المساهمون: Jae Won Jun, Yuri Seo, Sueng-Han Han, Jinu Han, Seo, Yuri

مصطلحات موضوعية: Adult, Child, Preschool, DNA, Mitochondrial / genetics, DNA-Binding Proteins / genetics, Exome Sequencing, Humans, Male, Mitochondrial Proteins / genetics, Optic Atrophy* / genetics, Optic Atrophy, Autosomal Dominant* / pathology, Retinal Degeneration* / diagnosis, Retinal Degeneration* / genetics, Retrospective Studies, SSBP1, dominant optic atrophy, genome sequencing, incomplete penetrance, inherited optic neuropathy

Relation: OPHTHALMIC GENETICS; J03734; OAK-2023-02214; OAK-2023-02215; OAK-2023-02216; https://ir.ymlib.yonsei.ac.kr/handle/22282913/195926; T202304062; OPHTHALMIC GENETICS, Vol.44(3) : 286-290, 2023-06

الاتاحة: https://ir.ymlib.yonsei.ac.kr/handle/22282913/195926
https://doi.org/10.1080/13816810.2022.2109685
https://www.tandfonline.com/doi/full/10.1080/13816810.2022.2109685

المؤلفون: Vassallo, James

مصطلحات موضوعية: Retinal degeneration -- Case studies, Retinal degeneration -- Diagnosis

Relation: Vassallo, J. (2019). Benign familial fleck retina with foveal involvement. Malta Medical Journal, 31(2), 33-34.; https://www.um.edu.mt/library/oar/handle/123456789/49482

الاتاحة: https://www.um.edu.mt/library/oar/handle/123456789/49482

المؤلفون: Santos, Ana Rita, Ribeiro, Luisa, Bandello, Francesco, Lattanzio, Rosangela, Egan, Catherine, Frydkjaer-Olsen, Ulrik, García-Arumí, José, Gibson, Jonathan, Grauslund, Jakob, Harding, Simon P, Lang, Gabriele E, Massin, Pascale, Midena, Edoardo, Scanlon, Peter, Aldington Hnd, Stephen J, Simão, Sílvia, Schwartz, Christian, Ponsati, Berta, Porta, Massimo, Costa, Miguel Ângelo, Hernández, Cristina, Cunha-Vaz, José, Simó, Rafael

المصدر: Santos , A R , Ribeiro , L , Bandello , F , Lattanzio , R , Egan , C , Frydkjaer-Olsen , U , García-Arumí , J , Gibson , J , Grauslund , J , Harding , S P , Lang , G E , Massin , P , Midena , E , Scanlon , P , Aldington Hnd , S J , Simão , S , Schwartz , C , Ponsati , B , Porta , M , Costa , M Â , Hernández , C , Cunha-Vaz , J , Simó , R & European ....

مصطلحات موضوعية: Journal Article, Electroretinography, Cross-Sectional Studies, Retinal Neurons/pathology, Humans, Middle Aged, Retinal Vessels/pathology, Male, Diabetes Mellitus, Type 2/complications, Retinal Degeneration/diagnosis, Female, Aged, Diabetic Retinopathy/diagnosis

وصف الملف: application/pdf

الاتاحة: https://portal.findresearcher.sdu.dk/da/publications/3da882ae-5c7e-44f2-bf71-ff003b2cbe08
https://doi.org/10.2337/db16-1453
https://findresearcher.sdu.dk/ws/files/141379950/Functional_and_Structural_Findings_of_Neurodegeneration_in_Early_Stages_of_Diabetic_Retinopathy.pdf

المؤلفون: Birtel, J., von Landenberg, C., Gliem, M., Gliem, C., Reimann, J., Kunz, W. S., Herrmann, P., Betz, C., Caswell, R., Nesbitt, V., Kornblum, C., Charbel Issa, P.

