المؤلفون: Tiffany J. Hwang, Solange Rios Salomão, Rubens Belfort, Alfredo A. Sadun, Jesse Gale, Rustum Karanjia, Adriana Berezovsky, Jeffrey Tran, Piero Barboni, Federico Sadun, Peter A. Quiros, Carlos Filipe Chicani, Carolina do V. F. Ramos, Valerio Carelli, Chiara La Morgia, Edward R. Chu, Milton N. Moraes-Filho, M. N. Moraes, A.M. DeNegri

المصدر: Ophthalmology. 124:843-850

مصطلحات موضوعية: medicine.medical_specialty, Visual acuity, genetic structures, Nerve fiber layer, Optic neuropathy, 03 medical and health sciences, chemistry.chemical_compound, Quadrant (abdomen), 0302 clinical medicine, Ophthalmology, Medicine, Prospective cohort study, business.industry, Leber's hereditary optic neuropathy, Retinal, medicine.disease, eye diseases, medicine.anatomical_structure, chemistry, Decreased Visual Acuity, 030221 ophthalmology & optometry, Optometry, sense organs, medicine.symptom, business, 030217 neurology & neurosurgery

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::51f680c10a99c14566218409b2c3676e
https://doi.org/10.1016/j.ophtha.2017.01.002

المؤلفون: Nivea Nunes Cavascan, Milton N. Moraes-Filho, Kirsten Anderson, M. N. Moraes, Rustum Karanjia, Carolina do V. F. Ramos, Adriana Berezovsky, Stuart G Coupland, Solange Rios Salomão, Rubens Belfort, Alfredo A. Sadun, Jeffrey Tran, A.M. DeNegri, Federico Sadun, H. Liu, Samir Nazarali, Sung EunSong Watanabe, Paula Yuri Sacai, Valerio Carelli, Chiara La Morgia, Piero Barboni

المساهمون: Karanjia, Rustum, Berezovsky, Adriana, Sacai, Paula Yuri, Cavascan, Nivea Nune, Liu, Henry Yuheng, Nazarali, Samir, Moraes filho, Milton Nune, Anderson, Kirsten, Tran, Jeffrey Show, Watanabe, Sung Eunsong, Moraes, Milton Nune, Sadun, Federico, Denegri, Anna Maria, Barboni, Piero, Do Val Ferreira Ramos, Carolina, LA MORGIA, Chiara, Carelli, Valerio, Belfort, Ruben, Coupland, Stuart Glenn, Salomao, Solange Rio, Sadun, Alfredo A.

مصطلحات موضوعية: Retinal Ganglion Cells, Adult, Male, medicine.medical_specialty, Heterozygote, genetic structures, DNA Mutational Analysis, Visual Acuity, Visual Field, Retinal Ganglion Cell, Optic Atrophy, Hereditary, Leber, DNA, Mitochondrial, Optic neuropathy, DNA Mutational Analysi, 03 medical and health sciences, Cellular and Molecular Neuroscience, Nerve Fibers, 0302 clinical medicine, Ophthalmology, medicine, Electroretinography, Humans, In patient, Subclinical infection, medicine.diagnostic_test, Color Vision, business.industry, Leber's hereditary optic neuropathy, Middle Aged, medicine.disease, eye diseases, medicine.anatomical_structure, Retinal ganglion cell, Negative response, Nerve Fiber, 030221 ophthalmology & optometry, Female, sense organs, Visual Fields, business, Sensory System, 030217 neurology & neurosurgery, Photic Stimulation, Photopic vision, Human

وصف الملف: STAMPA

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::813b6961178e90d9840046b27e75a2eb
http://hdl.handle.net/11585/610065

المؤلفون: M. N. Moraes, Ruwan A. Silva, Nanna Dahl Rendtorff, Valerio Carelli, Adriana Berezovsky, Marianne Lodahl, Thomas A. Albini, Rubens Belfort, Alfredo A. Sadun, Milton N. Moraes-Filho, Neil R. Miller, Solange Rios Salomão, Fred N. Ross-Cisneros, Lisbeth Tranebjærg, Billy X. Pan

المساهمون: F. N. Ross-Cisnero, B. X. Pan, R. A. Silva, N. R. Miller, T. A. Albini, L. Tranebjaerg, N. D. Rendtorff, M. Lodahl, M. N. Moraes-Filho, M. N. Morae, S. R. Salomao, A. Berezovsky, R. Belfort, V. Carelli, A. A. Sadun

المصدر: Mitochondrion. 13(6)

