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Projets de recherche
CANADA
Colombie-Britannique
VANCOUVER
Chronic childhood vasculitis: Characterizing the individual rare diseases to improve patient outcomes
British Columbia Children's Hospital
Division of pediatric rheumatology
CANADA
Colombie-Britannique
VANCOUVER
Immunological mechanisms in systemic vasculitis
Centre for Health Evaluation and Outcome Sciences (CHEOS)
Department of Nephrology
COREE, REPUBLIQUE DE
KOREA, REPUBLIC OF
KOREA
Factors associated with chronic and severe status of rare disease and health-related quality of life among rare disease patients
Korea National Institute of Health
COREE, REPUBLIQUE DE
KOREA, REPUBLIC OF
KOREA
Integrative study of epigenetic variations in rare diseases
Korea National Institute of Health
COREE, REPUBLIQUE DE
KOREA, REPUBLIC OF
SEOUL
Establishment and management of clinical research network for systemic vasculitis
Hanyang University
COREE, REPUBLIQUE DE
KOREA, REPUBLIC OF
SEOUL
Establishment and operation of the clinical research network for rare glomerular diseases
Yonsei University College of Medicine
ESPAGNE
Cataluña
BARCELONA
Clinical, genetic and allelic heterogeneity of early-onset hereditary kidney diseases: novel molecular causes of congenital anomalies of the kidney and urinary tract
Fundació Puigvert
Laboratorio de Biología Molecular
ESPAGNE
Cataluña
BARCELONA
Atmospheric monitoring and time series analysis of climate and pollution impact on vasculitis onset - ES
ISGlobal - Instituto de Salud Global de Barcelona
Programa de investigación de Clima y salud
ESPAGNE
Galicia
SANTIAGO DE COMPOSTELA
Strategic action in Galicia 2.0 for hereditary kidney disease: genetic diagnosis and establishment of a galician register of patients, a cost/efficient prevention measure
Hospital Clínico Universitario de Santiago
Fundación Pública Galega de Medicina Xenómica
SUEDE
Region Skåne
LUND
Bacterial virulence factors, innate immunity and prothrombotic mechanisms in renal disease
Skånes Universitetssjukhus
Department of Clinical Sciences, Division of Pediatrics
SUISSE
Suisse Alémanique
RÜSCHLIKON
Cross-Domain Data Fusion techniques for vasculitis prediction
IBM Research - Zurich
CANADA
Ontario
TORONTO
Beyond the Genome: Transcriptome Based Diagnostics for Rare Diseases and Cancer
Hospital for Sick Children, Research Institute
ESPAGNE
Madrid
MADRID
Bioinformatics developments based on network and systems biology to identify new candidate genes for rare genetic diseases
Fundación Jiménez Díaz
Área de Genética y Genómica
ETATS-UNIS
Washington
ADDRESS: NOT PROVIDED - US
A powerful web-based discovery platform for rare disease genetics
Institution: Information not provided - US
FRANCE
ILE-DE-FRANCE
PARIS
STaHR : Stimulation de la Recombinaison Homologue pour la Thérapie Génique - FR
Muséum National d'Histoire Naturelle
Laboratoire Structure et Instabilité des Génomes - INSERM U1154 - CNRS 7196
FRANCE
PAYS DE LA LOIRE
NANTES
FROGH : Etude Génétique de la Population Française - FR
Institut de Recherche en Santé - Université de Nantes
L'Institut du thorax - Inserm UMR 1087 / CNRS UMR 6291
IRLANDE
County Dublin
DUBLIN
Establishment of a scalable semantic data architecture for study of chronic disease
Trinity College Dublin
ADAPT Centre
IRLANDE
County Dublin
DUBLIN
Ensemble averaging for complex disease prediction in the large p small n domain from multiple data sources
Trinity College Dublin
School of Computer Science and Statistcs - O'Reilly Institute
JAPON
JAPAN
AICHI
Management ofthe clinical diagnostic centre for rare intractable diseases with genome instability and development of potential therapeutic medicine
Research Institute of Environmental Medicine, Nagoya University
JAPON
JAPAN
AICHI
Establishment of the Next-generation Muti-omics Clinical Diagnostic Centre for rare intractable diseases with genome instability
Research Institute of Environmental Medicine, Nagoya University
JAPON
JAPAN
TOKYO
Formation of integrated omics analysis base of refractory diseases in children and perinatal period
National Center for Child Health and Development
Research Institute
Projets de recherche multicentriques
- IRCCS Istituto G. Gaslini - Ospedale Pediatrico
- U.O.C. di Pediatria II - I.A.S. Malattie Autoinfiammatorie
- UMC Utrecht - Universitair Medisch Centrum Utrecht
- Polikliniek Immunologie
- Institut für Immunologie
- Institut für Immunologie der Universitätsmedizin Rostock
- Trinity College Dublin
- ADAPT Centre
- Trinity College Dublin
- Trinity Translational Medicine Institute
- Zentrum für Kinder- und Jugendmedizin - Angelika-Lautenschläger-Klinik
- Klinik für Kinderheilkunde I - Sektion Pädiatrische Nephrologie
- Cliniques universitaires Saint-Luc - UCLouvain
- Laboratory of Nephrology
- University of British Columbia
- Maternal Infant Child and Youth Research Network
- Muséum National d'Histoire Naturelle
- Laboratoire Structure et Instabilité des Génomes - INSERM U1154 - CNRS 7196
- Institut de Recherche en Santé - Université de Nantes
- L'Institut du thorax - Inserm UMR 1087 / CNRS UMR 6291
ITALIE
LIGURIA
GENOVA
PRINTO: Paediatric Rheumatology International Trials Organisation (Research)
PAYS-BAS
Utrecht
UTRECHT
SHARE: Single Hub and Access point for paediatric Rheumatology in Europe
ALLEMAGNE
Mecklenburg-Vorpommern
ROSTOCK
AUTOROME: from immune responses in rare autoimmune diseases to novel therapeutic intervention strategies-a personalized medicine approach (FINISHED)
IRLANDE
County Dublin
DUBLIN
HELICAL - Health Data Linkage for Clinical Benefit
IRLANDE
County Dublin
DUBLIN
HELICAL - Health Data Linkage for Clinical Benefit
ALLEMAGNE
Baden-Württemberg
HEIDELBERG
EURENOMICS: European Consortium for High-Throughput Research in Rare Kidney Diseases (TERMINATED)
BELGIQUE
ARRONDISSEMENT BRUSSELS-CAPITAL
BRUSSELS
EUNEFRON: the European network for the study of orphan nephropathies
CANADA
Colombie-Britannique
VANCOUVER
Maternal Infant Child and Youth Research Network (MICYRN)
FRANCE
ILE-DE-FRANCE
PARIS
STaHR : Stimulation de la Recombinaison Homologue pour la Thérapie Génique
FRANCE
PAYS DE LA LOIRE
NANTES