مصطلحات موضوعية: Adolescent, Adult, Aged, Electroretinography, Female, Fluorescein Angiography/*methods, Fundus Oculi, Humans, Male, Middle Aged, Mitochondrial Diseases/*diagnosis, Retinal Degeneration/*diagnosis, Retinal Pigment Epithelium/*pathology, Retrospective Studies, Visual Acuity, Young Adult, Autofluorescence, Genetics, Mitochondrial disease, oct, Retinal imaging

Relation: https://linkinghub.elsevier.com/retrieve/pii/S2468-6530(21)00071-3; Ophthalmol Retina. 2022 Jan;6(1):65-79. doi:10.1016/j.oret.2021.02.017. Epub 2021 Jul 10.; https://rde.dspace-express.com/handle/11287/622414; Ophthalmology Retina

الاتاحة: https://doi.org/10.1016/j.oret.2021.02.017
https://rde.dspace-express.com/handle/11287/622414

المساهمون: SUK HO BYEON, SUNG YONG KANG, Kang, Sung Yong, Byeon, Suk Ho

مصطلحات موضوعية: Fourier Analysis, Humans, Pilot Projects, Retina/pathology, Retinal Degeneration/diagnosis, Retinal Pigment Epithelium/pathology, Tomography, Optical Coherence, Visual Acuity

وصف الملف: 185~186

Relation: AMERICAN JOURNAL OF OPHTHALMOLOGY; J00097; OAK-2009-00115; https://ir.ymlib.yonsei.ac.kr/handle/22282913/103455; http://www.sciencedirect.com/science/article/pii/S000293940800706X; T200900181; AMERICAN JOURNAL OF OPHTHALMOLOGY, Vol.147(1) : 185-186, 2009

الاتاحة: https://ir.ymlib.yonsei.ac.kr/handle/22282913/103455
https://doi.org/10.1016/j.ajo.2008.09.009
http://www.sciencedirect.com/science/article/pii/S000293940800706X

المؤلفون: Cem Yildirim, Ibrahim Toprak, Volkan Yaylali

المصدر: Canadian Journal of Ophthalmology. 50:438-441

مصطلحات موضوعية: Aged, Basement Membrane/pathology, Diabetic Retinopathy/*diagnosis, Female, Humans, Male, Middle Aged, Ophthalmoscopes, Retinal Degeneration/*diagnosis, Retinal Photoreceptor Cell Inner Segment/*pathology, Retinal Pigment Epithelium/pathology, Retrospective Studies, Tomography, Optical Coherence, Tonometry, Ocular, Visual Acuity, Retinal degeneration, Visual acuity, visual acuity, genetic structures, clinical evaluation, ex vivo study, photoreceptor inner segment, retrospective study, retinal pigment epithelium, Basement Membrane, chemistry.chemical_compound, computer program, middle aged, External limiting membrane, comparative study, oculoplethysmography, clinical article, adult, Retinal Degeneration, General Medicine, Diabetic retinopathy, cohort analysis, external limiting membrane, female, medicine.anatomical_structure, visual system parameters, medicine.symptom, Photoreceptor inner segment, medicine.medical_specialty, Article, in vivo study, image analysis, Ophthalmology, medicine, controlled study, Retinal Photoreceptor Cell Inner Segment, human, Macular edema, optical coherence tomography, Diabetic Retinopathy, controlled clinical trial, nonproliferative diabetic retinopathy, business.industry, ophthalmoscope, Retinal, clinical assessment, medicine.disease, pigment epithelium, eye diseases, image processing, chemistry, retina degeneration, Optometry, pathology, sense organs, business

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9b8b515c5e87b8e1b6e6dae5288ad865
https://doi.org/10.1016/j.jcjo.2015.07.009

