Retinitis pigmentosa

This publication has 221 references indexed in Scilit:

• Assessment of Structure and Function Over a 3-year Period after Gene Transfer in RPE65−/− dogs
  Documenta Ophthalmologica, 2005
• Characterization of Usher syndrome type I gene mutations in an Usher syndrome patient population
  Human Genetics, 2005
• A novel in vitro retinal differentiation model by co-culturing adult human bone marrow stem cells with retinal pigmented epithelium cells
  Biochemical and Biophysical Research Communications, 2004
• Identification and molecular modelling of a mutation in the motor head domain of myosin VIIA in a family with autosomal dominant hearing impairment (DFNA11)
  Human Genetics, 2004
• Long-Term Protection of Retinal Structure but Not Function Using RAAV.CNTF in Animal Models of Retinitis Pigmentosa
  Molecular Therapy, 2001
• Segregation of a mutation in CNGB1 encoding the β-subunit of the rod cGMP-gated channel in a family with autosomal recessive retinitis pigmentosa
  Human Genetics, 2001
• Visual acuity impairment in patients with retinitis pigmentosa at age 45 years or older
  Ophthalmology, 1999
• Correlation between Goldmann perimetry and maximal electroretinogram response in retinitis pigmentosa
  Documenta Ophthalmologica, 1995
• Homozygous tandem duplication within the gene encoding the β-subunit of rod phosphodiesterase as a cause for autosomal recessive retinitis pigmentosa
  Human Mutation, 1995
• Molecular Analysis and Genetic Mapping of the Rhodopsin Gene in Families with Autosomal Dominant Retinitis Pigmentosa
  Genomics, 1993