المؤلفون: Carelli, V, Newman, NJ, Yu-Wai-Man, P, Biousse, V, Moster, ML, Subramanian, PS, Vignal-Clermont, C, Wang, AG, Donahue, SP, Leroy, Bart, Sergott, RC, Klopstock, T, Sadun, AA, Rebolleda Fernández, G, Chwalisz, BK, Banik, R, Girmens, JF, La Morgia, C, DeBusk, AA, Jurkute, N, Priglinger, C, Karanjia, R, Josse, C, Salzmann, J, Montestruc, F, Roux, M, Taiel, M, Sahel, JA, the LHON Study, Group

المصدر: OPHTHALMOLOGY AND THERAPY ; ISSN: 2193-8245 ; ISSN: 2193-6528

مصطلحات موضوعية: Medicine and Health Sciences, Visual acuity, Natural history, MT-ND4, LHON, Leber hereditary optic neuropathy, Gene therapy

وصف الملف: application/pdf

العلاقة: https://biblio.ugent.be/publication/01GQJ1SPSXTA8KWP5XWE98B4YXTest; http://hdl.handle.net/1854/LU-01GQJ1SPSXTA8KWP5XWE98B4YXTest; http://dx.doi.org/10.1007/s40123-022-00611-xTest; https://biblio.ugent.be/publication/01GQJ1SPSXTA8KWP5XWE98B4YX/file/01GQJ1XTVN3AF30Z5WA8FS39Y7Test

الإتاحة: https://doi.org/10.1007/s40123-022-00611-xTest
https://biblio.ugent.be/publication/01GQJ1SPSXTA8KWP5XWE98B4YXTest
http://hdl.handle.net/1854/LU-01GQJ1SPSXTA8KWP5XWE98B4YXTest
https://biblio.ugent.be/publication/01GQJ1SPSXTA8KWP5XWE98B4YX/file/01GQJ1XTVN3AF30Z5WA8FS39Y7Test

المؤلفون: Newman N. J., Schniederjan M., Mendoza P. R., Calkins D. J., Yu-Wai-Man P., Biousse V., Carelli V., Taiel M., Rugiero F., Singh P., Rogue A., Sahel J. -A., Ancian P.

المساهمون: Newman N.J., Schniederjan M., Mendoza P.R., Calkins D.J., Yu-Wai-Man P., Biousse V., Carelli V., Taiel M., Rugiero F., Singh P., Rogue A., Sahel J.-A., Ancian P.

مصطلحات موضوعية: Case report, Leber hereditary optic neuropathy, Lenadogene nolparvovec, ND4, qPCR assay, Recombinant adeno-associated virus vector 2 serotype 2, Viral vector transduction, Aged, Biopsy, Clinical Trials, Phase III as Topic, Dependoviru, Female, Follow-Up Studie, Human, Brain Neoplasm, Glioblastoma, Optic Atrophy, Hereditary, Leber

وصف الملف: ELETTRONICO

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/35820885; info:eu-repo/semantics/altIdentifier/wos/WOS:000824926700003; volume:22; issue:1; firstpage:1; lastpage:7; numberofpages:7; journal:BMC NEUROLOGY; https://hdl.handle.net/11585/903013Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85133893079; https://bmcneurol.biomedcentral.com/articles/10.1186/s12883-022-02787-yTest

الإتاحة: https://doi.org/10.1186/s12883-022-02787-yTest
https://hdl.handle.net/11585/903013Test

المؤلفون: Calkins D. J., Yu-Wai-Man P., Newman N. J., Taiel M., Singh P., Chalmey C., Rogue A., Carelli V., Ancian P., Sahel J. A.

المساهمون: Calkins D.J., Yu-Wai-Man P., Newman N.J., Taiel M., Singh P., Chalmey C., Rogue A., Carelli V., Ancian P., Sahel J.A.

