X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
index medicus (44) 44
humans (43) 43
ophthalmology (34) 34
male (31) 31
female (29) 29
mutation (25) 25
adult (21) 21
child (20) 20
electroretinography (17) 17
phenotype (17) 17
adolescent (16) 16
genetics & heredity (15) 15
pedigree (15) 15
retina (13) 13
genetic aspects (12) 12
middle aged (12) 12
eye diseases (11) 11
heterozygote (11) 11
retinitis-pigmentosa (11) 11
biochemistry & molecular biology (9) 9
eye proteins - genetics (9) 9
fundus oculi (9) 9
gene (9) 9
sense organs (9) 9
alleles (8) 8
animals (8) 8
blindness (8) 8
child, preschool (8) 8
genotype (8) 8
cis-trans-isomerases (7) 7
genetic structures (7) 7
infant (7) 7
mice (7) 7
mutations (7) 7
retinal degeneration - genetics (7) 7
young adult (7) 7
article (6) 6
carrier proteins - genetics (6) 6
fluorescence (6) 6
genetics (6) 6
leber congenital amaurosis (6) 6
lipofuscin (6) 6
optical coherence tomography (6) 6
polymorphism, single-stranded conformational (6) 6
rpe65 (6) 6
tomography, optical coherence (6) 6
visual acuity - physiology (6) 6
visual fields - physiology (6) 6
children (5) 5
dna mutational analysis (5) 5
dystrophy (5) 5
electrophysiology (5) 5
fundus autofluorescence (5) 5
gene-therapy (5) 5
genes, recessive (5) 5
genetic disorders (5) 5
genetic variation (5) 5
macular degeneration (5) 5
medicine (5) 5
medicine & public health (5) 5
night blindness - genetics (5) 5
polymerase chain reaction (5) 5
retinitis pigmentosa (5) 5
visual field tests (5) 5
causes of (4) 4
choroideremia - genetics (4) 4
degeneration (4) 4
diagnosis (4) 4
disease (4) 4
gene mutations (4) 4
genes (4) 4
mutation - genetics (4) 4
patients (4) 4
protein (4) 4
report (4) 4
retinal diseases - genetics (4) 4
retinal-pigment epithelium (4) 4
visual acuity (4) 4
adaptor proteins, signal transducing (3) 3
aged (3) 3
aipl1 (3) 3
albinism, oculocutaneous - genetics (3) 3
analysis (3) 3
blindness - congenital (3) 3
blindness - genetics (3) 3
choroideremia - diagnosis (3) 3
choroideremia - physiopathology (3) 3
cone-rod dystrophy (3) 3
consanguinity (3) 3
diseases (3) 3
eye diseases, hereditary - genetics (3) 3
eye proteins (3) 3
fluorescein angiography (3) 3
follow-up studies (3) 3
gene expression (3) 3
genetic counseling (3) 3
genetic diseases, x-linked - genetics (3) 3
genetic research (3) 3
genotype & phenotype (3) 3
guanylate cyclase - genetics (3) 3
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Graefe's Archive for Clinical and Experimental Ophthalmology, ISSN 0721-832X, 9/2019, Volume 257, Issue 9, pp. 2005 - 2014
The lateralis splitting technique has been an interesting option for treating large-angle exotropia due to complete 3rd nerve paralysis since its inception in... 
Lateral rectus nasal transposition | Paralytic strabismus | Ophthalmology | Medicine & Public Health | Lateral rectus splitting | Third nerve palsy | PARALYSIS | NERVE PALSY | MANAGEMENT | SUTURES | OPHTHALMOLOGY | FIXATION | Paralysis | Transposition | Splitting | Strabismus | Motility | Surgery | Retina | Binocular vision | Horizontal cells | Rectus muscle | Patients | Index Medicus
Journal Article
FASEB journal : official publication of the Federation of American Societies for Experimental Biology, ISSN 0892-6638, 07/2019, pp. fj201900914RR - fj201900914RR
We previously reported that inactivation of the transmembrane taurine transporter (TauT or solute carrier 6a6) causes early retinal degeneration in mice.... 
