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Punctiform and Polychromatic Pre-Descemet Corneal Dystrophy: Clinical Evaluation and Identification of the Genetic Basis.
Alió Del Barrio, Jorge L; Chung, Doug D; Al-Shymali, Olena; Barrington, Alice; Jatavallabhula, Kavya; Swamy, Vinay S; Yébana, Pilar; Angélica Henríquez-Recine, Maria; Boto-de-Los-Bueis, Ana; Alió, Jorge L; Aldave, Anthony J.
Afiliação
  • Alió Del Barrio JL; Cornea, Cataract and Refractive Surgery Unit, Vissum Corporación, Alicante, Spain; Division of Ophthalmology, School of Medicine, Universidad Miguel Hernández, Alicante, Spain.
  • Chung DD; Stein Eye Institute, David Geffen School of Medicine, University of California Los Angeles, Los Angeles, California, USA.
  • Al-Shymali O; Cornea, Cataract and Refractive Surgery Unit, Vissum Corporación, Alicante, Spain.
  • Barrington A; Stein Eye Institute, David Geffen School of Medicine, University of California Los Angeles, Los Angeles, California, USA.
  • Jatavallabhula K; Stein Eye Institute, David Geffen School of Medicine, University of California Los Angeles, Los Angeles, California, USA.
  • Swamy VS; Stein Eye Institute, David Geffen School of Medicine, University of California Los Angeles, Los Angeles, California, USA.
  • Yébana P; Cornea, Cataract and Refractive Surgery Unit, Vissum Corporación, Alicante, Spain.
  • Angélica Henríquez-Recine M; Ophthalmology Department, La Paz University Hospital, Madrid, Spain.
  • Boto-de-Los-Bueis A; Ophthalmology Department, La Paz University Hospital, Madrid, Spain.
  • Alió JL; Cornea, Cataract and Refractive Surgery Unit, Vissum Corporación, Alicante, Spain; Division of Ophthalmology, School of Medicine, Universidad Miguel Hernández, Alicante, Spain.
  • Aldave AJ; Stein Eye Institute, David Geffen School of Medicine, University of California Los Angeles, Los Angeles, California, USA. Electronic address: aldave@jsei.ucla.edu.
Am J Ophthalmol ; 212: 88-97, 2020 04.
Article em En | MEDLINE | ID: mdl-31782998
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Distrofias Hereditárias da Córnea / Mutação de Sentido Incorreto / Peroxirredoxina III Idioma: En Ano de publicação: 2020 Tipo de documento: Article
Texto completo
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XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Distrofias Hereditárias da Córnea / Mutação de Sentido Incorreto / Peroxirredoxina III Idioma: En Ano de publicação: 2020 Tipo de documento: Article