X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
index medicus (605) 605
humans (527) 527
male (352) 352
ophthalmology (336) 336
electroretinography (334) 334
night blindness - physiopathology (314) 314
female (301) 301
adult (272) 272
middle aged (210) 210
adolescent (166) 166
stationary night blindness (155) 155
animals (152) 152
night blindness - genetics (145) 145
dark adaptation (143) 143
child (133) 133
night blindness (119) 119
retina - physiopathology (116) 116
mutation (110) 110
visual acuity (101) 101
retina (97) 97
electroretinogram (92) 92
aged (91) 91
night blindness - congenital (89) 89
pedigree (86) 86
retinal degeneration - physiopathology (84) 84
mice (76) 76
night blindness - diagnosis (72) 72
visual fields (72) 72
night blindness - etiology (71) 71
retinitis pigmentosa - physiopathology (71) 71
retinal diseases - physiopathology (69) 69
child, preschool (67) 67
medicine & public health (67) 67
light (65) 65
photic stimulation (65) 65
gene (64) 64
fundus oculi (61) 61
myopia - physiopathology (61) 61
disease models, animal (60) 60
neurosciences (57) 57
photoreceptor cells - physiopathology (56) 56
retinal degeneration - genetics (56) 56
retinitis pigmentosa - genetics (52) 52
abridged index medicus (51) 51
mutations (49) 49
phenotype (48) 48
retinal degeneration (48) 48
retinitis pigmentosa (48) 48
retinitis-pigmentosa (46) 46
dark adaptation - physiology (45) 45
genetic structures (45) 45
retinal cone photoreceptor cells - physiopathology (45) 45
fluorescein angiography (44) 44
visual acuity - physiology (44) 44
sense organs (42) 42
analysis (40) 40
electroretinography - methods (40) 40
erg (40) 40
retina - pathology (40) 40
congenital stationary night blindness (38) 38
infant (38) 38
myopia - genetics (38) 38
genetic linkage (37) 37
blindness (36) 36
photopic electroretinogram (36) 36
tomography, optical coherence (36) 36
photoreceptors (35) 35
rod (35) 35
vision disorders - physiopathology (35) 35
b-wave (34) 34
eye diseases, hereditary - physiopathology (34) 34
genetic disorders (34) 34
genetics & heredity (34) 34
night blindness - complications (34) 34
genetic diseases, x-linked - physiopathology (33) 33
mice, inbred c57bl (33) 33
photoreceptor cells, vertebrate - physiology (33) 33
research (33) 33
dna mutational analysis (32) 32
eye diseases (32) 32
visual field tests (32) 32
retinal rod photoreceptor cells - physiopathology (31) 31
x chromosome (31) 31
genetic aspects (30) 30
syndrome (30) 30
young adult (30) 30
bipolar cells (29) 29
diagnosis, differential (29) 29
retinal rod photoreceptor cells - physiology (29) 29
vitamin a deficiency - physiopathology (29) 29
eye proteins - genetics (28) 28
nyctalopia (28) 28
sensory thresholds (27) 27
genetic diseases, x-linked - genetics (26) 26
retinal diseases - diagnosis (26) 26
eye diseases, hereditary - genetics (25) 25
polymerase chain reaction (25) 25
article (24) 24
degeneration (24) 24
electrooculography (24) 24
more...
Language Language
Language Language
X
Sort by Item Count (A-Z)
Filter by Count
English (581) 581
German (15) 15
Japanese (9) 9
French (6) 6
Spanish (3) 3
Chinese (1) 1
Hebrew (1) 1
Polish (1) 1
more...
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Journal Article
Journal Article
PLoS ONE, ISSN 1932-6203, 03/2014, Volume 9, Issue 3, pp. e90342 - e90342
Journal Article
The American Journal of Human Genetics, ISSN 0002-9297, 02/2012, Volume 90, Issue 2, pp. 331 - 339
Complete congenital stationary night blindness (cCSNB) is a clinically and genetically heterogeneous group of retinal disorders characterized by nonprogressive... 
