X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
index medicus (37) 37
ophthalmology (36) 36
humans (33) 33
cyp4v2 (31) 31
mutation (27) 27
female (24) 24
cyp4v2 gene (21) 21
male (21) 21
adult (20) 20
corneal dystrophies, hereditary - genetics (20) 20
retinal diseases - genetics (18) 18
mutations (17) 17
corneo-retinal dystrophy (16) 16
middle aged (16) 16
bietti crystalline dystrophy (15) 15
electroretinography (15) 15
cytochrome p-450 enzyme system - genetics (13) 13
cytochrome p450 family 4 (13) 13
dna mutational analysis (13) 13
genetic aspects (12) 12
tomography, optical coherence (12) 12
corneal dystrophies, hereditary - diagnosis (11) 11
cytochrome p-450 (11) 11
retinal dystrophy (11) 11
corneal dystrophies, hereditary - pathology (10) 10
cytochrome p450 family 4 - genetics (10) 10
eye diseases (10) 10
fluorescein angiography (10) 10
japanese patients (10) 10
retinal diseases - diagnosis (10) 10
retinal diseases - pathology (10) 10
dystrophy (9) 9
retinitis pigmentosa (9) 9
aged (8) 8
gene (8) 8
identification (8) 8
pedigree (8) 8
phenotype (8) 8
retinopathy (8) 8
cyp4v2 mutations (7) 7
metabolism (7) 7
patients (7) 7
retina (7) 7
sense organs (7) 7
bietti (6) 6
exons (6) 6
gene mutations (6) 6
genes (6) 6
genetic structures (6) 6
genotype (6) 6
retinal pigment epithelium - pathology (6) 6
young adult (6) 6
alleles (5) 5
analysis (5) 5
bietti crystalline corneoretinal dystrophy (5) 5
choroidal neovascularization (5) 5
corneal dystrophies, hereditary - physiopathology (5) 5
dna - genetics (5) 5
dna sequencing (5) 5
fundus oculi (5) 5
medicine, research & experimental (5) 5
nucleotide sequencing (5) 5
polymerase chain reaction (5) 5
retinal degeneration (5) 5
retinal diseases - physiopathology (5) 5
retinal pigment epithelium (5) 5
visual acuity (5) 5
atrophy (4) 4
care and treatment (4) 4
china (4) 4
cornea (4) 4
cytochrome p450 (4) 4
cytochrome p450 family 4 - metabolism (4) 4
diagnosis (4) 4
fatty-acids (4) 4
genetic testing (4) 4
genetics (4) 4
medical research (4) 4
medicine & public health (4) 4
medicine, experimental (4) 4
neovascularization (4) 4
optical coherence tomography (4) 4
research (4) 4
retinitis-pigmentosa (4) 4
tomography (4) 4
visual acuity - physiology (4) 4
visual field tests (4) 4
animals (3) 3
article (3) 3
asian continental ancestry group - genetics (3) 3
bietti's crystalline dystrophy (3) 3
choroid - pathology (3) 3
corneal dystrophies, hereditary - metabolism (3) 3
crystal structure (3) 3
crystalline dystrophy (3) 3
cyp (3) 3
deposits (3) 3
diagnosis, differential (3) 3
epithelium (3) 3
eye proteins - genetics (3) 3
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Journal Article
The British journal of ophthalmology, ISSN 0007-1161, 02/2018, Volume 102, Issue 2, pp. 187 - 194
Journal Article
International Journal of Molecular Medicine, ISSN 1107-3756, 4/2014, Volume 33, Issue 4, pp. 913 - 918
Journal Article
国际眼科杂志:英文版, ISSN 2222-3959, 2015, Volume 8, Issue 3, pp. 465 - 469
AIM: To analyze the CYP4V2 mutations in five unrelated Chinese patients with Bietti crystalline corneoretinal dystrophy(BCD) and to provide clinical features... 
corneoretinal | mutation | dystrophy | gene | CYP4V2 | Bietti’s | Bietti’s dystrophy | Corneoretinal dystrophy | Mutation | CYP4V2 gene | GENE | FAMILIES | OPHTHALMOLOGY | RETINOPATHY | CHOROIDAL NEOVASCULARIZATION | IDENTIFICATION | comeoretinal dystrophy | Bietti's dystrophy | corneoretinal dystrophy
Journal Article
Ophthalmic Genetics, ISSN 1381-6810, 10/2016, Volume 37, Issue 4, pp. 445 - 452
Journal Article
Journal Article
Journal Article
PLoS ONE, ISSN 1932-6203, 04/2014, Volume 9, Issue 4, pp. e94960 - e94960
Journal Article
International Ophthalmology, ISSN 0165-5701, 6/2013, Volume 33, Issue 3, pp. 269 - 276
Bietti crystalline corneoretinal dystrophy (BCD, MIM 210370) is a type of hereditary retinal disorder which commonly occurs in China. It is known that... 
Ophthalmology | Medicine & Public Health | Bietti crystalline dystrophy | CYP4V2 gene
Journal Article
Journal of Current Ophthalmology, ISSN 2452-2325, 06/2019, Volume 31, Issue 2, pp. 172 - 179
To report the genetic analysis of an Iranian Bietti crystalline dystrophy (BCD)-affected family, and to review previously reported mutations in the gene and... 
CYP4V2 mutations | BCD | p.Glu407 | Bietti crystalline dystrophy | CYP4V2
Journal Article
Investigative ophthalmology & visual science, ISSN 0146-0404, 03/2019, Volume 60, Issue 4, pp. 1044 - 1049
PURPOSE. We investigate whether choriocapillaris deficits can be visualized in patients with retinitis pigmentosa (RP) using wide-angle swept-source optical... 
swept-source OCT | BIETTI CRYSTALLINE DYSTROPHY | optical coherence tomography angiography | SPECTRAL-DOMAIN | choriocapillaris | retinitis pigmentosa | OPHTHALMOLOGY | MACULAR DEGENERATION | CYP4V2 MUTATIONS | retinal pigment epithelium | NEOVASCULARIZATION
Journal Article