X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
index medicus (422) 422
humans (415) 415
ophthalmology (344) 344
male (262) 262
female (226) 226
vitelliform macular dystrophy (224) 224
middle aged (172) 172
adult (160) 160
tomography, optical coherence (145) 145
fluorescein angiography (144) 144
bestrophins (136) 136
eye proteins - genetics (130) 130
mutation (128) 128
aged (114) 114
vitelliform macular dystrophy - diagnosis (104) 104
optical coherence tomography (103) 103
chloride channels - genetics (102) 102
degeneration (102) 102
macular degeneration (95) 95
visual acuity (94) 94
child (93) 93
eye diseases (91) 91
retina (90) 90
electrooculography (82) 82
vitelliform macular dystrophy - genetics (79) 79
retinal-pigment epithelium (78) 78
disease (77) 77
phenotype (76) 76
best vitelliform macular dystrophy (75) 75
electroretinography (74) 74
mutations (73) 73
adolescent (72) 72
pedigree (72) 72
fundus oculi (70) 70
animals (69) 69
best-disease (65) 65
gene (65) 65
sense organs (65) 65
vmd2 gene (65) 65
visual acuity - physiology (64) 64
chloride channels (63) 63
bestrophin (60) 60
choroidal neovascularization (59) 59
retrospective studies (57) 57
genetic structures (54) 54
vmd2 (54) 54
family (52) 52
macular degeneration - genetics (51) 51
dna mutational analysis (49) 49
article (48) 48
best disease (47) 47
aged, 80 and over (46) 46
dystrophy (46) 46
abridged index medicus (45) 45
retinal pigment epithelium (45) 45
tomography (45) 45
vitelliform macular dystrophy - physiopathology (45) 45
macular dystrophy (44) 44
young adult (44) 44
protein (43) 43
retinal pigment epithelium - pathology (43) 43
tomography, optical coherence - methods (42) 42
eye proteins - metabolism (41) 41
fundus autofluorescence (41) 41
vitelliform macular dystrophy - pathology (40) 40
chloride channels - metabolism (39) 39
membrane (39) 39
retinal degeneration (39) 39
fluorescence (38) 38
genetics & heredity (38) 38
vitelliform macular dystrophy - complications (37) 37
adult-onset foveomacular vitelliform dystrophy (35) 35
genetic aspects (34) 34
retinal diseases - genetics (34) 34
follow-up studies (33) 33
best1 (32) 32
diagnosis, differential (32) 32
genotype (32) 32
macular degeneration - diagnosis (32) 32
medical imaging (32) 32
research (32) 32
biochemistry & molecular biology (31) 31
child, preschool (31) 31
choroidal neovascularization - drug therapy (31) 31
pattern dystrophy (31) 31
retina - pathology (30) 30
bevacizumab (29) 29
channels (28) 28
lipofuscin (28) 28
macular degeneration - pathology (28) 28
patients (28) 28
choroidal neovascularization - etiology (27) 27
genetics (27) 27
physiology (27) 27
best's disease (26) 26
medicine & public health (26) 26
mutation, missense (26) 26
retinitis-pigmentosa (26) 26
analysis (25) 25
electrophysiology (25) 25
more...
Language Language
Language Language
X
Sort by Item Count (A-Z)
Filter by Count
English (520) 520
German (23) 23
Spanish (14) 14
French (7) 7
Czech (4) 4
Korean (3) 3
Chinese (1) 1
Italian (1) 1
Japanese (1) 1
Polish (1) 1
Portuguese (1) 1
Romanian (1) 1
Russian (1) 1
Slovak (1) 1
Turkish (1) 1
more...
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


The American Journal of Human Genetics, ISSN 0002-9297, 09/2013, Volume 93, Issue 3, pp. 571 - 578
Journal Article
Clinical Ophthalmology, ISSN 1177-5467, 2019, Volume 13, pp. 465 - 475
To determine the pupil response of Best vitelliform macular dystrophy (BVMD) patients for focal blue and red light stimuli presented at 76 test points in a... 
Perimetry | Pupillary light reflex | Pupilloperimetry | Best vitelliform macular dystrophy | Visual field | Tomography | Light emitting diodes | Photoreceptors | Mutation | Best Vitelliform Macular Dystrophy | Pupillary Light Reflex | BVMD
Journal Article
Retina, ISSN 0275-004X, 04/2017, Volume 38, Issue 5, pp. 1041 - 1046
Purpose: To provide a systematic classification of findings regarding the different stages of vitelliform macular dystrophy on spectral domain optical... 
best disease | vitelliform macular dystrophy | PATTERN | optical coherence tomography | FUNDUS AUTOFLUORESCENCE | OPHTHALMOLOGY | MUTATIONS | Eye diseases | Usage | Care and treatment | Diagnosis | Optical tomography | Index Medicus
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 3/2002, Volume 99, Issue 6, pp. 4008 - 4013
Vitelliform macular dystrophy (VMD/Best disease; ) is an early-onset autosomal dominant disorder in which accumulation of lipofuscin-like material within and... 
Vitelliform macular dystrophy | Electric potential | Biological Sciences | Transfection | Complementary DNA | Plasmids | Gluconates | Chloride channels | Cellular immunity | Pipettes | Electric current | BESTROPHIN | CA2 | BEST-DISEASE | VMD2 GENE | MULTIDISCIPLINARY SCIENCES | MUTATIONS | DEGENERATION | Protein Subunits | Caenorhabditis elegans Proteins - chemistry | Humans | Caenorhabditis elegans Proteins - metabolism | Eye Proteins - chemistry | Electric Conductivity | Chloride Channels - genetics | Drosophila Proteins - metabolism | Mutation, Missense - genetics | Cysteine - genetics | Bestrophins | Chlorides - metabolism | Cloning, Molecular | Protein Structure, Quaternary | Cysteine - metabolism | Eye Proteins - genetics | Cell Line | Calcium - pharmacology | Chloride Channels - chemistry | 4,4'-Diisothiocyanostilbene-2,2'-Disulfonic Acid - pharmacology | Retinal Degeneration - genetics | Models, Molecular | Drosophila Proteins - chemistry | Chloride Channels - metabolism | Caenorhabditis elegans | Animals | Eye Proteins - metabolism | Cell Membrane Permeability - drug effects | Drosophila Proteins - genetics | Caenorhabditis elegans Proteins - genetics | Drosophila melanogaster | Genes, Dominant - genetics | Ion Channel Gating - drug effects | Retinal degeneration | Genetic aspects | Research | Cytochemistry | Proteins | Neurology | Mutation | Disease | Eyes & eyesight | Bestrophin | retinal pigment epithelium | Index Medicus
Journal Article