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Forschungsprojekt(e)
FRANKREICH
HAUTS-DE-FRANCE
LILLE
Set up of SAP component scintigraphy for diagnosis and follow-up of amyloidosis
CHRU de Lille - Hôpital Claude Huriez
Service de médecine interne
FRANKREICH
HAUTS-DE-FRANCE
LILLE
Set up of SAP component scintigraphy for diagnosis and follow-up of amyloidosis
CHRU de Lille - Hôpital Roger Salengro
Service de Médecine nucléaire et imagerie fonctionnelle
PORTUGAL
SUL
LISBOA
Protein glycation and transthyretin amyloidogenesis in yeast: A model system of neurodegenerative amyloid diseases.
Faculdade de Cięncias da Universidade de Lisboa
Laboratório de Enzimologia
REPUBLIK KOREA
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
REPUBLIK KOREA
KOREA, REPUBLIC OF
SEOUL
Biology of cystatins: development of new drugs against amyloidosis based upon the structure of cystatin C
Seoul National University Hospital
Molecular Diagnostics Laboratory
REPUBLIK KOREA
KOREA, REPUBLIC OF
SEOUL
Management of clinical research network for amyloidosis and prognostic factor analysis
Sungkyunkwan University
SCHWEDEN
Region Uppsala
UPPSALA
Pathophysiological studies on AA, AL and TTR amyloidoses
Uppsala University
Department of immunology, Genetics and Pathology, IGP
SCHWEIZ
Suisse Alémanique
BERN
Bern Cardiac Amyloidosis REgistry (B-CARE)
Universitätsspital Inselspital
Universitätsklinik für Kardiologie
FRANKREICH
ILE-DE-FRANCE
PARIS
TRAJHISTORY project: assessing single cell TRAJectories and alterations of cell communication and tissue HISTOry to get causal insights into rare and catastrophic glomerular disease
PARCC - Paris-Centre de recherche Cardiovasculaire (U970)
Centre de Recherche Cardiovasculaire
KANADA
Colombie-Britannique
VICTORIA
Silent Genomes: Reducing health care disparities and improving diagnostic success for children with genetic diseases from Indigenous populations
University of Victoria
Community Genetics Research Program/Island Medical Program
KANADA
Ontario
TORONTO
Beyond the Genome: Transcriptome Based Diagnostics for Rare Diseases and Cancer
Hospital for Sick Children, Research Institute
REPUBLIK KOREA
KOREA, REPUBLIC OF
KOREA
Integrative study of epigenetic variations in rare diseases
Korea National Institute of Health
REPUBLIK KOREA
KOREA, REPUBLIC OF
SEOUL
Establishment and operation of the clinical research network for rare glomerular diseases
Yonsei University College of Medicine
SPANIEN
Cataluńa
BARCELONA
Catalan Interhospital Network of Genetic Variants to improve genetic diagnosis in rare diseases
Centro de Regulación Genómica
Archivo europeo de genomas y fenomas del CRG
SPANIEN
Cataluńa
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
SPANIEN
Cataluńa
BARCELONA
Catalan Interhospital Network of Genetic Variants to improve genetic diagnosis in rare diseases
Hospital Clínic de Barcelona
Servicio de Inmunologia
SPANIEN
Cataluńa
BARCELONA
Catalan Interhospital Network of Genetic Variants to improve genetic diagnosis in rare diseases
Hospital Universitari Vall d'Hebron
Laboratorio de Genética
SPANIEN
Cataluńa
BARCELONA
Catalan Interhospital Network of Genetic Variants to improve genetic diagnosis in rare diseases
Hospital de la Santa Creu i Sant Pau
Servicio de Genética
SPANIEN
Cataluńa
L'HOSPITALET DE LLOBREGAT
Catalan Interhospital Network of Genetic Variants to improve genetic diagnosis in rare diseases
Hospital Universitari de Bellvitge
Unidad de Genética Molecular
SPANIEN
Madrid
MADRID
Identification of new genes causing rare diseases in pediatric patients, searching of genetic pharmacological targets, and drugs discovery, the steps for a personalized medicine
Instituto de Investigación Hospital 12 de Octubre
Grupo de investigación en enfermedades raras, mitocondriales y neuromusculares
VEREINIGTE STAATEN
Washington
ADDRESS: NOT PROVIDED - US
A powerful web-based discovery platform for rare disease genetics
Institution: Information not provided - US
IRLAND
County Dublin
DUBLIN
Establishment of a scalable semantic data architecture for study of chronic disease
Trinity College Dublin
ADAPT Centre
IRLAND
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
Multizentrische Forschungsprojekte
- Uppsala University
- Department of immunology, Genetics and Pathology, IGP
- Zentrum für Kinder- und Jugendmedizin des Universitätsklinikums Heidelberg
- Klinik für Kinderheilkunde I - Sektion Pädiatrische Nephrologie
- Cliniques universitaires Saint-Luc - UCLouvain
- Laboratory of Nephrology
- Trinity College Dublin
- ADAPT Centre
SCHWEDEN
Region Uppsala
UPPSALA
EURAMY: systemic amyloidoses in Europe
DEUTSCHLAND
Baden-Württemberg
HEIDELBERG
EURENOMICS: European Consortium for High-Throughput Research in Rare Kidney Diseases (TERMINATED)
BELGIEN
ARRONDISSEMENT BRUSSELS-CAPITAL
BRUSSELS
EUNEFRON: the European network for the study of orphan nephropathies
IRLAND
County Dublin
DUBLIN