المؤلفون: Eckmann-Hansen, Christina, Bek, Toke, Sander, Birgit, Larsen, Michael

المصدر: Eckmann-Hansen , C , Bek , T , Sander , B & Larsen , M 2023 , ' Visual Function and Inner Retinal Structure in Relation to Birth Factors in Autosomal Dominant Optic Atrophy ' , Investigative Ophthalmology & Visual Science , vol. 64 , no. 10 , 32 . https://doi.org/10.1167/iovs.64.10.32

مصطلحات موضوعية: autosomal dominant optic atrophy (ADOA), inner retinal morphology, visual development, Humans, Child, Preschool, Retina, Visual Acuity, Retinal Ganglion Cells, Birth Weight, Optic Atrophy, Autosomal Dominant/genetics, Tomography, Optical Coherence/methods, GTP Phosphohydrolases/genetics, Infant, Newborn

Relation: https://pure.au.dk/portal/en/publications/b9bcf144-63e7-4187-aeb6-a45ad4fc4856

الاتاحة: https://pure.au.dk/portal/en/publications/b9bcf144-63e7-4187-aeb6-a45ad4fc4856
https://doi.org/10.1167/iovs.64.10.32
http://www.scopus.com/inward/record.url?scp=85165934539&partnerID=8YFLogxK

المؤلفون: Zeviani M., Carelli V.

المساهمون: Zeviani M., Carelli V.

مصطلحات موضوعية: Ataxia and retinitis pigmentosa (NARP), Autosomal dominant optic atrophy (ADOA), Kearns-Sayre syndrome, Leber’s hereditary optic neuropathy (LHON), Mitochondrial disorder, Mitochondrial DNA, MtDNA heteroplasmic deletion, Neurogenic muscle weakne, Optic atrophy, Retina, Retinitis pigmentosa, Animal, DNA, Mitochondrial, Human, Mitochondria, Mitochondrial Disease, Hereditary, Leber, Retinal Diseases

وصف الملف: ELETTRONICO

Relation: info:eu-repo/semantics/altIdentifier/pmid/35008635; info:eu-repo/semantics/altIdentifier/wos/WOS:000741736600001; volume:23; issue:1; firstpage:1; lastpage:33; numberofpages:33; journal:INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES; http://hdl.handle.net/11585/864469; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85121582783; https://doi.org/10.3390/ijms23010210

الاتاحة: http://hdl.handle.net/11585/864469
https://doi.org/10.3390/ijms23010210

المؤلفون: FORMICHI, PATRIZIA, RADI, ELENA, GALLUS, GIAN NICOLA, BRUNETTI, JLENIA, BATTISTI, CARLA, RUFA, ALESSANDRA, DOTTI, MARIA, FRANCESCHINI, ROSSELLA, BRACCI, LUISA, FEDERICO, ANTONIO, Giorgi, Eleonora

المساهمون: Formichi, Patrizia, Radi, Elena, Giorgi, Eleonora, Gallus, GIAN NICOLA, Brunetti, Jlenia, Battisti, Carla, Rufa, Alessandra, Dotti, Maria, Franceschini, Rossella, Bracci, Luisa, Federico, Antonio

مصطلحات موضوعية: 2-Deoxy-D-ribose (dRib), Apoptosi, Autosomal dominant optic atrophy (ADOA), Caspase 3, OPA1, Peripheral blood lymphocytes (PBLs)

Relation: info:eu-repo/semantics/altIdentifier/pmid/25796301; info:eu-repo/semantics/altIdentifier/wos/WOS:000353738200018; volume:351; issue:1-2; firstpage:99-108; lastpage:108; journal:JOURNAL OF THE NEUROLOGICAL SCIENCES; http://hdl.handle.net/11365/976816; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-84924897905; http://www.sciencedirect.com/science/article/pii/S0022510X15001276

الاتاحة: http://hdl.handle.net/11365/976816
https://doi.org/10.1016/j.jns.2015.02.047
http://www.sciencedirect.com/science/article/pii/S0022510X15001276

المؤلفون: Antonio Federico, Eleonora Giorgi, Elena Radi, Patrizia Formichi, Carla Battisti, Jlenia Brunetti, Maria Teresa Dotti, Luisa Bracci, Alessandra Rufa, Gian Nicola Gallus, Rossella Franceschini

مصطلحات موضوعية: Adult, Male, Autosomal dominant optic atrophy (ADOA), Apoptosis, Mitochondrion, Biology, Retinal ganglion, OPA1, GTP Phosphohydrolases, Optic neuropathy, Optic Atrophy, Autosomal Dominant, medicine, Humans, Protein Isoforms, Inner mitochondrial membrane, Aged, 2-Deoxy-D-ribose (dRib), Caspase 3, Middle Aged, medicine.disease, eye diseases, Peripheral blood lymphocytes (PBLs), Pedigree, Cell biology, Neurology, Biochemistry, mitochondrial fusion, Mutation, Optic nerve, Optic Atrophy 1, Female, Neurology (clinical)

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::13923f31f29c1676fe99575c40f42e89
http://hdl.handle.net/11365/976816

المؤلفون: Rumery, Travis, Kardon, Randy

المساهمون: Kathleen Digre, MD, Lanning Kline, MD

المصدر: 2010 North American Neuro-Ophthalmology Society Annual Meeting

مصطلحات موضوعية: Autosomal Dominant Optic Atrophy (ADOA), Non-arteritic Anterior Ischemic Optic Neuropathy (NAION), Optic Nerve Hypoplasia (ONH), Macula OCT, Retinal Layers

وصف الملف: application/pdf

Relation: NANOS 2010: Poster Presentations; Neuro-ophthalmology Virtual Education Library: NOVEL http://NOVEL.utah.edu; 20100309_nanos_posters_027.pdf; https://collections.lib.utah.edu/ark:/87278/s6mw5pf2

الاتاحة: https://collections.lib.utah.edu/ark:/87278/s6mw5pf2