Manuel Posada - Wissenschaftliche Veröffentlichungen

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Vol. 17, April of The European Journal of JSTOR

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Published by: Springer ... Karen Berg Brigham, Julio López-Bastida, Renata Linertová, Juan Oliva-Moreno, Pedro Serrano-Aguilar, Manuel Posada-de-la-Paz, ... › stable

National rare diseases registry in Spain: pilot study of the ...ojrd.biomedcentral.com › articles

ojrd.biomedcentral.com

Verónica Alonso; , Ignacio Abaitua; & Manuel Posada de la Paz. DG Salud Pública, FISABIO-Saud Pública, CIBERESP, ValenciaSpain. Óscar Zurriaga. Subdirección de Promoción de salud y Prevención, Consejería ...

Diagnostic delay in rare diseases: data from the Spanish rare ...

ojrd.biomedcentral.com

by J Benito-Lozano · — Juan Benito-Lozano, Greta Arias-Merino, Manuel Posada de la Paz & Verónica ... Springer Nature remains neutral with regard to jurisdictional ... › articles

EPIRARE survey on activities and needs of rare disease registries in...

ojrd.biomedcentral.com

... Sabina Gainotti,; Luciano Vittozzi,; Fabrizio Bianchi,; Monica Ensini and; Manuel Posada Part of Springer Science+Business Media.

Social and economic costs and health-related quality of life in...

bmchealthservres.biomedcentral.com

... de Salud Carlos III (Spain): Manuel Posada de la Paz, Manuel Hens Pérez, Ignacio Abaitua Part of Springer Science+Business Media. ⇑.

Severe alpha-1 antitrypsin deficiency in composite heterozygotes...

respiratory-research.biomedcentral.com

... Ilaria Ferrarotti, Francisco Rodriguez-Frias, Laura Perez, Irene Vazquez, Javier Alonso, Manuel Posada and Beatriz Martínez-Delgado*.

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Verónica Alonso
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Jörg Finsterseifer

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Wissenschaftliche Veröffentlichungen Manuel Posada

Vol. 17, April of The European Journal of JSTOR

National rare diseases registry in Spain: pilot study of the ...ojrd.biomedcentral.com › articles

Diagnostic delay in rare diseases: data from the Spanish rare ...

EPIRARE survey on activities and needs of rare disease registries in...

Social and economic costs and health-related quality of life in...

Severe alpha-1 antitrypsin deficiency in composite heterozygotes...