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Retinitis Pigmentosa: more books (45)

Retinitis Pigmentosa by John R. Heckenlively, 1987-12
Retinitis Pigmentosa Advances in Genetical Research by Peter Humphries, Shomi Bhattacharya, et all 1991-07-06
Retinitis Pigmentosa:Clinical Implications of Current Research (Advances in Experimental Medicine & Biology)
Retinitis Pigmentosa: Causes, Diagnosis and Treatment (Eye and Vision Research Developments)
Research in Retinitis Pigmentosa: Part 1 of the Proceedings of the 4th Congress of the International Retinitis Pigmentosa Association, Bad Nauheim, We ... of Pharmacology and Therapeutics) (v. 62) by International Retinitis Pigmentosa Assoc, 1987-01
Genetic eye diseases: Retinitis pigmentosa and other inherited eye disorders ; proceedings of the International Symposium on Genetics and Ophthalmology, ... 1981 (Birth defects original article series)
Retinitis Pigmentosa by William Toy Shoemaker, 2010-01-08
Retinitis Pigmentosa: Patients' Fight for Sight by F. Brunsmann, 1988-05-01
Retinitis pigmentosa and hypogammaglobulinemia.(Clinical report): An article from: Southern Medical Journal by John C. Starr, George W. Brasher, et all 2006-09-01
Retinitis pigmentosa and common variable immunodeficiency disease: associated or separate?(Editorial): An article from: Southern Medical Journal by Margaret M. DeAngelis, 2006-09-01
Retinitis Pigmentosa Medical Guide by Qontro Medical Guides, 2008-07-09
Gale Encyclopedia of Medicine: Retinitis pigmentosa by CGC Dorothy Elinor Stonely MS, 2002-01-01
An Ethnographic Study of the Village of Hosakerekodi, Karnataka, India, to Determine Potential Factors for Retinitis Pigmentosa in the Region by Lyn Gopalan, 1992
Gene therapy helps blind mice see: sight restored in cone cells impaired by retinitis pigmentosa.(Body & Brain): An article from: Science News by Gwyneth Dickey, 2010-07-17

lists with details

Introduction: Retinitis Pigmentosa - WrongDiagnosis.com
Introduction to retinitis pigmentosa as a medical condition including symptoms, diagnosis, misdiagnosis, treatment, prevention, and prognosis.
http://www.wrongdiagnosis.com/r/retinitis_pigmentosa/intro.htm

Extractions: Researching symptoms of Retinitis Pigmentosa: Further information about the symptoms of Retinitis Pigmentosa is available including a list of symptoms of Retinitis Pigmentosa , or alternatively return to research other symptoms in the symptom center Causes of Retinitis Pigmentosa: Research more detailed information about the causes of Retinitis Pigmentosa , other possibly hidden causes of Retinitis Pigmentosa , or other general information about Retinitis Pigmentosa Statistics and Retinitis Pigmentosa: Various sources and calculations are available in statistics about Retinitis Pigmentosa prevalence and incidence statistics for Retinitis Pigmentosa , and you can also research other medical statistics in our statistics center
Home
guide for finding information about retinitis pigmentosa on the Internet. retinitis pigmentosa is an inherited condition which results in gradual loss
http://iris.medoph.unimelb.edu.au/new/rp/

Extractions: home what is RP? genetics and inheritance treatment ... contact us About this site This site is designed to be a 'travel guide' for finding information about Retinitis Pigmentosa on the Internet. Retinitis Pigmentosa is an inherited condition which results in gradual loss of vision. When someone is diagnosed with RP, they or their family may feel confused, alone and frightened. We hope that by providing easy access to useful information it will help patients and their families understand the disease and adjust to the diagnosis. We welcome your feedback about this site.
BBC - Health - Conditions - Retinitis Pigmentosa
A guide to retinitis pigmentosa. retinitis pigmentosa (RP) is the name given to a group of hereditary diseases of the retina the light sensitive
http://www.bbc.co.uk/health/conditions/retinitispigmentosa1.shtml

