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Results of search for 'su:"Color Vision Defects"', page 148 of 202
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Authors
Alpern, M
Birch, J
Carroll, Joseph
Cole, Barry L
Hauswirth, William W
Ichikawa, H
Jaeger, W
Kohl, Susanne
Lanthony, P
Michaelides, Michel
Mollon, J D
Neitz, Jay
Neitz, Maureen
Pinckers, A
Pokorny, J
Sharpe, L T
Smith, V C
Verriest, G
Wissinger, Bernd
Zrenner, E
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Adolescent
Adult
Aged
Child
Color Perception
Color Perception Tests
Color Vision Defects
Electroretinography
Female
Humans
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Middle Aged
Visual Acuity
complications
diagnosis
etiology
genetics
methods
physiology
physiopathology
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2941.
A frameshift insertion in the cone cyclic nucleotide gated cation channel causes complete achromatopsia in a consanguineous family from a rural isolate.
[electronic resource]
by
Rojas, Cecilia V
María, Lorena Santa
Santos, José Luis
Cortés, Fanny
Alliende, María Angélica
Producer:
20030317
In:
European journal of human genetics : EJHG
vol. 10
Online resources:
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2942.
Color discrimination impairment in workers exposed to mercury vapor.
[electronic resource]
by
Urban, Pavel
Gobba, Fabriziomaria
Nerudová, Jana
Lukás, Edgar
Cábelková, Zdena
Cikrt, Miroslav
Producer:
20031027
In:
Neurotoxicology
vol. 24
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2943.
Visual dysfunction in HIV-positive patients without infectious retinopathy.
[electronic resource]
by
Plummer, D J
Sample, P A
Freeman, W R
Producer:
19980612
In:
AIDS patient care and STDs
vol. 12
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2944.
Tilted disc syndrome and colour vision.
[electronic resource]
by
Vuori, Marja-Liisa
Mäntyjärvi, Maija
Producer:
20071023
In:
Acta ophthalmologica Scandinavica
vol. 85
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2945.
Cone-mediated multifocal electroretinogram in early age-related maculopathy and its relationships with subjective macular function tests.
[electronic resource]
by
Feigl, Beatrix
Brown, Brian
Lovie-Kitchin, Jan
Swann, Peter
Producer:
20050228
In:
Current eye research
vol. 29
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2946.
Elephants and human color-blind deuteranopes have identical sets of visual pigments.
[electronic resource]
by
Yokoyama, Shozo
Takenaka, Naomi
Agnew, Dalen W
Shoshani, Jeheskel
Producer:
20060606
In:
Genetics
vol. 170
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2947.
[CONSIDERATIONS ON VISUAL DEFECTS FOUND IN THE SCHOOL POPULATION OF THE TOWN OF CARRARA IN THE SCHOOL-YEARS 1961-1962 AND 1962-1963].
[electronic resource]
by
BARGHINI, G
BASSANO, L
BASSANI, A
LAZZERINI, A
Producer:
19961201
In:
Rivista italiana d'igiene
vol. 23
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2948.
Long-term occupational exposure to organic solvents affects color vision, contrast sensitivity and visual fields.
[electronic resource]
by
Costa, Thiago Leiros
Barboni, Mirella Telles Salgueiro
Moura, Ana Laura de Araújo
Bonci, Daniela Maria Oliveira
Gualtieri, Mirella
de Lima Silveira, Luiz Carlos
Ventura, Dora Fix
Producer:
20130116
In:
PloS one
vol. 7
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2949.
Abnormal achromatic and chromatic contrast sensitivity in neurofibromatosis type 1.
[electronic resource]
by
Ribeiro, Maria José
Violante, Inês Ribeiro
Bernardino, Inês
Ramos, Fabiana
Saraiva, Jorge
Reviriego, Pablo
Upadhyaya, Meena
Silva, Eduardo Duarte
Castelo-Branco, Miguel
Producer:
20120402
In:
Investigative ophthalmology & visual science
vol. 53
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2950.
Association between Val66Met polymorphism of Brain-Derived Neurotrophic Factor (BDNF) gene and a deficiency of colour vision in alcohol-dependent male patients.
[electronic resource]
by
Serý, Omar
Sťastný, František
Zvolský, Petr
Hlinomazová, Zuzana
Balcar, Vladimir J
Producer:
20111107
In:
Neuroscience letters
vol. 499
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2951.
Blind to the risk: an analysis into the guidance offered to doctors and medical students with colour vision deficiency.
[electronic resource]
by
Raynor, Nicolas J
Hallam, Gemma
Hynes, Niamh K
Molloy, Brett T
Producer:
20210330
In:
Eye (London, England)
vol. 33
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2952.
[Pratical remarks on Farnsworth 100 Hue in acquired dyschromatopsies].
[electronic resource]
by
Biais, B
Guile, Y
Producer:
19760823
In:
Archives d'ophtalmologie
vol. 36
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2953.
Linkage disequilibrium for two X-linked genes in Sardinia and its bearing on the statistical mapping of the human X chromosome.
[electronic resource]
by
Filippi, G
Rinaldi, A
Palmarino, R
Seravalli, E
Siniscalco, M
Producer:
19770922
In:
Genetics
vol. 86
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2954.
Adrenoleukodystrophy: a complex chromosomal rearrangement in the Xq28 red/green-color-pigment gene region indicates two possible gene localizations.
[electronic resource]
by
Feil, R
Aubourg, P
Mosser, J
Douar, A M
Le Paslier, D
Philippe, C
Mandel, J L
Producer:
19920110
In:
American journal of human genetics
vol. 49
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2955.
Acquired color vision defects and self monitoring of blood sugar in diabetics.
[electronic resource]
by
Shute, D T
Oshinskie, L
Producer:
19870115
In:
Journal of the American Optometric Association
vol. 57
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2956.
Congenital adrenal hypoplasia--an X-linked disease.
[electronic resource]
by
Weiss, L
Mellinger, R C
Producer:
19710111
In:
Journal of medical genetics
vol. 7
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2957.
Relationship of color blindness to alcoholic liver damage.
[electronic resource]
by
Ugarte, G
Cruz-Coke, R
Rivera, L
Altschiller, H
Mardones, J
Producer:
19710210
In:
Pharmacology
vol. 4
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2958.
Further studies supporting the identity of congenital tritanopia and hereditary dominant optic atrophy.
[electronic resource]
by
Krill, A E
Smith, V C
Pokorny, J
Producer:
19710715
In:
Investigative ophthalmology
vol. 10
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2959.
Localisation of the Becker muscular dystrophy gene on the short arm of the X chromosome by linkage to cloned DNA sequences.
[electronic resource]
by
Kingston, H M
Sarfarazi, M
Thomas, N S
Harper, P S
Producer:
19840824
In:
Human genetics
vol. 67
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2960.
Achromatopsia. Clinical diagnosis and treatment.
[electronic resource]
by
O'Connor, P S
Tredici, T J
Ivan, D J
Mumma, J V
Shacklett, D E
Producer:
19831220
In:
Journal of clinical neuro-ophthalmology
vol. 2
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