مصطلحات موضوعية: biodistribution, Leber hereditary optic neuropathy, lenadogene nolparvovec, Lumevoq, ND4, qPCR assay, recombinant adeno-associated virus vector 2 serotype 2, transduction, viral vector

وصف الملف: STAMPA

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/34729378; info:eu-repo/semantics/altIdentifier/wos/WOS:000757164400008; volume:23; firstpage:307; lastpage:318; numberofpages:12; journal:MOLECULAR THERAPY. METHODS & CLINICAL DEVELOPMENT; http://hdl.handle.net/11585/864473Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85121632005; https://www.sciencedirect.com/science/article/pii/S2329050121001510?via=ihubTest

الإتاحة: https://doi.org/10.1016/j.omtm.2021.09.013Test
http://hdl.handle.net/11585/864473Test
https://www.sciencedirect.com/science/article/pii/S2329050121001510?via=ihubTest

المؤلفون: Newman N. J., Yu-Wai-Man P., Carelli V., Biousse V., Moster M. L., Vignal-Clermont C., Sergott R. C., Klopstock T., Sadun A. A., Girmens J. -F., La Morgia C., DeBusk A. A., Jurkute N., Priglinger C., Karanjia R., Josse C., Salzmann J., Montestruc F., Roux M., Taiel M., Sahel J. -A.

المساهمون: Newman N.J., Yu-Wai-Man P., Carelli V., Biousse V., Moster M.L., Vignal-Clermont C., Sergott R.C., Klopstock T., Sadun A.A., Girmens J.-F., La Morgia C., DeBusk A.A., Jurkute N., Priglinger C., Karanjia R., Josse C., Salzmann J., Montestruc F., Roux M., Taiel M., Sahel J.-A.

مصطلحات موضوعية: gene therapy, Leber hereditary optic neuropathy, natural history, ND4, visual acuity

وصف الملف: ELETTRONICO

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/34108929; info:eu-repo/semantics/altIdentifier/wos/WOS:000658318000001; volume:12; firstpage:1; lastpage:13; numberofpages:13; journal:FRONTIERS IN NEUROLOGY; https://hdl.handle.net/11585/864635Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85107371051; https://www.frontiersin.org/articles/10.3389/fneur.2021.662838/fullTest

الإتاحة: https://doi.org/10.3389/fneur.2021.662838Test
https://hdl.handle.net/11585/864635Test

المؤلفون: Yu-Wai-Man P., Newman N. J., Carelli V., La Morgia C., Biousse V., Bandello F. M., Clermont C. V., Campillo L. C., Leruez S., Moster M. L., Cestari D. M., Foroozan R., Sadun A., Karanjia R., Jurkute N., Blouin L., Taiel M., Sahel J. -A., Hussain R., Jorany R., Sheel P., DuBois L., Carbonelli M., Di Vito L., Romagnoli M., DeBusk A. A., Massini M., Hage R., Heilweil G., Tsui I., Garcia V., Morilla A., Barboni P., Cascavilla M. L., Battista M., Calcagno F., Pina A.

المساهمون: Yu-Wai-Man P., Newman N.J., Carelli V., La Morgia C., Biousse V., Bandello F.M., Clermont C.V., Campillo L.C., Leruez S., Moster M.L., Cestari D.M., Foroozan R., Sadun A., Karanjia R., Jurkute N., Blouin L., Taiel M., Sahel J.-A., Hussain R., Jorany R., Sheel P., DuBois L., Carbonelli M., Di Vito L., Romagnoli M., DeBusk A.A., Massini M., Hage R., Heilweil G., Tsui I., Garcia V., Morilla A., Barboni P., Cascavilla M.L., Battista M., Calcagno F., Pina A.

مصطلحات موضوعية: Leber Hereditary Optic Neuropathy, LHON

وصف الملف: ELETTRONICO

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/33911213; info:eu-repo/semantics/altIdentifier/wos/WOS:000645160400004; volume:36; issue:4; firstpage:1; lastpage:9; numberofpages:9; journal:EYE; https://hdl.handle.net/11585/864597Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85105133304; https://www.nature.com/articles/s41433-021-01535-9Test

الإتاحة: https://doi.org/10.1038/s41433-021-01535-9Test
https://hdl.handle.net/11585/864597Test
https://www.nature.com/articles/s41433-021-01535-9Test

المؤلفون: 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.

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.