COMPLETE FORM | LIGHT RESPONSE | CHANNEL | MGLUR6 | SYNAPTIC-TRANSMISSION | MOUSE MODEL | GENETICS & HEREDITY | NYCTALOPIN | RICH REPEAT PROTEIN | MUTATIONS | CONE ELECTRORETINOGRAM | Electroretinography - methods | Night Blindness - metabolism | Humans | Dark Adaptation - genetics | Retinal Rod Photoreceptor Cells - metabolism | Gene Knockdown Techniques - methods | Myopia - metabolism | Receptors, Metabotropic Glutamate - genetics | Retinal Bipolar Cells - physiology | Chromosome Mapping - methods | Genetic Diseases, X-Linked | Night Blindness - genetics | Retinal Bipolar Cells - metabolism | Eye Diseases, Hereditary | Signal Transduction | Mice, Inbred C57BL | Zebrafish | Mice, Inbred C3H | Myopia - genetics | Animals | Myopia - physiopathology | Pedigree | Night Blindness - physiopathology | Retinal Rod Photoreceptor Cells - physiology | Heterozygote | Mice | Receptors, G-Protein-Coupled - genetics | Mutation | Chromosome mapping | Usage | Gene mutations | Retinal bipolar cells | Causes of | Physiological aspects | Night blindness | Genetic aspects | Research | Analysis | Genetic disorders | Proteins | Rodents | Blindness | Gene expression | Cells | Index Medicus | Animal models | Antibodies | Insertion | stationary night blindness | Retina | Guanine nucleotide-binding protein | Electroretinograms | Depolarization | Signal transduction | Vision | Bipolar cells | Gene mapping | DNA sequencing | Report
Journal Article
Journal Article
Journal Article
Graefe's Archive for Clinical and Experimental Ophthalmology, ISSN 0721-832X, 10/2016, Volume 254, Issue 10, pp. 1951 - 1956
To describe congenital stationary night blindness (CSNB) with negative electroretinogram, hypoplastic discs, nystagmus and thinning of the inner nuclear layer... 
Optic disc hypoplasia | Full-field electroretinography | Congenital stationary night blindness | Ophthalmology | Medicine & Public Health | Optical coherence tomography | GENOTYPE | PHENOTYPE | OPHTHALMOLOGY | NYCTALOPIN | UPDATE | RICH | MUTATIONS | Retinal Bipolar Cells - pathology | Retinal Diseases - genetics | Diseases in Twins - genetics | Eye Abnormalities - diagnostic imaging | Frameshift Mutation | Humans | Nystagmus, Pathologic - genetics | Male | Retinal Diseases - diagnostic imaging | Dark Adaptation | Young Adult | Myopia - diagnosis | Polymerase Chain Reaction | Genetic Diseases, X-Linked - diagnostic imaging | Genetic Diseases, X-Linked - genetics | Retrospective Studies | Night Blindness - genetics | Visual Acuity - physiology | Genetic Diseases, X-Linked - physiopathology | Electroretinography | Myopia - diagnostic imaging | Eye Diseases, Hereditary - diagnostic imaging | Eye Diseases, Hereditary - physiopathology | Optic Disk - abnormalities | Tomography, Optical Coherence | Genotype | Nystagmus, Pathologic - physiopathology | Eye Abnormalities - genetics | Night Blindness - diagnostic imaging | Eye Diseases, Hereditary - genetics | Myopia - genetics | Myopia - physiopathology | Nystagmus, Pathologic - diagnosis | Pedigree | Night Blindness - physiopathology | TRPM Cation Channels - genetics | Eye Abnormalities - physiopathology | Consanguinity | Retinal Diseases - physiopathology | Genetic disorders | Index Medicus | Clinical Medicine | Medical and Health Sciences | Medicin och hälsovetenskap | Oftalmologi | Klinisk medicin
Journal Article
PLoS ONE, ISSN 1932-6203, 09/2015, Volume 10, Issue 9, pp. e0137072 - e0137072
Congenital stationary night blindness (CSNB) is a non-progressive, clinically and genetically heterogeneous disease of impaired night vision. We report a... 
