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The Natural History of Leber Congenital Amaurosis and Cone-Rod Dystrophy Associated with Variants in the GUCY2D Gene.
Hahn, Leo C; Georgiou, Michalis; Almushattat, Hind; van Schooneveld, Mary J; de Carvalho, Emanuel R; Wesseling, Nieneke L; Ten Brink, Jacoline B; Florijn, Ralph J; Lissenberg-Witte, Birgit I; Strubbe, Ine; van Cauwenbergh, Caroline; de Zaeytijd, Julie; Walraedt, Sophie; de Baere, Elfride; Mukherjee, Rajarshi; McKibbin, Martin; Meester-Smoor, Magda A; Thiadens, Alberta A H J; Al-Khuzaei, Saoud; Akyol, Engin; Lotery, Andrew J; van Genderen, Maria M; Ossewaarde-van Norel, Jeannette; van den Born, L Ingeborgh; Hoyng, Carel B; Klaver, Caroline C W; Downes, Susan M; Bergen, Arthur A; Leroy, Bart P; Michaelides, Michel; Boon, Camiel J F.
Afiliación
  • Hahn LC; Department of Ophthalmology, Amsterdam University Medical Centers, University of Amsterdam, Amsterdam, The Netherlands.
  • Georgiou M; Moorfields Eye Hospital National Health Service Foundation Trust, London, United Kingdom.
  • Almushattat H; Department of Ophthalmology, Amsterdam University Medical Centers, University of Amsterdam, Amsterdam, The Netherlands.
  • van Schooneveld MJ; Department of Ophthalmology, Amsterdam University Medical Centers, University of Amsterdam, Amsterdam, The Netherlands; Bartiméus Diagnostic Center for Complex Visual Disorders, Zeist, The Netherlands.
  • de Carvalho ER; Moorfields Eye Hospital National Health Service Foundation Trust, London, United Kingdom.
  • Wesseling NL; Department of Ophthalmology, Amsterdam University Medical Centers, University of Amsterdam, Amsterdam, The Netherlands.
  • Ten Brink JB; Department of Clinical Genetics, Amsterdam University Medical Centers, University of Amsterdam, Amsterdam, The Netherlands.
  • Florijn RJ; Department of Clinical Genetics, Amsterdam University Medical Centers, University of Amsterdam, Amsterdam, The Netherlands.
  • Lissenberg-Witte BI; Department of Epidemiology and Data Science, Amsterdam University Medical Centers, Vrije Universiteit Amsterdam, Amsterdam, The Netherlands.
  • Strubbe I; Department of Ophthalmology, Ghent University Hospital, Ghent University, Ghent, Belgium.
  • van Cauwenbergh C; Department of Ophthalmology, Ghent University Hospital, Ghent University, Ghent, Belgium; Center for Medical Genetics Ghent, Ghent University Hospital & Ghent University, Ghent, Belgium.
  • de Zaeytijd J; Department of Ophthalmology, Ghent University Hospital, Ghent University, Ghent, Belgium.
  • Walraedt S; Department of Ophthalmology, Ghent University Hospital, Ghent University, Ghent, Belgium.
  • de Baere E; Department of Ophthalmology, Ghent University Hospital, Ghent University, Ghent, Belgium; Center for Medical Genetics Ghent, Ghent University Hospital & Ghent University, Ghent, Belgium.
  • Mukherjee R; Department of Ophthalmology, St James's University Hospital, Leeds, United Kingdom.
  • McKibbin M; Department of Ophthalmology, St James's University Hospital, Leeds, United Kingdom.
  • Meester-Smoor MA; Department of Ophthalmology, Erasmus Medical Center, Rotterdam, The Netherlands.
  • Thiadens AAHJ; Department of Ophthalmology, Erasmus Medical Center, Rotterdam, The Netherlands.
  • Al-Khuzaei S; Oxford Eye Hospital, John Radcliffe Hospital, Oxford University Hospitals National Health Service Foundation Trust, & Nuffield Laboratory of Ophthalmology, University of Oxford, Oxford, United Kingdom.
  • Akyol E; Eye Unit, University Hospital Southampton, Southampton, United Kingdom.
  • Lotery AJ; Eye Unit, University Hospital Southampton, Southampton, United Kingdom.
  • van Genderen MM; Bartiméus Diagnostic Center for Complex Visual Disorders, Zeist, The Netherlands; Department of Ophthalmology, University Medical Center Utrecht, Utrecht, The Netherlands.
  • Ossewaarde-van Norel J; Department of Ophthalmology, University Medical Center Utrecht, Utrecht, The Netherlands.
  • van den Born LI; The Rotterdam Eye Hospital and the Rotterdam Ophthalmic Institute, Rotterdam, The Netherlands.
  • Hoyng CB; Department of Ophthalmology, Radboud University Medical Center, Nijmegen, The Netherlands.
  • Klaver CCW; Department of Ophthalmology, Erasmus Medical Center, Rotterdam, The Netherlands; Department of Ophthalmology, Radboud University Medical Center, Nijmegen, The Netherlands.
  • Downes SM; Oxford Eye Hospital, John Radcliffe Hospital, Oxford University Hospitals National Health Service Foundation Trust, & Nuffield Laboratory of Ophthalmology, University of Oxford, Oxford, United Kingdom.
  • Bergen AA; Department of Clinical Genetics, Amsterdam University Medical Centers, University of Amsterdam, Amsterdam, The Netherlands; The Netherlands Institute for Neuroscience (NIN-KNAW), Amsterdam, The Netherlands.
  • Leroy BP; Department of Ophthalmology, Ghent University Hospital, Ghent University, Ghent, Belgium; Center for Medical Genetics Ghent, Ghent University Hospital & Ghent University, Ghent, Belgium; Division of Ophthalmology and Center for Cellular and Molecular Therapeutics, Children's Hospital of Philadel
  • Michaelides M; Moorfields Eye Hospital National Health Service Foundation Trust, London, United Kingdom; UCL Institute of Ophthalmology, University College London, London, United Kingdom.
  • Boon CJF; Department of Ophthalmology, Amsterdam University Medical Centers, University of Amsterdam, Amsterdam, The Netherlands; Department of Ophthalmology, Leiden University Medical Center, Leiden, The Netherlands. Electronic address: Camiel.boon@amsterdamumc.nl.
Ophthalmol Retina ; 6(8): 711-722, 2022 08.
Article en En | MEDLINE | ID: mdl-35314386
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Amaurosis Congénita de Leber / Distrofias de Conos y Bastones Tipo de estudio: Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: Ophthalmol Retina Año: 2022 Tipo del documento: Article País de afiliación: Países Bajos Pais de publicación: Estados Unidos
Texto completo
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Amaurosis Congénita de Leber / Distrofias de Conos y Bastones Tipo de estudio: Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: Ophthalmol Retina Año: 2022 Tipo del documento: Article País de afiliación: Países Bajos Pais de publicación: Estados Unidos