PubMed (OMIM) for id: 5148

Year	Number of Results
1949	2
1953	1
1961	1
1966	1
1967	1
1980	1
1981	2
1982	3
1983	1
1984	1
1985	2
1986	1
1987	1
1989	1
1990	6
1991	2
1992	2
1993	1
1995	1
1996	2
1997	1
1998	1
1999	1
2000	4
2001	2
2003	2
2004	2
2005	1
2006	1
2007	2
2008	1
2010	2
2015	2
2024	0

1

Nonsyndromic retinitis pigmentosa is highly prevalent in the Jerusalem region with a high frequency of founder mutations.

Sharon D, Banin E. Sharon D, et al. Mol Vis. 2015 Jul 17;21:783-92. eCollection 2015. Mol Vis. 2015. PMID: 26261414 Free PMC article.

2

Charles Bonnet Syndrome in Advanced Retinitis Pigmentosa.

O'Hare F, Bentley SA, Wu Z, Guymer RH, Luu CD, Ayton LN. O'Hare F, et al. Ophthalmology. 2015 Sep;122(9):1951-3. doi: 10.1016/j.ophtha.2015.03.006. Epub 2015 Apr 11. Ophthalmology. 2015. PMID: 25870080 No abstract available.

3

Autosomal-recessive early-onset retinitis pigmentosa caused by a mutation in PDE6G, the gene encoding the gamma subunit of rod cGMP phosphodiesterase.

Dvir L, Srour G, Abu-Ras R, Miller B, Shalev SA, Ben-Yosef T. Dvir L, et al. Am J Hum Genet. 2010 Aug 13;87(2):258-64. doi: 10.1016/j.ajhg.2010.06.016. Epub 2010 Jul 22. Am J Hum Genet. 2010. PMID: 20655036 Free PMC article.

4

Genetic reactivation of cone photoreceptors restores visual responses in retinitis pigmentosa.

Busskamp V, Duebel J, Balya D, Fradot M, Viney TJ, Siegert S, Groner AC, Cabuy E, Forster V, Seeliger M, Biel M, Humphries P, Paques M, Mohand-Said S, Trono D, Deisseroth K, Sahel JA, Picaud S, Roska B. Busskamp V, et al. Science. 2010 Jul 23;329(5990):413-7. doi: 10.1126/science.1190897. Epub 2010 Jun 24. Science. 2010. PMID: 20576849 Free article.

5

The retinitis pigmentosa 2 gene product is a GTPase-activating protein for Arf-like 3.

Veltel S, Gasper R, Eisenacher E, Wittinghofer A. Veltel S, et al. Nat Struct Mol Biol. 2008 Apr;15(4):373-80. doi: 10.1038/nsmb.1396. Epub 2008 Mar 23. Nat Struct Mol Biol. 2008. PMID: 18376416

6

[Another Swiss family tree of dominant inherited retinitis pigmentosa].

REHSTEINER K. REHSTEINER K. Ophthalmologica. 1949 Jan;117(1):51-9. doi: 10.1159/000300644. Ophthalmologica. 1949. PMID: 18115690 German. No abstract available.

7

Recurrent mutation in the first zinc finger of the orphan nuclear receptor NR2E3 causes autosomal dominant retinitis pigmentosa.

Coppieters F, Leroy BP, Beysen D, Hellemans J, De Bosscher K, Haegeman G, Robberecht K, Wuyts W, Coucke PJ, De Baere E. Coppieters F, et al. Am J Hum Genet. 2007 Jul;81(1):147-57. doi: 10.1086/518426. Epub 2007 May 24. Am J Hum Genet. 2007. PMID: 17564971 Free PMC article.

8

Multifocal ERG reveals several patterns of cone degeneration in retinitis pigmentosa with concentric narrowing of the visual field.

Janáky M, Pálffy A, Deák A, Szilágyi M, Benedek G. Janáky M, et al. Invest Ophthalmol Vis Sci. 2007 Jan;48(1):383-9. doi: 10.1167/iovs.06-0661. Invest Ophthalmol Vis Sci. 2007. PMID: 17197558

9

Retinitis pigmentosa.

Hartong DT, Berson EL, Dryja TP. Hartong DT, et al. Lancet. 2006 Nov 18;368(9549):1795-809. doi: 10.1016/S0140-6736(06)69740-7. Lancet. 2006. PMID: 17113430 Review.

10

Histopathologic-genotypic correlations in retinitis pigmentosa and allied diseases.

Ben-Arie-Weintrob Y, Berson EL, Dryja TP. Ben-Arie-Weintrob Y, et al. Ophthalmic Genet. 2005 Jun;26(2):91-100. doi: 10.1080/13816810590968032. Ophthalmic Genet. 2005. PMID: 16020312

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