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The validation of inherited retinal disease-specific patient-reported outcome measures in adolescent patients.
Selvan, Kavin; Abuzaitoun, Rebhi; Abalem, Maria Fernanda; Vincent, Ajoy; Andrews, Chris A; Lacy, Gabrielle D; Farjo, Rafid; Kao, Karissa; Kao, Krystal; Dagnelie, Gislin; Musch, David C; Jayasundera, K Thiran; Héon, Elise.
Affiliation
  • Selvan K; Genetics and Genome Biology (GGB) Program, The Hospital for Sick Children Research Institute, Toronto, Ontario, Canada.
  • Abuzaitoun R; Department of Ophthalmology and Vision Sciences, The Hospital for Sick Children, University of Toronto, Toronto, Ontario, Canada.
  • Abalem MF; Institute of Medical Science, Temerty Faculty of Medicine, University of Toronto, Toronto, Ontario, Canada.
  • Vincent A; Department of Ophthalmology and Visual Sciences, University of Michigan Medical School, Ann Arbor, Michigan, USA.
  • Andrews CA; Department of Ophthalmology and Visual Sciences, University of Michigan Medical School, Ann Arbor, Michigan, USA.
  • Lacy GD; Department of Ophthalmology and Otolaryngology, University of Sao Paulo Medical School, Sao Paulo, Brazil.
  • Farjo R; Genetics and Genome Biology (GGB) Program, The Hospital for Sick Children Research Institute, Toronto, Ontario, Canada.
  • Kao K; Department of Ophthalmology and Vision Sciences, The Hospital for Sick Children, University of Toronto, Toronto, Ontario, Canada.
  • Kao K; Institute of Medical Science, Temerty Faculty of Medicine, University of Toronto, Toronto, Ontario, Canada.
  • Dagnelie G; Department of Ophthalmology and Visual Sciences, University of Michigan Medical School, Ann Arbor, Michigan, USA.
  • Musch DC; Department of Ophthalmology and Visual Sciences, University of Michigan Medical School, Ann Arbor, Michigan, USA.
  • Jayasundera KT; Department of Ophthalmology and Visual Sciences, University of Michigan Medical School, Ann Arbor, Michigan, USA.
  • Héon E; Department of Ophthalmology and Visual Sciences, University of Michigan Medical School, Ann Arbor, Michigan, USA.
Ophthalmic Genet ; 44(3): 218-225, 2023 06.
Article in En | MEDLINE | ID: mdl-36974468

Full text: 1 Database: MEDLINE Main subject: Retinal Degeneration / Activities of Daily Living Type of study: Prognostic_studies Limits: Humans Language: En Journal: Ophthalmic Genet Journal subject: GENETICA MEDICA / OFTALMOLOGIA Year: 2023 Type: Article Affiliation country: Canada

Full text: 1 Database: MEDLINE Main subject: Retinal Degeneration / Activities of Daily Living Type of study: Prognostic_studies Limits: Humans Language: En Journal: Ophthalmic Genet Journal subject: GENETICA MEDICA / OFTALMOLOGIA Year: 2023 Type: Article Affiliation country: Canada