Medicine and Dentistry
Patient
100%
Electroretinography
44%
Family
31%
Retinal Detachment
27%
Surgery
22%
Autofluorescence
21%
Retinitis pigmentosa
21%
Retinopathy
20%
Syndrome
19%
Sibling
19%
Follow up
19%
Disease
18%
Therapeutic Procedure
18%
Congenital Stationary Night Blindness
14%
Retina Degeneration
14%
Age
13%
Vitelliform Macular Dystrophy
13%
Pars Plana Vitrectomy
13%
Male
12%
Retina
12%
Injection
11%
Examination
10%
Female
10%
Visual Impairment
9%
Retina Dystrophy
9%
Genotype
9%
High Myopia
9%
Retinal Imaging
8%
Exudative Retinal Detachment
8%
Child
7%
Hospital
7%
Association
7%
Vitrectomy
7%
Spectral Domain Optical Coherence Tomography
6%
Lesion
6%
Respiratory Distress Syndrome
6%
Genetic Analysis
6%
Case Report
6%
Cataract Surgery
5%
Multimodal Imaging
5%
Laser Coagulation
5%
Retinal Disease
5%
Gene Therapy
5%
Triamcinolone Acetonide
5%
Visual Acuity
5%
Clinical Examination
5%
Gene Mutation
5%
Intraocular Pressure
5%
Biochemistry, Genetics and Molecular Biology
Gene
30%
Optics
17%
Genetic Screening
16%
Missense
16%
Genetics
12%
Molecular Genetics
11%
Next Generation Sequencing
10%
Retinitis pigmentosa
10%
Phenotype
9%
Autosomal Recessive Inheritance
8%
Genotyping
6%
Exon
6%
RPE65
6%
Vision
5%
Reduction (Chemistry)
5%
