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1دورية أكاديمية
المؤلفون: Vignal-ClermoḤ, Catherine, Yu-Wai-Man, Patrick, Sadun, Alfredo A, Klopstock, Thomas, Sergott, Robert C, Fernández, Gema Rebolleda, Chwalisz, Bart K, Banik, Rudrani, Taiel, Magali, Roux, Michel, Sahel, José-Alain, Group, LHON Study, Newman, Nancy J, Carelli, Valerio, Moster, Mark L, Biousse, Valerie, Subramanian, Prem S, Wang, An-Guor, Donahue, Sean P, Leroy, Bart P
المصدر: American journal of ophthalmology 249, 108 - 125 (2023). doi:10.1016/j.ajo.2022.11.026
مصطلحات موضوعية: info:eu-repo/classification/ddc/610, Humans, Optic Atrophy, Hereditary, Leber: drug therapy, Leber: genetics, Genetic Vectors, Parvovirinae: genetics, Genetic Therapy, Inflammation: etiology, Leber hereditary optic neuropathy, intravitreal gene therapy, safety
جغرافية الموضوع: DE
العلاقة: info:eu-repo/semantics/altIdentifier/issn/0002-9394; info:eu-repo/semantics/altIdentifier/pmid/pmid:36496192; info:eu-repo/semantics/altIdentifier/issn/1879-1891; https://pub.dzne.de/record/169155Test; https://pub.dzne.de/search?p=id:%22DZNE-2023-00034%22Test
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2دورية أكاديمية
المؤلفون: Newman, Nancy J, Yu-Wai-Man, Patrick, DeBusk, Adam A, Girmens, Jean François, Rudolph, Günther, Karanjia, Rustum, Taiel, Magali, Blouin, Laure, Smits, Gerard, Katz, Barrett, Sahel, José-Alain, Group, LHON Study, Carelli, Valerio, Vignal, Catherine, Hage, Rabih, Catarino, Claudia B, Priglinger, Claudia, Priglinger, Siegfried, Thurau, Stephan, von Livonius, Bettina, Muth, Daniel, Wolf, Armin, Al-Tamami, Jasmina, Moster, Mark L, Pressler, Angelika, Schertler, Cosima, Hildebrandt, Martin, Neuenhahn, Michael, Heilweil, Gad, Tsui, Irena, Hubbard, G Baker, Hendrick, Andrew, Dattilo, Michael, Peragallo, Jason, Biousse, Valerie, Hawy, Eman, DuBois Med, Lindreth, Gibbs, Deborah, Filho, Alcides Fernandes, Dobbs, Jannah, Carbonelli, Michele, Di Vito, Lidia, Contin, Manuela, Mohamed, Susan, La Morgia, Chiara, Vignal-Clermont, Catherine, Silvestri, Sara, Acheson, James, Eleftheriadou, Maria, Esposti, Simona, Gemenetzi, Maria, Leitch-Devlin, Lauren, Tucker, William R, Jurkute, Neringa, SantaMaria, Melissa, Tollis, Heather, Sergott, Robert C, Haller, Julie A, Massini, Maria, Klopstock, Thomas, Sadun, Alfredo A, Barboni, Piero
المصدر: Ophthalmology 128(5), 649 - 660 (2021). doi:10.1016/j.ophtha.2020.12.012
مصطلحات موضوعية: info:eu-repo/classification/ddc/610, Adolescent, Adult, Aged, DNA, Mitochondrial: genetics, Dependovirus: genetics, Double-Blind Method, Electroretinography, Female, Follow-Up Studies, Genetic Therapy, Genetic Vectors, Humans, Intravitreal Injections, Male, Middle Aged, Mutation, Optic Atrophy, Hereditary, Leber: diagnosis, Leber: genetics, Leber: psychology, Leber: therapy, Quality of Life: psychology, Time Factors, Treatment Outcome, Visual Acuity: physiology, Visual Field Tests, Visual Fields: physiology
جغرافية الموضوع: DE
العلاقة: info:eu-repo/semantics/altIdentifier/issn/1549-4713; info:eu-repo/semantics/altIdentifier/issn/0161-6420; info:eu-repo/semantics/altIdentifier/pmid/pmid:33451738; https://pub.dzne.de/record/157825Test; https://pub.dzne.de/search?p=id:%22DZNE-2021-01282%22Test
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3
المؤلفون: Moster, Mark L, Sergott, Robert C, Sadun, Alfredo A, DeBusk, Adam A, Carbonelli, Michele, Hage, Rabih, Priglinger, Siegfried, Karanjia, Rustum, Blouin, Laure, Taiel, Magali, Katz, Barrett, Sahel, José Alain, Newman, Nancy J, group, LHON study, Yu-Wai-Man, Patrick, Carelli, Valerio, Bryan, Molly Scannell, Smits, Gerard, Biousse, Valérie, Vignal-Clermont, Catherine, Klopstock, Thomas
المساهمون: Moster M.L., Sergott R.C., Newman N.J., Yu-Wai-Man P., Carelli V., Bryan M.S., Smits G., Biousse V., Vignal-Clermont C., Klopstock T., Sadun A.A., DeBusk A.A., Carbonelli M., Hage R., Priglinger S., Karanjia R., Blouin L., Taiel M., Katz B., Sahel J.A.
