Investigación sobre Anomalías Congénitas

The risk of re-identification versus the need to identify individuals in rare disease research. Eur J Hum Genet. 2016 Nov;24(11):1553-1558

Hansson MG, Lochmüller H, Riess O, Schaefer F, Orth M, Rubinstein Y, Molster C, Dawkins H, Taruscio D, Posada de la Paz M, Woods S.

PUBMED DOI

Rare Diseases: Joining Mainstream Research and Treatment Based on Reliable Epidemiological Data. Adv Exp Med Biol. 2017;1031:3-21

Groft SC, Posada de la Paz M.

PUBMED DOI

Linked Registries: Connecting Rare Diseases Patient Registries through a Semantic Web Layer. Biomed Res Int. 2017;2017:8327980

Sernadela P, González-Castro L, Carta C, van der Horst E, Lopes P, Kaliyaperumal R, Thompson M, Thompson R, Queralt-Rosinach N, Lopez-Martín E, Wood L, Robertson A, Lamanna C, Gilling M, Orth M, Merino-Martinez R, Posada de la Paz M, Taruscio D, Lochmüller H, Robinson P, Roos M, Oliveira JL.

PUBMED DOI

Preparing Data at the Source to Foster Interoperability across Rare Disease Resources. Adv Exp Med Biol. 2017;1031:165-179

Roos M, López-Martin E, Wilkinson MD.

PUBMED DOI

Investigación

Investigación sobre Anomalías Congénitas

Líneas de investigación

Content with Investigacion Epidemiología, Salud Pública y Salud Global .

Publicaciones destacadas

The risk of re-identification versus the need to identify individuals in rare disease research. Eur J Hum Genet. 2016 Nov;24(11):1553-1558

Rare Diseases: Joining Mainstream Research and Treatment Based on Reliable Epidemiological Data. Adv Exp Med Biol. 2017;1031:3-21

Linked Registries: Connecting Rare Diseases Patient Registries through a Semantic Web Layer. Biomed Res Int. 2017;2017:8327980

Preparing Data at the Source to Foster Interoperability across Rare Disease Resources. Adv Exp Med Biol. 2017;1031:165-179

Content with Investigacion Epidemiología, Salud Pública y Salud Global .

Información adicional

Content with Investigacion Epidemiología, Salud Pública y Salud Global .

Resultados de investigación