METABOTROPIC GLUTAMATE-RECEPTOR | LIGHT RESPONSE | RABBIT RETINA | MULTIDISCIPLINARY SCIENCES | DEPOLARIZING BIPOLAR | SYNAPTIC-TRANSMISSION | ROD BIPOLAR CELLS | GENE-EXPRESSION | FRAMESHIFT MUTATION | RETINITIS-PIGMENTOSA | MAMMALIAN RETINA | RGS Proteins - genetics | Night Blindness - metabolism | Humans | Heterotrimeric GTP-Binding Proteins - metabolism | Male | Heterotrimeric GTP-Binding Proteins - genetics | Myopia - metabolism | Night Blindness - pathology | RGS Proteins - metabolism | Female | Genetic Diseases, X-Linked - genetics | Night Blindness - genetics | Genetic Diseases, X-Linked - physiopathology | Disease Models, Animal | Genetic Predisposition to Disease - genetics | Eye Diseases, Hereditary - pathology | Eye Diseases, Hereditary - physiopathology | Retina - physiopathology | Gene Expression Regulation | Retinal Cone Photoreceptor Cells - physiology | Proteoglycans - metabolism | Myopia - pathology | Presynaptic Terminals - physiology | Genetic Diseases, X-Linked - metabolism | Eye Diseases, Hereditary - genetics | Myopia - genetics | Animals | Calcium Channels, L-Type - genetics | Myopia - physiopathology | Pedigree | Night Blindness - physiopathology | Dogs | Genetic Diseases, X-Linked - pathology | Presynaptic Terminals - metabolism | Calcium Channels, L-Type - metabolism | Retinal Cone Photoreceptor Cells - metabolism | Eye Diseases, Hereditary - metabolism | Proteoglycans - genetics | Immunohistochemistry | Veterinary colleges | Protein kinase C | Disease | Genes | Antibodies | Retina | Labelling | Rods | Nyctalopia | Veterinary medicine | Homozygosity | Modulators | Defects | Gene sequencing | Proteins | Signal transduction | Rodents | Bipolar cells | Synaptic ribbons | Dendrites | Terminals | University graduates | Night vision | Phenotypes | Congenital diseases | Immunomodulation | Gene expression | Electron microscopy | Spherules | Cones | Vision | Blindness | Photoreceptors | Mutation | Gene mapping | Stationary night blindness | Cellular structure | Pharmaceuticals | Index Medicus
Journal Article
Clinical Genetics, ISSN 0009-9163, 06/2016, Volume 89, Issue 6, pp. 690 - 699
Congenital stationary night blindness ( CSNB ) is a clinically and genetically heterogeneous retinal disorder which represents rod photoreceptor dysfunction or... 
SLC24A1 | high‐throughput sequencing | congenital stationary night blindness | humans | Congenital stationary night blindness | High-throughput sequencing | Humans | RHODOPSIN GENE | ALPHA-SUBUNIT | CHANNEL | PATHOGENIC MECHANISMS | ROD TRANSDUCIN | GENETICS & HEREDITY | MISSENSE MUTATION | ELECTRORETINOGRAM | CONE DYSTROPHY | NA/CA-K EXCHANGER | NA+/CA2+-K+ EXCHANGERS | high-throughput sequencing | Eye Diseases, Hereditary - diagnosis | Family Health | Male | Sodium-Calcium Exchanger - genetics | Base Sequence | Myopia - diagnosis | Female | Genetic Diseases, X-Linked - genetics | High-Throughput Nucleotide Sequencing - methods | Night Blindness - genetics | Genetic Diseases, X-Linked - physiopathology | Electroretinography | Amino Acid Sequence | Genetic Predisposition to Disease - genetics | Eye Diseases, Hereditary - physiopathology | Night Blindness - diagnosis | Genes, Recessive | Genetic Diseases, X-Linked - diagnosis | Eye Diseases, Hereditary - genetics | Myopia - genetics | Sequence Homology, Amino Acid | Homozygote | Exome - genetics | Myopia - physiopathology | Pedigree | Night Blindness - physiopathology | Mutation | Analysis | Genomics | Genetic disorders | Retina | Photoreceptors | Eye diseases | Congenital diseases | Blindness | Index Medicus | Life Sciences | Human health and pathology | Genetics
Journal Article
Chemical Senses, ISSN 0379-864X, 07/2013, Volume 38, Issue 6, pp. 509 - 517
Sight is undoubtedly not only important for food identification and selection but also for the modulation of gustatory sensitivity. We can, therefore, assume... 
Multisensory integration | Food neophobia | Intuitive eating | Taste thresholds | Vision | Plasticity | EATING BEHAVIOR | PHYSIOLOGY | FOOD SCIENCE & TECHNOLOGY | HUMANS | intuitive eating | plasticity | NEUROSCIENCES | food neophobia | CHILDREN | vision | MONOSODIUM GLUTAMATE | taste thresholds