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INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, ISSN 0146-0404, 04/2019, Volume 60, Issue 5, pp. 1491 - 1500
PURPOSE. To provide a histopathologic, morphometric analysis of the retina in Alzheimer's disease (AD). METHODS. Human postmortem retinas from eight patients... 
retinal biomarkers | NERVE-FIBER LAYER | VISUAL IMPAIRMENT | histopathology | GANGLION-CELL LOSS | MODEL | MILD COGNITIVE IMPAIRMENT | DEGENERATION | OPHTHALMOLOGY | morphometric analysis | Alzheimer's disease | THICKNESS | LIFE | Index Medicus
Journal Article
Alzheimer's & Dementia: The Journal of the Alzheimer's Association, ISSN 1552-5260, 07/2018, Volume 14, Issue 7, pp. P731 - P732
Journal Article
Alzheimer's & Dementia: The Journal of the Alzheimer's Association, ISSN 1552-5260, 07/2018, Volume 14, Issue 7, pp. P1456 - P1456
Journal Article
Alzheimer's & Dementia: The Journal of the Alzheimer's Association, ISSN 1552-5260, 07/2018, Volume 14, Issue 7, pp. P214 - P215
Journal Article
Alzheimer's & Dementia: The Journal of the Alzheimer's Association, ISSN 1552-5260, 07/2018, Volume 14, Issue 7, pp. P317 - P317
Journal Article
Alzheimer's & Dementia: The Journal of the Alzheimer's Association, ISSN 1552-5260, 07/2018, Volume 14, Issue 7, pp. P1123 - P1123
Journal Article
Canadian Journal of Ophthalmology/Journal canadien d'ophtalmologie, ISSN 0008-4182, 02/2019, Volume 54, Issue 1, pp. e27 - e30
Journal Article
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 12/2012, Volume 109, Issue 49, pp. 20065 - 20070
An animal model of Leber hereditary optic neuropathy (LHON) was produced by introducing the human optic atrophy mtDNA ND6 P25L mutation into the mouse. Mice... 
Axons | Mitochondria | Optic atrophy | Optic nerve | Leber hereditary optic atrophy | Cell lines | Mitochondrial DNA | Biochemistry | Synaptosomes | Genetic mutation | Neurodegenerative disease | Ophthalmology | Oxidative phosphorylation | Maternal inheritance | LIFE-SPAN | neurodegenerative disease | MULTIDISCIPLINARY SCIENCES | MITOCHONDRIAL-DNA MUTATION | CELL LINES | maternal inheritance | oxidative phosphorylation | GLUTAMATE TRANSPORT | ENCEPHALOPATHY | RESPIRATORY COMPLEX I | ophthalmology | MICE | CYBRIDS | DYSFUNCTION | SUPEROXIDE-DISMUTASE | Electroretinography | Optic Nerve - pathology | Optic Atrophy, Hereditary, Leber - complications | Reactive Oxygen Species - metabolism | Age Factors | Humans | Oxidative Stress - physiology | Immunoblotting | NADH Dehydrogenase - genetics | Optic Atrophy, Hereditary, Leber - genetics | Synaptosomes - metabolism | Mutation, Missense - genetics | Animals | DNA, Mitochondrial - genetics | Adenosine Triphosphate - metabolism | Demyelinating Diseases - etiology | Mice | Demyelinating Diseases - pathology | Optic Atrophy, Hereditary, Leber - physiopathology | Retina - pathology | Disease Models, Animal | Development and progression | Genetic aspects | Gene mutations | Health aspects | Oxidative stress | Rodents | Retina | Mutation | Adenosine triphosphatase | Index Medicus | Biological Sciences
Journal Article
Brain, ISSN 0006-8950, 01/2011, Volume 134, Issue 1, pp. 220 - 234
Journal Article
Brain, ISSN 0006-8950, 08/2010, Volume 133, Issue 8, pp. 2426 - 2438
Journal Article
Brain, ISSN 0006-8950, 2014, Volume 137, Issue 2, pp. 335 - 353
Journal Article
Frontiers in Neurology, ISSN 1664-2295, 05/2017, Volume 8
There is increasing awareness on the role played by circadian rhythm abnormalities in neurodegenerative disorders such as Alzheimer’s disease (AD) and... 
melanopsin | retinal ganglion cells | Alzheimer’s disease | circadian rhythms | optic nerve | Parkinson’s disease
Journal Article
Journal Article