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GENETIC RISK FACTORS IN ACUTE CENTRAL SEROUS CHORIORETINOPATHY.
Mohabati, Danial; Schellevis, Rosa L; van Dijk, Elon H C; Altay, Lebriz; Fauser, Sascha; Hoyng, Carel B; De Jong, Eiko K; Boon, Camiel J F; Yzer, Suzanne.
Afiliação
  • Mohabati D; Department of Ophthalmology, Leiden University Medical Center, Leiden, the Netherlands.
  • Schellevis RL; Department of Ophthalmology, Rotterdam Ophthalmic Institute, Rotterdam, the Netherlands.
  • van Dijk EHC; Department of Ophthalmology, Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Center, Nijmegen, the Netherlands.
  • Altay L; Department of Ophthalmology, Leiden University Medical Center, Leiden, the Netherlands.
  • Fauser S; Department of Ophthalmology, University Hospital of Cologne, Cologne, Germany.
  • Hoyng CB; Department of Ophthalmology, University Hospital of Cologne, Cologne, Germany.
  • De Jong EK; Department of Ophthalmology, Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Center, Nijmegen, the Netherlands.
  • Boon CJF; Department of Ophthalmology, Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Center, Nijmegen, the Netherlands.
  • Yzer S; Department of Ophthalmology, Leiden University Medical Center, Leiden, the Netherlands.
Retina ; 39(12): 2303-2310, 2019 Dec.
Article em En | MEDLINE | ID: mdl-30300269
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Proteínas / Receptores de Mineralocorticoides / Predisposição Genética para Doença / Polimorfismo de Nucleotídeo Único / Coriorretinopatia Serosa Central Tipo de estudo: Diagnostic_studies / Etiology_studies / Observational_studies / Risk_factors_studies Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Retina Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Holanda
Texto completo
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Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Proteínas / Receptores de Mineralocorticoides / Predisposição Genética para Doença / Polimorfismo de Nucleotídeo Único / Coriorretinopatia Serosa Central Tipo de estudo: Diagnostic_studies / Etiology_studies / Observational_studies / Risk_factors_studies Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Retina Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Holanda