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Research projects
GERMANY
Sachsen
DRESDEN
Perturbed type I interferon responses in pediatric autoinflammatory diseases with vascular inflammation (TRR 237: Nucleic Acid Immunity B18)
Universitätsklinikum Carl Gustav Carus an der TU Dresden
Klinik und Poliklinik für Kinder- und Jugendmedizin
UNITED STATES
Washington
ADDRESS: NOT PROVIDED - US
Applying bioinformatics to research in immune; muscle; and bone diseases
Institution: Information not provided - US
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
AUSTRIA
WIEN
WIEN
iDysChart: Charting key molecules and mechanisms of human immune Dysregulation
AKH BT 25.3
Ludwig Boltzmann Institute for Rare and Undiagnosed Diseases
BELGIUM
ARRONDISSEMENT BRUSSELS-CAPITAL
BRUSSELS
GENODERM: Development of a Genetic Analysis Method by Mendeliomes and Genomes in the Diagnosis of Genodermatoses and Rare Genetic Diseases With Cutaneous Expression
Hôpital Universitaire des Enfants Reine Fabiola - HUDERF
Dermatologie
CANADA
Colombie-Britannique
VANCOUVER
Immunological mechanisms in systemic vasculitis
Centre for Health Evaluation and Outcome Sciences (CHEOS)
Department of Nephrology
CANADA
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
CANADA
Ontario
TORONTO
Beyond the Genome: Transcriptome Based Diagnostics for Rare Diseases and Cancer
Hospital for Sick Children, Research Institute
FRANCE
ILE-DE-FRANCE
PARIS
FAIRVASC: FAIRVASC - building registry interoperability to inform clinical care - FR
AP-HP.Centre - Université de Paris - Hôpital Cochin
Unité fonctionnelle de Médecine interne et centre de référence maladies rares
GERMANY
Schleswig-Holstein
LÜBECK
FAIRVASC: FAIRVASC - building registry interoperability to inform clinical care -DE
Universitätsklinikum Schleswig-Holstein - Campus Lübeck
Klinik für Rheumatologie und Klinische Immunologie
ITALY
LAZIO
ROMA
Characterization of the innate immune response and identification of prognostic factors in patients with fever of unknown origin
IRCCS Ospedale Pediatrico Bambino Gesů - SEDE GIANICOLO
U.O. di Reumatologia
KOREA, REPUBLIC OF
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
KOREA, REPUBLIC OF
KOREA, REPUBLIC OF
SEOUL
Establishment and management of clinical research network for systemic vasculitis
Hanyang University
SPAIN
Cataluńa
BARCELONA
Diagnosis and follow-up of undefined autoinflammatory diseases through the application of transcriptomic and advanced genomic technologies
Hospital Clínic de Barcelona
Servicio de Inmunologia
SPAIN
Cataluńa
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
SPAIN
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
SWEDEN
Region Skĺne
LUND
FAIRVASC: FAIRVASC - building registry interoperability to inform clinical care - SE
Lund University
Department of Clinical Sciences
SWEDEN
Region Skĺne
LUND
Bacterial virulence factors, innate immunity and prothrombotic mechanisms in renal disease
Lund University
Department of Clinical Sciences - Division of Pediatrics
SWITZERLAND
Suisse Alémanique
RÜSCHLIKON
Cross-Domain Data Fusion techniques for vasculitis prediction
IBM Research - Zurich
UNITED STATES
Washington
ADDRESS: NOT PROVIDED - US
A powerful web-based discovery platform for rare disease genetics
Institution: Information not provided - US
AUSTRIA
WIEN
WIEN
Molecular studies of key molecules in immune signaling - Identification of novel players & rescue strategies in natural killer cell cytotoxicity
AKH BT 25.3
Ludwig Boltzmann Institute for Rare and Undiagnosed Diseases
BELGIUM
OOST-VLAANDEREN
GENT
Unraveling pathophysiologic and genetic causes of primary immune deficiencies with a focus on antibody disorders (common variable immunodeficiency= CVID) and disorders of anti-fungal immunity (chronic mucocutaneous candidiasis = CMC)
PID research lab (PIRL), UZ Gent - MRBII - Entrance 38
Center for Primary Immunodeficiencies Ghent, Jeffrey Modell Foundation diagnostic and research center
FINLAND
Finland
HELSINKI
Genetics of primary immunodeficiency diseases
HUS - Helsinki University Hospital
FRANCE
AUVERGNE-RHONE-ALPES
ADDRESS: NOT PROVIDED - FR
Nutrient transporters: a new tool for characterization of hematopoietic progenitors with optimal transplantation potential
