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index medicus (129) 129
humans (127) 127
male (75) 75
female (66) 66
usher syndrome (49) 49
adult (46) 46
ophthalmology (46) 46
retinitis pigmentosa (42) 42
retinitis pigmentosa - complications (38) 38
usher's syndrome (38) 38
child (37) 37
syndrome (35) 35
deafness (34) 34
middle aged (34) 34
usher syndromes - complications (33) 33
adolescent (31) 31
hearing loss (30) 30
genetics & heredity (28) 28
usher-syndrome (27) 27
otorhinolaryngology (24) 24
child, preschool (23) 23
prevalence (22) 22
usher syndromes - genetics (22) 22
mutation (21) 21
pedigree (21) 21
hearing loss, sensorineural - complications (20) 20
retinitis-pigmentosa (20) 20
deafness - complications (19) 19
aged (18) 18
genetic aspects (18) 18
diagnosis (17) 17
hearing loss, sensorineural - genetics (17) 17
research (17) 17
retinitis pigmentosa - genetics (17) 17
animals (16) 16
children (16) 16
complications and side effects (16) 16
gene (16) 16
electroretinography (15) 15
young adult (15) 15
genetics (14) 14
eye diseases (13) 13
hearing loss, sensorineural - diagnosis (13) 13
usher syndromes (13) 13
usher syndromes - diagnosis (13) 13
care and treatment (12) 12
dna mutational analysis (12) 12
health aspects (12) 12
mutations (12) 12
pediatrics (12) 12
retinitis pigmentosa - diagnosis (12) 12
abridged index medicus (11) 11
cochlear implants (11) 11
hearing impairment (11) 11
infant (11) 11
medicine, research & experimental (11) 11
molecular sequence data (11) 11
retrospective studies (11) 11
usher syndromes - pathology (11) 11
visual acuity (11) 11
analysis (10) 10
leber congenital amaurosis (10) 10
myosin viia (10) 10
optical coherence tomography (10) 10
phenotype (10) 10
risk factors (10) 10
usher syndromes - physiopathology (10) 10
vision (10) 10
vision disorders - complications (10) 10
article (9) 9
base sequence (9) 9
cochlear implantation (9) 9
gene therapy (9) 9
identification (9) 9
localization (9) 9
mice (9) 9
retinal degeneration (9) 9
sense organs (9) 9
diagnosis, differential (8) 8
gene mutations (8) 8
genes (8) 8
genetic structures (8) 8
genotype (8) 8
medicine (8) 8
neurosciences (8) 8
retina (8) 8
vision disorders - diagnosis (8) 8
visual acuity - physiology (8) 8
biochemistry & molecular biology (7) 7
blindness (7) 7
cohort studies (7) 7
deaf (7) 7
deafness - genetics (7) 7
edema (7) 7
extracellular matrix proteins - genetics (7) 7
follow-up studies (7) 7
genetic research (7) 7
hearing (7) 7
heterogeneity (7) 7
homozygote (7) 7
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Journal Article
Journal Article
Journal of Neuroscience, ISSN 0270-6474, 07/2015, Volume 35, Issue 28, pp. 10188 - 10201
Journal Article
Journal Article
Journal of Glaucoma, ISSN 1057-0829, 08/2012, Volume 21, Issue 6, pp. 392 - 393
Journal Article
Journal of pediatric ophthalmology and strabismus, 2015, Volume 52, pp. e26 - e29
Journal Article
Journal of Medical Case Reports, ISSN 1752-1947, 03/2015, Volume 9, Issue 1, pp. 1 - 4
Usher syndrome is a genetically heterogeneous condition and represents the most common cause of inherited combined vision and hearing loss. Deficits manifest... 
Keratic precipitates | Retinitis pigmentosa | Usher syndrome | Granulomatous uveitis | Uveitis, Anterior - etiology | Humans | Middle Aged | Female | Endothelium, Corneal - pathology | Usher Syndromes - complications | Uveitis, Anterior - pathology | Visual Acuity | Medicine, Experimental | Medical research | Medical examination | Blood | Uveitis | Index Medicus
Journal Article
Graefe's Archive for Clinical and Experimental Ophthalmology, ISSN 0721-832X, 10/2010, Volume 248, Issue 10, pp. 1481 - 1485
Journal Article
PLoS One, ISSN 1932-6203, 2011, Volume 6, Issue 3, pp. e15669 - e15669
The LEW/Ztm-ci2 rat is an animal model for syndromal deafness that arose from a spontaneous mutation. Homozygous animals show locomotor abnormalities like... 
HEARING-LOSS | HAIR-CELLS | WHIRLIN | GENE | MULTIDISCIPLINARY SCIENCES | MOUSE | UNCONVENTIONAL MYOSIN | CIRCLING BEHAVIOR | DEAFNESS DFNB3 | MODEL | RETINITIS-PIGMENTOSA | Humans | Molecular Sequence Data | Male | RNA, Messenger - metabolism | Vision, Ocular - radiation effects | In Situ Hybridization | Usher Syndromes - genetics | Rats, Mutant Strains | Base Sequence | Light | Female | Usher Syndromes - complications | Usher Syndromes - physiopathology | Electroretinography | Amino Acid Sequence | Retinal Rod Photoreceptor Cells - radiation effects | RNA, Messenger - genetics | Rats | Exons - genetics | Retinal Degeneration - physiopathology | Mutation - genetics | Myosins - chemistry | Reverse Transcriptase Polymerase Chain Reaction | Myosins - genetics | Phenotype | Animals | Retinal Rod Photoreceptor Cells - physiology | Gene Expression Regulation - radiation effects | Environment | Retinal Degeneration - pathology | Retinal Degeneration - complications | Deafness | Amino acids | Genetic aspects | RNA | Muscle proteins | Myosin | Pathogenesis | Zoology | Proline | Retina | mRNA | Leucine | Medical schools | Amino acid substitution | Proteins | Degeneration | Phenotypes | Abnormalities | Animal sciences | Environmental factors | Hearing impairment | Hearing loss | Animal behavior | Retinal degeneration | Photoreceptors | Mutation | Laboratory animals | Index Medicus
Journal Article
Journal Article