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Case 21-2019: A 31-Year-Old Woman with Vision Loss.
Matiello, Marcelo; Juliano, Amy F; Bowley, Michael; Karaa, Amel.
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  • Matiello M; From the Departments of Neurology (M.M., M.B.) and Pediatrics (A.K.), Massachusetts General Hospital, the Departments of Neurology (M.M., M.B.), Radiology (A.F.J.), and Pediatrics (A.K.), Harvard Medical School, and the Department of Radiology, Massachusetts Eye and Ear Infirmary (A.F.J.) - all in B
  • Juliano AF; From the Departments of Neurology (M.M., M.B.) and Pediatrics (A.K.), Massachusetts General Hospital, the Departments of Neurology (M.M., M.B.), Radiology (A.F.J.), and Pediatrics (A.K.), Harvard Medical School, and the Department of Radiology, Massachusetts Eye and Ear Infirmary (A.F.J.) - all in B
  • Bowley M; From the Departments of Neurology (M.M., M.B.) and Pediatrics (A.K.), Massachusetts General Hospital, the Departments of Neurology (M.M., M.B.), Radiology (A.F.J.), and Pediatrics (A.K.), Harvard Medical School, and the Department of Radiology, Massachusetts Eye and Ear Infirmary (A.F.J.) - all in B
  • Karaa A; From the Departments of Neurology (M.M., M.B.) and Pediatrics (A.K.), Massachusetts General Hospital, the Departments of Neurology (M.M., M.B.), Radiology (A.F.J.), and Pediatrics (A.K.), Harvard Medical School, and the Department of Radiology, Massachusetts Eye and Ear Infirmary (A.F.J.) - all in B
N Engl J Med ; 381(2): 164-172, 2019 Jul 11.
Article em En | MEDLINE | ID: mdl-31291520
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Transtornos da Visão / Atrofia Óptica Hereditária de Leber Idioma: En Ano de publicação: 2019 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Transtornos da Visão / Atrofia Óptica Hereditária de Leber Idioma: En Ano de publicação: 2019 Tipo de documento: Article