Extractions: Send it to a friend! Dr Trisha Macnair Retinitis pigmentosa (RP) is the name given to a group of hereditary diseases of the retina - the light sensitive tissue in the back of the eye. About 25,000 families in the UK are affected. How's the retina affected? Genetic influences Further help In these conditions the retina slowly degenerates and gradually loses its ability to transmit images to the brain, resulting in a progressive loss in vision. Cells from the pigmented layer of the retina migrate into the nerve cell containing layer, causing a typical pattern of black or brown star shapes in the retina that give the diseases their name. Symptoms usually become apparent between the ages of ten and 30 (although they develop much earlier in life in some types of RP, and much, much later in others). Visual loss may be slow or rapid. Often the first symptom is night blindness followed by a narrowing of side vision leading to 'tunnel' vision. In one type of RP the loss of vision begins in the central area (macular dystrophy) interfering with reading and detailed work. There may be associated syndromes such as Usher syndrome (hearing and sight loss). Dozens of different gene mutations that may lead to RP have been described. The condition results from inheriting one or two of these abnormal genes, depending on the type of RP.
Eye Conditions - Retinitis Pigmentosa
retinitis pigmentosa (RP) is the collective name for a range of diseases that damage the retina and cause vision to fade. There is no cure,
http://www.betterhealth.vic.gov.au/bhcv2/bhcarticles.nsf/pages/Eye_conditions_re
The DRM WebWatcher: Retinitis Pigmentosa (RP)
A Disability Resources Monthly guide to the best online resources about retinitis pigmentosa.
http://www.disabilityresources.org/RP.html

Extractions: Home WebWatcher Regional Librarians ... Contact Us The DRM WebWatcher Retinitis Pigmentosa (RP) Updated 1/5/2004 A B C D ... About/Hint/Link Retinitis Pigmentosa (RP) is an hereditary, progressive eye disease that affects a person's night and peripheral vision. See these sites for more information. Australian Retinitis Pigmentosa and Retinal Degeneration Good resources from down under! This site includes information and links relating to computer access and adaptive equipment, international and Australian RP and low vision support organizations, links to research sites and sites by persons with RP, chat, mailing lists, and more. Focus Focus is a "a grass-roots group of RP patients calling for new and expanded directions in scientific research and applied medicine for their condition." Its website provides information about alternative treatments and current research and studies, which are provided on "an information only basis and do not intend or imply that they are the correct or only course of treatments that should be administered." The site includes extensive information about RP and nutrition, FAQs, and a newsletter. As always, DRM recommends viewing medical and legal information on personal websites with caution. RP - Retinitis Pigmentosa John Wenberg, the author of this personal homepage, has compiled an extensive guide to RP and RP resources online. Topics covered include RP links, RP E-Pals, mailing lists, research, RP Internet chat, the inheritance of retinal degeneration, online articles, contacts, FAQs, personal experiences, and more. As always, DRM recommends viewing medical and legal information on personal websites with caution.
Usher Syndrome & Retinitis Pigmentosa: Information & Referrals
Usher Syndrome retinitis pigmentosa Information Referrals.
http://www.deafblind.com/nidcd.html

Extractions: About 3-6 percent of all deaf children and perhaps an equal number of hard-of-hearing children have Usher syndrome (US), which itself is more than one genetic condition. On the basis of clinical findings, at least three types exist . Gene localization studies show that one clinical type may be due to several different genes located on different chromosomes. The most important clinical distinctions are based on the differences in hearing and balance. The retinitis pigmentosa (RP) may look the same even to an experienced eye doctor except that the symptoms can begin earlier in Type I. Usher syndrome is one of several conditions in which both hearing loss and retinitis pigmentosa are present. In this article, the symptoms of RP and the various forms of Usher syndrome will be discussed. Suggestions will be given on where to go for further diagnosis and information. Retinitis Pigmentosa (RP) Other Hearing Loss/Retinitis Pigmentosa (RP) Conditions.
Retinitis Pigmentosa, UPMC | University Of Pittsburgh Medical Center, Pittsburgh
Information about diagnosis, treatment options, and current research for retinitis pigmentosa from the health care experts at UPMC.
http://eye.upmc.com/RetinitisPigmentosa/
Elsevier.com - Retinitis Pigmentosa Patients Fight For Sight
The promotion of research by the German retinitis pigmentosa Society (DRPV), Methods for monitoring treatment in retinitis pigmentosa, R Hennekes.
http://www.elsevier.com/wps/product/cws_home/26638

Extractions: Home Site map Regional Sites Advanced Product Search ... Retinitis Pigmentosa: Patients' Fight for Sight Book information Product description Audience Author information and services Ordering information Bibliographic and ordering information Conditions of sale Book related information Submit your book proposal Other books in same subject area About Elsevier Select your view RETINITIS PIGMENTOSA: PATIENTS' FIGHT FOR SIGHT This volume covers the social and medical aspects of patient care in retinitis pigmentosa (RP), experiences of patients as well as national and international activities of the RP societies. The patient-related problems include such topics as genetic counselling, technical aids for blind and visually handicapped, therapy trials, human services, psychological, social, vocational and familial problems.
Retina Hong Kong
This is the Home Page of Retina Hong Kong (formerly known as Hong Kong retinitis pigmentosa Society ). We offer information in English and Chinese coded in
http://www.retina.org.hk/