Index Medicus
Journal Article
Klinische Monatsblatter fur Augenheilkunde, ISSN 0023-2165, 03/2018, Volume 235, Issue 3, pp. 281 - 289
Journal Article
JAMA Ophthalmology, ISSN 2168-6165, 08/2014, Volume 132, Issue 8, pp. 996 - 1001
IMPORTANCE: We describe novel ocular phenotypic features caused by mutations in ADAMTS18. The exact role of ADAMTS18 in ocular disease is unclear, and our work... 
OPHTHALMOLOGY | ECTOPIA LENTIS | GENE | KNOBLOCH-SYNDROME | Phenotype | Humans | Adolescent | ADAMTS Proteins | Adult | Male | Mutation | ADAM Proteins - genetics | Eye Abnormalities - genetics | Gene mutations | Analysis | Phenotypic plasticity | Causes of | Eye diseases | Genetic aspects | Research | Index Medicus | Abridged Index Medicus
Journal Article
Klinische Monatsblatter fur Augenheilkunde, ISSN 0023-2165, 03/2016, Volume 233, Issue 3, pp. 243 - 250
Journal Article
Ophthalmic Research, ISSN 0030-3747, 2017, Volume 58, Issue 4, pp. 243 - 243
Journal Article
Ophthalmic Research, ISSN 0030-3747, 2017, Volume 58, Issue 4, pp. I - IV
Journal Article
Klinische Monatsblatter fur Augenheilkunde, 03/2019, Volume 236, Issue 3, p. 244
Inherited retinal diseases (IRDs) may be caused by variations in genes affecting the connecting cilium of photoreceptor cells and intraflagellar transport,... 
Journal Article
Molecular Vision, ISSN 1090-0535, 2011, Volume 17, Issue 104, pp. 939 - 948
Background: A broad spectrum of pigmentation of the skin and hair is found among patients diagnosed with ocular albinism (OA) and oculocutaneous albinism... 
TYROSINASE GENE | EYED-DILUTION LOCUS | RECESSIVE OCULAR ALBINISM | OCULOCUTANEOUS ALBINISM | OA1 GENE | BIOCHEMISTRY & MOLECULAR BIOLOGY | OPHTHALMOLOGY | MELANOCORTIN-1 RECEPTOR | CHINESE FAMILY | HUMAN PIGMENTATION | P-GENE | RED HAIR | Eye - pathology | Hypopigmentation - congenital | Genetic Testing | Hypopigmentation - metabolism | Membrane Glycoproteins - metabolism | Humans | Nystagmus, Congenital - complications | Child, Preschool | Infant | Male | Nystagmus, Congenital - genetics | Receptor, Melanocortin, Type 1 - metabolism | Monophenol Monooxygenase - metabolism | Polymorphism, Single-Stranded Conformational | Genes, X-Linked | Membrane Transport Proteins - genetics | Nystagmus, Congenital - metabolism | Albinism, Oculocutaneous - genetics | Base Sequence | Adult | Female | Membrane Transport Proteins - metabolism | Monophenol Monooxygenase - genetics | Eye Proteins - genetics | Child | Hypopigmentation - complications | Albinism, Ocular - genetics | Eye - metabolism | Hypopigmentation - genetics | Albinism, Oculocutaneous - metabolism | Genetic Association Studies | Receptor, Melanocortin, Type 1 - genetics | Visual Acuity - genetics | Albinism, Ocular - complications | Membrane Glycoproteins - genetics | Albinism, Oculocutaneous - complications | Phenotype | Eye Proteins - metabolism | Pedigree | Adolescent | Alleles | Albinism, Ocular - metabolism | Mutation | Fundus Oculi | Index Medicus
Journal Article
JAMA Ophthalmology, ISSN 2168-6165, 08/2014, Volume 132, Issue 8, p. 996
  We describe novel ocular phenotypic features caused by mutations in ADAMTS18. The exact role of ADAMTS18 in ocular disease is unclear, and our work further... 
Proteins | Genotype & phenotype | Eye diseases | Mutation | Ophthalmology
Journal Article
No results were found for your search.

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