المصدر: Journal of Neuro-Ophthalmology
Journal of neuro-ophthalmology 41(3), 298-308 (2021). doi:10.1097/WNO.0000000000001316مصطلحات موضوعية: Male, Retinal Ganglion Cells, methods [Tomography, Optical Coherence], Visual acuity, genetic structures, Cross-sectional study, physiology [Visual Fields], Genetic enhancement, Nerve fiber layer, Visual Acuity, Phases of clinical research, Retinal Ganglion Cell, chemistry.chemical_compound, Medicine, Contrast (vision), media_common, physiopathology [Optic Atrophy, Hereditary, Leber], Middle Aged, genetics [DNA, Mitochondrial], medicine.anatomical_structure, Clinical Research: Epidemiology Meets Neuro-Ophthalmology, Female, medicine.symptom, Tomography, Optical Coherence, Human, Adult, LEBER HEREDITARY OPTIC NEUROPATHY, medicine.medical_specialty, Adolescent, media_common.quotation_subject, Visual Field, Optic Atrophy, Hereditary, Leber, therapy [Optic Atrophy, Hereditary, Leber], pathology [Retinal Ganglion Cells], DNA, Mitochondrial, Young Adult, methods [Genetic Therapy], Double-Blind Method, Ophthalmology, Humans, ddc:610, Aged, Cross-Sectional Studie, business.industry, Retinal, Genetic Therapy, eye diseases, Cross-Sectional Studies, chemistry, genetics [Optic Atrophy, Hereditary, Leber], Neurology (clinical), Visual Fields, business
وصف الملف: STAMPA
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1a859b80cf449813d0a2a3e53babfd2bTest
http://europepmc.org/articles/PMC8366757Test -
4
المؤلفون: Vignal-ClermoḤ, Catherine, Yu-Wai-Man, Patrick, Sadun, Alfredo A, Klopstock, Thomas, Sergott, Robert C, Fernández, Gema Rebolleda, Chwalisz, Bart K, Banik, Rudrani, Taiel, Magali, Roux, Michel, Sahel, José-Alain, Group, LHON Study, Newman, Nancy J, Carelli, Valerio, Moster, Mark L, Biousse, Valerie, Subramanian, Prem S, Wang, An-Guor, Donahue, Sean P, Leroy, Bart P
المساهمون: Vignal-ClermoḤ, Catherine, Yu-Wai-Man, Patrick, Newman, Nancy J, Carelli, Valerio, Moster, Mark L, Biousse, Valerie, Subramanian, Prem S, Wang, An-Guor, Donahue, Sean P, Leroy, Bart P, Sadun, Alfredo A, Klopstock, Thoma, Sergott, Robert C, Fernández, Gema Rebolleda, Chwalisz, Bart K, Banik, Rudrani, Taiel, Magali, Roux, Michel, Sahel, José-Alain
المصدر: American journal of ophthalmology 249, 108-125 (2023). doi:10.1016/j.ajo.2022.11.026
مصطلحات موضوعية: genetics [Parvovirinae], safety, Ophthalmology, genetics [Optic Atrophy, Hereditary, Leber], etiology [Inflammation], Genetic Vectors, Humans, intravitreal gene therapy, drug therapy [Optic Atrophy, Hereditary, Leber], ddc:610, Genetic Therapy, Leber hereditary optic neuropathy
وصف الملف: STAMPA
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e04af6889f4d7c4cb47ed839f60bcde7Test
https://pubmed.ncbi.nlm.nih.gov/36496192Test -
5
المؤلفون: Biousse, Valérie, Newman, Nancy J, Esposti, Simona, La Morgia, Chiara, Priglinger, Claudia, Karanja, Rustum, Blouin, Laure, Taiel, Magali, Sahel, José-Alain, Group, LHON Study, Yu-Wai-Man, Patrick, Carelli, Valerio, Moster, Mark L, Vignal-Clermont, Catherine, Klopstock, Thomas, Sadun, Alfredo A, Sergott, Robert C, Hage, Rabih
المساهمون: Biousse V., Newman N.J., Yu-Wai-Man P., Carelli V., Moster M.L., Vignal-Clermont C., Klopstock T., Sadun A.A., Sergott R.C., Hage R., Esposti S., La Morgia C., Priglinger C., Karanja R., Blouin L., Taiel M., Sahel J.-A., Emory University School of Medicine, Emory University [Atlanta, GA], University College of London [London] (UCL), Istituti di Ricovero e Cura a Carattere Scientifico (IRCCS), Jefferson (Philadelphia University + Thomas Jefferson University), Centre Hospitalier National d'Ophtalmologie des Quinze-Vingts (CHNO), Ludwig-Maximilians-Universität München (LMU), University of California [Los Angeles] (UCLA), University of California, National Institute for Health Research Moorfields Biomedical Research Centre at Moorfields Eye Hospital and UCL Institute of Ophthalmology, London, GenSight Biologics, Institut de la Vision, Centre National de la Recherche Scientifique (CNRS)-Sorbonne Université (SU)-Institut National de la Santé et de la Recherche Médicale (INSERM)