مصطلحات موضوعية: Adult, Male, Pathology, medicine.medical_specialty, genetic structures, Wolfram syndrome, Axonal loss, Adult, Axons, Humans, Male, Membrane Protein, Retinal ganglion, Optic neuropathy, medicine, pathology, Wolfram Syndrome, Humans, Molecular Biology, genetics, Mutation, Optic Nerve, Retina, business.industry, Membrane Proteins, Optic Nerve, Wolfram Syndrome, Cell Biology, Anatomy, medicine.disease, eye diseases, Axons, medicine.anatomical_structure, Retinal ganglion cell, Mutation, Optic nerve, Molecular Medicine, pathology, sense organs, Mitochondrial optic neuropathies, business

وصف الملف: STAMPA

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::59df099cb94ac771d7277230aad7e038
https://pubmed.ncbi.nlm.nih.gov/23748048

المؤلفون: Pasquale Montagna, M. N. Moraes, Gaetano Cantalupo, Elisa Sancisi, Poul Kjer, Piero Barboni, Vilma Mantovani, Alfredo A. Sadun, D. Milea, Alessandra Munarini, Steffen Heegaard, Valerio Carelli, Chiara La Morgia, Milton N. Moraes-Filho, Jens Hannibal, Fred N. Ross-Cisneros, Solange Rios Salomão, Kevin R. Tozer

المساهمون: La Morgia C., Ross-Cisneros F.N., Sadun A.A., Hannibal J., Munarini A., Mantovani V., Barboni P., Cantalupo G., Tozer K.R., Sancisi E., Salomao S.R., Moraes M.N., Moraes-Filho M.N., Heegaard S., Milea D., Kjer P., Montagna P., Carelli V.

مصطلحات موضوعية: Adult, Male, Retinal Ganglion Cells, Melanopsin, Circadian rhythms, Neuro-ophthalmology, Mitochondrial disease, Leber Hereditary Optic Neuropathy (LHON), Dominant Optic Atrophy (DOA), Neuropathology, Aging, Mitochondrial Diseases, genetic structures, Hypothalamus, Giant retinal ganglion cells, Optic Atrophy, Hereditary, Leber, Biology, Retinal ganglion, Retina, Optic neuropathy, Optic Atrophy, Autosomal Dominant, medicine, Humans, Visual Pathways, Aged, 80 and over, Intrinsically photosensitive retinal ganglion cells, Rod Opsins, Original Articles, Middle Aged, medicine.disease, eye diseases, medicine.anatomical_structure, Case-Control Studies, Nerve Degeneration, Female, sense organs, Neurology (clinical), Mitochondrial optic neuropathies, Neuroscience, Retinohypothalamic tract

وصف الملف: ELETTRONICO

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d7fb1ea53220ca681386043f83b1e3b7
http://hdl.handle.net/11562/429963

المؤلفون: M N Moraes, S Cronemberger, P C Lana, I D Castro, N Calixto

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::954efc541179c7b41098d3e95a51c226

المؤلفون: Adriana Berezovsky, Solange Rios Salomão, Fred N. Ross-Cisneros, M. N. Moraes, Rubens Belfort, Alfredo A. Sadun, Kelly S. Rue, Valerio Carelli, Milton N. Moraes-Filho, Billy X. Pan

المساهمون: B. X. Pan, F. N. Ross-Cisnero, V. Carelli, K. S. Rue, S. R. Salomao, M. N. Moraes-Filho, M. N. Morae, A. Berezovsky, R. Belfort, A. A. Sadun

المصدر: Investigative Opthalmology & Visual Science. 53:7608

مصطلحات موضوعية: Male, Retinal Ganglion Cells, congenital, hereditary, and neonatal diseases and abnormalities, medicine.medical_specialty, genetic structures, Mitochondrial disease, pathology, Optic Nerve, Nerve fiber layer, Axonal loss, Optic Atrophy, Hereditary, Leber, Optic neuropathy, Ophthalmology, Humans, Medicine, Aged, Leber, business.industry, Leber's hereditary optic neuropathy, Optic Nerve, Articles, Anatomy, Middle Aged, Models, Theoretical, pathology, Disease Progression, Female, Humans, Male, Mathematics, Middle Aged, Model, medicine.disease, Axons, eye diseases, Hereditary, medicine.anatomical_structure, Optical Coherence, Disease Progression, Optic nerve, Female, pathology, Retinal Ganglion Cell, sense organs, pathology, Tomography, Mitochondrial optic neuropathies, business, Mathematics, Tomography, Optical Coherence, Optic nerve disorder, Aged, Axon, Theoretical, Optic Atrophy

وصف الملف: ELETTRONICO

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::606236a271d29184edcb8d8fec8de45e
https://doi.org/10.1167/iovs.12-10452