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Phenotypic Variability of Retinal Disease Among a Cohort of Patients With Variants in the CLN Genes.
Kolesnikova, Masha; Lima de Carvalho, Jose Ronaldo; Oh, Jin Kyun; Soucy, Megan; Demirkol, Aykut; Kim, Angela H; Tsang, Stephen H; Breazzano, Mark P.
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  • Kolesnikova M; Jonas Children's Vision Care and Bernard & Shirlee Brown Glaucoma Laboratory, New York-Presbyterian Hospital, New York, New York, United States.
  • Lima de Carvalho JR; College of Medicine at the State University of New York at Downstate Medical Center, Brooklyn, New York, United States.
  • Oh JK; Department of Ophthalmology, Hospital das Clínicas de Pernambuco, Empresa Brasileira de Serviços Hospitalares, Federal University of Pernambuco, Recife, Pernambuco, Brazil.
  • Soucy M; Department of Ophthalmology, Edward S. Harkness Eye Institute, Columbia University Medical Center, New York-Presbyterian Hospital, New York, New York, United States.
  • Demirkol A; Department of Pathology and Cell Biology, Columbia University Irving Medical Center, New York, New York, United States.
  • Kim AH; Jonas Children's Vision Care and Bernard & Shirlee Brown Glaucoma Laboratory, New York-Presbyterian Hospital, New York, New York, United States.
  • Tsang SH; Usküdar University Vocational School of Health Services, Department of Opticianry, Istanbul, Turkey.
  • Breazzano MP; Jonas Children's Vision Care and Bernard & Shirlee Brown Glaucoma Laboratory, New York-Presbyterian Hospital, New York, New York, United States.
Invest Ophthalmol Vis Sci ; 64(3): 23, 2023 03 01.
Article en En | MEDLINE | ID: mdl-36912596
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Pruebas Genéticas / Distrofias Retinianas Tipo de estudio: Diagnostic_studies / Prognostic_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: Invest Ophthalmol Vis Sci Año: 2023 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Estados Unidos
Texto completo
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Pruebas Genéticas / Distrofias Retinianas Tipo de estudio: Diagnostic_studies / Prognostic_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: Invest Ophthalmol Vis Sci Año: 2023 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Estados Unidos