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Next generation phenotyping using narrative reports in a rare disease clinical data warehouse.
Garcelon, Nicolas; Neuraz, Antoine; Salomon, Rémi; Bahi-Buisson, Nadia; Amiel, Jeanne; Picard, Capucine; Mahlaoui, Nizar; Benoit, Vincent; Burgun, Anita; Rance, Bastien.
Afiliación
  • Garcelon N; Institut Imagine, Paris Descartes Paris Descartes-Sorbonne Paris Cité University, Paris, France. nicolas.garcelon@institutimagine.org.
  • Neuraz A; Institut National de la Santé et de la Recherche Médicale (INSERM), Centre de Recherche des Cordeliers, UMR 1138 Equipe 22, Paris Descartes, Sorbonne Paris Cité University, Paris, France. nicolas.garcelon@institutimagine.org.
  • Salomon R; Imagine - Institute of Genetic Diseases, 24 boulevard du Montparnasse, 75015, Paris, France. nicolas.garcelon@institutimagine.org.
  • Bahi-Buisson N; Institut National de la Santé et de la Recherche Médicale (INSERM), Centre de Recherche des Cordeliers, UMR 1138 Equipe 22, Paris Descartes, Sorbonne Paris Cité University, Paris, France.
  • Amiel J; Department of Medical Informatics, Necker-Enfants Malades Hospital, Assistance Publique des Hôpitaux de Paris (AP-HP), Paris, France.
  • Picard C; Institut Imagine, Paris Descartes Paris Descartes-Sorbonne Paris Cité University, Paris, France.
  • Mahlaoui N; Pediatric Nephrology, Necker Enfants Malades Hospital AP-HP, Université Paris Descartes, Paris, France.
  • Benoit V; Institut Imagine, Paris Descartes Paris Descartes-Sorbonne Paris Cité University, Paris, France.
  • Burgun A; Pediatric Neurology, Necker Enfants Malades Hospital AP-HP, Université Paris Descartes, Paris, France.
  • Rance B; Institut Imagine, Paris Descartes Paris Descartes-Sorbonne Paris Cité University, Paris, France.
Orphanet J Rare Dis ; 13(1): 85, 2018 05 31.
Article en En | MEDLINE | ID: mdl-29855327

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Enfermedades Raras / Data Warehousing Límite: Humans Idioma: En Revista: Orphanet J Rare Dis Asunto de la revista: MEDICINA Año: 2018 Tipo del documento: Article País de afiliación: Francia

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Enfermedades Raras / Data Warehousing Límite: Humans Idioma: En Revista: Orphanet J Rare Dis Asunto de la revista: MEDICINA Año: 2018 Tipo del documento: Article País de afiliación: Francia