Visual Acuity, Vitrectomy, Scleral buckle, Young Adult, Ophthalmology, medicine, Humans, Macula Lutea, Young adult, Retrospective Studies, Surgical repair, business.industry, Retinal Detachment, Retinal detachment repair, Retinal detachment, General Medicine, medicine.disease, eye diseases, Scleral Buckling, medicine.anatomical_structure, Female, medicine.symptom, business, Tomography, Optical Coherence, Follow-Up Studies
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c52d1b02e6bcefb880fb33d1185d7c56Test
https://doi.org/10.1111/aos.14783Test -
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المؤلفون: Mor Hanany, Hadas Newman, Tamar Ben-Yosef, Eedy Mezer, Frans P.M. Cremers, Eyal Banin, Alexey Obolensky, Itay Chowers, Samer Khateb, Muhammad Imran Khan, Avigail Beryozkin, Dror Sharon, Carlos Alberto Idrobo-Robalino
المصدر: Scientific Reports, Vol 10, Iss 1, Pp 1-12 (2020)
Scientific Reports, 10, 1
Scientific Reports, 10
Scientific Reportsمصطلحات موضوعية: Male, 0301 basic medicine, Visual acuity, genetic structures, Visual Acuity, lcsh:Medicine, Diseases, Sensory disorders Donders Center for Medical Neuroscience [Radboudumc 12], Cohort Studies, 0302 clinical medicine, Night Blindness, Israel, Child, Signs and symptoms, lcsh:Science, Aged, 80 and over, education.field_of_study, Multidisciplinary, Clinical pathology, medicine.diagnostic_test, Middle Aged, medicine.anatomical_structure, Child, Preschool, Female, medicine.symptom, Retinitis Pigmentosa, Tomography, Optical Coherence, Adult, medicine.medical_specialty, Adolescent, Fundus Oculi, Population, Nonsense mutation, Genes, Recessive, Article, Young Adult, 03 medical and health sciences, Medical research, All institutes and research themes of the Radboud University Medical Center, Ophthalmology, Retinitis pigmentosa, Electroretinography, medicine, Genetics, Humans, Allele, Eye Proteins, Outer nuclear layer, education, Alleles, Aged, business.industry, lcsh:R, medicine.disease, eye diseases, 030104 developmental biology, Jews, Mutation, 030221 ophthalmology & optometry, lcsh:Q, sense organs, Visual Fields, business
وصف الملف: application/pdf
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::827c9bb9588d9d53c56e9c32f3396dfaTest
http://link.springer.com/article/10.1038/s41598-020-72028-0Test -
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المؤلفون: Michal Macarov, Karen Hendler, Anat Blumenfeld, Claudia Yahalom, Orly Wussuki-Lior, Samer Khateb, Mordechai Shohat
المصدر: Graefe's Archive for Clinical and Experimental Ophthalmology. 256:2157-2164
مصطلحات موضوعية: Adult, Male, 0301 basic medicine, congenital, hereditary, and neonatal diseases and abnormalities, medicine.medical_specialty, Visual acuity, PAX6 Transcription Factor, genetic structures, Mutation, Missense, Visual Acuity, Vision, Low, 030105 genetics & heredity, Blindness, Refraction, Ocular, Young Adult, 03 medical and health sciences, Cellular and Molecular Neuroscience, 0302 clinical medicine, Ophthalmology, Humans, Medicine, Child, Aniridia, Aged, Retrospective Studies, Genetic testing, medicine.diagnostic_test, business.industry, Corectopia, Genetic heterogeneity, Eye Diseases, Hereditary, Middle Aged, medicine.disease, eye diseases, Sensory Systems, Hypoplasia, Pedigree, Phenotype, Child, Preschool, 030221 ophthalmology & optometry, Female, sense organs, PAX6, medicine.symptom, Differential diagnosis, business
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d2fccc4f3bac13608bfc16e55cedb6c8Test
https://doi.org/10.1007/s00417-018-4119-1Test -
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المؤلفون: Samer Khateb, Shekhar Jha, Kapil Bharti, Eyal Banin
