Your browser doesn't support javascript.
loading
Optic nerve involvement in CACNA1F-related disease: observations from a multicentric case series.
Marziali, Elisa; Van Den Broeck, Filip; Bargiacchi, Sara; Fortunato, Pina; Caputo, Roberto; Sodi, Andrea; De Zaeytijd, Julie; Murro, Vittoria; Mucciolo, Dario Pasquale; Giorgio, Dario; Passerini, Ilaria; Palazzo, Viviana; Peluso, Francesca; de Baere, Elfride; Zeitz, Christina; Leroy, Bart P; Secci, Jacopo; Bacci, Giacomo M.
Afiliación
  • Marziali E; Pediatric Ophthalmology Unit, Meyer Children's Hospital, University of Florence, Florence, Italy.
  • Van Den Broeck F; Department of Ophthalmology and Center for Medical Genetics Ghent, Ghent University Hospital, Ghent, Belgium.
  • Bargiacchi S; Medical Genetics Unit, Meyer Children's Hospital, University of Florence, Florence, Italy.
  • Fortunato P; Pediatric Ophthalmology Unit, Meyer Children's Hospital, University of Florence, Florence, Italy.
  • Caputo R; Pediatric Ophthalmology Unit, Meyer Children's Hospital, University of Florence, Florence, Italy.
  • Sodi A; Department of Neuroscience, Psychology, Drug Research and Child Health, University of Florence, Florence, Italy.
  • De Zaeytijd J; Department of Ophthalmology and Center for Medical Genetics Ghent, Ghent University Hospital, Ghent, Belgium.
  • Murro V; Department of Neuroscience, Psychology, Drug Research and Child Health, University of Florence, Florence, Italy.
  • Mucciolo DP; Department of Neuroscience, Psychology, Drug Research and Child Health, University of Florence, Florence, Italy.
  • Giorgio D; Department of Neuroscience, Psychology, Drug Research and Child Health, University of Florence, Florence, Italy.
  • Passerini I; Department of Genetic Diagnosis, Careggi Teaching Hospital, Florence, Italy.
  • Palazzo V; Medical Genetics Unit, Meyer Children's Hospital, University of Florence, Florence, Italy.
  • Peluso F; Medical Genetics Unit, Azienda USL-IRCCS di Reggio Emilia, Reggio Emilia, Italy.
  • de Baere E; Center for Medical Genetics, Ghent University and Ghent University Hospital, Ghent, Belgium.
  • Zeitz C; INSERM, CNRS, Institut de la Vision, Sorbonne Université, Paris, France.
  • Leroy BP; Department of Ophthalmology and Center for Medical Genetics Ghent, Ghent University Hospital, Ghent, Belgium.
  • Secci J; Center for Medical Genetics, Ghent University and Ghent University Hospital, Ghent, Belgium.
  • Bacci GM; Division of Ophthalmology and Center for Cellular and Molecular Therapeutics, Inc, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
Ophthalmic Genet ; 44(2): 152-162, 2023 04.
Article en En | MEDLINE | ID: mdl-36469668
Asunto(s)
Palabras clave
Texto completo
Añadir a Mi BVS
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Enfermedades de la Retina / Ceguera Nocturna / Miopía Límite: Humans Idioma: En Revista: Ophthalmic Genet Asunto de la revista: GENETICA MEDICA / OFTALMOLOGIA Año: 2023 Tipo del documento: Article País de afiliación: Italia Pais de publicación: Reino Unido
Texto completo
Añadir a Mi BVS
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Enfermedades de la Retina / Ceguera Nocturna / Miopía Límite: Humans Idioma: En Revista: Ophthalmic Genet Asunto de la revista: GENETICA MEDICA / OFTALMOLOGIA Año: 2023 Tipo del documento: Article País de afiliación: Italia Pais de publicación: Reino Unido