Institution: Information not provided - FR
FRANCE
ILE-DE-FRANCE
PARIS
Rho GTPases and rare skin diseases
IMAGINE - Institut des Maladies Génétiques
Institut IMAGINE - INSERM U1163
GERMANY
Bayern
GARMISCH-PARTENKIRCHEN
The importance of motion diagnostics to promote early physical activity in children with rheumatic diseases
Kinderklinik Garmisch-Partenkirchen gGmbH
Deutsches Zentrum für Kinder- und Jugendrheumatologie
GERMANY
Niedersachsen
HANNOVER
German Centre for Infection Research: Infections of the immunocompromised Host - Investigation of genetic susceptibility and identification of diagnostic biomarkers of infection control
Medizinische Hochschule Hannover
Abteilung für Virologie
GERMANY
Nordrhein-Westfalen
SANKT AUGUSTIN
Depressive symptoms and association with disease activity, pain and disability in juvenile patients with chronic rheumatic diseases
Asklepios Kinderklinik Sankt Augustin GmbH
Abteilung für Allgemeine Kinder- und Jugendmedizin
NORWAY
Řstlandet
OSLO
Functional consequences of genetic variations in primary immunodeficiencies and immune dysregulation (FUNPID)
Oslo Universitetssykehus HF, Rikshospitalet
Nasjonal behandlingstjeneste for screening av nyfřdte og avansert laboratoriediagnostikk ved medfřdte stoffskiftesykdommer
SPAIN
Cataluńa
BARCELONA
Integrating genome and transcriptome profiling for the identification of novel genetic basis of primary immunodeficiencies
Vall d'Hebron Institut de Recerca VHIR
Vall d'Hebron Institut de Recerca
SWEDEN
Region Stockholm
HUDDINGE
Genetic basis of immunodeficiency diseases
Karolinska Institutet - Huddinge
Department of laboratory medicine (LABMED)
SWITZERLAND
Suisse Alémanique
BASEL
The role of ZNF74 in the generation and maintenance of immunological memory
Universitätsspital Basel
Departement Biomedizin
SWITZERLAND
Suisse Alémanique
SCHLIEREN
Pathophysiology of Inborn Immunodeficiencies
Institute for Regenerative Medicine
Department Gene and Cell Therapy
SWITZERLAND
Suisse Alémanique
SCHLIEREN
Towards Identification of New Inborn Errors of Immunity by Whole Exome/Genome Sequencing
Institute for Regenerative Medicine
Department Gene and Cell Therapy
SWITZERLAND
Suisse Alémanique
ZÜRICH
Genetic Study of Immunodeficiency: Search for New Genetic Causes for Primary Immunodeficiencies
Universitäts - Kinderspital Zürich - Eleonorenstiftung
Immunologie
UNITED KINGDOM
Cambridgeshire
CAMBRIDGE
NIHR BioResource - Rare Disease: PID - Primary Immune Disorders
Addenbrooke's Hospital
Department of Medicine - Renal services
ITALY
LAZIO
ROMA
Diverse rare diseases caused by functional dysregulation of Rho GTPase-related proteins
ISS - Istituto Superiore di Sanitŕ
Centro Nazionale Malattie Rare
Multicentric Research projects
- Trinity College Dublin
- ADAPT Centre
- Istituto Dermopatico dell'Immacolata - IRCCS
- Laboratorio di Biologia Molecolare e Cellulare
- IRCCS Istituto G. Gaslini - Ospedale Pediatrico
- U.O.C. di Pediatria II - I.A.S. Malattie Autoinfiammatorie
- IRCCS Istituto G. Gaslini - Ospedale Pediatrico
- U.O.C. di Pediatria II - I.A.S. Malattie Autoinfiammatorie
- Azienda Ospedaliera Universitaria Anna Meyer
- S.C. Nefrologia e Dialisi
- CCI am Universitätsklinikum Freiburg
- Centrum für Chronische Immundefizienz
- Lund University
- Department of Experimental Medical Science
- Istituto San Raffaele Telethon per la Terapia Genica - TIGET
- Istituto San Raffaele Telethon per la Terapia Genica
IRELAND
County Dublin
DUBLIN
HELICAL - Health Data Linkage for Clinical Benefit
ITALY
LAZIO
ROMA
GENESKIN: European network on rare genetic skin diseases
ITALY
LIGURIA
GENOVA
PRINTO: Paediatric Rheumatology International Trials Organisation (Research)
ITALY
LIGURIA
GENOVA
INSAID: A comprehensive clinical and experimental approach to personalized molecular medicine in patients with defined and undefined autoinflammatory disorders
ITALY
TOSCANA
FIRENZE
FAIRVASC: FAIRVASC - building registry interoperability to inform clinical care
GERMANY
Baden-Württemberg
FREIBURG
EURO-PADNET: the pathophysiology and natural course of patients with Primary Antibody Deficiencies
SWEDEN
Region Skĺne
LUND
IDR: ImmunoDeficiency Resource
ITALY
LOMBARDIA
MILANO