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

الإتاحة: https://doi.org/10.1016/j.ajo.2022.11.026Test
https://pub.dzne.de/record/169155Test
https://pub.dzne.de/search?p=id:%22DZNE-2023-00034%22Test

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

الإتاحة: https://doi.org/10.1016/j.ophtha.2020.12.012Test
https://pub.dzne.de/record/157825Test
https://pub.dzne.de/search?p=id:%22DZNE-2021-01282%22Test

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.0000000000001316

مصطلحات 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

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

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.0000000000001367

مصطلحات 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

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

الإتاحة: https://doi.org/10.1097/WNO.0000000000001367Test
https://pub.dzne.de/record/164175Test
https://pub.dzne.de/search?p=id:%22DZNE-2022-00831%22Test