المصدر: Journal of Neuro-Ophthalmology
Journal of Neuro-Ophthalmology, Lippincott, Williams & Wilkins, 2020, 41 (3), pp.309-315. ⟨10.1097/wno.0000000000001367⟩
Journal of neuro-ophthalmology 41(3), 309-315 (2021). doi:10.1097/WNO.0000000000001367مصطلحات موضوعية: Male, Visual acuity, Time Factors, genetic structures, Genetic enhancement, Visual Acuity, NADH dehydrogenase subunit 4, 0302 clinical medicine, Quality of life, education.field_of_study, metabolism [NADH Dehydrogenase], physiopathology [Optic Atrophy, Hereditary, Leber], Original Contribution, Recombinant Protein, Middle Aged, genetics [DNA, Mitochondrial], Recombinant Proteins, Intravitreal Injections, ComputingMethodologies_DOCUMENTANDTEXTPROCESSING, [SDV.NEU]Life Sciences [q-bio]/Neurons and Cognition [q-bio.NC], Female, medicine.symptom, Tomography, Optical Coherence, Human, Adult, medicine.medical_specialty, LEBER HEREDITARY OPTIC NEUROPATHY, Composite score, Time Factor, Adolescent, Long term follow up, Population, Optic Atrophy, Hereditary, Leber, therapy [Optic Atrophy, Hereditary, Leber], DNA, Mitochondrial, Follow-Up Studie, 03 medical and health sciences, Young Adult, methods [Genetic Therapy], Double-Blind Method, Ophthalmology, administration & dosage [Recombinant Proteins], medicine, Humans, ddc:610, [SDV.MHEP.OS]Life Sciences [q-bio]/Human health and pathology/Sensory Organs, education, Aged, business.industry, Intravitreal Injection, NADH Dehydrogenase, Genetic Therapy, eye diseases, Clinical trial, genetics [Optic Atrophy, Hereditary, Leber], Mutation, 030221 ophthalmology & optometry, Quality of Life, Neurology (clinical), Visual Fields, genetics [NADH Dehydrogenase], business, 030217 neurology & neurosurgery, Follow-Up Studies
وصف الملف: STAMPA
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e4f70ac6a14ffd36a34ac106985e191dTest
http://europepmc.org/articles/PMC8366761Test -
6دورية أكاديمية
المؤلفون: Biousse, Valérie, Newman, Nancy J, Esposti, Simona, La Morgia, Chiara, Priglinger, Claudia, Karanja, Rustum, Blouin, Laure, Taiel, Magali, Sahel, José-Alain, Group, LHON Study, Yu-Wai-Man, Patrick, Carelli, Valerio, Moster, Mark L, Vignal-Clermont, Catherine, Klopstock, Thomas, Sadun, Alfredo A, Sergott, Robert C, Hage, Rabih
المصدر: Journal of neuro-ophthalmology 41(3), 309 - 315 (2021). doi:10.1097/WNO.0000000000001367
مصطلحات موضوعية: info:eu-repo/classification/ddc/610, Adolescent, Adult, Aged, DNA, Mitochondrial: genetics, Double-Blind Method, Female, Follow-Up Studies, Genetic Therapy: methods, Humans, Intravitreal Injections, Male, Middle Aged, Mutation, NADH Dehydrogenase: genetics, NADH Dehydrogenase: metabolism, Optic Atrophy, Hereditary, Leber: genetics, Leber: physiopathology, Leber: therapy, Quality of Life, Recombinant Proteins: administration & dosage, Time Factors, Tomography, Optical Coherence, Visual Acuity, Visual Fields, Young Adult
جغرافية الموضوع: DE
العلاقة: info:eu-repo/semantics/altIdentifier/issn/1070-8022; info:eu-repo/semantics/altIdentifier/issn/1536-5166; info:eu-repo/semantics/altIdentifier/pmid/pmid:34415265; https://pub.dzne.de/record/164175Test; https://pub.dzne.de/search?p=id:%22DZNE-2022-00831%22Test