المؤلفون: Jonsson, Karoline Boegeberg, Frydkjaer-Olsen, Ulrik, Grauslund, Jakob

المصدر: Jonsson , K B , Frydkjaer-Olsen , U & Grauslund , J 2016 , ' Vascular Changes and Neurodegeneration in the Early Stages of Diabetic Retinopathy : Which Comes First? ' , Ophthalmic Research , vol. 56 , no. 1 , pp. 1-9 . https://doi.org/10.1159/000444498

مصطلحات موضوعية: Diabetic retinopathy, Multifocal electroretinography, Neurodegeneration, Optical coherence tomography, Vasculopathy, Electroretinography, Humans, Retinal Vessels/pathology, Nerve Fibers/pathology, Retinal Degeneration/diagnosis, Tomography, Optical Coherence/methods, Retinal Ganglion Cells/pathology, Diabetic Retinopathy/complications

Relation: https://portal.findresearcher.sdu.dk/da/publications/28f317ce-8bc7-4f99-9f01-be804e081612

الاتاحة: https://portal.findresearcher.sdu.dk/da/publications/28f317ce-8bc7-4f99-9f01-be804e081612
https://doi.org/10.1159/000444498

المؤلفون: Benedetto Falsini, Anthony G. Robson, Naheed W. Khan, Mineo Kondo

المصدر: Journal of Ophthalmology, Vol 2017 (2017)
Journal of Ophthalmology

مصطلحات موضوعية: 0301 basic medicine, Retinal degeneration, Article Subject, business.industry, Settore MED/30 - MALATTIE APPARATO VISIVO, MEDLINE, Outcome measures, Genetics disease, medicine.disease, Bioinformatics, 03 medical and health sciences, Ophthalmology, Editorial, 030104 developmental biology, 0302 clinical medicine, lcsh:Ophthalmology, lcsh:RE1-994, medicine, retinal degeneration, diagnosis, genetics, business, 030217 neurology & neurosurgery

وصف الملف: text/xhtml

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fdc1055867ae21168e36e0caba1a0410
https://doi.org/10.1155/2017/2109014

المؤلفون: Sunyer Grau, Bernat

المساهمون: Universitat Politècnica de Catalunya. Departament d'Òptica i Optometria, Sánchez Herrero, Eulalia, Gispets Parcerisas, Joan, sánchez herr

مصطلحات موضوعية: Àrees temàtiques de la UPC::Ciències de la visió::Optometria, Retinal degeneration--Diagnosis, Retina--Diseases--Diagnosis, Degeneració macular, Retina -- Malalties -- Diagnòstic

جغرافية الموضوع: east=2.0526060461997986, north=41.556424796922215, name=Hospital, Espanya

Time: name=Hospital, 08227, Barcelona, Espanya

Relation: http://hdl.handle.net/2117/89742

الاتاحة: http://hdl.handle.net/2117/89742

المؤلفون: Vincent, A., Munier, F.L., Vandenhoven, C.C., Wright, T., Westall, C.A., Héon, E.

المصدر: Retina, vol. 32, no. 8, pp. 1643-1651

مصطلحات موضوعية: Adult, Aged, Collagen/genetics, Corneal Dystrophies, Hereditary/diagnosis, Disease Progression, Electrooculography, Electroretinography, Female, Humans, Male, Middle Aged, Optic Atrophy/diagnosis, Pedigree, Phenotype, Retina/physiopathology, Retinal Degeneration/diagnosis, Retinal Degeneration/genetics, Retinal Drusen/diagnosis, Retinal Pigment Epithelium/pathology, Tomography, Optical Coherence, Visual Acuity/physiology, Visual Fields/physiology

Relation: info:eu-repo/semantics/altIdentifier/pmid/22277927; info:eu-repo/semantics/altIdentifier/eissn/1539-2864; https://serval.unil.ch/notice/serval:BIB_7F3F7BC8A534

الاتاحة: https://serval.unil.ch/notice/serval:BIB_7F3F7BC8A534
https://doi.org/10.1097/IAE.0b013e318240a574

