المؤلفون: Kutluer M., Huang L., Marigo V.

المساهمون: Kutluer, M., Huang, L., Marigo, V.

مصطلحات موضوعية: achromatopsia, calcium, calpain, calpastatin, congenital stationary night blindne, Leber's congenital amaurosi, retinitis pigmentosa, stargardt disease

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/32246618; info:eu-repo/semantics/altIdentifier/wos/WOS:000526946300002; volume:15; issue:10; firstpage:1784; lastpage:1791; journal:NEURAL REGENERATION RESEARCH; info:eu-repo/grantAgreement/EC/H2020/MSCA-ITN-2017-765441; http://hdl.handle.net/11380/1201647Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85083250691

الإتاحة: https://doi.org/10.4103/1673-5374.280303Test
http://hdl.handle.net/11380/1201647Test

المؤلفون: Testa, Francesco, Maguire, Albert M, Rossi, Settimio, Marshall, Kathleen, AURICCHIO, ALBERTO, MELILLO, PAOLO, Bennett, Jean, SIMONELLI, FRANCESCA

المساهمون: Testa, Francesco, Maguire, Albert M, Rossi, Settimio, Marshall, Kathleen, Auricchio, Alberto, Melillo, Paolo, Bennett, Jean, Simonelli, Francesca

مصطلحات موضوعية: Binocular computerized visual field, Gene therapy, Leber’s Congenital Amaurosi, Microperimetry, Optical coherence tomography, Biochemistry, Genetics and Molecular Biology (all), Medicine (all)

العلاقة: info:eu-repo/semantics/altIdentifier/wos/WOS:000369715400071; ispartofbook:ADV EXP MED BIOL; volume:854; firstpage:533; lastpage:539; numberofpages:7; http://hdl.handle.net/11588/623788Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-84943327793; http://www.springer.com/series/5584Test

الإتاحة: https://doi.org/10.1007/978-3-319-17121-0_71Test
http://hdl.handle.net/11588/623788Test
http://www.springer.com/series/5584Test

المؤلفون: Kathleen A. Marshall, Albert M. Maguire, Alberto Auricchio, Settimio Rossi, Paolo Melillo, Francesco Testa, Jean Bennett, Francesca Simonelli

المساهمون: Testa F, Maguire AM, Rossi S, Marshall K, Auricchio A, Melillo P, Bennett J.b , Simonelli F., Testa, Francesco, Maguire, Albert M, Rossi, Settimio, Marshall, Kathleen, Auricchio, Alberto, Melillo, Paolo, Bennett, Jean, Simonelli, Francesca

المصدر: Retinal Degenerative Diseases ISBN: 9783319171203

مصطلحات موضوعية: 0301 basic medicine, Retinal degeneration, medicine.medical_specialty, Visual acuity, genetic structures, Microperimetry, Leber’s Congenital Amaurosi, 03 medical and health sciences, 0302 clinical medicine, Gene therapy, Ophthalmology, Medicine, Biochemistry, Genetics and Molecular Biology (all), Optical coherence tomography, business.industry, Medicine (all), medicine.disease, eye diseases, Visual field, Clinical trial, 030104 developmental biology, Cis-trans-Isomerases, 030221 ophthalmology & optometry, Optometry, Leber's congenital amaurosis, medicine.symptom, business, Binocular vision, Binocular computerized visual field

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a84191443e72386ed71bc83c7ff647f4Test
http://hdl.handle.net/11591/355132Test

المؤلفون: Maguire AM, High KA, Auricchio A, Wright JF, Pierce EA, TESTA, Francesco, Mingozzi F, Bennicelli JL, Ying GS, ROSSI, Settimio, Fulton A, Marshall KA, BANFI, Sandro, Chung DC, Morgan, JI, Hauck B, Zelenaia O, Zhu X, Raffini L, Coppieters F, De Baere E, Shindler KS, Volpe NJ, Surace EM, Acerra C, Lyubarsky A, Redmond TM, Stone E, Sun J, Mcdonnell JW, Leroy BP, SIMONELLI, Francesca, Bennett J.

المساهمون: Maguire, Am, High, Ka, Auricchio, A, Wright, Jf, Pierce, Ea, Testa, Francesco, Mingozzi, F, Bennicelli, Jl, Ying, G, Rossi, Settimio, Fulton, A, Marshall, Ka, Banfi, Sandro, Chung, Dc, Morgan, Ji, Hauck, B, Zelenaia, O, Zhu, X, Raffini, L, Coppieters, F, De Baere, E, Shindler, K, Volpe, Nj, Surace, Em, Acerra, C, Lyubarsky, A, Redmond, Tm, Stone, E, Sun, J, Mcdonnell, Jw, Leroy, Bp, Simonelli, Francesca, Bennett, J.

