Literature DB >> 1495768

Investigation of disease mechanisms in retinitis pigmentosa.

A C Bird1.   

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Year:  1992        PMID： 1495768     DOI： 10.3109/13816819209087605

Source DB:  PubMed          Journal:  Ophthalmic Paediatr Genet        ISSN： 0167-6784


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  8 in total

1.  Self-complementary AAV-mediated gene therapy restores cone function and prevents cone degeneration in two models of Rpe65 deficiency.

Authors:  J Pang; S E Boye; B Lei; S L Boye; D Everhart; R Ryals; Y Umino; B Rohrer; J Alexander; J Li; X Dai; Q Li; B Chang; R Barlow; W W Hauswirth
Journal:  Gene Ther       Date:  2010-03-18       Impact factor: 5.250

2.  Structural and functional correlates in color vision deficiency.

Authors:  A Gupta; G Laxmi; M G Nittala; R Raman
Journal:  Eye (Lond)       Date:  2011-04-15       Impact factor: 3.775

Review 3.  Molecular genetics of macular dystrophies.

Authors:  K Zhang; H Yeon; M Han; L A Donoso
Journal:  Br J Ophthalmol       Date:  1996-11       Impact factor: 4.638

4.  Short-term outcomes of subtenon triamcinolone acetonide injections in patients with retinitis pigmentosa-associated cystoid macular edema unresponsive to carbonic anhydrase inhibitors.

Authors:  Buğra Karasu
Journal:  Int Ophthalmol       Date:  2019-11-26       Impact factor: 2.031

5.  Defective intracellular transport is the molecular basis of rhodopsin-dependent dominant retinal degeneration.

Authors:  N J Colley; J A Cassill; E K Baker; C S Zuker
Journal:  Proc Natl Acad Sci U S A       Date:  1995-03-28       Impact factor: 11.205

6.  Screening for homozygosity by descent in families with autosomal recessive retinitis pigmentosa.

Authors:  Kota Lalitha; Subhadra Jalali; Tejas Kadakia; Chitra Kannabiran
Journal:  J Genet       Date:  2002-08       Impact factor: 1.166

7.  Intravitreal and subtenon depot triamcinolone as treatment of retinitis pigmentosa associated cystoid macular edema.

Authors:  Sidnei Barge; Renata Rothwell; Paula Sepúlveda; Luís Agrelos
Journal:  Case Rep Ophthalmol Med       Date:  2013-12-23

8.  Complexity of the Class B Phenotype in Autosomal Dominant Retinitis Pigmentosa Due to Rhodopsin Mutations.

Authors:  Samuel G Jacobson; David B McGuigan; Alexander Sumaroka; Alejandro J Roman; Michaela L Gruzensky; Rebecca Sheplock; Judy Palma; Sharon B Schwartz; Tomas S Aleman; Artur V Cideciyan
Journal:  Invest Ophthalmol Vis Sci       Date:  2016-09-01       Impact factor: 4.799
  8 in total

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