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Retinal vein occlusion in child with rare mutations in genes for thrombophilia.
Giancotta, C; Sanseviero, M; Talarico, V; La Rosa, M A; Galati, M C; Raiola, G; Miniero, R.
Affiliation
  • Giancotta C; Department of Pediatrics, "Pugliese-Ciaccio" Hospital, Catanzaro.
  • Sanseviero M; Department of Pediatrics, "Pugliese-Ciaccio" Hospital, Catanzaro.
  • Talarico V; Department of Pediatrics, "Pugliese-Ciaccio" Hospital, Catanzaro.
  • La Rosa MA; Unit of Genetic and Pediatric Immunology, University-Hospital "G. Martino", Messina.
  • Galati MC; Department of Pediatric Onco-hematology, "Pugliese-Ciaccio" Hospital, Catanzaro, Italy.
  • Raiola G; Department of Pediatrics, "Pugliese-Ciaccio" Hospital, Catanzaro.
  • Miniero R; Department of Pediatrics, "Pugliese-Ciaccio" Hospital, Catanzaro.
Clin Ter ; 170(3): e163-e167, 2019.
Article in En | MEDLINE | ID: mdl-31173043
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Retinal Vein Occlusion / Thrombophilia / Bevacizumab Limits: Adolescent / Female / Humans Language: En Journal: Clin Ter Year: 2019 Document type: Article
Fulltext
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PubMed Links
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Retinal Vein Occlusion / Thrombophilia / Bevacizumab Limits: Adolescent / Female / Humans Language: En Journal: Clin Ter Year: 2019 Document type: Article