المصدر: Age-related Macular Degeneration ISBN: 9783030660130
مصطلحات موضوعية: Retina, medicine.medical_specialty, Retinal pigment epithelium, genetic structures, business.industry, Cell, Macular degeneration, medicine.disease, Embryonic stem cell, eye diseases, Photoreceptor cell, Transplantation, 03 medical and health sciences, 0302 clinical medicine, medicine.anatomical_structure, Ophthalmology, medicine, sense organs, 030212 general & internal medicine, Induced pluripotent stem cell, business
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::c6e088e0cdfe16bc6596ef53abc03dbcTest
https://doi.org/10.1007/978-3-030-66014-7_11Test -
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المؤلفون: Hamzah Aweidah, Tamar Ben-Yosef, Oscar Iguzquiza, Frans P.M. Cremers, Roque Daniel Carrero Valenzuela, Myriam Berman, Muhammad Imran Khan, Dror Sharon, Radgonde Amer, Samer Khateb, Avigail Beryozkin, Anand Swaroop, Eyal Banin
المصدر: Frontiers in Cell and Developmental Biology, 9
Frontiers in Cell and Developmental Biology, Vol 9 (2021)
Frontiers in Cell and Developmental Biologyمصطلحات موضوعية: Retinal degeneration, medicine.medical_specialty, Visual acuity, genetic structures, QH301-705.5, Posterior pole, genotype-phenotype correlation, Sensory disorders Donders Center for Medical Neuroscience [Radboudumc 12], Cell and Developmental Biology, Ophthalmology, Retinitis pigmentosa, Medicine, Missense mutation, RPGRIP1, Biology (General), Original Research, medicine.diagnostic_test, business.industry, Dystrophy, Cell Biology, medicine.disease, eye diseases, natural history, retinal degeneration, mutation spectrum, sense organs, Age of onset, medicine.symptom, business, Developmental Biology, Electroretinography
وصف الملف: application/pdf
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::91bc64e58addb9fbf8c489471a9aa339Test
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المؤلفون: Diego Almeida, Radgonde Amer, Itay Chowers, Sarah Elbaz-Hayoun, Samer Khateb, Batya Rinsky, Shira Hagbi-Levi, Michelle Grunin, Gala Beykin, Liran Tiosano
المصدر: Investigative Ophthalmology & Visual Science
مصطلحات موضوعية: Male, Proteome, Visual Acuity, Enzyme-Linked Immunosorbent Assay, Serpin, Proteomics, Retina, Aqueous Humor, Endopeptidase activity, Platelet degranulation, Humans, Cellular protein metabolic process, Eye Proteins, age- related macular degeneration, Aged, Aged, 80 and over, Clusterin, biology, Molecular biology, eye diseases, ROC Curve, Wet Macular Degeneration, retinal degeneration, biology.protein, Biomarker (medicine), Female, sense organs, Biomarkers
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f4af9d926e619df2c5821fdad4816991Test
https://doi.org/10.1167/iovs.62.10.18Test -
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المؤلفون: Prasanthi, Namburi, Samer, Khateb, Segev, Meyer, Tom, Bentovim, Rinki, Ratnapriya, Alisa, Khramushin, Anand, Swaroop, Ora, Schueler-Furman, Eyal, Banin, Dror, Sharon
المصدر: Molecular Vision
مصطلحات موضوعية: Adult, Heterozygote, Georgia, Genotype, Color Vision Defects, Retinal Dystrophies, Exome Sequencing, Electroretinography, Humans, Genetic Testing, Fluorescein Angiography, Child, Phylogeny, Sequence Deletion, Aged, 80 and over, Corneal Dystrophies, Hereditary, Histone-Lysine N-Methyltransferase, Middle Aged, eye diseases, Pedigree, Electrooculography, Phenotype, Complement Factor H, Jews, Female, Tomography, Optical Coherence, Transcription Factors, Research Article
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=pmid________::1a358d9afc956ed9a446477c85acc510Test
https://pubmed.ncbi.nlm.nih.gov/32476814Test