Edukad projektid

eesti keeles / in English
Leidsin 15 projekti. programm [ FP7 ]  otsingusõna [ INSTITUT NATIONAL DE LA SANTE ET DE LA RECHERCHE MEDICALE (INSERM) ]

Partner-riigid (projektides osaluse arv)
projekti nr akronüüm ja pealkiri kestus
FP7 - 305299 AgedBrainSYSBIO - SYSTEMS BIOLOGY OF PATHWAYS INVOLVING BRAIN AGEING 2013-2016
FP7 - 212111 BBMRI - Biobanking and Biomolecular Resources Research Infrastructure 2008-2011
FP7 - 313010 BBMRI-LPC - BBMRI - Large Prospective Cohorts 2013-2017
FP7 - 306031 BestAgeing - Biomarker Research Alliance for Diagnosing Heart Disease in the Ageing European Population 2013-2017
FP7 - 259882 EPICE - Effective Perinatal Intensive Care in Europe: translating knowledge into evidence based practice 2011-2015
FP7 - 217817 ETHICSWEB - Inter-connected European Information and Documentation System for Ethics and Science: European Ethics Documentation Centre 2008-2011
FP7 - 244519 EURECNET - European Research Ethics Committees’ Network 2011-2014
FP7 - 278709 EUROHYP-1 - European multicentre, randomised, phase III clinical trial of hypothermia plus best medical treatment versus best medical treatment alone for acute ischaemic stroke 2012-2017
FP7 - 201068 HEALTH-NCP-NET - Coordination Action for Reinforcing the Health National Contact Points Network 2008-2013
FP7 - 249697 HIVERA - Harmonizing, Integrating and Vitalizing European Research on hiv/Aids 2010-2014
FP7 - 223576 MYOAGE - Understanding and combating human age-related muscle weakness 2009-2012
FP7 - 242146 NEOMERO - European multicenter network to evaluate pharmacokinetics, safety and efficacy of Meropenem in neonatal sepsis and meningitis 2010-2013
FP7 - 602041 NeoVanc - Treatment of late onset bacterial sepsis caused by vancomycin susceptible bacteria in neonates and infants aged under three months 2014-2019
FP7 - 201230 RAREDISEASEPLATFORM - A European Platform of Integrated Information Services for Researchers in the Field of Rare Diseases and Orphan Drugs Supporting Team and Project Building. 2008-2011
FP7 - 223143 TECHGENE - High throughput molecular diagnostics in individual patients for genetic diseases with heterogeneous clinical presentation 2009-2012