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OCULAR MANIFESTATIONS OF ASP38ALA AND THR59LYS FAMILIAL TRANSTHYRETIN AMYLOIDOSIS.
Choi, Kyung Jun; Son, Ki Young; Kang, Se Woong; Kim, Darae; Choi, Jin Oh; Kim, Hee Jin; Kim, Jung Sun; Jeon, Eun Seok; Kim, A Young; Kang, Min Chae; Kim, Sang Jin.
Afiliación
  • Choi KJ; Department of Ophthalmology, Samsung Medical Center, School of Medicine, Sungkyunkwan University Seoul, Republic of Korea.
  • Son KY; Department of Ophthalmology, Samsung Medical Center, School of Medicine, Sungkyunkwan University Seoul, Republic of Korea.
  • Kang SW; Department of Ophthalmology, Samsung Medical Center, School of Medicine, Sungkyunkwan University Seoul, Republic of Korea.
  • Kim D; Division of Cardiology, Department of Medicine, Heart Vascular Stroke Institute, Samsung Medical Center, School of Medicine, Sungkyunkwan University, Seoul, Republic of Korea.
  • Choi JO; Division of Cardiology, Department of Medicine, Heart Vascular Stroke Institute, Samsung Medical Center, School of Medicine, Sungkyunkwan University, Seoul, Republic of Korea.
  • Kim HJ; Department of Laboratory Medicine and Genetics, Samsung Medical Center, School of Medicine, Sungkyunkwan University, Seoul, Republic of Korea.
  • Kim JS; Department of Pathology, Samsung Medical Center, School of Medicine, Sungkyunkwan University, Seoul, Republic of Korea; and.
  • Jeon ES; Division of Cardiology, Department of Medicine, Heart Vascular Stroke Institute, Samsung Medical Center, School of Medicine, Sungkyunkwan University, Seoul, Republic of Korea.
  • Kim AY; Department of Ophthalmology, Ewha Womans University Medical Center, School of Medicine, Ewha Womans University, Seoul, Republic of Korea.
  • Kang MC; Department of Ophthalmology, Samsung Medical Center, School of Medicine, Sungkyunkwan University Seoul, Republic of Korea.
  • Kim SJ; Department of Ophthalmology, Samsung Medical Center, School of Medicine, Sungkyunkwan University Seoul, Republic of Korea.
Retina ; 42(2): 396-403, 2022 02 01.
Article en En | MEDLINE | ID: mdl-34483316
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Enfermedades de la Retina / Prealbúmina / Mutación Puntual / Neuropatías Amiloides Familiares / Cápsula del Cristalino / Enfermedades del Cristalino Tipo de estudio: Observational_studies Límite: Female / Humans / Male / Middle aged Idioma: En Revista: Retina Año: 2022 Tipo del documento: Article
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Enfermedades de la Retina / Prealbúmina / Mutación Puntual / Neuropatías Amiloides Familiares / Cápsula del Cristalino / Enfermedades del Cristalino Tipo de estudio: Observational_studies Límite: Female / Humans / Male / Middle aged Idioma: En Revista: Retina Año: 2022 Tipo del documento: Article