Extractions: This is the Home Page of Retina Hong Kong (formerly known as "Hong Kong Retinitis Pigmentosa Society"). We offer information in English and Chinese coded in BIG5 and GB. You can view all of our information under Operating System of such codes. If you want to know more about Retinal Degenerative Diseases and Retina Hong Kong, please make your choice: His hope for sight...... Depends on our support, and your help! 101, Lai Huen House, Lai Kok Estate,
The Foundation Fighting Blindess - Retinitis Pigmentosa
Visit Dr. Yousef Matuk s site to learn about retinitis pigmentosa from a Click Here, What is retinitis pigmentosa? retinitis pigmentosa (RP) is the name
http://www.ffb.ca/disease_rp.php?hc=0
Retinitis Pigmentosa - The Foundation Fighting Blindness - Canada
You are in the Diseases section on the retinitis pigmentosa page. What is retinitis pigmentosa? retinitis pigmentosa (RP) is the name given to a group of
http://www.ffb.ca/disease_rp-txt.html
Retinitis Pigmentosa Definition - Medical Dictionary Definitions Of Popular Medi
Online Medical Dictionary and glossary with medical definitions.
http://www.medterms.com/script/main/art.asp?articlekey=22264
Retinitis Pigmentosa
retinitis pigmentosa is the name given to a group of diseases that affect the retina. In retinitis pigmentosa, the retina begins to degenerate,
http://ww3.komotv.com/global/story.asp?s=1230586
BCAO :: :: Retinitis Pigmentosa (RP)
Your eye health Common Vision Problems retinitis pigmentosa (RP) retinitis pigmentosa is a group of inherited diseases developing inside the pigmented
http://www.optometrists.bc.ca/content2/Retinitis_pigmentosa/104/0/58

Extractions: select one Allergies Amblyopia Astigmatism Blepharitis Cataracts Colour deficiency Computer Vision Syndrome Conjunctivitis Corneal ulceration Diabetes Diabetic retinopathy Drooping eyelids Dry eyes Farsightedness Glaucoma Iritis or anterior uveitis Keratitis Keratoconus Light sensitivity Low vision Macular degeneration Nearsightedness Neovascularization Ocular hypertension Pinguecula Presbyopia Pterygium Retinal detachment Retinitis pigmentosa Strabismus Styes Take Your B.C. Eye Test Your eye health > Common Vision Problems > Retinitis pigmentosa (RP) Retinitis pigmentosa is a group of inherited diseases developing inside the pigmented area of the retina of the eye. They tend to become apparent between age 10 and 30, although some types of retinitis pigmentosa occur in childhood or later in life. Vision changes include night blindness, loss of side vision, and "tunnel vision. The most common symptom of retinitis pigmentosa is a personal history of visual problems at dusk or in low light. This problem cannot be helped by corrective lenses, however, because the retina itself is deteriorating. Your B.C. Optometrist can help you adapt to living with retinitis pigmentosa.
Retinitis Pigmentosa
retinitis pigmentosa Information about Retinitis Pgimentosa, including treatment, prevention, diagnosis. Retina International -.
http://www.ability.org.uk/Retinitis_Pigmentosa.html

Extractions: "see the ability, not the disability" You to can help support the Ability Project by: Our Aims ... Z Retinitis Pigmentosa Retinitis Pigmentosa - Information about Retinitis Pgimentosa, including treatment, prevention, diagnosis. Retina International -. Supports research into the cause and treatments of these eye diseases. British Retinitis Pigmentosa Society Samuel R. Evans, LPC, CRC, NCC-counseling - a counselor and advocate for people with physical and psychiatric disabilities. Webmaster . Site Design by Ability "see the ability, not the disability" Acknowledgments
Connotea: Vferraz's Bookmarks Matching Tag "retinitis Pigmentosa"
vferraz s bookmarks matching tag retinitis pigmentosa . Gene mutations in retinitis pigmentosa and their clinical implications. (info). DY Wang et al.
http://www.connotea.org/user/vferraz/tag/retinitis pigmentosa

Extractions: Home Latest News ... Contact Us By Usage Ablepharon-macrostom... Angelman angelman syndrome ... therapy vferraz vferraz's bookmarks matching tag "retinitis pigmentosa" Gene mutations in retinitis pigmentosa and their clinical implications. info D Y Wang et al. Clin Chim Acta Jan 2005 PMID: 15563868 doi:10.1016/j.cccn.2004.08.004 Posted by vferraz to retinitis pigmentosa ophthalmic genetics on Thu Mar 03 2005 at 01:23 UTC Add a bookmark Create a new group Create a tag note Rename a tag ... Edit my registration
Retinitis Pigmentosa - Wikipedia, The Free Encyclopedia
The same view with tunnel vision from retinitis pigmentosa. retinitis pigmentosa, or RP, is a genetic eye condition. Generally, night blindness precedes
http://en.wikipedia.org/wiki/Retinitis_pigmentosa