مصطلحات موضوعية: RPE65 gene, Leber’s congenital amaurosi, gene therapy

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/19854499; info:eu-repo/semantics/altIdentifier/wos/WOS:000271674600033; volume:374; issue:9701; firstpage:1597; lastpage:1605; numberofpages:9; journal:THE LANCET; http://hdl.handle.net/11591/181549Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-70350620424; http://www.journals.elsevier.com/the-lancetTest/

الإتاحة: https://doi.org/10.1016/S0140-6736Test(09)61836-5
http://hdl.handle.net/11591/181549Test
http://www.journals.elsevier.com/the-lancetTest/

المؤلفون: Jean Bennett, Jessica I. W. Morgan, Carmela Acerra, Kathleen A. Marshall, Katherine A. High, Daniel C. Chung, Xiaosong Zhu, Alberto Auricchio, Enrico Maria Surace, Bernd Hauck, Frauke Coppieters, Gui-Shuang Ying, Albert M. Maguire, Kenneth S. Shindler, Sandro Banfi, Jenni Fer Uvellman Mcdonnell, Nicholas J. Volpe, Arkady Lyubarsky, Ann Fulton, Leslie Raffini, Eric A. Pierce, Elfride De Baere, Olga Zelenaia, Jeannette L. Bennicelli, J. Fraser Wright, Francesco Testa, T. Michael Redmond, Junwei Sun, Edwin M. Stone, Federico Mingozzi, Francesca Simonelli, Bart P. Leroy, Settimio Rossi

المساهمون: Maguire, Am, High, Ka, Auricchio, A, Wright, Jf, Pierce, Ea, Testa, Francesco, Mingozzi, F, Bennicelli, Jl, Ying, G, Rossi, Settimio, Fulton, A, Marshall, Ka, Banfi, Sandro, Chung, Dc, Morgan, Ji, Hauck, B, Zelenaia, O, Zhu, X, Raffini, L, Coppieters, F, De Baere, E, Shindler, K, Volpe, Nj, Surace, Em, Acerra, C, Lyubarsky, A, Redmond, Tm, Stone, E, Sun, J, Mcdonnell, Jw, Leroy, Bp, Simonelli, Francesca, Bennett, J., Auricchio, Alberto, Testa, F, Rossi, S, Banfi, S, Surace, Enrico Maria, Simonelli, F

المصدر: Lancet (London, England). 374(9701)

مصطلحات موضوعية: Retinal degeneration, Male, Visual acuity, genetic structures, Visual Acuity, Blindness, chemistry.chemical_compound, Mice, Medicine, Child, media_common, Age Factors, General Medicine, Dependovirus, gene therapy, Leber’s congenital amaurosi, Treatment Outcome, Disease Progression, Leber's congenital amaurosis, Female, medicine.symptom, Safety, Retinopathy, Adult, cis-trans-Isomerases, medicine.medical_specialty, Adolescent, Genetic Vectors, Dark Adaptation, Optic Atrophy, Hereditary, Leber, Article, Injections, Young Adult, Nystagmus, Physiologic, Ophthalmology, Electroretinography, media_common.cataloged_instance, Animals, Humans, European union, Eye Proteins, Dose-Response Relationship, Drug, business.industry, Infant, Newborn, Retinal, Genetic Therapy, medicine.disease, eye diseases, Disease Models, Animal, RPE65 gene, RPE65, chemistry, Cis-trans-Isomerases, Mutation, business, Carrier Proteins

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::83e3ef7f273825996ee1f6bcdf200da5Test
https://pubmed.ncbi.nlm.nih.gov/19854500Test

المؤلفون: Uggetti, C, Egitto, Mg, Pichiecchio, A, Zappoli, F, FAZZI, Elisa Maria, SIGNORINI, SARA, LANZI, Gaetana

المساهمون: Uggetti, C, Fazzi, Elisa Maria, Signorini, Sara, Egitto, Mg, Pichiecchio, A, Zappoli, F, Lanzi, Gaetana

مصطلحات موضوعية: Leber's congenital amaurosi, retinal dystrophy, magnetic resonance imaging

العلاقة: info:eu-repo/semantics/altIdentifier/wos/WOS:000186177400028; volume:16; issue:3; firstpage:481; lastpage:483; numberofpages:3; journal:RIVISTA DI NEURORADIOLOGIA; http://hdl.handle.net/11379/482657Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-0141960954

الإتاحة: http://hdl.handle.net/11379/482657Test