المؤلفون: Catherine Cassiman, Thomy de Ravel, Elfride De Baere, Ingele Casteels, Werner Spileers

المساهمون: Clinical sciences, Medical Genetics

مصطلحات موضوعية: Retinal degeneration, Male, Pathology, medicine.medical_specialty, Eye Diseases, Hereditary/diagnosis, genetic structures, Fundus Oculi, DNA Mutational Analysis, Retinal Degeneration/diagnosis, Vision Disorders, Consanguinity, Fundus (eye), Vision Disorders/diagnosis, Retina, Night Blindness/diagnosis, Night Blindness, Pathognomonic, Exons/genetics, Orphan Nuclear Receptors/genetics, medicine, Electroretinography, Humans, Genetics (clinical), medicine.diagnostic_test, business.industry, Retina/abnormalities, Retinal Degeneration, Homozygote, Infant, Eye Diseases, Hereditary, Exons, Orphan Nuclear Receptors, medicine.disease, eye diseases, Visual field, Ophthalmology, Electrophysiology, medicine.anatomical_structure, Phenotype, Codon, Nonsense, Pediatrics, Perinatology and Child Health, sense organs, business

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6e823debed8ee6df45fddc91998185ad
https://biblio.vub.ac.be/vubir/peculiar-fundus-abnormalities-and-pathognomonic-electrophysiological-findings-in-a-14monthold-boy-with-nr2e3-mutations(25a27283-39d8-40a5-8a2d-b47a6698adcd).html

المؤلفون: Mataftsi, A., Schorderet, D.F., Chachoua, L., Boussalah, M., Nouri, M.T., Barthelmes, D., Borruat, F.X., Munier, F.L.

المصدر: Investigative Ophthalmology & Visual Science, vol. 48, no. 11, pp. 5160-5167

مصطلحات موضوعية: Adult, Blindness/congenital, Blindness/diagnosis, Child, Preschool, Chromosome Mapping, Chromosomes, Human, Pair 6/genetics, Consanguinity, DNA Mutational Analysis, Electroretinography, Eye Proteins/genetics, Female, Genes, Duplicate/genetics, Humans, Male, Microsatellite Repeats, Mutation, Myopia/genetics, Nystagmus, Congenital/genetics, Pedigree, Retinal Degeneration/diagnosis, Retinal Degeneration/genetics, Tomography, Optical Coherence, Vision Disorders/genetics

Relation: info:eu-repo/semantics/altIdentifier/pmid/17962469; info:eu-repo/semantics/altIdentifier/pissn/0146-0404; https://serval.unil.ch/notice/serval:BIB_AAFE612770E1

الاتاحة: https://serval.unil.ch/notice/serval:BIB_AAFE612770E1
https://doi.org/10.1167/iovs.06-1013

المؤلفون: Mantel, I., Brantley, M.A., Bellmann, C., Robson, A.G., Holder, G.E., Taylor, A., Anderson, G., Moore, A.T.

المصدر: Klinische Monatsblätter für Augenheilkunde, vol. 221, no. 5, pp. 427-430

مصطلحات موضوعية: Blindness/diagnosis, Blindness/genetics, Child, Chromosome Deletion, Chromosomes, Human, Pair 16, Corneal Dystrophies, Hereditary/diagnosis, Hereditary/genetics, DNA Mutational Analysis, Disease Progression, Electroretinography, Female, Fluorescein Angiography, Homozygote, Humans, Male, Membrane Glycoproteins/genetics, Molecular Chaperones/genetics, Neuronal Ceroid-Lipofuscinoses/diagnosis, Neuronal Ceroid-Lipofuscinoses/genetics, Night Blindness/diagnosis, Night Blindness/genetics, Phenotype, Retinal Degeneration/diagnosis, Retinal Degeneration/genetics

Relation: info:eu-repo/semantics/altIdentifier/pmid/15162299; info:eu-repo/semantics/altIdentifier/pissn/0023-2165; https://serval.unil.ch/notice/serval:BIB_33330

الاتاحة: https://serval.unil.ch/notice/serval:BIB_33330
https://doi.org/10.1055/s-2004-812819

المؤلفون: Gabriel Coscas

Resource Type: eBook.

