X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
index medicus (38) 38
ophthalmology (36) 36
cyp4v2 (34) 34
humans (34) 34
mutation (27) 27
female (25) 25
cyp4v2 gene (22) 22
male (22) 22
adult (21) 21
corneal dystrophies, hereditary - genetics (20) 20
retinal diseases - genetics (18) 18
corneo-retinal dystrophy (17) 17
middle aged (17) 17
mutations (17) 17
bietti crystalline dystrophy (15) 15
electroretinography (15) 15
cytochrome p450 family 4 (14) 14
cytochrome p-450 enzyme system - genetics (13) 13
dna mutational analysis (13) 13
genetic aspects (13) 13
cytochrome p-450 (12) 12
tomography, optical coherence (12) 12
corneal dystrophies, hereditary - diagnosis (11) 11
cytochrome p450 family 4 - genetics (11) 11
retinal dystrophy (11) 11
corneal dystrophies, hereditary - pathology (10) 10
eye diseases (10) 10
fluorescein angiography (10) 10
japanese patients (10) 10
retinal diseases - diagnosis (10) 10
retinal diseases - pathology (10) 10
aged (9) 9
dystrophy (9) 9
retinitis pigmentosa (9) 9
gene (8) 8
identification (8) 8
metabolism (8) 8
pedigree (8) 8
phenotype (8) 8
retinopathy (8) 8
cyp4v2 mutations (7) 7
patients (7) 7
retina (7) 7
sense organs (7) 7
bietti (6) 6
bietti crystalline corneoretinal dystrophy (6) 6
cytochrome p450 (6) 6
exons (6) 6
gene mutations (6) 6
genes (6) 6
genetic structures (6) 6
genotype (6) 6
medicine, research & experimental (6) 6
retinal pigment epithelium - pathology (6) 6
young adult (6) 6
alleles (5) 5
analysis (5) 5
choroidal neovascularization (5) 5
corneal dystrophies, hereditary - physiopathology (5) 5
cytochrome p450 family 4 - metabolism (5) 5
diagnosis (5) 5
dna - genetics (5) 5
dna sequencing (5) 5
fundus oculi (5) 5
nucleotide sequencing (5) 5
polymerase chain reaction (5) 5
research (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
fatty-acids (4) 4
genetic testing (4) 4
genetics (4) 4
genetics & heredity (4) 4
medical research (4) 4
medicine & public health (4) 4
medicine, experimental (4) 4
neovascularization (4) 4
optical coherence tomography (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
biochemistry & molecular biology (3) 3
choroid - pathology (3) 3
corneal dystrophies, hereditary - metabolism (3) 3
crystal structure (3) 3
crystalline dystrophy (3) 3
cyp (3) 3
cytochrome (3) 3
deposits (3) 3
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Current Genomics, ISSN 1389-2029, 08/2006, Volume 7, Issue 5, pp. 273 - 282
Journal Article
JAPANESE JOURNAL OF OPHTHALMOLOGY, ISSN 0021-5155, 09/2006, Volume 50, Issue 5, pp. 426 - 431
Purpose: To identify CYP4V2 mutations in three unrelated Japanese patients with Bietti crystalline corneoretinal dystrophy (BCD). Methods: The three cases were... 
Bietti crystalline corneoretinal dystrophy | CYP4V2 | gene mutation | OPHTHALMOLOGY | MUTATIONS | CYP4V2 GENE | CORNEO-RETINAL DYSTROPHY
Journal Article
European Journal of Ophthalmology, ISSN 1120-6721, 05/2010, Volume 20, Issue 3, pp. 612 - 614
Journal Article
Clinical and Experimental Optometry, ISSN 0816-4622, 05/2011, Volume 94, Issue 3, pp. 302 - 308
Journal Article
Case Reports in Ophthalmology, ISSN 1663-2699, 09/2011, Volume 2, Issue 3, pp. 296 - 301
Purpose: To describe the clinical and genetic characteristics of a Japanese family in which one member exhibited Bietti’s crystalline corneoretinal dystrophy... 
Published: September 2011 | Biettiߣs crystalline corneoretinal dystrophy | Retinitis pigmentosa | Retinal dystrophy | CYP4V2 gene
Journal Article
Case Reports in Ophthalmology, 09/2011, Volume 2, Issue 3, pp. 296 - 301
To describe the clinical and genetic characteristics of a Japanese family in which one member exhibited Bietti's crystalline corneoretinal dystrophy (BCD).... 
Bietti's crystalline corneoretinal dystrophy | Retinitis pigmentosa | Retinal dystrophy | CYP4V2 gene
Journal Article
Bioinformation, 2011, Volume 7, Issue 7, p. 360
Cytochromes P450 (CYPs) are a super family of heme-containing enzymes well-known for their monooxgenase reaction. There are 57 CYP isoenzymes found in human... 
Journal Article
Journal Article
Journal Article
No results were found for your search.

Cannot display more than 1000 results, please narrow the terms of your search.