Extractions: You did it! Over US$240,000 was donated in the 21 day fund drive. Thank you for your generosity! You are still welcome to make a donation or purchase Wikimedia merchandise Normal vision. Courtesy NIH National Eye Institute The same view with tunnel vision from retinitis pigmentosa Retinitis pigmentosa , or RP , is a genetic eye condition. Generally, night blindness precedes tunnel vision by years or even decades. Many people with RP do not become legally blind until their 40s or 50s and retain some sight all their life. Others go completely blind from RP, in some cases as early as childhood. Progression of RP is different in each case. RP is a group of inherited disorders in which abnormalities of the photoreceptors rods and cones ) or the retinal pigment epithelium (RPE) of the retina lead to progressive visual loss. Affected individuals first experience defective dark adaptation or nyctalopia (night blindness), followed by constriction of the peripheral visual field and, eventually, loss of central vision late in the course of the disease. edit Mottling of the retinal pigment epithelium with bone-spicule pigmentation is typically pathognomonic for retinis pigmentosa. Other ocular features include waxy pallor of the optic nerve head, attenuated retinal vessels, cellophane maculopathy, cystic macular edema, and posterior subcapsular cataract.
Institute Of Ophthalmology
The Institute of Ophthalmology retinitis pigmentosa Page the condition, treatment options, research underway at the Institute of Ophthalmology, etc.
http://www.ucl.ac.uk/ioo/eyedisease/rp.htm

Extractions: Three forms of biological treatment are being developed at the Institute of Ophthalmology, namely the use of drugs to delay cell death, gene therapy and cell transplantation. The progressive nature of retinal degenerations, and the ability to make the diagnosis genetically before any visual impairment has become apparent, make it possible to intervene earlier and prevent the loss of rods and cones. In experimental systems we are exploring different ways of achieving this. The closest to application in patients is the use of so-called survival factors, which are injected into the eye on a monthly basis. Additionally, other drug-based strategies are being examined. As retinal degenerations have a genetic basis we have a large programme designing ways of replacing defective genes with those that function normally. Delivering the gene to the right group of cells, installing it and then ensuring it is controlled properly whilst not causing any serious side effects, is a colossal challenge. However, the potential benefits are so great that the considerable investment of time and money that will be required will be well worthwhile. One day it may be possible to replace degenerated rods and cones by transplantation and early studies are in progress to explore this exciting possibility. More immediately, transplantation is likely to have a role in the delivery of factors that will aid the survival of photoreceptors.
RPlist Home Page
The most common forms are Macular Degeneration and retinitis pigmentosa (or RP, which gave its name to RPlist); other forms include Usher syndrome,
http://www.dixonvision.com/rplist/

Extractions: the retinal degeneration discussion list. See here how you can make these pages easier to read. This is the official web site of RPlist, the Retinal Degeneration Mailing List. It gives information about this mailing list only. For information about retinal degenerations, refer to the links page RPlist is an electronic mailing list , i.e. a group of people who use electronic mail (e-mail) on the Internet to exchange ideas and information. Any e-mail message sent to the list's address is automatically forwarded to all members (subscribers). Anyone with a valid Internet e-mail address can join or leave the group at any time. Participation is entirely free of charge. RPlist is dedicated to discussions related to retinal degenerations . It is open to people personally effected by these conditions, their family and friends, people working in the eye care or low vision fields, and more generally anyone who wants to learn or share experience in relation with retinal conditions. back to top What is a Retinal Degeneration?
Genome.gov | Learning About Retinitis Pigmentosa
What do we know about heredity and retinitis pigmentosa? retinitis pigmentosa (RP) is the name given to a group of inherited eye diseases that affect
http://www.genome.gov/13514348

Extractions: Print Version What is Retinitis Pigmentosa? What are the symptoms of Retinitis Pigmentosa? What causes Retinitis Pigmentosa? How is Retinitis Pigmentosa treated? ... Additional Resources for Retinitis Pigmentosa Retinitis pigmentosa (RP) is the name given to a group of inherited eye diseases that affect the retina (the light-sensitive part of the eye). RP causes the breakdown of photoreceptor cells (cells in the retina that detect light). Photoreceptor cells capture and process light helping us to see. As these cells breakdown and die, patients experience progressive vision loss. The most common feature of all forms of RP is a gradual breakdown of rods (retinal cells that detect dim light) and cones (retinal cells that detect light and color). Most forms of RP first cause the breakdown of rod cells. These forms of RP, sometimes called rod-cone dystrophy, usually begin with night blindness. Night blindness is somewhat like the experience normally sighted individuals encounter when entering a dark movie theatre on a bright, sunny day. However, patients with RP cannot adjust well to dark and dimly lit environments. Top of page What are the symptoms of Retinitis Pigmentosa?

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