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         Achromatopsia:     more detail
  1. My Blindy Girl - A Mother's Journey Through Achromatopsia by Ellen Tomaszewski, 2009
  2. Achromatopsia: A Medical Dictionary, Bibliography, And Annotated Research Guide To Internet References by Icon Health Publications, 2004-08-20
  3. My Blindy Girl - A Mother's Journey Through Achromatopsia by Ellen Tomaszewski, 2008
  4. My Blindy Girl - a mother's journey through achromatopsia by Ellen Tomaszewski, 2010-01-17
  5. Visual Disturbances and Blindness: Color Blindness, Alice Walker, Macular Degeneration, Achromatopsia, Akinetopsia, Low Vision, Amblyopia
  6. Understanding and coping with achromatopsia by Frances Futterman, 1998
  7. Achromatopsia

81. Retina International's Scientific Newsletter - Cone Cyclic Nucleotide-gated Cati
achromatopsia, Pro 163 Leu, CT, 0528, 5, NlaIV, Homozygous, (1).achromatopsia, Arg 283 Trp, CT, 0887, 7, -MspI, Homozygous, (1). achromatopsia,
http://www.retina-international.org/sci-news/cnga3mut.htm
Retina International's Scientific Newsletter
Mutation Database
Mutations of the Cone Cyclic Nucleotide-gated Cation Channel
Recent update from: 18.07.99 Phenotype Mutation Basechange Nucleotide Exon Restriction Site Classification
Mutation Database OMIM Reference Achromatopsia Pro 163 Leu C-T -NlaIV Homozygous
Achromatopsia Arg 283 Trp C-T -MspI Homozygous
Achromatopsia Arg 283 Gln G-A
Heterozygous
Achromatopsia Thr 291 Arg C-G
Heterozygous
Achromatopsia Arg 411 Trp C-T +NlaIII Heterozygous
Achromatopsia Val 529 Met G-A +NcoI Heterozygous Achromatopsia Phe 547 Leu C-A Heterozygous Achromatopsia Gly 557 Arg G-A Heterozygous Polymorphism IVS4+91g-c g-c Polymorphism IVS2+46g-t g-t Polymorphism IVS2+16g-a g-a Polymorphism Asp 24 Asp C-T Polymorphism Thr 66 Thr C-T Polymorphism Thr 153 Met C-T -BbsI References 1. Kohl, S., Marx, T., Giddings, I., Jagle, H., Jacobson, S.G., Apfelstedt-Sylla, E., Zrenner, E., Sharpe, L.T., and Wissinger, B. Total colourblindness is caused by mutations in the gene encoding the alpha-subunit of the cone photoreceptor cGMP-gated cation channel. 1998; Nat.Genet. 19: 257 - 259. Goto Top Link to PudMed Return to Retina International's Scientific Newsletter ... Return to pagehead Contact the editor: irpamp@irpa.org

82. Internet Public Library: Vision And Eye Conditions
achromatopsia Network http//www.achromat.org/ The achromatopsia Network is an informationand support network for individuals and families concerned with the
http://www.ipl.org/div/aon/browse/hea14.70.00/
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Achromatopsia Network
http://www.achromat.org/
The Achromatopsia Network is "an information and support network for individuals and families concerned with the rare inherited vision disorder achromatopsia, including both rod monochromacy and blue cone monochromacy." This website contains a description of achromatopsia, the mission and purpose of the Achromatopsia Network, special needs of people with achromatopsia, information on becoming a member, a list of informational materials available through the Network and partial contents of The Achromatopsia Network Newsletter.
The American Academy of Ophthalmology
http://www.eyenet.org/

83. The Macula
the color deficiency is “monochromatism.” Very few people (about 3 in a million)have total “color blindness” or “achromatopsia”; they see things
http://www.tedmontgomery.com/the_eye/macula.html
The Macula
Anatomy, Physiology and
Pathology of the Human Eye
Ted M. Montgomery,
Optometric Physician
Click on a selection here fovea centralis color vision color deficiency color vision testing macular degeneration Amsler grid cystoid macular edema central serous retinopathy , or scroll down the page.
Full Page View

The macula lutea is the small, yellowish central portion of the retina , and it is the area providing the clearest, most distinct vision. When one looks directly at something, the light from that object forms an image on one’s macula. A healthy macula ordinarily is capable of achieving at least 20/20 (“normal”) vision or visual acuity, even if this is with a correction in glasses or contact lenses. Not uncommonly, an eye’s best visual acuity is 20/15; in this case, that eye can perceive the same detail at 20 feet that a 20/20 eye must move up to 15 feet to see as distinctly. Some people are even capable of 20/10 vision, which is twice as good as 20/20. Vision this acute may be due to there being more cones per square millimeter of the macula than in the average eye, enabling that eye to distinguish much greater detail.
fovea centralis
The very center of the macula is called the fovea centralis , an area where all of the photoreceptors are cones ; there are no rods in the fovea. The fovea is the point of sharpest, most acute visual acuity. (The center of the fovea is the “foveola.”) Because the fovea has no rods, small dim objects in the dark cannot be seen if one looks directly at them. For this reason, to detect faint stars in the sky, one must look just to the side of them so that their light falls on a retinal area, containing numerous rods, outside of the macular zone.

84. Achromatopsia Website Results :: Linkspider UK
achromatopsia Websites from the Linkspider UK. achromatopsia Directory.Complete Results for achromatopsia Related Topics. achromatopsia
http://www.linkspider.co.uk/Health/ConditionsandDiseases/EyeDisorders/ColorBlind
Achromatopsia Websites from Linkspider UK Keyword: Achromatopsia Linkspider UK Directory
Achromatopsia
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85. The Psych3120 2000-September Archive By Subject
Kelly Symes; Psych3120 achromatopsia FCS SLC; Psych3120 achromatopsiaCatherineW123@aol.com; Psych3120 achromatopsia CatherineW123
http://lists.csbs.utah.edu/pipermail/psych3120/2000-September/subject.html
2000-September Archives by Subject
Starting: Thu Aug 31 18:32:31 2000
Ending: Sat Sep 30 15:47:04 2000
Messages:

86. Nature Publishing Group
Their ancestors have a high incidence of the autosomal recessive disorder achromatopsia,or total colorblindness, and genetic analysis of the Pingelapese has
http://www.nature.com/cgi-taf/DynaPage.taf?file=/nm/journal/v6/n7/full/nm0700_74

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