Factor leading to macular dege macular degeneration. Medical search. Frequent questions

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Anatomy26

Retinal Pigment Epithelium Choroid Bruch Membrane Pigment Epithelium of Eye Retina Macula Lutea Fundus Oculi Fovea Centralis Photoreceptor Cells, Vertebrate Exudates and Transudates Cells, Cultured Subretinal Fluid Retinal Photoreceptor Cell Outer Segment Vitreous Body Eye Photoreceptor Cells Intervertebral Disc Retinal Vessels Retinal Cone Photoreceptor Cells Chromosomes, Human, Pair 10 Retinal Rod Photoreceptor Cells Axons Retinal Neurons Retinal Photoreceptor Cell Inner Segment Rod Cell Outer Segment Cell Line

Organisms3

Mice, Inbred C57BL Mice, Transgenic Mice, Knockout

Diseases40

Macular Degeneration Wet Macular Degeneration Choroidal Neovascularization Retinal Drusen Retinal Degeneration Geographic Atrophy Nerve Degeneration Optic Disk Drusen Wallerian Degeneration Choroid Diseases Retinal Neovascularization Intervertebral Disc Degeneration Chronic Disease Scotoma Postoperative Complications Retinal Diseases Eye Diseases Vision Disorders Vision, Low Retinal Detachment Retinal Hemorrhage Disease Models, Animal Blindness Retinitis Pigmentosa Eye Diseases, Hereditary Frontotemporal Lobar Degeneration Cataract Atrophy Genetic Predisposition to Disease Disease Progression Optic Atrophy Retinoschisis Retrograde Degeneration Glaucoma Spinocerebellar Degenerations Diabetic Retinopathy Neovascularization, Pathologic Angiomatosis Retinal Dystrophies Paraneoplastic Cerebellar Degeneration

Chemicals and Drugs38

Complement Factor H Lipofuscin Lutein Angiogenesis Inhibitors Eye Proteins Xanthophylls Antibodies, Monoclonal, Humanized Complement Factor B Indocyanine Green Vascular Endothelial Growth Factor A Complement C2 Photosensitizing Agents Retinoids Retinal Pigments Porphyrins Pyridinium Compounds Complement C3 Tissue Inhibitor of Metalloproteinase-3 Aptamers, Nucleotide Complement Factor I Complement C3b Inactivator Proteins Serine Endopeptidases Rhodopsin Triamcinolone Peripherins Triamcinolone Acetonide Coloring Agents Antioxidants Proteins cis-trans-Isomerases ATP-Binding Cassette Transporters Complement Membrane Attack Complex beta Carotene RNA, Messenger Complement C1 Inactivator Proteins Complement Factor D Extracellular Matrix Proteins Antibodies, Monoclonal

Analytical, Diagnostic and Therapeutic Techniques and Equipment42

Fluorescein Angiography Risk Factors Visual Acuity Intravitreal Injections Retrospective Studies Case-Control Studies Tomography, Optical Coherence Prospective Studies Electroretinography Cohort Studies Prevalence Incidence Photochemotherapy Treatment Outcome Ophthalmoscopy Photography Questionnaires Disease Models, Animal Laser Coagulation Vision Tests Light Coagulation Injections, Intraocular Visual Field Tests Diagnostic Techniques, Ophthalmological Lasers Injections Follow-Up Studies Sensory Aids Blotting, Western Contrast Sensitivity Immunohistochemistry Reverse Transcriptase Polymerase Chain Reaction Fluorescent Antibody Technique, Indirect Ophthalmoscopes Pedigree Ophthalmologic Surgical Procedures Odds Ratio Cataract Extraction Reproducibility of Results Polymerase Chain Reaction Eye Protective Devices Microscopy, Electron

Psychiatry and Psychology6

Visual Acuity Frontotemporal Lobar Degeneration Visual Fields Contrast Sensitivity Vision, Ocular Smoking

Phenomena and Processes30

Visual Acuity Time Factors Aging Polymorphism, Single Nucleotide Genotype Genetic Predisposition to Disease Eye Color Haplotypes Dark Adaptation Mutation Oxidative Stress Visual Fields Chromosomes, Human, Pair 10 Complement Activation Alleles Complement Pathway, Alternative Light Phenotype Gene Frequency Contrast Sensitivity Linkage Disequilibrium Vision, Ocular Homozygote Apoptosis Odds Ratio Gene Expression Regulation Cell Survival Fluorescence Cell Death Infrared Rays

Disciplines and Occupations2

Immunohistochemistry Ophthalmology

Anthropology, Education, Sociology and Social Phenomena1

National Eye Institute (U.S.)

Technology, Industry, Agriculture2

Eye Protective Devices Dietary Supplements

Information Science4

Prevalence Incidence Questionnaires Reading

Named Groups2

Visually Impaired Persons Asian Continental Ancestry Group

Health Care16

Risk Factors Retrospective Studies Case-Control Studies Prospective Studies Age Factors Cohort Studies Prevalence Incidence Treatment Outcome Questionnaires Eye Banks Follow-Up Studies National Eye Institute (U.S.)Odds Ratio Reproducibility of Results Infrared Rays

Geographicals1

Anatomy Organisms Diseases Chemicals and Drugs Analytical, Diagnostic and Therapeutic Techniques and Equipment Psychiatry and Psychology Phenomena and Processes Disciplines and Occupations Anthropology, Education, Sociology and Social Phenomena Technology, Industry, Agriculture Information Science Named Groups Health Care Geographicals

Macular Degeneration Wet Macular Degeneration Choroidal Neovascularization Retinal Drusen Retinal Pigment Epithelium Retinal Degeneration Geographic Atrophy Fluorescein Angiography Risk Factors Choroid Visual Acuity Nerve Degeneration Complement Factor H Bruch Membrane Pigment Epithelium of Eye Intravitreal Injections Retina Macula Lutea Lipofuscin Time Factors Optic Disk Drusen Retrospective Studies Fundus Oculi Wallerian Degeneration Case-Control Studies Tomography, Optical Coherence Choroid Diseases Lutein Fovea Centralis Photoreceptor Cells, Vertebrate Prospective Studies Angiogenesis Inhibitors Age Factors Retinal Neovascularization Electroretinography Cohort Studies Prevalence Incidence Exudates and Transudates Photochemotherapy Eye Proteins Treatment Outcome Cells, Cultured Intervertebral Disc Degeneration Ophthalmoscopy Xanthophylls Chronic Disease Photography Subretinal Fluid Questionnaires Scotoma Postoperative Complications Retinal Diseases Aging Antibodies, Monoclonal, Humanized Eye Diseases Vision Disorders Vision, Low Retinal Detachment Retinal Hemorrhage Complement Factor B Polymorphism, Single Nucleotide Indocyanine Green Disease Models, Animal Genotype Laser Coagulation Blindness Vision Tests Vascular Endothelial Growth Factor A Retinitis Pigmentosa Complement C2 Photosensitizing Agents Eye Diseases, Hereditary Frontotemporal Lobar Degeneration Cataract Retinoids Retinal Pigments Porphyrins Atrophy Genetic Predisposition to Disease Light Coagulation Retinal Photoreceptor Cell Outer Segment Eye Banks Eye Color Vitreous Body Pyridinium Compounds Injections, Intraocular Visual Field Tests Disease Progression Mice, Inbred C57BL Diagnostic Techniques, Ophthalmological Eye Optic Atrophy Photoreceptor Cells Intervertebral Disc Retinal Vessels Haplotypes Complement C3 Lasers Retinal Cone Photoreceptor Cells

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