مصطلحات موضوعية: Adolescent, Adult, Aged, Cross-Sectional Studie, DNA, Mitochondrial, Double-Blind Method, Female, Genetic Therapy, Human, Male, Middle Aged, Optic Atrophy, Hereditary, Leber, Retinal Ganglion Cell, Tomography, Optical Coherence, Visual Field, Young Adult, Visual Acuity

وصف الملف: STAMPA

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/34310464; info:eu-repo/semantics/altIdentifier/wos/WOS:000711807500012; volume:41; issue:3; firstpage:298; lastpage:308; numberofpages:11; journal:JOURNAL OF NEURO-OPHTHALMOLOGY; https://hdl.handle.net/11585/864483Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85114845943; https://journals.lww.com/jneuro-ophthalmology/Fulltext/2021/09000/Cross_Sectional_Analysis_of_Baseline_Visual.4.aspxTest

الإتاحة: https://doi.org/10.1097/WNO.0000000000001316Test
https://hdl.handle.net/11585/864483Test
https://journals.lww.com/jneuro-ophthalmology/Fulltext/2021/09000/Cross_Sectional_Analysis_of_Baseline_Visual.4.aspxTest

المؤلفون: 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.

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.

مصطلحات موضوعية: Adolescent, Adult, Aged, DNA, Mitochondrial, Double-Blind Method, Female, Follow-Up Studie, Genetic Therapy, Human, Intravitreal Injection, Male, Middle Aged, Mutation, NADH Dehydrogenase, Optic Atrophy, Hereditary, Leber, Quality of Life, Recombinant Protein, Time Factor, Tomography, Optical Coherence, Young Adult, Visual Acuity, Visual Fields

وصف الملف: STAMPA

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/34415265; info:eu-repo/semantics/altIdentifier/wos/WOS:000711807500016; volume:41; issue:3; firstpage:309; lastpage:315; numberofpages:7; journal:JOURNAL OF NEURO-OPHTHALMOLOGY; https://hdl.handle.net/11585/864514Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85114846151; https://journals.lww.com/jneuro-ophthalmology/Fulltext/2021/09000/Long_Term_Follow_Up_After_Unilateral_Intravitreal.5.aspxTest

الإتاحة: https://doi.org/10.1097/WNO.0000000000001367Test
https://hdl.handle.net/11585/864514Test
https://journals.lww.com/jneuro-ophthalmology/Fulltext/2021/09000/Long_Term_Follow_Up_After_Unilateral_Intravitreal.5.aspxTest

المؤلفون: Newman, NJ, Yu-Wai-Man, P, Carelli, V, Moster, ML, Biousse, V, Vignal-Clermont, C, Sergott, RC, Klopstock, T, Sadun, AA, Barboni, P, DeBusk, AA, Girmens, JF, Rudolph, G, Karanjia, R, Taiel, M, Blouin, L, Smits, G, Katz, B, Sahel, J-A, Vignal, C, Hage, R, Catarino, CB, Priglinger, C, Priglinger, S, Thurau, S, von Livonius, B, Muth, D, Wolf, A, Al-Tamami, J, Pressler, A, Schertler, C, Hildebrandt, M, Neuenhahn, M, Heilweil, G, Tsui, I, Hubbard, GB, Hendrick, A, Dattilo, M, Peragallo, J, Hawy, E, DuBois, Med L, Gibbs, D, Filho, AF, Dobbs, J, Carbonelli, M, Di Vito, L, Contin, M, Mohamed, S, La Morgia, C, Silvestri, S, Acheson, J, Eleftheriadou, M, Esposti, S, Gemenetzi, M, Leitch-Devlin, L, Tucker, WR, Jurkute, N, SantaMaria, M, Tollis, H, Haller, JA, Massini, M.

المساهمون: Newman, NJ, Yu-Wai-Man, P, Carelli, V, Moster, ML, Biousse, V, Vignal-Clermont, C, Sergott, RC, Klopstock, T, Sadun, AA, Barboni, P, DeBusk, AA, Girmens, JF, Rudolph, G, Karanjia, R, Taiel, M, Blouin, L, Smits, G, Katz, B, Sahel, J-A, Vignal, C, Hage, R, Catarino, CB, Priglinger, C, Priglinger, S, Thurau, S, von Livonius, B, Muth, D, Wolf, A, Al-Tamami, J, Pressler, A, Schertler, C, Hildebrandt, M, Neuenhahn, M, Heilweil, G, Tsui, I, Hubbard, GB, Hendrick, A, Dattilo, M, Peragallo, J, Hawy, E, DuBois, Med L, Gibbs, D, Filho, AF, Dobbs, J, Carbonelli, M, Di Vito, L, Contin, M, Mohamed, S, La Morgia, C, Silvestri, S, Acheson, J, Eleftheriadou, M, Esposti, S, Gemenetzi, M, Leitch-Devlin, L, Tucker, WR, Jurkute, N, SantaMaria, M, Tollis, H, Haller, JA, Massini, M.

