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Subclinical Leber's hereditary optic neuropathy with pediatric acute spinal cord onset: more than meets the eye.
Mauri, Eleonora; Dilena, Robertino; Boccazzi, Antonio; Ronchi, Dario; Piga, Daniela; Triulzi, Fabio; Gagliardi, Delia; Brusa, Roberta; Faravelli, Irene; Bresolin, Nereo; Magri, Francesca; Corti, Stefania; Comi, Giacomo P.
Afiliação
  • Mauri E; Department of Pathophysiology and Transplantation, Dino Ferrari Centre, University of Milan, Milan, Italy.
  • Dilena R; Foundation IRCCS Ca' Granda Ospedale Maggiore Policlinico, Unit of Neurophysiopathology, Milan, Italy.
  • Boccazzi A; Foundation IRCCS Ca' Granda Ospedale Maggiore Policlinico, Pediatric Unit "Media Intensità di Cura", Milan, Italy.
  • Ronchi D; Department of Pathophysiology and Transplantation, Dino Ferrari Centre, University of Milan, Milan, Italy.
  • Piga D; Foundation IRCCS Ca' Granda Ospedale Maggiore Policlinico, Neurology Unit, Milan, Italy.
  • Triulzi F; Foundation IRCCS Ca' Granda Ospedale Maggiore Policlinico, Neuroradiology Unit, Milan, Italy.
  • Gagliardi D; Department of Pathophysiology and Transplantation, Dino Ferrari Centre, University of Milan, Milan, Italy.
  • Brusa R; Department of Pathophysiology and Transplantation, Dino Ferrari Centre, University of Milan, Milan, Italy.
  • Faravelli I; Department of Pathophysiology and Transplantation, Dino Ferrari Centre, University of Milan, Milan, Italy.
  • Bresolin N; Department of Pathophysiology and Transplantation, Dino Ferrari Centre, University of Milan, Milan, Italy.
  • Magri F; Foundation IRCCS Ca' Granda Ospedale Maggiore Policlinico, Neurology Unit, Milan, Italy.
  • Corti S; Department of Pathophysiology and Transplantation, Dino Ferrari Centre, University of Milan, Milan, Italy.
  • Comi GP; Foundation IRCCS Ca' Granda Ospedale Maggiore Policlinico, Neurology Unit, Milan, Italy.
BMC Neurol ; 18(1): 220, 2018 Dec 27.
Article em En | MEDLINE | ID: mdl-30591017
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Medula Espinal / Transtornos da Visão / Atrofia Óptica Hereditária de Leber Tipo de estudo: Prognostic_studies Limite: Child, preschool / Female / Humans Idioma: En Ano de publicação: 2018 Tipo de documento: Article
Texto completo
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XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Medula Espinal / Transtornos da Visão / Atrofia Óptica Hereditária de Leber Tipo de estudo: Prognostic_studies Limite: Child, preschool / Female / Humans Idioma: En Ano de publicação: 2018 Tipo de documento: Article