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         Retinitis Pigmentosa:     more books (45)
  1. Retinitis Pigmentosa by John R. Heckenlively, 1987-12
  2. Retinitis Pigmentosa Advances in Genetical Research by Peter Humphries, Shomi Bhattacharya, et all 1991-07-06
  3. Retinitis Pigmentosa:Clinical Implications of Current Research (Advances in Experimental Medicine & Biology)
  4. Retinitis Pigmentosa: Causes, Diagnosis and Treatment (Eye and Vision Research Developments)
  5. 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
  6. 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)
  7. Retinitis Pigmentosa by William Toy Shoemaker, 2010-01-08
  8. Retinitis Pigmentosa: Patients' Fight for Sight by F. Brunsmann, 1988-05-01
  9. Retinitis pigmentosa and hypogammaglobulinemia.(Clinical report): An article from: Southern Medical Journal by John C. Starr, George W. Brasher, et all 2006-09-01
  10. Retinitis pigmentosa and common variable immunodeficiency disease: associated or separate?(Editorial): An article from: Southern Medical Journal by Margaret M. DeAngelis, 2006-09-01
  11. Retinitis Pigmentosa Medical Guide by Qontro Medical Guides, 2008-07-09
  12. Gale Encyclopedia of Medicine: Retinitis pigmentosa by CGC Dorothy Elinor Stonely MS, 2002-01-01
  13. An Ethnographic Study of the Village of Hosakerekodi, Karnataka, India, to Determine Potential Factors for Retinitis Pigmentosa in the Region by Lyn Gopalan, 1992
  14. 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

101. HealthCentral - General Encyclopedia - Retinitis Pigmentosa
General Health Encyclopedia, retinitis pigmentosa. The risk factors are a family history of retinitis pigmentosa. It is a rare condition.
http://www.healthcentral.com/mhc/top/001029.cfm
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102. Retinitis Pigmentosa (RP)
retinitis pigmentosa (RP). What causes it? As of yet, the cause of retinitis pigmentosa has not been found, but research into the disease is ongoing.
http://www.irishhealth.com/?level=4&con=196

103. Usher Syndrome & Retinitis Pigmentosa: Information & Referrals
Go Back to The Archives Page. Usher Syndrome retinitis pigmentosa Information Referrals. This retinitis pigmentosa (RP). Retinitis
http://www.deafblind.com/nidcd.html

This information is from the National Institute on Deafness and Other Communication Disorders (NIDCD) Hereditary Hearing Impairment Resource Registry (HHIRR).
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.

104. Www.heim2.tu-clausthal.de/PROJEKT/SOZIALES/RP/index-d.html
retinitis pigmentosa Contact a Family for families with printer friendly, retinitis pigmentosa, BRITISH retinitis pigmentosa SOCIETY. British retinitis pigmentosa Society PO Box 350 Buckingham
http://www.heim2.tu-clausthal.de/PROJEKT/SOZIALES/RP/index-d.html

105. HHMI News: Ion Channel Malfunctions In Form Of Retinitis Pigmentosa
Ion Channel Malfunctions in Form of retinitis pigmentosa. The more we know about the fundamental processes that underlie these diseases
http://www.hhmi.org/news/zagotta.html
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Ion Channel Malfunctions in Form of Retinitis Pigmentosa
"The more we know about the fundamental processes that underlie these diseases, the closer we are to being able to intervene in an intelligent way," said HHMI investigator William N. Zagotta. HHMI researchers have identified a molecular malfunction that causes a form of retinitis pigmentosa (RP), an inherited disease that causes progressive loss of vision and ultimately blindness. Mutations in any one of 19 genes can cause RP. Although the researchers studied a specific mutation that alters only one of the 19 genes, their studies may offer a broad explanation for how the rod photoreceptor cells in the eye slowly die, which can ultimately lead to blindness. The studies were reported in an article published in the April 11, 2002, issue of the journal

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