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Retinitis pigmentosa

  • Masqueraders of Age-Related Macular Degeneration

    Masqueraders of Age-Related Macular Degeneration

  • Genetic Defects of CHM and Visual Acuity Outcome in 24 Choroideremia

    Genetic Defects of CHM and Visual Acuity Outcome in 24 Choroideremia

  • Retinitis Pigmentosa Precision Panel Overview Indications Clinical

    Retinitis Pigmentosa Precision Panel Overview Indications Clinical

  • Retinitis Pigmentosa: a Brief Review of the Genetic and Clinical Aspects

    Retinitis Pigmentosa: a Brief Review of the Genetic and Clinical Aspects

  • Retinitis Pigmentosa and Allied Disorders Yog Raj Sharma, P

    Retinitis Pigmentosa and Allied Disorders Yog Raj Sharma, P

  • Stargardt Disease

    Stargardt Disease

  • Nicole Marie Psaltis, O.D. WJB Dorn VAMC, Columbia SC Residents Day Proposal August 30, 2010

    Nicole Marie Psaltis, O.D. WJB Dorn VAMC, Columbia SC Residents Day Proposal August 30, 2010

  • Colour Vision Deficiency

    Colour Vision Deficiency

  • Retinitis Pigmentosa, Ataxia, and Peripheral Neuropathy

    Retinitis Pigmentosa, Ataxia, and Peripheral Neuropathy

  • Gene Therapy for Inherited Retinal Diseases

    Gene Therapy for Inherited Retinal Diseases

  • Leber Congenital Amaurosis (LCA) Refers WHAT IS the RETINA? to a Group of Diseases That Cause Severe Vision Loss in Infancy

    Leber Congenital Amaurosis (LCA) Refers WHAT IS the RETINA? to a Group of Diseases That Cause Severe Vision Loss in Infancy

  • (LCA9) for Leber's Congenital Amaurosis on Chromosome 1P36

    (LCA9) for Leber's Congenital Amaurosis on Chromosome 1P36

  • Leber Congenital Amaurosis

    Leber Congenital Amaurosis

  • Color Blindness (Color Vision Deficiency–Daltonism)

    Color Blindness (Color Vision Deficiency–Daltonism)

  • Prevalence of Posterior Subcapsular Lens Opacities in Patients with Retinitis Pigmentosa

    Prevalence of Posterior Subcapsular Lens Opacities in Patients with Retinitis Pigmentosa

  • Evaluating Structural Progression of Retinitis Pigmentosa After Cataract Surgery

    Evaluating Structural Progression of Retinitis Pigmentosa After Cataract Surgery

  • Retinal Dystrophies and Variants in PRPH2

    Retinal Dystrophies and Variants in PRPH2

  • Unilateral Retinitis Pigmentosa in One Eye and Tilted Hypoplastic Disc in the Other Eye (Two in One Disease)

    Unilateral Retinitis Pigmentosa in One Eye and Tilted Hypoplastic Disc in the Other Eye (Two in One Disease)

Top View
  • Primary Angle Closure As a Presenting Feature of Retinitis Pigmentosa: a Rare Case Report
  • Clinical and Molecular Characterization of Achromatopsia Patients: a Longitudinal Study
  • PRPH2-Related Retinal Diseases: Broadening the Clinical Spectrum and Describing a New Mutation
  • Seeing Through Their Eyes: Lived Experiences of People with Retinitis
  • Teaching Children with a Colour Vision Deficiency (Colour Blindness)
  • Primary Focus: Blindness and Regeneration
  • The Socioeconomic Impact of Inherited Retinal Dystrophies (Irds) in the United Kingdom Retina International August 2019
  • No Wonder You Don't See Well
  • Optic Nerve Disorders ANATOMY
  • Achromatopsia Achromatopsia Is a Rare Hereditary Vision Disorder
  • Cataract Extraction in Retinitis Pigmentosa Patients
  • Retinitis Pigmentosa* by R
  • Retinal Inflammation, Cell Death and Inherited Retinal Dystrophies
  • Retinitis Pigmentosa and Education Issues
  • Survival Analysis of Visual Improvement After Cataract Surgery
  • Therapy Approaches for Stargardt Disease
  • Leber Congenital Amaurosis/Early-Onset Severe
  • Outcome of Cataract Surgery in Patients with Retinitis Pigmentosa


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