مصطلحات موضوعية: best-corrected visual acuity, bilateral visual improvement, contrast sensitivity, efficacy, Humphrey visual field perimetry, intravitreal gene therapy, Leber Hereditary Optic Neuropathy, Phase 3 randomized double-masked clinical trial, Quality of life, retinal anatomic measure, safety, Adolescent, Adult, Aged, DNA, Mitochondrial, Dependoviru, Double-Blind Method, Electroretinography, Female, Follow-Up Studie, Genetic Vector, Human, Intravitreal Injection, Male, Middle Aged, Mutation, Optic Atrophy, Hereditary, Leber

وصف الملف: STAMPA

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/33451738; info:eu-repo/semantics/altIdentifier/wos/WOS:000642151600003; volume:128; issue:5; firstpage:649; lastpage:660; numberofpages:12; journal:OPHTHALMOLOGY; https://hdl.handle.net/11585/864738Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85099580418; https://www.sciencedirect.com/science/article/pii/S0161642020311878?via=ihubTest

الإتاحة: https://doi.org/10.1016/j.ophtha.2020.12.012Test
https://hdl.handle.net/11585/864738Test
https://www.sciencedirect.com/science/article/pii/S0161642020311878?via=ihubTest

المؤلفون: Yu-Wai-Man P., Newman N. J., Carelli V., Moster M. L., Biousse V., Sadun A. A., Klopstock T., Vignal-Clermont C., Sergott R. C., Rudolph G., la Morgia C., Karanjia R., Taiel M., Blouin L., Burguiere P., Smits G., Chevalier C., Masonson H., Salermo Y., Katz B., Picaud S., Calkins D. J., Sahel J. -A.

المساهمون: Yu-Wai-Man P., Newman N.J., Carelli V., Moster M.L., Biousse V., Sadun A.A., Klopstock T., Vignal-Clermont C., Sergott R.C., Rudolph G., la Morgia C., Karanjia R., Taiel M., Blouin L., Burguiere P., Smits G., Chevalier C., Masonson H., Salermo Y., Katz B., Picaud S., Calkins D.J., Sahel J.-A.

مصطلحات موضوعية: gene therapy, LHON, Leber's hereditary optic neuropathy, visual improvement

وصف الملف: ELETTRONICO

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/33298565; info:eu-repo/semantics/altIdentifier/wos/WOS:000597340700002; volume:12; issue:573; firstpage:1; lastpage:10; numberofpages:10; journal:SCIENCE TRANSLATIONAL MEDICINE; https://hdl.handle.net/11585/794045Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85095991918

الإتاحة: https://doi.org/10.1126/scitranslmed.aaz7423Test
https://hdl.handle.net/11585/794045Test

المؤلفون: Newman, NJ, Yu-Wai-Man, P, Carelli, V, Biousse, V, Moster, ML, Vignal-Clermont, C, Sergott, RC, Klopstock, T, Sadun, AA, Girmens, JF, La Morgia, C, DeBusk, AA, Jurkute, N, Priglinger, C, Karanjia, R, Josse, C, Salzmann, J, Montestruc, F, Roux, M, Taiel, M, Sahel, JA

المصدر: Frontiers in Neurology , 12 , Article 662838. (2021)

وصف الملف: text

العلاقة: https://discovery.ucl.ac.uk/id/eprint/10130004/1/Jurkute_Intravitreal%20Gene%20Therapy%20vs.%20Natural%20History%20in%20Patients%20With%20Leber%20Hereditary%20Optic%20Neuropathy%20Carrying%20the%20m.11778G%3EA%20ND4%20Mutation_VoR.pdfTest; https://discovery.ucl.ac.uk/id/eprint/10130004Test/

الإتاحة: https://discovery.ucl.ac.uk/id/eprint/10130004/1/Jurkute_Intravitreal%20Gene%20Therapy%20vs.%20Natural%20History%20in%20Patients%20With%20Leber%20Hereditary%20Optic%20Neuropathy%20Carrying%20the%20m.11778G%3EA%20ND4%20Mutation_VoR.pdfTest
https://discovery.ucl.ac.uk/id/eprint/10130004Test/