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  3. Research By Disease

Disease: Bullous dystrophy macular type

  • Blaschkoid Skin Lesions in a Young Girl
  • Central thickness in corneal disorders
  • Choroidal neovascularisation secondary toX-linked retinoschisis
  • Clinical and genetic features of retinoschisis in 120 families with <em>RS1</em> mutations
  • Comments based on 256 intraocular implants placed after extracapsular extraction of the crystalline lens
  • Complications of Descemet's stripping with automated endothelial keratoplasty: survey of 118 eyes at One Institute
  • Eight years experience with the Worst Medallion two loop lens
  • Penetrating keratoplasty for pseudophakic bullous keratopathy associated with closed-loop anterior chamber intraocular lenses
  • Penetrating keratoplasty in Iceland 1981-1996.
  • Postoperative complications in cataract surgery
  • Results from the multicenter Boston Type 1 Keratoprosthesis Study
  • The gene for hereditary bullous dystrophy, X-linked macular type, maps to the Xq27.3-qter region
  • Visual Recovery and Endothelial Cell Survival After Descemet Stripping Automated Endothelial Keratoplasty for Failed Penetrating Keratoplasty Grafts—A Cohort Study
  • X-linked mental retardation, microcephaly, and growth delay associated with hereditary bullous dystrophy macular type: report of a second family
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CheckOrphan is a non-profit organization located in Basel, Switzerland and Santa Cruz, California that is dedicated to rare, orphan and neglected diseases. CheckOrphan offers users an interactive and dynamic platform for all these diseases. This strategy allows visitors to be updated daily on all the latest news and interact with people internationally. This is essential, because due to the nature of these diseases, there is not a large concentration of individuals within any given proximity.
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