الموضوعات: Retinal degeneration--Diagnosis, Optical coherence tomography

Categories: MEDICAL / Ophthalmology

المؤلفون: Bernasconi, O.R., Piguet, B.

المصدر: Klinische Monatsblätter für Augenheilkunde, vol. 208, no. 5, pp. 291-293

مصطلحات موضوعية: Adult, Aged, Chromosome Aberrations/genetics, Chromosome Disorders, Corneal Dystrophies, Hereditary/classification, Hereditary/diagnosis, Diagnosis, Differential, Fluorescein Angiography, Genes, Dominant/genetics, Humans, Macula Lutea/pathology, Male, Phenotype, Pigment Epithelium of Eye/pathology, Retinal Degeneration/classification, Retinal Degeneration/diagnosis, Retinal Neovascularization/classification, Retinal Neovascularization/diagnosis, Vitreoretinopathy, Proliferative/classification, Proliferative/diagnosis

Relation: info:eu-repo/semantics/altIdentifier/pmid/8766030; info:eu-repo/semantics/altIdentifier/pissn/0023-2165; https://serval.unil.ch/notice/serval:BIB_5346

الاتاحة: https://serval.unil.ch/notice/serval:BIB_5346
https://doi.org/10.1055/s-2008-1035218

المؤلفون: Sunyer Grau, Bernat

المساهمون: Universitat Politècnica de Catalunya. Departament d'Òptica i Optometria, Sánchez Herrero, Eulalia, Gispets Parcerisas, Joan, sánchez herr

المصدر: Recercat. Dipósit de la Recerca de Catalunya
instname
UPCommons. Portal del coneixement obert de la UPC
Universitat Politècnica de Catalunya (UPC)

مصطلحات موضوعية: Ciències de la visió::Optometria [Àrees temàtiques de la UPC], Retinal degeneration--Diagnosis, Retina -- Malalties -- Diagnòstic, Retina--Diseases--Diagnosis, Degeneració macular

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::e00642a91445f16235cb6d919194815b
http://hdl.handle.net/2117/89742

المؤلفون: Khan, Naheed W, Falsini, Benedetto, Kondo, Mineo, Robson, Anthony G., Falsini, Benedetto (ORCID:0000-0002-3569-4968)

مصطلحات الفهرس: retinal degeneration, diagnosis, genetics, Settore MED/30 - MALATTIE APPARATO VISIVO, info:eu-repo/semantics/article

URL: http://hdl.handle.net/10807/109073
info:eu-repo/semantics/altIdentifier/pmid/29098082
info:eu-repo/semantics/altIdentifier/wos/WOS:000412557700001
volume:2017
issue:N/A
firstpage:N/A
lastpage:N/A
issueyear:N/A
journal:JOURNAL OF OPHTHALMOLOGY

Additional Titles: Comparison of MAIA microperimetry and the Amsler grid in the detection of scotomas and metamorphopsia in patients with macular alteration
Estudio comparativo de la microperimetria mediante MAIA y la rejilla de Amsler en la detección de escotomas y metamorfopsias en individuos con afectación macular

المؤلفون: Universitat Politècnica de Catalunya. Departament d'Òptica i Optometria, Sánchez Herrero, Eulalia, Gispets Parcerisas, Joan, sánchez herr, Sunyer Grau, Bernat

مصطلحات الفهرس: Àrees temàtiques de la UPC::Ciències de la visió::Optometria, Retinal degeneration--Diagnosis, Retina--Diseases--Diagnosis, Degeneració macular, Retina -- Malalties -- Diagnòstic, Bachelor thesis

URL: http://hdl.handle.net/2117/89742