X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
index medicus (31) 31
humans (27) 27
female (22) 22
ophthalmology (22) 22
male (21) 21
adult (18) 18
middle aged (16) 16
aged (14) 14
genetics & heredity (13) 13
dna mutational analysis (11) 11
mutation (9) 9
adolescent (8) 8
animals (7) 7
pedigree (7) 7
phenotype (7) 7
treatment outcome (7) 7
visual acuity (7) 7
child (6) 6
fluorescein angiography (6) 6
photosensitizing agents - therapeutic use (6) 6
porphyrins - therapeutic use (6) 6
prospective studies (6) 6
aged, 80 and over (5) 5
alleles (5) 5
alpha-subunit (5) 5
base sequence (5) 5
biochemistry & molecular biology (5) 5
dystrophy (5) 5
eye (5) 5
follow-up studies (5) 5
genetic aspects (5) 5
genetics (5) 5
locus (5) 5
retina (5) 5
total colourblindness (5) 5
verteporfin (5) 5
amino acid sequence (4) 4
choroidal neovascularization - drug therapy (4) 4
choroidal neovascularization - etiology (4) 4
electrophysiology (4) 4
eye diseases (4) 4
eye proteins - genetics (4) 4
genes (4) 4
genetic research (4) 4
mutation - genetics (4) 4
mutations (4) 4
optic atrophies, hereditary - genetics (4) 4
photochemotherapy (4) 4
research (4) 4
retinitis-pigmentosa (4) 4
achromatopsia (3) 3
age of onset (3) 3
analysis (3) 3
articles (3) 3
cat retina (3) 3
choroid neoplasms - drug therapy (3) 3
clonal deletion (3) 3
color vision defects - genetics (3) 3
exons (3) 3
exons - genetics (3) 3
genetic structures (3) 3
genetic testing (3) 3
macular degeneration (3) 3
macular degeneration - genetics (3) 3
medical and health sciences (3) 3
medicin och hälsovetenskap (3) 3
molecular sequence data (3) 3
neurosciences (3) 3
optic nerve response (3) 3
phenotypes (3) 3
photodynamic therapy (3) 3
photoreceptors (3) 3
polymorphism, single-stranded conformational (3) 3
retina - metabolism (3) 3
retinal degeneration (3) 3
retinitis pigmentosa (3) 3
retinitis pigmentosa - genetics (3) 3
safety (3) 3
surgery (3) 3
visual acuity - physiology (3) 3
acetylcholine receptors (2) 2
acuity (2) 2
adenosine (2) 2
age (2) 2
amacrine cells (2) 2
basic medicine (2) 2
bietti (2) 2
biochemistry, general (2) 2
cats (2) 2
cells (2) 2
child, preschool (2) 2
choroidal neovascularization (2) 2
chromosome mapping (2) 2
color blindness (2) 2
cones (2) 2
conserved sequence (2) 2
copy number (2) 2
crystalline dystrophy (2) 2
cyclic nucleotide phosphodiesterases, type 6 - genetics (2) 2
cyclic nucleotide-gated cation channels (2) 2
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Klinische Monatsblatter fur Augenheilkunde, ISSN 0023-2165, 1995, Volume 206, Issue 5, pp. 380 - 383
Journal Article
Vision Research, ISSN 0042-6989, 03/1996, Volume 36, Issue 6, pp. 797 - 816
To identify cholinergically mediated components in the optic nerve response (ORN) we studied effects of cholinergic agonists and antagonists in the arterially... 
Journal Article
Klinische Monatsblatter fur Augenheilkunde, ISSN 0023-2165, 1997, Volume 210, Issue 1, pp. 1 - 18
Journal Article
Vision Research, ISSN 0042-6989, 1999, Volume 39, Issue 6, pp. 1059 - 1068
The function of A1- and A2a-adenosine receptors in the control of vascular resistance and in the modulation of light-evoked neuronal activity was investigated... 
Electrophysiology | Cat retina | Optic nerve response | Adenosine | Vascular
Journal Article
The American Journal of Human Genetics, ISSN 0002-9297, 2000, Volume 67, Issue 4, pp. 800 - 813
Journal Article
European Journal of Human Genetics, ISSN 1018-4813, 2000, Volume 8, Issue 4, pp. 286 - 292
Journal Article
Journal Article
The American Journal of Human Genetics, ISSN 0002-9297, 2001, Volume 69, Issue 4, pp. 722 - 737
Journal Article
Human Mutation, ISSN 1059-7794, 11/2002, Volume 20, Issue 5, pp. 405 - 405
RGPR was the first gene found to be mutated in XLRP, the subtype of RP displaying the most severe form of retinal degeneration with partial or complete... 
retinitis pigmentosa | retinal degeneration | XLRP | RP3 | RPGR | Frameshift Mutation | Exons | Europe | Humans | Open Reading Frames | Retinitis Pigmentosa - genetics | Male | Carrier Proteins - genetics | Female | Genetic Diseases, X-Linked - genetics | Polymorphism, Single Nucleotide | Mutation | Eye Proteins | Index Medicus
Journal Article
No results were found for your search.

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