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Correlation of retinal vascular characteristics with laboratory and ocular findings in Fabry disease: exploring ocular diagnostic biomarkers.
Lindziute, Migle; Kaufeld, Jessica; Hufendiek, Karsten; Volkmann, Ingo; Brockmann, Dorothee; Hosari, Sami; Hohberger, Bettina; Christian, Mardin; Framme, Carsten; Jan, Tode; Hufendiek, Katerina.
Afiliação
  • Lindziute M; University Eye Hospital, Hannover Medical School, Hannover, Germany. Lindziute.Migle@mh-hannover.de.
  • Kaufeld J; Division of Nephrology, Center for Internal Medicine, Hannover Medical School, Hannover, Germany.
  • Hufendiek K; University Eye Hospital, Hannover Medical School, Hannover, Germany.
  • Volkmann I; University Eye Hospital, Hannover Medical School, Hannover, Germany.
  • Brockmann D; University Eye Hospital, Hannover Medical School, Hannover, Germany.
  • Hosari S; Department of Surgery, Friedrich-Alexander-University of Erlangen-Nuremberg, Erlangen, Germany.
  • Hohberger B; Department of Ophthalmology, Friedrich-Alexander-University of Erlangen-Nuremberg, Erlangen, Germany.
  • Christian M; Department of Ophthalmology, Friedrich-Alexander-University of Erlangen-Nuremberg, Erlangen, Germany.
  • Framme C; University Eye Hospital, Hannover Medical School, Hannover, Germany.
  • Jan T; University Eye Hospital, Hannover Medical School, Hannover, Germany.
  • Hufendiek K; University Eye Hospital, Hannover Medical School, Hannover, Germany. Hufendiek.Katerina@mh-hannover.de.
Orphanet J Rare Dis ; 18(1): 314, 2023 10 08.
Article em En | MEDLINE | ID: mdl-37807078
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Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Distrofias Hereditárias da Córnea / Doença de Fabry Tipo de estudo: Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Revista: Orphanet J Rare Dis Assunto da revista: MEDICINA Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Alemanha
Texto completo
Adicionar na Minha BVS
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Distrofias Hereditárias da Córnea / Doença de Fabry Tipo de estudo: Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Revista: Orphanet J Rare Dis Assunto da revista: MEDICINA Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Alemanha